ARGINASE INHIBITORS AND METHODS OF USE THEREOF

Title:

ARGINASE INHIBITORS AND METHODS OF USE THEREOF

Document Type and Number:

WIPO Patent Application WO/2019/159120

Kind Code:

Abstract:

Disclosed are compounds of formula (Ia) or a pharmaceutically acceptable salt thereof, pharmaceutical compositions comprising compounds of formula (Ia) and methods of using the same for treating cancer or a respiratory inflammatory disease and inhibiting arginase, wherein R1 is -NHR1a; R1a is -H or -C(O)CH(R1b)NHR1c; and R1b is selected from -H, -(C1-C4 ) alkyl and CH2OR1d and R1cis -H; or R1b and R1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and R1d is H or -CH3.

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Inventors:

MLYNARSKI SCOTT NATHAN (US)
GREBE TYLER (US)
KAWATKAR SAMEER (US)
FINLAY MAURICE RAYMOND VERSCHOYLE (GB)
SIMPSON IAIN (GB)
WANG JIANYAN (US)
COOK STEVE (US)

Application Number:

PCT/IB2019/051236

Publication Date:

August 22, 2019

Filing Date:

February 15, 2019

Export Citation:

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Assignee:

ASTRAZENECA AB (SE)

International Classes:

A61P29/00; A61K31/69; A61P35/00; C07F5/02

Domestic Patent References:

WO2011133653A1	2011-10-27
WO2016210106A1	2016-12-29
WO2018089490A1	2018-05-17

Other References:

"Remington's Pharmaceutical Sciences", 1985, MACK PUBLISHING COMPANY
BERGE ET AL., J. PHARM. SCI., vol. 66, 1977, pages 1 - 19
STAHL; WERMUTH: "Handbook of Pharmaceutical Salts: Properties, Selection, and Use", 2002, WILEY-VCH
CORWIN HANSCH: "Comprehensive Medicinal Chemistry", vol. 5, 1990, PERGAMON PRESS

Attorney, Agent or Firm:

NESS, Mark (GB)

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Claims:

Claims

1 . A compound of formula (I), or a pharmaceutically acceptable salt thereof:

wherein

R¹ is -NHR^1a;

R^1a is -H or -C(0)CH(R^1b)NHR^1c; and

R^1b is selected from -H, -(C₁-C₄) alkyl and CH₂OR^1d and R^1c is -H; or

R^1b and R^1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and

R^1d is H or -CHs.

2. A compound of formula (II), or a pharmaceutically acceptable salt thereof:

wherein

R² is -OH or -NHR^2a;

R^2a is -H or -C(0)CH(R^2b)NHR^2c;

R^2b is selected from -H, -(C₁-C₄) alkyl and CH₂OR^2d and R^2c is -H; or

R^2b and R^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R^2d is -H or -CHs.

3. A compound of formula (III), or a pharmaceutically acceptable salt thereof:

wherein

R³ is selected from -H, -(C₁-C₄) alkyl and -CH₂OR^3a; and

R^3a is -H or -CHs.

4. A compound of formula (IV), or a pharmaceutically acceptable salt thereof:

wherein R⁴ is -OH or -NH_:

5. A compound of formula (V), or a pharmaceutically acceptable salt thereof:

6. A compound of formula (VI), or a pharmaceutically acceptable salt thereof:

wherein

R^6a is -H or -CHs; R^6b is -C(0)C(R^6cR^6d)NH₂; or -(C1-C3) alkyl which is substituted with 0 or 1 amino or - OR^6e; and

R^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OR^6f;

R^6d is H or -CH₃; and

R^6e and R^6f are independently -H or -CH₃.

7. A compound of formula (VI), or a pharmaceutically acceptable salt thereof; wherein R^6a is -H or -CH₃; and R^6b is -(CrC₃) alkyl which is substituted with 0 or 1 amino; or alternatively,

R^6a is -H or -CH₃; R^6b is -C(0)C(R^6cR^6d)NH₂; R^6c is -(Ci-C₃) alkyl which is substituted with 0 or 1 amino or -OH; and R^6d is H or -CH₃.

8. A compound of formula (lb), or a pharmaceutically acceptable salt thereof:

wherein

R¹ is -NHR^1a;

R^1a is -H or -C(0)CH(R^1b)NHR^1c; and

R^1b is selected from -H, -(C₁-C₄) alkyl and CH₂OR^1d and R^1c is -H; or

R^1b and R^1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and

R^1d is H or -CHs.

9. A compound of formula (lib), or a pharmaceutically acceptable salt thereof:

wherein

R² is -OH or -NHR^2a; R^2a is -H or -C(0)CH(R^2b)NHR^2c;

R^2b is selected from -H, -(C₁-C₄) alkyl and CH₂OR^2d and R^2c is -H; or

R^2b and R^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R^2d is -H or -CHs.

10. A compound of formula (lllb), or a pharmaceutically acceptable salt thereof:

wherein

R³ is selected from -H, -(C₁-C₄) alkyl and -CH₂OR^3a; and

R^3a is -H or -CHs.

1 1 . A compound of formula (IVb), or a pharmaceutically acceptable salt thereof:

wherein R⁴ is -OH or -NH_:

12. A compound of formula (Vb), or a pharmaceutically acceptable salt thereof:

13. A compound of formula (Vlb), or a pharmaceutically acceptable salt thereof:

wherein

R^6a is -H or -CH₃;

R^6b is -C(0)C(R^6cR^6d)NH₂; or -(C₁-C₃) alkyl which is substituted with 0 or 1 amino or - OR^6e; and

R^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OR^6f;

R^6d is H or -CH₃; and

R^6e and R^6f are independently -H or -CH₃.

14. A compound of formula (Vlb), or a pharmaceutically acceptable salt thereof; wherein R^6a is -H or -CH₃; and R^6b is -(C₁-C₃) alkyl which is substituted with 0 or 1 amino; or alternatively,

R^6a is -H or -CH₃; R^6b is -C(0)C(R^6cR^6d)NH₂; R^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OH; and R^6d is H or -CH3.

15. A compound of Table 1 , or a pharmaceutically acceptable salt thereof.

16. A pharmaceutical composition comprising a compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

17. A method of treating cancer comprising a compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof.

18. A compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, for treating cancer.

19. A compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in treating cancer.

20. A pharmaceutical composition comprising a compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, for use in treating cancer.

21 . A method of treating a respiratory inflammatory disease comprising a compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof.

22. A compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, for treating a respiratory inflammatory disease.

23. A compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in treating a respiratory inflammatory disease.

24. A pharmaceutical composition comprising a compound of any one of Claims 1 to 15, or a pharmaceutically acceptable salt thereof, for use in treating a respiratory inflammatory disease.

Description:

ARGINASE INHIBITORS AND METHODS OF USE THEREOF

Background

Arginase is a manganese metalloenzyme that catalyzes the conversion of L-arginine to urea and L-ornithine. Two isoforms exist: Arginase 1 is a cytosolic enzyme predominantly found in hepatocytes where it plays a critical role in removing ammonia through urea synthesis, and Arginase 2, a mitochondrial enzyme highly expressed in kidney involved in production of ornithine, a precursor for polyamines and prolines important for cell proliferation and collagen production, respectively.

Although L-arginine is not an essential amino acid as it can be provided through protein turnover in healthy adults, increased expression and secretion of arginases results in reduced L- arginine levels in various physiologic and pathologic conditions ( e.g ., pregnancy, auto-immune diseases, cancer). Immune cells, in particular, are sensitive to reduced L-arginine levels. T- cells, when faced with a low L-arginine microenvironment, reduce their proliferation rate and lower the expression of Oϋ3z chain, IFNy, and lytic enzymes resulting in impaired T-cell responsiveness. Dendritic cells respond to low L-arginine conditions by reducing their ability to present antigens, and natural killer cells reduce both proliferation and expression of lytic enzymes.

Tumors use multiple immune suppressive mechanisms to evade the immune system. One of these is the reduction of L-arginine through increased levels of circulating arginase, increased expression and secretion of arginase by tumor cells, and recruitment of arginase expressing and secreting myeloid derived suppressor cells. Together, these lead to a reduction of L-arginine in the tumor microenvironment and an immune-suppressive phenotype.

Pharmacologic inhibition of arginase activity has been shown to reverse the low L-arginine induced immune suppression in animal models. As such, there is a need for potent and selective arginase inhibitors to reverse immune suppression and re-activate anti-cancer immunity in patients, either as single agent, or in combination with therapies reversing additional immune-suppressive mechanisms. Summary

In one embodiment, disclosed is a compound of formula (I), or a pharmaceutically acceptable salt thereof:

wherein

R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NH ₂; and

R ^1b is -CHs or -CH(CH ₃) ₂.

In one embodiment, disclosed is a compound of formula (la), or a pharmaceutically acceptable salt thereof:

wherein

R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NHR ^1c; and

R ^1b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^1d and R ^1c is -H; or

R ^1b and R ^1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and

R ^1d is H or -CHs.

In one embodiment, disclosed is a compound of formula (lb), or a pharmaceutically acceptable salt thereof:

wherein

R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NHR ^1c; and

R ^1b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂0R ^1d and R ^1c is -H; or

R ^1b and R ^1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and

R ^1d is H or -CHs.

In one embodiment, disclosed is a compound of formula (II), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NH ₂; and

R ^2b is -CHs or -CH(CH ₃) ₂.

In one embodiment, disclosed is a compound of formula (lla), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NHR ^2c;

R ^2b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^2d and R ^2c is -H; or

R ^2b and R ^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R ^2d is -H or -CHs. In one embodiment, disclosed is a compound of formula (lib), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NHR ^2c;

R ^2b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^2d and R ^2c is -H; or

R ^2b and R ^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R ^2d is -H or -CHs.

In some embodiments, disclosed is a compound of formula (III), or a pharmaceutically acceptable salt thereof:

wherein R ³ is -CH ₃ or -CH(CH ₃) ₂.

In some embodiments, disclosed is a compound of formula (Ilia), or a pharmaceutically acceptable salt thereof:

wherein

R ³ is selected from -H, -(C ₁-C ₄) alkyl and -CH ₂OR ^3a; and

R ^3a is -H or -CHs. In one embodiment, disclosed is a compound of formula (lllb), or a pharmaceutically acceptable salt thereof:

wherein

R ³ is selected from -H, -(C ₁-C ₄) alkyl and -CH ₂OR ^3a; and

R ^3a is -H or -CHs.

In some embodiments, disclosed is a compound of formula (IV), or a pharmaceutically acceptable salt thereof:

wherein R ⁴ is -OH or -NH ₂.

In one embodiment, disclosed is a compound of formula (IVb), or a pharmaceutically acceptable salt thereof:

wherein R ⁴ is -OH or -NH ₂.

In some embodiments, disclosed is a compound of formula (V), or a pharmaceutically acceptable salt thereof:

In one embodiment, disclosed is a compound of formula (Vb), or a pharmaceutically acceptable salt thereof:

In one embodiment, disclosed is a compound of formula (VI), or a pharmaceutically acceptable salt thereof:

wherein

R ^6a is -H or -CH ₃;

R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; or -(C1-C3) alkyl which is substituted with 0 or 1 amino or - OR ^6e; and

R ^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OR ^6f;

R ^6d is H or -CH ₃; and

R ^6e and R ^6f are independently -H or -CH ₃.

In one embodiment, disclosed is a compound of formula (Vlb), or a pharmaceutically acceptable salt thereof:

wherein

R ^6a is -H or -CH ₃;

R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; or -(C1-C3) alkyl which is substituted with 0 or 1 amino or - OR ^6e; and

R ^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OR ^6f;

R ^6d is H or -CH ₃; and

R ^6e and R ^6f are independently -H or -CH ₃.

In some embodiments, disclosed are the compounds of Table 1 , or a pharmaceutically acceptable salt thereof.

In some embodiments, disclosed are pharmaceutical compositions comprising a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI),

(Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, and a pharmaceutically acceptable carrier.

In some embodiments, disclosed are methods of treating cancer comprising a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI),

(Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof.

In some embodiments, disclosed are compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for treating cancer.

In some embodiments, disclosed is the use of a compound of (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof in the manufacture of a medicament for use in treating cancer.

In some embodiments, disclosed are pharmaceutical compositions comprising a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI),

(Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in treating cancer.

In some embodiments, disclosed are methods of treating a respiratory inflammatory disease comprising a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof.

In some embodiments, disclosed are pharmaceutical compositions comprising a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI),

(Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in treating a respiratory inflammatory disease.

In some embodiments, the aforementioned respiratory inflammatory disease is chronic obstructive pulmonary disease (COPD) or asthma.

Brief Description of Drawings

Figure 1 shows NMR spectra depicting the conversion of compound B to compound A where compound B is prepared in 100% d6-DMSO (labeled A), 75% D ₂0 in d6-DMSO (labeled B), 50% D ₂0 in d6-DMSO (labeled C), 25% D ₂0 in d6-DMSO (labeled E) and 100% D ₂0 (labeled F).

Figure 2 shows the NMR spectrum (in 0.1 M DCI in D ₂0) of compound B depicting how acidification yields almost complete conversion to compound A.

Figure 3 compares NMR spectra of amorphous material in d6-DMSO (Labeled B) with crystalline compound B in d6-DMSO (Labeled A) showing that both materials have the same cyclic structure as crystalline compound B.

Detailed Description

Compounds

In one embodiment, disclosed is a compound of formula (I), or a pharmaceutically acceptable salt thereof:

wherein R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NH ₂; and

R ^1b is -CHs or -CH(CH ₃) ₂.

In one embodiment, disclosed is a compound of formula (I). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (I).

In some embodiments of formula (I), R ¹ is -NHR ^1a and R ^1a is -H.

In some embodiments of formula (I), R ¹ is -NHR ^1a, R ^1a is -C(0)CH(R ^{1 b})NH ₂ and R ^{1 b} is

-CHs.

In some embodiments of formula (I), R ¹ is -NHR ^1a, R ^1a is -C(0)CH(R ^{1 b})NH ₂ and R ^{1 b} is -CH(CH ₃) ₂.

In one embodiment, disclosed is a compound of formula (la), or a pharmaceutically acceptable salt thereof:

wherein

R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NHR ^1c; and

R ^1b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^1d; and R ^1c is -H; or

R ^1b and R ^1c, together with the atom to which they are attached, form a 5-membered ring; and

R ^1d is H or -CHs.

In one embodiment, disclosed is a compound of formula (la). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (la).

In some embodiments, a compound of formula (la) is represented by formula (Ia1 ) or

(Ia2) :

wherein R ¹ is the same as defined above.

In some embodiments of formula (la), R ^1a is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is -H and R ^1c is -H. In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is CH ₂0R ^1d; R ^1c is -H and R ^1d is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is CH ₂OR ^1d; R ^1c is -H and R ^1d is -CH ₃.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is -(C1-C4) alkyl and R ^1c is -H. In some embodiments, the C1 -C4 alkyl is selected from methyl, ethyl, isopropyl, sec-butyl, tert- buty and isobutyl.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is methyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is ethyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is isopropyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is sec-butyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is isobutyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is terf-butyl; and R ^1c is -H.

In some embodiments of formula (la), R ^1a is -C(0)CH(R ^1b)NHR ^1c and R ^{1 b} and R ^1c, together with the atom to which they are attached, form a 5-membered ring.

In one embodiment, disclosed is a compound of formula (lb), or a pharmaceutically acceptable salt thereof:

wherein

R ¹ is -NHR ^1a;

R ^1a is -H or -C(0)CH(R ^1b)NHR ^1c; and R ^1b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^1d; and R ^1c is -H; or

R ^1b and R ^1c, together with the atom to which they are attached, form a 5-membered heterocyclic ring; and

R ^1d is H or -CHs.

In one embodiment, disclosed is a compound of formula (lb). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (lb).

In some embodiments, a compound of formula (lb) is represented by formula (Ib1 ) or

(Ib2) :

wherein R ¹ is the same as defined above.

In some embodiments of formula (lb), R ^1a is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is -H and R ^1c is -H. In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is CH ₂OR ^1d; R ^1c is -H and R ^1d is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is CH ₂OR ^1d; R ^1c is -H and R ^1d is -CH ₃.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is -(C ₁-C ₄) alkyl and R ^1c is -H. In some embodiments, the C ₁-C ₄ alkyl is selected from methyl, ethyl, isopropyl, sec-butyl, tert- buty and isobutyl.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is methyl; and R ^1c is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is ethyl; and R ^1c is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is isopropyl; and R ^1c is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is sec-butyl; and R ^1c is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is isobutyl; and R ^1c is -H. In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c; R ^1b is terf-butyl; and R ^1c is -H.

In some embodiments of formula (lb), R ^1a is -C(0)CH(R ^1b)NHR ^1c and R ^{1 b} and R ^1c, together with the atom to which they are attached, form a 5-membered ring.

In one embodiment, disclosed is a compound of formula (II), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NH ₂; and

R ^2b is -CHs or -CH(CH ₃) ₂.

In one embodiment, disclosed is a compound of formula (II). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (II).

In some embodiments of formula (II), R ² is -OH.

In some embodiments of formula (II), R ² is -NHR ^2a and R ^2a is -H.

In some embodiments of formula (II), R ² is -NHR ^2a, R ^2a is -C(0)CH(R ^2b)NH ₂ and R ^2b is

-CHs.

In some embodiments of formula (II), R ² is -NHR ^2a, R ^2a is -C(0)CH(R ^2b)NH ₂ and R ^2b is -CH(CHS) ₂.

In one embodiment, disclosed is a compound of formula (lla), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NHR ^2c; R ^2b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^2d; and R ^2c is -H; or

R ^2b and R ^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R ^2d is H or -CHs.

In one embodiment, disclosed is a compound of formula (lla). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (lla).

In one embodiment of formula (lla), R ² is -OH.

In one embodiment of formula (lla), R ² is -NHR ^2a; and R ^2a is -H.

In one embodiment of formula (lla), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is H and R ^2c is H.

In one embodiment of formula (lla), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -CH ₂OR ^2d; R ^2c is H and R ^2d is H.

In one embodiment of formula (lla), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -CH ₂OR ^2d; R ^2c is H and R ^2d is -CH ₃.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -(C ₁-C ₄) alkyl and R ^2c is -H. In some embodiments, the C ₁-C ₄ alkyl is selected from methyl, ethyl, isopropyl, sec-butyl, terf-butyl, and isobutyl.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is methyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is ethyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is isopropyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a _; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is sec-butyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is isobutyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is terf-butyl; and R ^2c is -H.

In some embodiments of formula (lla), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c and R ^2b and R ^2c, together with the atom to which they are attached, form a 5-membered ring.

In one embodiment, disclosed is a compound of formula (lib), or a pharmaceutically acceptable salt thereof:

wherein

R ² is -OH or -NHR ^2a;

R ^2a is -H or -C(0)CH(R ^2b)NHR ^2c;

R ^2b is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^2d; and R ^2c is -H; or

R ^2b and R ^2c, together with the atoms to which they are attached, form a 5-membered heterocyclic ring; and

R ^2d is -H or -CHs.

In one embodiment, disclosed is a compound of formula (lib). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (lib).

In one embodiment of formula (lib), R ² is -OH.

In one embodiment formula (lib), R ² is -NHR ^2a; and R ^2a is -H.

In one embodiment formula (lib), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is H and R ^2c is H.

In one embodiment formula (lib), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -CH ₂OR ^2d; R ^2c is H and R ^2d is H.

In one embodiment formula (lib), R ² is -NHR ^2a; and R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -CH ₂OR ^2d; R ^2c is H and R ^2d is -CH ₃.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is -(C ₁-C ₄) alkyl and R ^2c is -H. In some embodiments, the C ₁-C ₄ alkyl is selected from methyl, ethyl, isopropyl, sec-butyl, terf-butyl, and isobutyl.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is methyl; and R ^2c is -H.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is ethyl; and R ^2c is -H.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is isopropyl; and R ^2c is -H.

In some embodiments formula (lib), R ² is -NHR ^2a _; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is sec- butyl; and R ^2c is -H. In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is isobutyl; and R ^2c is -H.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c; R ^2b is tert- butyl; and R ^2c is -H.

In some embodiments formula (lib), R ² is -NHR ^2a; R ^2a is -C(0)CH(R ^2b)NHR ^2c and R ^2b and R ^2c, together with the atom to which they are attached, form a 5-membered ring.

In some embodiments, disclosed is a compound of formula (III), or a pharmaceutically acceptable salt thereof:

wherein

In one embodiment, disclosed is a compound of formula (III). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (III).

In some embodiments of formula (III), R ³ is -CH ₃.

In some embodiments of formula (III), R ³ is -CH(CH ₃)2.

In some embodiments, disclosed is a compound of formula (Ilia), or a pharmaceutically acceptable salt thereof:

wherein

R ³ is selected from -H, -(C ₁-C ₄) alkyl and CH ₂OR ^3a; and

R ^3a is -H or -CHs.

In one embodiment, disclosed is a compound of formula (Ilia). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (Ilia).

In one embodiment of formula (Ilia), R ³ is -H.

In one embodiment formula (Ilia), R ³ is -Ch OR ³³ and R ^3a is -H. In one embodiment formula (Ilia), R ³ s -CH ₂OR ^3a and R ^3a is -CH ₃.

In one embodiment formula (Ilia), R ³ s -(C ₁-C ₄) alkyl. In some embodiments, the -(C ₁-C ₄) alkyl is selected from methyl, ethyl, sopropyl, sec-butyl and isobutyl

In one embodiment formula (Ilia), R ³ s methyl

In one embodiment formula (Ilia), R ³ s ethyl

In one embodiment formula (Ilia), R ³ s isopropyl

In one embodiment formula (Ilia), R ³ s sec-butyl

In one embodiment formula (Ilia), R ³ s isobutyl.

In one embodiment formula (Ilia), R ³ is terf-butyl.

In some embodiments, disclosed is a compound of formula (lllb), or a pharmaceutically acceptable salt thereof:

wherein

R ³ is selected from -H, -(C ₁-C ₄) alkyl and -CH ₂OR ^3a; and

R ^3a is -H or -CHs.

In one embodiment, disclosed is a compound of formula (lllb). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (lllb).

In one embodiment formula (lllb), R ³ s -H.

In one embodiment formula (lllb), R ³ s -CH ₂OR ^3a and R ^3a is -H.

In one embodiment formula (lllb), R ³ s -CH ₂OR ^3a and R ^3a is -CH ₃.

In one embodiment formula (lllb), R ³ s -(C ₁-C ₄) alkyl. In some embodiments, the -(C ₁-C ₄) alkyl is selected from methyl, ethyl, sopropyl, sec-butyl and isobutyl

In one embodiment formula (lllb), R ³ s methyl

In one embodiment formula (lllb), R ³ s ethyl

In one embodiment formula (lllb), R ³ s isopropyl

In one embodiment formula (lllb), R ³ s sec-butyl

In one embodiment formula (lllb), R ³ s isobutyl

In one embodiment formula (lllb), R ³ s tert- butyl. In some embodiments, disclosed is a compound of formula (IV), or a pharmaceutically acceptable salt thereof:

wherein R ⁴ is -OH or -NH ₂.

In one embodiment, disclosed is a compound of formula (IV). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (IV).

In some embodiments formula (IV), R ⁴ is -OH.

In some embodiments formula (IV), R ⁴ is -NH ₂.

In some embodiments, disclosed is a compound of formula (IVb), or a pharmaceutically acceptable salt thereof:

wherein R ⁴ is -OH or -NH ₂.

In one embodiment, disclosed is a compound of formula (IVb). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (IVb).

In some embodiments formula (IVb), R ⁴ is -OH.

In some embodiments formula (IVb), R ⁴ is -NH ₂.

In some embodiments, disclosed is a compound of formula (V), or a pharmaceutically acceptable salt thereof:

In one embodiment, disclosed is a compound of formula (V). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (V). In some embodiments, disclosed is a compound of formula (Vb), or a pharmaceutically acceptable salt thereof:

In one embodiment, disclosed is a compound of formula (Vb). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (Vb).

In some embodiments, disclosed is a compound of formula (VI), or a pharmaceutically acceptable salt thereof:

wherein

R ^6a is -H or -CH ₃;

R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; or -(C ₁-C ₃) alkyl which is substituted with 0 or 1 amino or - OR ^6e; and

R ^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OR ^6f;

R ^6d is H or -CH ₃; and

R ^6e and R ^6f are independently -H or -CH ₃.

In one embodiment, disclosed is a compound of formula (VI). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (VI).

In some embodiments of formula (VI), R ^6a is -H or -CH ₃; and R ^6b is -(C ₁-C ₃) alkyl which is substituted with 0 or 1 amino.

In some embodiments of formula (VI), R ^6a is -H or -CH ₃; R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; R ^6c is -(C1-C3) alkyl which is substituted with 0 or 1 amino or -OH; and R ^6d is H or -CH ₃.

In some embodiments, a compound of formula (VI) is represented by formula (Vla1 ) or

(Vla2):

wherein R ^6a and R ^6b are the same as defined above.

In one embodiment, disclosed is a compound of formula (Vla1 ). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (Vla1 ).

In one embodiment, disclosed is a compound of formula (Vla2). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (Vla2).

In one embodiment of Formula (VI), R ^6b is -CH ₃ or -CH ₂CH ₂NH ₂.

In some embodiments, disclosed is a compound of formula (Vlb), or a pharmaceutically acceptable salt thereof:

wherein

R ^6a is -H or -CH ₃;

R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; or -(CrC ₃) alkyl which is substituted with 0 or 1 amino or - OR ^6e; and

R ^6c is -(Ci-C ₃) alkyl which is substituted with 0 or 1 amino or -OR ^6f;

R ^6d is H or -CH ₃; and

R ^6e and R ^6f are independently -H or -CH ₃.

In one embodiment, disclosed is a compound of formula (Vlb). In another embodiment, disclosed is a pharmaceutically acceptable salt of the compound of formula (Vlb).

In one embodiment of formula (Vlb), R ^6b is -CH ₃ or -CH ₂CH ₂NH ₂.

In some embodiments of formula (Vlb), R ^6a is -H or -CH ₃; and R ^6b is -(Ci-C ₃) alkyl which is substituted with 0 or 1 amino.

In some embodiments of formula (Vlb), R ^6a is -H or -CH ₃; R ^6b is -C(0)C(R ^6cR ^6d)NH ₂; R ^6c is -(Ci-C ₃) alkyl which is substituted with 0 or 1 amino or -OH; and R ^6d is H or -CH ₃. In some embodiments, a compound of formula (Vlb) is represented by formula (Vlb1 ) or

(Vlb2):

wherein R ^6a and R ^6b are the same as defined above.

In some embodiments, the compounds of formula (I), (la), (II), (lla), (III), (Ilia), (IV), (V), and (VI) including species thereof are converted to the compounds of formula (lb), (Mb), (lllb), (IVb), (Vb), and (Vlb) including species thereof via intramolecular cyclization, and vice versa. That is, it is an interconversion process. The compounds of formula (I), (la), (II), (lla), (III), (Ilia), (IV), (V), and (VI) including species thereof and the compounds of formula (lb), (lib), (lllb), (IVb), (Vb), and (Vlb) including species thereof are each converted into the other partially or completely depending on the conditions, such as temperature, pressure, humidity, the pH and/or composition of medium (e.g., solvents), and etc. It is illustrated in the scheme below:

wherein R ¹ is the same as defined in formula (la) and (lb) above.

In some embodiments, disclosed are compounds of Table 1 , or a pharmaceutically salt thereof:

Table 1

The language“C ₁-C ₄ alkyl” includes acyclic alkyl moieties having 1 -4 carbon atoms. Examples of C ₁-C ₄ alkyl moieties include methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, and terf-butyl.

The language“pharmaceutically acceptable salt” includes acid addition or base addition salts that retain the biological effectiveness and properties of the compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (Nib), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 and, which typically are not biologically or otherwise undesirable.

In many cases, the compounds of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 are capable of forming acid and/or base salts by virtue of the presence of basic and/or carboxyl groups or groups similar thereto.

Pharmaceutically acceptable acid addition salts can be formed with inorganic acids and organic acids, e.g., acetate, aspartate, benzoate, besylate, bromide/hydrobromide,

bicarbonate/carbonate, bisulfate/sulfate, camphorsulfonate, chloride/hydrochloride,

chlortheophyllonate, citrate, ethanedisulfonate, fumarate, gluceptate, gluconate, glucuronate, hippurate, hydroiodide/iodide, isethionate, lactate, lactobionate, laurylsulfate, malate, maleate, malonate, mandelate, mesylate, methylsulfate, naphthoate, napsylate, nicotinate, nitrate, octadecanoate, oleate, oxalate, palmitate, palmoate, phosphate/hydrogen

phosphate/dihydrogen phosphate, polygalacturonate, propionate, stearate, succinate, subsalicylate, sulfate/hydrogensulfate, tartrate, tosylate and trifluoroacetate salts. Inorganic acids from which salts can be derived include, for example, hydrochloric acid, hydrobromic acid, sulfuric acid, nitric acid, phosphoric acid, and the like. Organic acids from which salts can be derived include, for example, acetic acid, propionic acid, glycolic acid, oxalic acid, maleic acid, malonic acid, succinic acid, fumaric acid, tartaric acid, citric acid, benzoic acid, mandelic acid, methanesulfonic acid, ethanesulfonic acid, toluenesulfonic acid, trifluoroacetic acid,

sulfosalicylic acid, and the like. Pharmaceutically acceptable base addition salts can be formed with inorganic and organic bases. Inorganic bases from which salts can be derived include, for example, ammonia and salts of ammonium and metals from columns I to XII of the periodic table. In certain

embodiments, the salts are derived from sodium, potassium, ammonium, calcium, magnesium, iron, silver, zinc, and copper; particularly suitable salts include ammonium, potassium, sodium, calcium and magnesium salts. Organic bases from which salts can be derived include, for example, primary, secondary, and tertiary amines, substituted amines including naturally occurring substituted amines, cyclic amines, basic ion exchange resins, and the like. Certain organic amines include isopropylamine, benzathine, cholinate, diethanolamine, diethylamine, lysine, meglumine, piperazine and tromethamine.

The pharmaceutically acceptable salts of the compounds of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 can be synthesized from a basic or acidic moiety, by conventional chemical methods. Generally, such salts can be prepared by reacting free acid forms of these

compounds with a stoichiometric amount of the appropriate base (such as Na ⁺, Ca ²⁺, Mg ²⁺, or K ⁺ hydroxide, carbonate, bicarbonate or the like), or by reacting free base forms of these compounds with a stoichiometric amount of the appropriate acid. Such reactions are typically carried out in water or in an organic solvent, or in a mixture of the two. Generally, use of non- aqueous media like ether, ethyl acetate, ethanol, isopropanol, or acetonitrile is desirable, where practicable. Lists of additional suitable salts can be found, e.g., in“Remington's Pharmaceutical Sciences,” 20th ed., Mack Publishing Company, Easton, Pa., (1985); Berge et al., "J. Pharm. Sci., 1977, 66, 1 -19 and in“Handbook of Pharmaceutical Salts: Properties, Selection, and Use” by Stahl and Wermuth (Wiley-VCH, Weinheim, Germany, 2002).

Any formula given herein is also intended to represent unlabeled forms as well as isotopically labeled forms for the compounds of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 . Isotopically labeled compounds have structures depicted by the formulas given herein except that one or more atoms are replaced by an atom of the same element but with differing mass number. Examples of isotopes that can be incorporated into the compounds of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 and their pharmaceutically acceptable salts include isotopes of hydrogen, carbon, nitrogen, oxygen, phosphorous, sulfur, fluorine, chlorine and iodine, such as ²H, ³H, ¹¹C, ¹³C, ¹⁴C, ¹⁵N, ³⁵S, ³⁶CI and ¹²⁵l. Isotopically labeled compounds of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 can generally be prepared by conventional techniques known to those skilled in the art or by processes analogous to those described in the accompanying Examples using appropriate isotopically labeled reagents in place of the non-labeled reagents previously employed.

The compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (Nib), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 may have different isomeric forms. The language“optical isomer,”“stereoisomer” or“diastereoisomer” refers to any of the various stereoisomeric configurations which may exist for a given compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 . It is understood that a substituent may be attached at a chiral center of a carbon atom and, therefore, the disclosed compounds include enantiomers, diastereomers and racemates. The term“enantiomer” includes pairs of stereoisomers that are non-superimposable mirror images of each other. A 1 :1 mixture of a pair of enantiomers is a racemic mixture. The term is used to designate a racemic mixture where appropriate. The terms“diastereomers” or“diastereoisomers” include stereoisomers that have at least two asymmetric atoms, but which are not mirror images of each other. The absolute stereochemistry is specified according to the Cahn-lngold-Prelog R-S system. When a compound is a pure enantiomer, the stereochemistry at each chiral center may be specified by either R or S. Resolved compounds whose absolute configuration is unknown can be designated (+) or (-) depending on the direction (dextro- or levorotatory) which they rotate plane polarized light at the wavelength of the sodium D line. Certain of the compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 contain one or more asymmetric centers or axes and may thus give rise to enantiomers, diastereomers or other stereoisomeric forms that may be defined, in terms of absolute stereochemistry, as (R)- or (S)-. The present disclosure is meant to include all such possible isomers, including racemic mixtures, optically pure forms and intermediate mixtures. Optically active (R)- and (S)-isomers may be prepared using chiral synthons or chiral reagents, or resolved using conventional techniques well known in the art, such as chiral HPLC.

Also disclosed herein the Intermediates 1 -48 in the Examples, and salts thereof.

Pharmaceutical Compositions

In some embodiments, disclosed are pharmaceutical compositions comprising a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , and a pharmaceutically acceptable carrier.

The language“pharmaceutically acceptable carrier” includes compounds, materials, compositions, and/or dosage forms which are, within the scope of sound medical judgment, suitable for use in contact with the tissues of human beings and animals without excessive toxicity, irritation, allergic response, or other problem or complication, as ascertained by one of skill in the art.

The disclosed compositions may be in a form suitable for oral use (for example, as tablets, lozenges, hard or soft capsules, aqueous or oily suspensions, emulsions, dispersible powders or granules, syrups or elixirs), for topical use (for example, as creams, ointments, gels, or aqueous or oily solutions or suspensions), for administration by inhalation (for example, as a finely divided powder or a liquid aerosol), for administration by insufflation (for example, as a finely divided powder) or for parenteral administration (for example, as a sterile aqueous or oily solution for intravenous, subcutaneous, intramuscular or intramuscular dosing or as a suppository for rectal dosing).

The amount of active ingredient that is combined with one or more pharmaceutically acceptable carriers to produce a single dosage form will necessarily vary depending upon the host treated and the particular route of administration. For further information on Routes of Administration and Dosage Regimes the reader is referred to Chapter 25.3 in Volume 5 of Comprehensive Medicinal Chemistry (Corwin Hansch; Chairman of Editorial Board), Pergamon Press 1990.

Therapeutic Utilities

The present compounds are useful as arginase inhibitors in therapies.

In one aspect, disclosed are methods for treating cancer in a subject in need thereof, comprising administering to the subject an effective amount of a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (Nib), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof.

In one aspect, disclosed are methods for treating a respiratory inflammatory disease in a subject in need thereof, comprising administering to the subject an effective amount of a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof.

In one aspect, disclosed is a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in treating cancer.

In one aspect, disclosed is a compound of formula (I), (la), (lb), (II), ( 11 a) , (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in treating a respiratory inflammatory disease.

In one aspect, disclosed is the use of a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt, in the manufacture of a medicament for treating cancer.

In one aspect, disclosed are pharmaceutical compositions comprising a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in treating cancer.

The term“cancer” includes, for example, renal cell carcinoma, head and neck squamous cell carcinoma, lung cancer ( e.g ., small cell lung cancer (SCLC), non-small cell lung cancer (NSCLC), mesothelioma), pancreatic cancer, colorectal cancer, breast cancer, acute myeloid leukemia (AML), prostate cancer, gastric cancer, bladder cancer, melanoma, renal cancer and ovarian cancer. In some embodiments, the cancer has metastasized. In some embodiments, the cancer is associated with Arginase 1 and/or Arginase 2 modulation.

In some embodiments, the cancer is associated with increased plasma Arginase 1 levels. In some embodiments, the cancer is associated with decreased plasma arginine levels. In some embodiments, the cancer is associated with both increased plasma Arginase 1 levels and decreased plasma arginine levels. In some embodiments, the cancer associated with increased plasma Arginase 1 levels and/or decreased plasma arginine levels includes renal cell carcinoma, head and neck squamous cell carcinoma, lung cancer (e.g., small cell lung cancer (SCLC), non-small cell lung cancer (NSCLC), mesothelioma), pancreatic cancer, colorectal cancer and breast cancer.

In some embodiments, the cancer secretes Arginase 2, for example, acute myeloid leukemia and prostate cancer.

In some embodiments, the cancer is associated with Arginase 1 positive tumor infiltrating immune cells, for example, lung cancer (small cell lung cancer (SCLC), non-small cell lung cancer (NSCLC), gastric cancer, bladder cancer, colorectal cancer, melanoma, head and neck squamous cell carcinoma, breast cancer, prostate cancer, ovarian cancer, pancreatic cancer and renal cancer.

The term“a respiratory inflammatory disease” refers to inflammatory conditions or disorders that affect the airspaces, pulmonary vasculature, pulmonary interstitium, or a combination thereof. They can be isolated to the lung or involve multiple organs. In one embodiment, the respiratory inflammatory disease is an inflammatory lung disease. In another embodiment, the inflammatory lung disease is noninfectious.

In some embodiments, the respiratory inflammatory disease is asthma, chronic obstructive pulmonary disease (COPD), chemically-induced lung fibrosis, idiopathic pulmonary fibrosis, cystic fibrosis, or a combination thereof. In some embodiments, the respiratory inflammatory disease is chronic obstructive pulmonary disease (COPD) or asthma.

In one aspect, disclosed are methods for inhibiting arginase in a subject in need thereof, comprising administering to the subject an effective amount of a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (Nib), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof.

In one aspect, disclosed is a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, for use in inhibiting arginase.

In one aspect, disclosed is the use of a compound of formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , or a pharmaceutically acceptable salt thereof, in the manufacture of a medicament for inhibiting arginase.

The term“arginase” includes manganese-containing enzymes belonging to the uerohydrolase family that catalyze the fifth and final step in the urea cycle converting L-arginine into L-ornithine and urea. The term“arginase” includes the two isozymes of the enzyme, e.g., Arginase 1 , which functions in the urea cycle, and is located primarily in the cytoplasm of the liver, and Arginase 2, which is located in the mitochondria of several tissues in the body and is implicated in the regulation of arginine/ornithine concentrations in the cell. In some

embodiments, the compounds of formula (I), (la), (lb), (II), ( 11 a) , (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 , or a

pharmaceutically acceptable salt thereof, are selective for arginase 1 . In some embodiments, the compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 , or a pharmaceutically acceptable salt thereof, are selective for Arginase 2. In some embodiments, the compounds of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 , or a pharmaceutically acceptable salt thereof, are inhibit both Arginase 1 and Arginase 2.

The language“effective amount” includes an amount of a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 that will elicit a biological or medical response in a subject, for example, the reduction or inhibition of enzyme or protein activity related to arginase or cancer, amelioration of symptoms of cancer or the slowing or delaying of progression of cancer. In some embodiments, the language“effective amount” includes the amount of a compound of formula (I), (la), (lb), (II), (lla), (Mb), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, or Table 1 , that when administered to a subject, is effective to at least partially alleviate, inhibit, and/or ameliorate cancer or inhibit arginase, and/or reduce or inhibit the growth of a tumor or proliferation of cancerous cells in a subject.

The term“subject” includes warm blooded mammals, for example, primates, dogs, cats, rabbits, rats, and mice. In some embodiments, the subject is a primate, for example, a human. In some embodiments, the subject is suffering from cancer. In some embodiments, the subject is in need of treatment (e.g., the subject would benefit biologically or medically from treatment). In some embodiments, the patient is suffering from cancer. In some embodiments, the subject has increased plasma Arginase 1 levels. In some embodiments, the subject has decreased arginine levels. In some embodiments, the patient has both increased plasma Arginase 1 levels and decreased arginine levels. In some embodiments, the subject has a cancer secreting Arginase 2 (e.g., acute myeloid leukemia or prostate cancer). In some embodiments, the subject has Arginase 1 positive tumor infiltrating immune cells. The language“inhibit,”“inhibition” or“inhibiting” includes a decrease in the baseline activity of a biological activity or process. In some embodiments, the compounds of formula formula (I), (la), (lb), (II), (lla), (lib), (III), (Ilia), (lllb), (IV), (IVb), (V), (Vb), (VI), (Vlb), including any subgenera or species thereof, and Table 1 inhibit arginase.

The language“treat,”“treating” and“treatment” includes the reduction or inhibition of enzyme or protein activity related to arginase or in a subject, amelioration of one or more symptoms of a cancer, or the slowing or delaying of progression of cancer in a subject. The language“treat,”“treating” and“treatment” also includes the reduction or inhibition of the growth of a tumor or proliferation of cancerous cells in a subject.

Aspects of the present disclosure can be further defined by reference to the following non limiting examples, which describe in detail preparation of certain compounds and intermediates of the present disclosure and methods for using compounds of the present disclosure. It will be apparent to those skilled in the art that many modifications, both to materials and methods, can be practiced without departing from the scope of the present disclosure.

Unless stated otherwise:

(i) all syntheses were carried out at ambient temperature, i.e. in the range 17 to 25°C and under an atmosphere of an inert gas such as nitrogen unless otherwise stated;

(ii) evaporations were carried out by rotary evaporation or utilising Genevac equipment or Biotage v10 evaporator in vacuo and work-up procedures were carried out after removal of residual solids by filtration;

(iii) flash chromatography purifications were performed on an automated Teledyne Isco CombiFlash® Rf or Teledyne Isco CombiFlash® Companion® using prepacked RediSep Rf Gold™ Silica Columns (20-40 pm, spherical particles), GraceResolv™ Cartridges (Davisil® silica) or Silicycle cartridges (40 - 63 pm).

(iv) preparative chromatography was performed on a Gilson prep HPLC instrument with UV collection; alternatively, preparative chromatography was performed on a Waters

AutoPurification HPLC-MS instrument with MS- and UV- triggered collection;

(v) chiral preparative chromatography was performed on a Gilson instrument with UV collection (233 injector / fraction collector, 333 & 334 pumps, 155 UV detector) or a Varian Prep Star instrument (2 x SD1 pumps, 325 UV detector, 701 fraction collector) pump running with Gilson 305 injection; alternatively, chiral preparative chromatography was performed on a Waters Prep 100 SFC-MS instrument with MS- and UV- triggered collection or a Thar

MultiGram III SFC instrument with UV collection.

(vi) yields, where present, are not necessarily the maximum attainable;

(vii) in general, the structures of end-products of the Formula I were confirmed by nuclear magnetic resonance (NMR) spectroscopy; NMR chemical shift values were measured on the delta scale [proton magnetic resonance spectra were determined using a Bruker Avance III 600 (600 MHz), Bruker Avance 400 (400 MHz), Bruker Avance 300 (300 MHz) or Bruker DRX 500 (500 MHz) instrument]; measurements were taken at ambient temperature unless otherwise specified; the following abbreviations have been used: s, singlet; d, doublet; t, triplet; q, quartet; m, multiplet; dd, doublet of doublets; ddd, doublet of doublet of doublet; dt, doublet of triplets; bs, broad signal.

(viii) in general, end-products of the Formula I were also characterized by mass spectroscopy following liquid chromatography (LCMS or UPLC); UPLC was carried out using a Waters UPLC fitted with a Waters SQ mass spectrometer (Column temp 40 °C, UV = 220-300 nm or 190-400 nm, Mass Spec = ESI with positive/negative switching) at a flow rate of 1 mL/min using a solvent system of 97% A + 3% B to 3% A + 97% B over 1 .50 min (total run time with equilibration back to starting conditions, etc., 1 .70 min), where A = 0.1 % formic acid or 0.05% trifluoroacetic acid in water (for acidic work) or 0.1 % ammonium hydroxide in water (for basic work) and B = acetonitrile. For acidic analysis the column used was a Waters Acquity HSS T3 (1 .8 pm, 2.1 x 50 mm), for basic analysis the column used was a Waters Acquity BEH C18 (1 .7 pm 2.1 x50 mm). Alternatively, UPLC was carried out using a Waters UPLC fitted with a Waters SQ mass spectrometer (Column temp 30 °C, UV = 210-400 nm, Mass Spec = ESI with positive/negative switching) at a flow rate of 1 mL/min using a solvent gradient of 2 to 98%

B over 1 .5 mins (total run time with equilibration back to starting conditions 2 min), where A = 0.1 % formic acid in water and B = 0.1 % formic acid in acetonitrile (for acidic work) or A = 0.1 % ammonium hydroxide in water and B = acetonitrile (for basic work). For acidic analysis the column used was a Waters Acquity HSS T3 (1 .8 pm, 2.1 x30 mm), for basic analysis the column used was a Waters Acquity BEH C18 (1 .7 pm, 2.1 x30 mm); LCMS was carried out using a Waters Alliance HT (2795) fitted with a Waters ZQ ESCi mass spectrometer and a Phenomenex Gemini-NX C18 (5 pm,1 10A, 2.1 x50 mm column at a flow rate of 1 .1 mL/min 95% A to 95% B over 4 min with a 0.5 min hold where A = 0.1 % formic acid and B = 0.1 % formic acid in acetonitrile (for acidic work) or A = 0.1 % ammonium hydroxide in water and B = acetonitrile (for basic work). Additionally, LCMS was carried out using a Shimadzu UFLC fitted with a Shimadzu LCMS-2020 mass spectrometer and a Waters HSS C18 (1 .8 pm, 2.1 x50 mm) or Shim-pack XR- ODS (2.2 pm, 3.0x50 mm) or Phenomenex Gemini-NX C18 (3 pm, 3.0x50 mm) column at a flow rate of 0.7ml_/min (for Waters HSS C18 column), 1 .OmL/min (for Shim-pack XR-ODS column) or 1 2mL/min (for Phenomenex Gemini-NX C18), 95% A to 95% B over 2.2 min with a 0.6 min hold, where A = 0.1 % formic acid or 0.05% trifluoroacetic acid in water (for acidic work) or 0.1 % ammonium hydroxide or 6.5 mM ammonium carbonate in water (for basic work) and B = acetonitrile. The reported molecular ion corresponds to the [M+H]+ unless otherwise specified; for molecules with multiple isotopic patterns (Br, Cl, etc.) the reported value is the one obtained for the lowest isotope mass unless otherwise specified.

(ix) ion exchange purification was generally performed using an SCX-2 (Biotage) cartridge.

(x) intermediate purity was assessed by thin layer chromatographic, mass

spectroscopy, LCMS, UPLC/MS, HPLC (high performance liquid chromatography) and/or NMR analysis;

(xi) the following abbreviations have been used:-

EtOH: ethanol

EtOAc: ethyl acetate

LDA: lithium diisopropylamide

MeOH: methanol

TFA: trifluoroacetic acid

MeCN: acetonitrile

LCMS: liquid chromatography-mass spectrometry rt or RT : room temperature

aq: aqueous

THF: tetrahydrofuran

KHMDS: potassium bis(trimethylsilyl)amide

DCM: dichloromethane

DMF: dimethylformamide

HATU: (1 -[Bis(dimethylamino)methylene]-1 H-1 ,2,3-triazolo[4,5- b]pyridinium 3-oxid hexafluorophosphate)

BOC: tert-butoxycarbonyl

DTNB: 5,5' -dithiobis(2-nitrobenzoic acid

TNB: 2-nitro-5-thiobenzoic acid

HEPES: (4-(2-hydroxyethyl)-1 -piperazineethanesulfonic acid) Example 1 : (fl)-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Intermediate 1 : ( 3S , 7aR)-3-(trichloromethyl)tetrahvdroDyrrolol 1 ,2-cloxazol- 1 (3H)-one

2,2,2-trichloroethane-1 ,1 -diol (2.155 g, 13.03 mmol) was added to a solution of D-proline

(1 .00 g, 8.69 mmol) in CHCI ₃ (100 mL) under nitrogen. The reaction flask was equipped with a reverse Dean-Stark trap and the reaction mixture was heated to reflux with stirring for 48 h. The reaction mixture was, cooled to room temperature, diluted with DCM (100 mL), and washed sequentially with water (2 x 200 mL) and saturated brine (2 x 200 mL). The organic layer was dried over Na ₂S0 ₄, filtered and evaporated to afford crude product. The crude material was purified by crystallisation from EtOH to give product (Intermediate 1 , 1 .13 g, 53.2% yield) as a white solid. ¹ H NMR (300 MHz, CDCI ₃) d 1 .66 - 2.41 (4H, m), 3.05 - 3.20 (1 H, m), 3.40 - 3.50 (1 H, m), 4.10 - 4.20 (1 H, m), 5.18 (1 H, s). Intermediate 2: (3S,7aS)-7a-((E)-4-bromobut-2-enyl)-3-(trichloromethyl)tetra hvdroDyrrolof1 ,2- cloxazol- 1 (3H)-one

A solution of LDA (2.0 M in THF/heptane/ethylbenzene, 2.05 mL, 4.09 mmol) was added dropwise to a solution of (3S,7af?)-3-(trichloromethyl)tetrahydropyrrolo[1 ,2-c]oxazol-1 (3H)-one (Intermediate 1 , 1 .00 g, 4.09 mmol) in THF (500 mL) at -78°C under an atmosphere of nitrogen. The resulting solution was stirred at -78 °C for 20 minutes. (£)- 1 ,4-dibromobut-2-ene (875 mg, 4.09 mmol) was added to the reaction mixture dropwise as a solution in THF (2 mL). The reaction mixture was stirred at -78°C for 30 minutes and then warmed to room temperature with stirring for an additional 2 h. The reaction mixture was evaporated to dryness and the resulting residue was diluted in EtOAc (20 mL) and washed sequentially with water (2 x 20 mL) and saturated brine (2 x 20 mL). The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography

(hexanes/EtOAc) to afford the product (Intermediate 2, 760 mg, 49% yield). ¹H NMR (300 MHz, CDCIs) d 1 .55 - 1 .75 (1 H, m), 1 .85 - 2.25 (3H, m), 2.52 - 2.73 (2H, m), 3.14 - 3.32 (2H, m), 3.89 - 4.10 (2H, m), 5.01 (1 H, s), 5.79 - 5.99 (2H, m); m/z (ES ⁺) [M+H] ⁺ =378.

Intermediate 3: (3S,7aS)-7aJ(E)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2- yl)but-2-enyl)-3-

( trichloromethvDtetrahvdropyrrolof 1,2-c]oxazol- 1 (3H)-one

Pd2(dba)3 (85.0 mg, 0.0928 mmol) was added to a solution of (3S,7aS)-7a-((E)-4- bromobut-2-enyl)-3-(trichloromethyl)tetrahydropyrrolo[1 ,2-c]oxazol-1 (3H)-one (Intermediate 2, 700 mg, 1 .85 mmol) and bis(pinacolato)diboron (942 mg, 3.71 mmol) in THF (30 mL) under an atmosphere of nitrogen. The resulting mixture was heated to 60 °C and stirred for 5 h. The reaction mixture was cooled to room temperature and concentrated to dryness. The resulting residue was diluted with EtOAc (50 mL) and washed sequentially with water and saturated brine. The organic layer was dried over Na ₂S0 ₄, filtered and concentrated to dryness. The resulting crude material was purified by silica gel chromatography to afford the product

(Intermediate s, 510 mg, 65% yield). ¹ H NMR (300 MHz, CDCI ₃) d 1 .28 (12H, s), 1 .58 - 1 .80 (2H, m), 1 .83 - 2.12 (3H, m) 2.42 - 2.65 (1 H, m), 3.20 (1 H, dd), 3.47 (1 H, q), 3.71 (1 H, t), 3.90 (1 H, t), 4.98 (1 H, s), 5.38 - 5.53 (1 H, m), 5.64 - 5.83 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 424.

Intermediate 4: (3S,7aR)-7a-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl) butyl)-3-

(trichloromethyl)tetrahydropyrrolof 1,2-cloxazol- 1 (3H)-one

Pd/C (10% wt, 125 mg, 0.12 mmol) was added to a solution of (3S,7aS)-7a-((E)-4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)but-2-enyl)-3-(trichloromethyl)tetrah ydropyrrolo[1 ,2- c]oxazol-1 (3H)-one (Intermediate 3, 500 mg, 1 .18 mmol) in MeOH (5 mL). The reaction flask was equipped with a balloon of H2 and the suspension stirred at room temperature for 30 min. The reaction mixture was filtered through diatomaceous earth and washed with MeOH. The filtrate was concentrated to dryness to afford crude product (Intermediate 4, 390 mg, 78% yield) which was used without further purification m/z (ES ⁺) [M+H] ⁺ = 426.

Example 1: ( R)-2-(4-bcrcncbutyl)pyrrclidine-2-carbcxylic acid

Concentrated aqueous HCI (1 .00 mL, 12.0 mmol) was added to a solution of ( 3SJaR )- 7a-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)-3- (trichloromethyl)tetrahydropyrrolo[1 ,2-c]oxazol-1 (3H)-one (Intermediate 4, 300 mg, 0.703 mmol) and phenylboronic acid (172 mg, 1 .41 mmol) in 1 ,4-dioxane (20 mL). The resulting solution was heated to 80 °C for 15 h. The reaction mixture was cooled to room temperature and concentrated to dryness. Crude material was purified by preparative LCMS (XBridge Prep C18 OBD column, 5m silica, 19 x 150 mm, H ₂0 (w/ 0.05% TFA/MeCN). Pure fractions were collected and concentrated to dryness to afford (F?)-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid (Example 1 , 85 mg, 37% yield) as a white solid. ¹ H NMR (400 MHz, D ₂0) d 0.63 - 0.74 (2H, m), 1 .09 - 1 .27 (2H, m), 1 .27 - 1 .37 (2H, m), 1 .65 - 1 .75 (1 H, m), 1 .77 - 2.08 (4H, m), 2.25 - 2.37 (1 H, m), 3.21 - 3.37 (2H, m); m/z (ES+) [M+H] ⁺ = 216.

Example 2: (2ff.4S)-2-(4-boronobutyl)-4-hvdroxypyrrolidine-2-carboxylic acid

Intermediate 5 Intermediate 6

Intermediate 7 Major Isomer Minor Isomer

Intermediate 8 Example 2

Intermediate 5: (2S,4S)-2-benzyl 1-tert-butyl 4-(benzyloxy)Dyrrolidine-1 ,2-dicarboxylate

(2S,4S)-1 -(terf-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid (5.00 g, 21 .6 mmol) was dissolved in DMF (73 mL) and the solution was cooled to 0 °C. Sodium hydride (60% dispersion in mineral oil) (1 .81 g, 45.3 mmol) was added portionwise and the suspension stirred at 0 °C for 1 h. Benzyl bromide (12.9 mL, 108 mmol) was added and the reaction mixture stirred overnight while slowly warming to RT. The crude reaction mixture was diluted with ethyl acetate (250 mL) and washed sequentially with citric acid (10% aq) and water. The organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude product was purified by silica gel chromatography (hexanes/EtOAc) to afford the product as a mixture of rotamers (Intermediate 5, 5.5 g, 62% yield). ¹ H NMR (300 MHz, DMSO-de) d 1 .28 -1 .40 (9H, s x2) rotamers, 2.20 (1 H, dd), 2.36 - 2.45 (1 H, m), 3.37 (1 H, dd), 3.51 - 3.58 (1 H, m), 4.14 (1 H, br s), 4.33 - 4.50 (3H, m), 4.94 - 5.17 (2H, m), 7.25 - 7.32 (1 OH, m); m/z (ES ⁺) [M+H] ⁺ = 412.

Intermediate 6: ( 4S)-2-benzyl 1 -tert-butyl 4-(benzyloxy)-2-(but-2-enyl)pyrrolidine-1 ,2-

(2S,4S)-2-Benzyl 1 -terf-butyl 4-(benzyloxy)pyrrolidine-1 ,2-dicarboxylate (Intermediate 5, 2.75 g, 6.68 mmol) and crotyl bromide (1 .03 mL, 10.0 mmol) were dissolved in THF (45 mL) and the solution was cooled to - 78 °C under an atmosphere of N ₂. The solution was treated with dropwise addition of a solution of KHMDS (0.5M in toluene, 20.1 mL, 10.0 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 3 h. The crude reaction mixture was quenched with water and the volatiles were removed in vacuo. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂S04, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford the product as a mixture of rotamers and E/Z olefins (Intermediate 6, 2.54 g, 82% yield). ¹H NMR (300 MHz, DMSO-de) d 1 .20 - 1 .41 (9H, s x2) rotamers, 1 .54 - 1 .62 (3H, m), 2.10 - 2.59 (3H, m), 2.67 - 2.97 (1 H, m), 3.10 - 3.43 (1 H, m), 3.50 - 3.78 (1 H, m), 3.98 - 4.15 (1 H, m), 4.34 - 4.49 (2H, m), 4.94 - 5.13 (2H, m), 5.18 - 5.30 (1 H, m), 5.38 - 5.63 (1 H, m), 7.25 - 7.36 (1 OH, m); m/z (ES ⁺) [M+H] ⁺ = 466.

Intermediate 8: (2R,4S)-1-(tert-butoxycarbonyl)-4-hydroxy-2-(4-(4,4,5,5-tetr amethyl-1,3,2- dioxaborolan-2-vl)butvl)pvrrolidine-2-carboxylic acid

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (0.366 g, 0.550 mmol) and

bis(diphenylphosphino)methane (0.419 g, 1 .09 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (31 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (1 .74 mL, 12.0 mmol) was added slowly to the solution. The reaction stirred at room temperature for 10 min. (4S)-2-Benzyl 1 -terf-butyl 4- (benzyloxy)-2-(but-2-enyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 6, 2.54 g, 5.46 mmol) was added to the reaction as a solution in DCM (21 mL) and the reaction mixture stirred overnight. The reaction mixture was diluted with DCM and quenched with water. The layers were separated and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (4S)-2-benzyl 1 -terf-butyl 4-(benzyloxy)-2- (4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 7, 2.0 g, 61 % yield) as a mixture of rotamers. Purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 21 .2 x 250 mm, 5 pm, Temperature = 23 °C, Mobile phase = 0-15% MeOH:C02, UV detection @ 220 nm, loading = 33 mg/inj, cone = 220 ng/mL in MeOH, flow rate = 75 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry for the major isomer was assigned as the anti-addition product and the minor isomer was assigned as the syn-addition product. The minor isomer (368 mg, 0.620 mmol) was dissolved in ethyl acetate (6.2 mL) and treated with Pd/C (10% wt, 132 mg, 0.124 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford (2F?,4S)-1 -(terf-butoxycarbonyl)-4-hydroxy-2-(4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 8, 228 mg, 98% yield) as a mixture of rotamers which was used without further purification. ¹ H NMR (300MHz, DMSO-de) d 0.57 - 0.74 (2H, m), 1 .17 (12 H, s), 1 .24 - 1 .47 (13H, m), 1 .59 - 1 .78 (1 H, m), 1 .78 - 1 .96 (1 H, m), 2.01 - 2.20 (2H, m), 2.84 - 3.09 (1 H, m), 3.58 - 3.73 (1 H, m), 4.14 - 4.31 (1 H, m), 4.98 - 5.09 (1 H, m), 12.20 - 12.60 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 414.

Example 2: (2R,4S)-2-(4-boronobutyl)-4-hydroxypyrrolidine-2-carboxylic acid

Trifluoroacetic acid (0.65 mL, 8.4 mmol) was added to a solution of (2F?,4S)-1 -(terf- butoxycarbonyl)-4-hydroxy-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 8, 175 mg, 0.423 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (3 mL) and 1 M aq HCI (3 mL). Phenylboronic acid (103 mg, 0.847 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10% to 100% acetonitrile in water) to obtain (2F?,4S)-2-(4-boronobutyl)-4-hydroxypyrrolidine-2- carboxylic acid (Example 2, 33 mg, 33% yield) as a white solid. ¹H NMR (400MHz, D ₂0) d 0.67 - 0.78 (2H, m), 1 .08 - 1 .41 (4H, m), 1 .81 - 2.12 (3H, m), 2.51 (1 H, dd), 3.22 - 3.37 (2H, m), 4.46 - 4.56 (1 H, m) ; m/z (ES ⁺) [M+H] ⁺ = 232. Example 3: (2ff,4fl)-2-(4-boronobutyl)-4-hvdroxypyrrolidine-2-carboxyli c acid

Intermediate 9 Intermediate 10

Intermediate 11 Minor Isomer Major Isomer

Intermediate 12 Example 3

Intermediate 9: (2S,4R)-2-benzy! 1-tert-butyl 4-(benzyloxy)Dyrrolidine-1 ,2-dicarboxylate

(2S,4F?)-1 -(tert-butoxycarbonyl)-4-hydroxypyrrolidine-2-carboxylic acid (5.00 g, 21 .6 mmol) was dissolved in DMF (73 mL) and the solution was cooled to 0 °C. Sodium hydride (60% wt in mineral oil, 1 .81 g, 45.4 mmol) was added portionwise and the suspension stirred at 0 °C for 1 h. Benzyl bromide (12.86 mL, 108.1 mmol) was added and the reaction mixture stirred overnight while slowly warming to RT. The crude reaction mixture was diluted with ethyl acetate (250 mL) and washed sequentially with citric acid (10% aq) and water. The organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford product (Intermediate 9, 5.9 g, 66% yield) as a mixture of rotamers. ¹ H NMR (300MHz, DMSO-d6) d 1 .27 - 1 .39 (9H, s x2) rotamers, 1 .95 - 2.08 (1 H, m), 2.34 - 2.47 (1 H, m), 3.41 - 3.53 (2H, m), 4.17 (1 H, br s), 4.28 (1 H, q), 4.43 - 4.55 (2H, m), 5.06 - 5.22 (2H, m), 7.25 - 7.41 (10H, m); m/z (ES ⁺) [M+H] ⁺ = 412.

Intermediate 10: (4R)-2-benzy! 1 -tert-butyl 4-(benzyloxy)-2-(but-2-enyl)Dyrrolidine-1 ,2- dicarboxylate

(2S,4F?)-2-Benzyl 1 -fert-butyl 4-(benzyloxy)pyrrolidine-1 ,2-dicarboxylate (Intermediate 9, 2.75 g, 6.68 mmol) and crotyl bromide (1 .03 mL, 10.0 mmol) were dissolved in THF (45 mL) and the solution was cooled to - 78 °C under an atmosphere of N ₂. The solution was treated with dropwise addition of a solution of KHMDS (0.5M in toluene, 20.1 mL, 10.0 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 3 h. The crude reaction mixture was quenched with water and the volatiles were removed in vacuo. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford product (Intermediate 10, 1 .23 g, 40% yield) as a mixture of rotamers and E/Z olefins. ¹H NMR (300MHz, DMSO-de) d 1 .25 - 1 .34 (9H, s x2) rotamers, 1 .45 - 1 .63 (3H, m), 2.12 - 2.64 (2H, m), 2.64 - 3.04 (1 H, m), 3.06 - 3.19 (1 H, m), 3.31 - 3.45 (1 H, m), 3.46 - 3.81 (1 H, m), 4.03 - 4.21 (1 H, m), 4.30 - 4.55 (2H, m), 4.90 - 5.16 (2H, m), 5.16 - 5.34 (1 H, m), 5.38 - 5.68 (1 H, m), 7.25 - 7.41 (1 OH, m). m/z (ES ⁺) [M+H] ⁺ = 466.

Intermediate 12: (2R,4R)- 1 -(tert-butoxycarbonyi)-4-hydroxy-2-(4-(4,4,5,5-tetramethyi- 1,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (177 mg, 0.264 mmol) and

bis(diphenylphosphino)methane (203 mg, 0.527 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (15 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (0.84 mL, 5.8 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. (4f?)-2-Benzyl 1 -terf-butyl 4- (benzyloxy)-2-(but-2-enyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 10, 1 .23 g, 2.64 mmol) was added to the reaction as a solution in DCM (10 mL) and the reaction mixture stirred overnight. The reaction mixture was diluted with DCM and quenched with water. The layers were separated and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (4f?)-2-benzyl 1 -terf-butyl 4-(benzyloxy)-2- (4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate

(Intermediate 11 , 950 mg, 60% yield). Purified material was subjected to chiral SFC

[(S,S)Whelk-01 column, 21 .2 x 250 mm, 5 pm, Temperature = 23 °C, Mobile phase = 0-15% MeOH:C02, UV detection @ 220 nm, loading = 33 mg/inj, cone = 220 ng/mL in MeOH, flow rate = 75 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry for the major isomer was assigned as the anti-addition product and the minor isomer was assigned as the syn-addition product. The major isomer (385 mg, 0.649 mmol) was dissolved in ethyl acetate (6.4 mL) and treated with Pd/C (10% wt, 138 mg, 0.130 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford the product (Intermediate 12, 249 mg, 93% yield) as a mixture of rotamers. ¹ H NMR (300 MHz, DMSO-de) d 0.61 - 0.73 (2H, m), 0.97 - 1 .1 1 (1 H, m), 1 .12 - 1 .23 (12H, m), 1 .25 - 1 .44 (12H, m), 1 .51 - 1 .71 (1 H, m), 1 .84 - 2.04 (2H, m), 2.05 - 2.19 (2H, m), 3.12 - 3.29 (1 H, m), 3.37 - 3.59 (1 H, m), 4.09 - 4.23 ( ¹ H, m); m/z (ES ⁺) [M+H] ⁺ = 414.

Example 3: (2RAR)-2-(4-boronobutyl)-4-hvdroxyDyrrolidine-2-carboxylic acid

Trifluoroacetic acid (0.65 mL, 8.5 mmol) was added to a solution of (2R,4R)- -(tert- butoxycarbonyl)-4-hydroxy-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 12, 197 mg, 0.179 mmol) in DCM (3 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (3 mL) and 1 M aq HCI (3 mL). Phenylboronic acid (102 mg, 0.837 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10% acetonitrile in water) to afford (2P?,4/ ^:?)-2-(4-boronobutyl)-4-hydroxypyrrolidine-2-carboxylic acid (Example 3, 25 mg, 25% yield) as a white solid. ¹ H NMR (300MHz, D ₂0) d 0.68 - 0.78 (2H, m), 1 .13 - 1 .43 (4H, m), 1 .64 - 1 .79 (1 H, m), 1 .94 - 2.14 (2H, m), 2.47 (1 H, d), 3.39 (2H, m), 4.46 - 4.53 (1 H, m). m/z (ES ⁺) [M+H] ⁺ = 232.

Example 4: (2S.4S)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Intermediate 13 Intermediate 14

Intermediate 15 Intermediate 16 Intermediate 17

Intermediate 18 Example 4

Intermediate 13: (2SAS)-2-benzyl 1-tert-butyl 4-azidoDyrrolidine-1 ,2-dicarboxylate

Methanesulfonyl chloride (0.71 mL, 9.2 mmol) was added dropwise to a solution of 2- benzyl l -(terf-butyl) (2S,4F?)-4-hydroxypyrrolidine-1 ,2-dicarboxylate (2.45 g, 7.26 mmol) and triethylamine (1 .27 mL, 9.15 mmol) in DCM (9.6 mL) at 0 °C. The reaction mixture stirred at 0 °C for 1 h before warming to room temperature with stirring for an additional 1 h. The reaction mixture was diluted with dichloromethane and washed with water. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness to afford 2-benzyl l -(terf-butyl) (2S,4F?)-4- ((methylsulfonyl)oxy)pyrrolidine-1 ,2-dicarboxylate (2.9 g, 95% yield) which was used without further purification m/z (ES ⁺) [M+H] ⁺ = 400. Sodium azide (1 .65 g, 25.4 mmol) was added to a solution of 2-benzyl l -(terf-butyl) (2S,4f?)-4-((methylsulfonyl)oxy)pyrrolidine-1 ,2-dicarboxylate (2.90 g, 7.26 mmol) in DMF (7.2 mL). The reaction mixture was heated to 50 °C and stirred overnight. The reaction mixture was cooled to room temperature and concentrated. The resulting residue was diluted with EtOAc and washed with water. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. Crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford the product (Intermediate 13, 2.00 g, 80% yield) as a mixture of rotamers. ¹ H NMR (300MHz, DMSO-de) d 1 .27 and 1 .40 (9H, s x2) rotamers, 1 .96 - 2.02 (1 H, m), 2.53 - 2.63 (1 H, m), 3.24 - 3.29 (1 H, m), 3.58 - 3.66 (1 H, m), 4.32 - 4.41 (2H, m), 5.06 - 5.22 (2H, m), 7.33-7.39 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 347. Intermediate 14: ( 4S)-2-benzyl 1-tert-butyl 4-azido-2-(but-2-enyl)pyrrolidine-1,2-dicarboxylate

(2S,4S)-2-benzyl 1 -tert-butyl 4-azidopyrrolidine-1 ,2-dicarboxylate (Intermediate 13, 1 .00 g, 2.89 mmol) and crotyl bromide (0.44 mL, 4.3 mmol) were dissolved in THF (20 mL) and the solution was cooled to -78 °C under an atmosphere of N ₂. The solution was treated with dropwise addition of a solution of KHMDS (0.5M in toluene, 8.66 mL, 4.33 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 3 h. The crude reaction mixture was quenched with water and the volatiles were removed in vacuo. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford the product (Intermediate 14, 750 mg, 65% yield) as a mixture of rotamers and E/Z olefins. ¹H NMR (300MHz, DMSO-de) d 1 .25 - 1 .34 (9H, s x2) rotomers, 1 .55 - 1 .64 (3H, m), 1 .99 - 2.15 (1 H, m), 2.33 - 2.62 (2H, m), 2.73 - 3.10 (1 H, m), 3.26 - 3.39 (1 H, m), 3.52 - 3.84 (1 H, m), 4.24 - 4.33 (1 H, m), 5.03 - 5.21 (2H, m), 5.28 - 5.35 (1 H, m), 5.49 - 5.65 (1 H, m), 7.31 - 7.36 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 401 .

Intermediate 16: (2S,4S)-2-benzyl 1-tert-butyl 4-azido-2-(4-(4, 4,5, 5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1,2-dicarboxylate and Intermediate 17: ( 2R,4S)-2-benzyl 1- tert-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (126 mg, 0.188 mmol) and

bis(diphenylphosphino)methane (144 mg, 0.375 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (10 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (0.60 mL, 4.1 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. (4S)-2-benzyl 1 -tert-butyl 4- azido-2-(but-2-enyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 14, 750 mg, 1 .87 mmol) was added to the reaction as a solution in DCM (8 mL) and the reaction mixture stirred overnight at room temperature. The reaction mixture was diluted with DCM and quenched with water. The layers were separated and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (4S)-2-benzyl 1 -fert-butyl 4-azido-2-(4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 15, 678 mg, 68% yield). Purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 21 .2 x 250 mm, 5 pm, Temperature = 23 °C, Mobile phase = 0-15% MeOH:C02, UV detection @ 220 nm, loading = 33 mg/inj, cone = 220 ng/mL in MeOH, flow rate = 75 mL/min, Outlet Pressue = 100 bar] to give two diastereomers. The stereochemistry for the major isomer was assigned as the anti-addition product Intermediate 16 and the minor isomer the syn-addition product Intermediate 17.

Intermediate 16 (Isomer 1 , 608 mg): (2S,4S)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (500MHz, DMSO-de) d 0.64 - 0.72 (2H, m), 1 .04 - 1 .12 (1 H, m), 1 .13 - 1 .20 (12H, m), 1 .22 - 1 .39 (12H, m),

1 .69 - 1 .80 (1 H, m), 2.01 - 2.23 (2H, m), 2.36 - 2.48 (1 H, m), 3.35 - 3.42 (1 H, m), 3.58 - 3.69 (1 H, m), 4.33 (1 H, quin), 5.05 - 5.17 (2H, m), 7.31 - 7.40 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 529.

Intermediate 17 (Isomer 2, 220 mg): (2f?,4S)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate.

Intermediate 18: (2S,4S)-4-Amino-1-(tert-butoxycarbonyl)-2-(4-(4,4,5,5-tetram ethyl-1,3,2- dioxaborolan-2-yl)butvl)pvrrolidine-2-carboxylic acid

(2S,4S)-2-Benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 16, 255 mg, 0.483 mmol) was dissolved in ethyl acetate (5 mL) and methanol (5 mL) and treated with Pd/C (10% wt, 128 mg, 0.120 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford the product

(Intermediate 18, 190 mg, 95% yield) as a mixture of rotamers which was used without further purification. ¹H NMR (300MHz, DMSO-de) d 0.66 (2H, t), 0.88-1 .03 (1 H, m), 1 .16 (12H, s), 1 .24- 1 .38 (13H, m), 1 .40 - 1 .56 (1 H, m), 1 .80 - 1 .91 (1 H, m), 2.00-2.15 (2H, m), 3.17-3.28 (1 H, m), 3.58 - 3.61 (1 H, m), 3.80 (1 H, dd), 9.01 (2H, br s); m/z (ES+) [M+H]+ = 413.

Example 4: (2S,4S)-4-Aminc-2-(4-bcrcncbutyl)pyrrclidine-2-carbcxylic acid

Trifluoroacetic acid (0.71 mL, 9.2 mmol) was added to a solution of (2S,4S)-4-amino-1 - (terf-butoxycarbonyl)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 18, 190 mg, 0.461 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (3 mL) and 1 M aq HCI (3 mL). Phenylboronic acid (1 12 mg, 0.919 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10% acetonitrile in water) to afford (2S,4S)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid (Example 4, 40 mg, 37% yield) as a white solid. ¹ H NMR (300MHz, D2O) d 0.73 (2H, t),

1 .10 - 1 .42 (4H, m), 1 .69 (1 H, ddd), 1 .86 - 1 .99 (1 H, m), 2.10 - 2.30 (2H, m), 3.05 (1 H, dd), 3.44 (1 H, dd), 3.69 (1 H, quin); m/z (ES ⁺) [M+H] ⁺ = 231 .

Example 5: (2/?,4S)-4-Amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Intermediate 17 Intermediate 19 Example 5

Intermediate 19: (2R.4S)-4-amino-1-(tert-butoxycarbonyl)-2-(4-(4.4.5.5-tetram ethyl-1.3.2- dioxaborolan-2-yl)butyl)Dyrrolidine-2-carboxylic acid

(2f?,4S)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 17, 220 mg, 0.416 mmol) was dissolved in ethyl acetate (5 mL) and methanol (5 mL) and treated with Pd/C (10% wt, 1 1 1 mg, 0.104 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford the product

(Intermediate 19, 150 mg, 87% yield) as a mixture of rotamers which was used without further purification. ¹H NMR (300MHz, DMSO-de) d 0.64-0.71 (2H, m), 1 .17 (12H, s), 1 .31 -1 .40 (15H, m), 1 .49 - 1 .93 (3H, m), 2.02 - 2.26 (3H, m), 3.38-3.47 (1 H, m), 3.72 - 3.81 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 413.

Example 5: (2RAS)-4-amino-2-(4-boronobutyl)Dyrrolidine-2-carboxylic acid

Trifluoroacetic acid (0.56 mL, 7.3 mmol) was added to a solution of (2f?,4S)-4-amino-1 - (terf-butoxycarbonyl)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 19, 150 mg, 0.364 mmol) in DCM (3 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (2 mL) and 1 M aq HCI (2 mL). Phenylboronic acid (99 mg, 0.81 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10%0 to 100% acetonitrile in water) to afford (2F?,4S)-4-amino-2-(4-boronobutyl)pyrrolidine-2- carboxylic acid (Example 5, 33 mg, 39% yield) as a white solid. ¹ H NMR (400MHz, D ₂0) d 0.72 (1 H, m), 1 .1 1 - 1 .39 (3H, m), 1 .46 - 1 .55 (1 H, m), 1 .63 - 1 .79 (2H, m), 1 .95 - 2.05 (1 H, m), 2.58 - 2.65 (1 H, m), 2.87 - 2.95 (1 H, m), 3.48 - 3.58 (3H, m); m/z (ES ⁺) [M+H] ⁺ = 231 .

Example 6: (2S.4ff)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Intermediate 20 Intermediate 21 Intermediate 22

Intermediate 23 Intermediate 24 Intermediate 25

Intermediate 26 Example 6

Intermediate 20: (2S,4R)-1 -tert-butyl 2-methyl 4-azidoDyrrolidine-1,2-dicarboxylate

Methanesulfonyl chloride (2.86 mL, 36.7 mmol) was added dropwise to a solution of

(25.45)-1 -terf-butyl 2-methyl 4-hydroxypyrrolidine-1 ,2-dicarboxylate (7.50 g, 30.6 mmol) and triethylamine (5.1 1 mL, 36.7 mmol) in DCM (38 mL) at 0 °C. The reaction mixture stirred at 0 °C for 1 h before warming to room temperature with stirring for an additional 1 h. The reaction mixture was diluted with dichloromethane and washed with water. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness to afford afford l -(terf-butyl) 2-methyl

(25.45)-4-((methylsulfonyl)oxy)pyrrolidine-1 ,2-dicarboxylate (9.9 g, 100% yield) which was used without further purification m/z (ES ⁺) [M+NH ₄] ⁺ = 341 .

Sodium azide (5.96 g, 91 .7 mmol) was added to a solution of 1 -(terf-butyl) 2-methyl

(2S,4S)-4-((methylsulfonyl)oxy)pyrrolidine-1 ,2-dicarboxylate (9.89 g, 30.6 mmol) in DMF (30 mL). The reaction mixture was heated to 50 °C and stirred overnight. The reaction mixture was cooled to room temperature and concentrated. The resulting residue was diluted with EtOAc and washed with water. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. Crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford the product (Intermediate 20, 5.95 g, 72% yield) as a mixture of rotamers. ¹ H NMR (300MHz, DMSO-de) d 1 .33 and 1 .40 (9H, s x2) rotamers, 2.08 - 2.22 (1 H, m), 2.26- 2.41 (1 H, m), 3.41 (1 H, dt), 3.48 - 3.61 (1 H, m), 3.65 and 3.68 (3H, s x2) rotamers, 4.22 (1 H, dd), 4.30 - 4.43 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 271 .

Intermediate 21: (2S,4R)-2-benzyl 1-tert-butyl 4-azidopyrrolidine-1 ,2-dicarboxylate

A solution of sodium hydroxide (5.28 g, 132 mmol) in water (22 mL) was added dropwise to a solution of (2S,4f?)-1 -terf-butyl 2-methyl 4-azidopyrrolidine-1 ,2-dicarboxylate (Intermediate 20, 5.95 g, 22.0 mmol) in THF (44 mL) and MeOH (22 mL) at 0 °C. The reaction mixture stirred overnight while slowly warming to room temperature. The volatiles were removed in vacuo and the aqueous layer was acidified to pH ~3 with 5 M HCI and extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness to afford (2S,4F?)-4- azido-1 -(terf-butoxycarbonyl)pyrrolidine-2-carboxylic acid (5.64 g, 100% yield) as a mixture of rotamers which was used without further purification. ¹H NMR (300MHz, DMSO-d ⁶) d 1 .35 and 1 .40 (9H, s x2) rotamers, 2.07 - 2.18 (1 H, m), 2.26- 2.38 (1 H, m), 3.34 - 3.44 (1 H, m), 3.48 - 3.63 (1 H, m), 4.09-4.17 (1 H, m), 4.30 - 4.37 (1 H, m); m/z (ES ) [M+HCOO] = 301 .

Benzyl bromide (2.83 mL, 23.8 mmol) was added dropwise to a solution of (2S,4F?)-4- azido-1 -(terf-butoxycarbonyl)pyrrolidine-2-carboxylic acid (5.19 g, 19.9 mmol) and triethylamine (3.46 mL, 24.8 mmol) in DMF (60 mL) and the reaction mixture stirred overnight at room temperature. The volatiles were removed in vacuo and the resulting residue was dissolved in EtOAc and washed with water. The organic layer was dried over Na2S04, filtered and concentrated to dryness. Crude material was purified by silica gel chromatography

(hexanes/EtOAc) to afford the product (Intermediate 21 , 5.09 g, 74% yield). ¹H NMR (300MHz, DMSO-de) d 1 .26 and 1 .39 (9H, s x2) rotamers, 2.1 1 - 2.23 (1 H, m), 2.31 -2.43 (1 H, m), 3.43 (1 H, ddd), 3.50 -3.59 (1 H, m), 4.25-4.40 (2H, m), 5.07-5.22 (2H, m), 7.31 -7.40 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 347.

Intermediate 22: (4R)-2-benzyl 1-tert-butyl 4-azido-2-(but-2-enyl)pyrrolidine- 1 ,2-dicarboxylate

(2S,4F?)-2-benzyl 1 -terf-butyl 4-azidopyrrolidine-1 ,2-dicarboxylate (Intermediate 21 , 5.09 g, 14.7 mmol) and crotyl bromide (2.27 mL, 22.0 mmol) were dissolved in THF (100 mL) and the solution was cooled to - 78 °C under an atmosphere of N ₂. The solution was treated with dropwise addition of a solution of KHMDS (0.5M in toluene, 44.1 mL, 22.0 mmol). The reaction mixture was slowly warmed to room temperature and stirred for 3 h. The crude reaction mixture was quenched with water and the volatiles were removed in vacuo. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂S04, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford the product (Intermediate 22, 4.6 g, 78% yield) as a mixture of rotamers and E/Z olefins. ¹H NMR (300MHz, DMSO-de) d 1 .26 - 1 .43 (9H, m), 1 .59 - 1 .66 (3H, m), 2.07 - 2.17 (1 H, m), 2.32 - 2.48 (2H, m), 2.57 - 3.12 (2H, m), 3.35 - 3.82 (1 H, m), 4.20 - 4.38 (1 H, m), 5.02 - 5.22 (2H, m), 5.24 - 5.41 (1 H, m), 5.46 - 5.68 (1 H, m), 7.28 - 7.42 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 401 .

Intermediate 24: (2S,4R)-2-benzyl 1-tert-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1,2-dicarboxylate and Intermediate 25: (2R,4R)-2-benzyl 1- tert-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (772 mg, 1 .15 mmol) and

bis(diphenylphosphino)methane (883 mg, 2.30 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (66 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (3.67 mL, 25.3 mmol) was slowly added to the solution. The reaction stirred at room temperature for 10 min. (4f?)-2-benzyl 1 -tert-butyl 4- azido-2-(but-2-enyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 22, 4.60 g, 1 1 .5 mmol) was added to the reaction as a solution in DCM (44 mL) and the reaction mixture stirred overnight. The reaction mixture was diluted with DCM and quenched with water. The layers were separated and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (4f?)-2-benzyl 1 -tert-butyl 4-azido-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 23, 2.7 g, 44% yield). The purified material was subjected to chiral SFC (Chiralpak IG column, 21 .2 x 250 mm, 5 pm, Temperature = 23 °C, Mobile phase = 0-7% MeOH (w/ 0.2% NH ₄0H):C0 ₂, UV detection @ 220 nm, loading = 16.8 mg/inj, cone = 1 12.5 ng/mL in MeOH, flow rate = 70 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry for the major diastereomer Intermediate 25 was assigned as the anti-addition product and the minor diastereomer Intermediate 24 the syn-addition product. Intermediate 24 (436 mg): (2S,4f?)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (400MHz, DMSO-de) d 0.58 - 0.70 (2H, m), 1 .17 (12H, s), 1 .25 -1 .40 (13 H, m), 1 .74-1 .83 (1 H, s), 2.00 - 2.1 1 (2H, m), 2.38-2.47 (1 H, m), 3.07 - 3.16 (1 H, m), 3.81 (1 H, m), 4.29 - 4.34 (1 H, m), 5.04 - 5.17 (2H, m), 7.34 - 7.39 (m, 5H); m/z (ES ⁺) [M+H] ⁺ = 529.

Intermediate 25 (1 .60 g): (2f?,4f?)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5- tetramethyl-1 ,3, 2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (400MHz, DMSO-de) d 0.56 - 0.73 (2H, m), 0.98 - 1 .13 (1 H, m), 1 .17 (12H, s), 1 .26 - 1 .37 (13H, m), 1 .66 - 1 .79 (1 H, m), 2.01 - 2.22 (2H, m), 2.34 - 2.47 (1 H, m), 3.60 (1 H, br dd), 4.29 - 4.35 (1 H, m), 5.04 - 5.18 (2H, m), 7.31 - 7.40 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 529.

Intermediate 26: (2S,4R)-4-amino-1-(tert-butoxycarbonyl)-2-(4-(4,4,5,5Jetrame thyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid

(2S,4f?)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 24, 236 mg, 0.447 mmol) was dissolved in ethyl acetate (4.5 mL) and treated with Pd/C (10% wt, 1 19 mg, 0.1 12 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford the product (Intermediate 26, 275 mg,

100% yield) which was used without further purification. ¹H NMR (300MHz, DMSO-de) d 0.64 - 0.71 (2H, M), 1 .17 (12H, s), 1 .27 -1 .40 (15H, m), 1 .57 - 1 .82 (4H, m), 1 .98-2.08 (3H, m), 3.70 - 3.78 (1 H, m) ; m/z (ES ⁺) [M+H] ⁺ = 413.

Example 6: (2S,4R)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Trifluoroacetic acid (0.69 mL, 8.9 mmol) was added to a solution of (2S,4f?)-4-amino-1 - (terf-butoxycarbonyl)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 26, 184 mg, 0.446 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (2 mL) and 1 M aq HCI (2 mL). Phenylboronic acid (109 mg, 0.894 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 100% acetonitrile in water) to afford (2S,4fi)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid (Example 6, 38 mg, 37% yield) as a white solid. ¹H NMR (400MHz, D ₂0) d 0.72 (2H, td), 1 .09 - 1 .19 (1 H, m), 1 .22 - 1 .39 (3H, m), 1 .65 - 1 .76 (2H, m), 1 .95 - 2.04 (1 H, m), 2.58 - 2.64 (1 H, m), 2.87 - 2.94 (1 H, m), 3.48 - 3.57 (2H, m); m/z (ES ⁺) [M+H] ⁺ = 231 .

Example 7: (2ff.4ff)-4-amino-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid

Intermediate 25 Intermediate 27 Example 7

Intermediate 27: (2R,4R)-4-amino-1-(tert-butoxycarbonyl)-2-(4-(4,4,5,5Jetrame thyl-1 ,3,2- dioxaborolan-2-yl)butyl)Dyrrolidine-2-carboxylic acid

(2f?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 25, 688 mg, 1 .30 mmol) was dissolved in ethyl acetate (13 mL) and methanol (4 mL) and treated with Pd/C (10% wt, 346 mg, 0.325 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with methanol. The filtrate was concentrated under reduced pressure to afford the product (Intermediate 27, 500 mg, 93% yield) which was used without further purification. ¹ H NMR (300MHz, DMSO-de) d 0.67 (2H, t), 0.94-1 .00 (1 H, m), 1 .17 (12H, s), 1 .22 -1 .38 (1 1 H, m), 1 .43 - 1 .53 (1 H, m), 1 .85 (1 H, d), 2.00 - 2.15 (2H, m), 3.23 (2H, dd), 3.58 - 3.61 (1 H, m), 3.80 - 3.88 (1 H, m), 8.96 (2H, m); m/z (ES ⁺) [M+H] ⁺ = 413.

Example 7: (2RAR)-4-amino-2-(4-boronobutyl)Dyrrolidine-2-carboxylic acid

Trifluoroacetic acid (1 .02 mL, 13.3 mmol) was added to a solution of (2fl,4fl)-4-amino-1 - (terf-butoxycarbonyl)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 27, 275 mg, 0.667 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (2 mL) and 1 M aq HCI (2 mL). Phenylboronic acid (163 mg, 1 .34 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10% to 100% acetonitrile in water) to afford (2f?,4/ ^:?)-4-amino-2-(4-boronobutyl)pyrrolidine-2- carboxylic acid (Example 7, 53 mg, 34% yield) as a white solid. ¹H NMR (400MHz, D20) d 0.76 (2H, dt), 1 .10 - 1 .46 (4H, m), 1 .62 - 1 .71 (1 H, m), 1 .84 - 1 .96 (1 H, m), 2.10 - 2.21 (1 H, m), 2.22 - 2.32 (1 H, m), 3.07 (1 H, dd), 3.46 (1 H, dd), 3.71 (1 H, quin) ; m/z (ES ⁺) [M+H] ⁺ = 231 .

Example 8: (2fl,4fl)-4-((S)-2-aminopropanamido)-2-(4-boronobutyl)pyrrol idine-2- carboxylic acid

Intermediate 27 Intermediate 28 Example 8

Intermediate 28: (2R,4R)-1-(tert-butoxycarbonvi)-4-((S)-2-(tert- butoxycarbonylamino)Dropanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)Dyrrolidine-2-carboxylic acid

Triethylamine (0.18 mL, 1 .3 mmol) and HATU (213 mg, 0.560 mmol) were added sequentially to a solution of Boc-Ala-OH (106 mg, 0.560 mmol) in DMF (2.4 mL) and the reaction stirred at room temperature for 30 min. (2F?,4/ ^:?)-4-amino-1 -(te/f-butoxycarbonyl)-2-(4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 27, 210 mg, 0.509 mmol) was added to the reaction mixture as a solution in DMF (2.4 mL). The reaction stirred at room temperature overnight. The crude reaction mixture was concentrated and directly purified by silica gel chromatography (hexanes/EtOAc) to afford the product

(Intermediate 28, 236 mg, 79% yield) as a mixture of rotamers. ¹ H NMR (300MHz, DMSO-de) d 0.65-0.72 (2H, m), 1 .1 1 - 1 .18 (18H, m), 1 .26-1 .37 (20H, m), 1 .63 - 1 .73 (1 H, m), 2.02 - 2.25 (2H, m), 3.09 - 3.20 (1 H, m), 3.59 - 3.72 (1 H, m), 3.83 - 3.94 (1 H, m), 4.18 - 4.29 (1 H, m), 6.80 (1 H, br s), 7.96 (1 H, s), 13.78 (1 H, br s); m/z (ES ⁺) [M+H] ⁺ = 584.

Example 8: (2R,4R)-4-((S)-2-aminoDroDanamido)-2-(4-boronobutyl)Dyrrolid ine-2-carboxylic acid

Trifluoroacetic acid (0.62 mL, 8.1 mmol) was added to a solution of (2R,4R)- -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)propanami do)-2-(4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 28, 236 mg, 0.404 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (2 mL) and 1 M aq HCI (2 ml_). Phenylboronic acid (99 mg, 0.81 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase

chromatography (RediSep Rf Gold® C18Aq, 0 to 10% acetonitrile in water) to afford (2R?,4R?)-4- ((S)-2-aminopropanamido)-2-(4-boronobutyl)pyrrolidine-2-carb oxylic acid (Example 8, 18 mg, 15% yield) as a white solid and mixture of rotamers. ¹ H NMR (500 MHz, D ₂0) d 0.69 (2H, dt), 1 .05 - 1 .14 (1 H, m), 1 .21 (3H, d), 1 .23-1 .35 (3H, m), 1 .65 (1 H, dt), 1 .91 -1 .96 (1 H, m), 2.17 (1 H, dd), 2.35 (1 H, dd), 3.26 (1 H, dd), 3.46 - 3.57 (2H, m), 4.29 - 4.34 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 302.

Example 9: (2/?,4/?)-4-((S)-2-amino-3-methylbutanamido)-2-(4-boronobuty l)pyrrolidine-2- carboxylic acid

Intermediate 27 Intermediate 29 Example 9

Intermediate 29: (2R,4R)-1-(tert-butoxycarbonyl)-4-((S)-2-(tert-butoxycarbony lamino)-3- methylbutanamido)-2-(4-(4,4,5,5Jetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)Dyrrolidine-2- carboxylic acid

Triethylamine (0.21 mL, 1 .5 mmol) and HATU (254 mg, 0.668 mmol) were added sequentially to a solution of Boc-Val-OH (145 mg, 0.668 mmol) in DMF (2.9 mL) and the reaction was stirred at room temperature for 30 min. (2P?,4/ ^:?)-4-amino-1 -(terf-butoxycarbonyl)- 2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid

(Intermediate 27, 250 mg, 0.606 mmol) was added to the reaction mixture as a solution in DMF (2.9 mL). The reaction stirred at room temperature overnight. The crude reaction mixture was concentrated and directly purified by silica gel chromatography (hexanes/EtOAc) to afford the product (Intermediate 29, 250 mg, 67% yield) as a mixture of rotamers. ¹H NMR (300MHz, DMSO-de) d 0.64 - 0.73 (2H, m), 0.73 - 0.85 (6H, m), 1 .13 - 1 .14 (1 H, m), 1 .17 (12H, s), 1 .22 - 1 .42 (22H, m), 1 .56 - 1 .75 (1 H, m), 1 .79 - 1 .97 (1 H, m), 2.00 - 2.26 (2H, m), 3.08 - 3.24 (1 H, m), 3.54 - 3.77 (2H, m), 4.12 - 4.36 (1 H, m), 6.58 (1 H, t), 7.96 - 8.03 (2H, m); m/z (ES ⁺) [M+H] ⁺ = 584. Example 9: (2R.4R)-4-((S)-2-amino-3-methylbutanamido)-2-(4-boronobutyl) DyrroHdine-2- carboxylic acid

Trifluoroacetic acid (0.63 mL, 8.2 mmol) was added to a solution (2f?,4/ ^:?)-1 -(tert- butoxycarbonyl)-4-((S)-2-(te/i-butoxycarbonylamino)-3-methyl butanamido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 29, 250 mg, 0.409 mmol) in DCM (4 mL). The resulting solution stirred at room temperature for 1 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (2 mL) and 1 M aq HCI (2 mL). Phenylboronic acid (99 mg, 0.81 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyopholized and purified by ion exchange chromatography (PoraPak Rxn CX 60 cc column). The desired product was eluted from the column using 2M ammonia/methanol. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 10% acetonitrile in water) to afford (2P?,4/ ^:?)-4-((S)-2-amino-3-methylbutanamido)-2-(4-boronobutyl )pyrrolidine-2-carboxylic acid (Example 9, 28 mg, 20% yield) as a white solid and a mixture of rotamers. ¹H NMR (300MHz, D ₂0) d 0.66 - 0.76 (2H, m), 0.85 (6H, dd), 1 .07 - 1 .43 (4H, m), 1 .55 - 1 .68 (1 H, m), 1 .77 - 1 .97 (2H, m), 2.13 - 2.33 (2H, m), 3.07 (1 H, d), 3.08 - 3.16 (1 H, m), 3.37 - 3.48 (1 H, m), 4.27 - 4.40 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 330.

Example 10: (2ff,4ff)-4-((fl)-2-amino-3-methylbutanamido)-2-(4-boronobut yl)pyrrolidine-2- carboxylic acid

Intermediate 25 Intermediate 30 Intermediate 31

Intermediate 32 Example 10 Intermediate 30: (2R,4R)-2-benzyl 1-tert-butyl 4-amine-2-(4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine- 1 ,2-dicarboxylate

Lindlar catalyst (5% wt, 0.275 g, 2.58 mmol) was added to a solution of (2fl,4fl)-2-benzyl 1 -tert- butyl 4-azido-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 25, 1 .56 g, 2.95 mmol) in THF (25 mL). The suspension was stirred under a hydrogen atmosphere (balloon, flask evacuated and back-filled with hydrogen x3) at room temperature for 8.5 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and the filtrate was concentrated to dryness. The crude material was purified by silica gel chromatography (1 to 15% MeOH in DCM) to afford (2fl,4fl)-2-benzyl 1 - tert-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 1 .01 g, 68% yield) as a gum and as a mixture of rotamers. ¹H NMR (500MHz, CD ₂CI ₂) d 0.74 (2H, q), 1 .20 - 1 .22 (14H, m), 1 .23 - 1 .29 (2H, m), 1 .32 (6H, s),

1 .37 - 1 .42 (5H, m), 1 .74 - 1 .83 (1 H, m), 1 .83 - 1 .93 (1 H, m), 2.1 1 - 2.19 (0.6H, m), 2.21 - 2.32 (1 4H, m), 3.19 (0.4H, dd), 3.28 (0.6H, dd), 3.44 - 3.51 (1 H, m), 3.63 (1 H, dd), 5.07 - 5.20 (2H, m), 7.28 - 7.34 (1 H, m), 7.34 - 7.41 (4H, m); m/z (ES ⁺) [M+H] ⁺ = 503.

Intermediate 31: (2R,4R)-2-benzyl 1-tert-butyl 4-((R)-2-(tert-butoxycarbonylamino)-3- methylbutanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborol an-2-yl)butyl)pyrrolidine-1,2-

A/,/V-Diisopropylethylamine (0.235 mL, 1 .34 mmol) was added slowly to a stirred solution of HATU (245 mg, 0.64 mmol) and Boc-D-Val-OH (1 17 mg, 0.54 mmol) in DMF (2 mL) at room temperature. The solution was stirred for 20 min and then a solution of (2F?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 270 mg, 0.54 mmol) in DMF (2 mL) was added. The reaction was stirred for 2.5 h, diluted with DCM (30 mL) and washed sequentially with water (3 x 25 mL) and saturated aqueous sodium chloride (30 mL). The organic layer was dried over MgSC , filtered and concentrated to dryness. The crude material was purified by silica gel

chromatography (5 to 65% EtOAc in hexanes) to afford (2fl,4fl)-2-benzyl 1 -tert-butyl 4-((F?)-2- (tert-butoxycarbonylamino)-3-methylbutanamido)-2-(4-(4,4,5,5 -tetramethyl-1 ,3,2-dioxaborolan- 2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 31 , 239 mg, 63% yield) as a colorless foam and as a mixture of rotamers. ¹ H NMR (500MHz, CD ₂CI ₂) d 0.74 - 0.81 (2H, m), 0.84 (3H, d), 0.87 - 0.94 (3H, m), 1 .24 (12H, s), 1 .26 - 1 .34 (2H, m), 1 .37 (5H, s), 1 .40 - 1 .43 (2H, m), 1 .45 (4H, s), 1 .46 (9H, s), 1 .78 - 1 .89 (1 H, m), 1 .95 - 2.07 (2H, m), 2.21 - 2.29 (0.6H, m), 2.31 - 2.46 (1 4H, m), 3.51 - 3.60 (1 .5H, m), 3.65 (0.5H, br d), 3.72 (1 H, br dd), 4.49 - 4.58 (1 H, m), 5.01 (1 H, br d), 5.19 - 5.29 (2H, m), 6.93 - 7.09 (1 H, m), 7.36 - 7.40 (1 H, m), 7.43 (4H, app d); m/z (ES ⁺) [M+H] ⁺ = 702.

Intermediate 32: (2R,4R)-1-(tert-butoxycarbonyl)-4-((R)-2-(tert-butoxycarbony lamino)-3- methylbutanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborol an-2-yl)butyl)pyrrolidine-2- carboxylic acid

Pd/C (10% wt, 25 mg, 0.23 mmol) was added to a solution of (2fl,4fl)-2-benzyl 1 -tert- butyl 4-((f?)-2-(te/f-butoxycarbonylamino)-3-methylbutanamido)-2-( 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 31 , 239 mg, 0.34 mmol) in EtOAc (4 mL). The suspension was stirred under a hydrogen atmosphere (balloon, flask evacuated and back-filled with hydrogen x3) at room temperature for 2 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and the filtrate was concentrated to dryness. The crude material was purified by silica gel chromatography (2 to 15% MeOH in DCM) to afford (2P?,4/ ^:?)-1 -(te/f-butoxycarbonyl)-4-((/ ^:?)-2-(fe/f-butoxycarbonylamino)-3- methylbutanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 32, 196 mg, 94% yield) as a white solid and as a mixture of rotamers. ¹ H NMR (500MHz, DMSO-de) d 0.63 - 0.71 (2H, m), 0.75 - 0.82 (6H, m), 1 .15 (12H, s), 1 .21 - 1 .30 (2H, m), 1 .32 (6H, s), 1 .36 (13H, br s), 1 .61 - 1 .72 (1 H, m), 1 .81 - 1 .90 (1 H, m),

1 .92 - 2.05 (2H, m), 2.05 - 2.13 (0.6H, m), 2.13 - 2.28 (1 .4H, m), 3.03 - 3.14 (1 H, m), 3.62 (0.6H, t), 3.66 (1 .4H, t), 4.18 - 4.29 (1 H, m), 6.59 (1 H, d), 7.99 (1 H, br s), 12.48 (0.4H, br s), 12.65 (0.6H, br s); m/z (ES ⁺) [M+H] ⁺ = 612.

Example 10: (2R,4R)-4-((R)-2-amino-3-methylbutanamido)-2-(4-boronobutyl) pyrrolidine-2- carboxylic acid

Trifluoroacetic acid (0.37 mL, 4.8 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((/ ^:?)-2-(fert-butoxycarbonylamino)-3-methylbutanamido)-2- (4- (4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 32, 195 mg, 0.32 mmol) in DCM (2 mL). The reaction solution was stirred at room temperature for 22 h and was then concentrated under reduced pressure. The crude amino acid was dissolved in 1 M HCI aq (2 mL) and Et2<D (2 mL). Phenylboronic acid (1 17 mg, 0.96 mmol) was added and the clear biphasic solution stirred at room temperature for 5 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL), and the layers were separated. The aqueous layer was washed with Et ₂0 and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and purified by ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 0 to 80% acetonitrile in water) to afford (2fl,4fl)-4-((fl)-2-amino-3- methylbutanamido)-2-(4-boronobutyl)pyrrolidine-2-carboxylic acid (Example 10, 46 mg, 44% yield) as a white solid. ¹H NMR (500MHz, D ₂0) d 0.73 - 0.80 (2H, m), 0.90 (6H, app t), 1 .13 - 1 .25 (1 H, m), 1 .26 - 1 .35 (1 H, m), 1 .40 (2H, quin), 1 .68 - 1 .80 (1 H, m), 1 .85 - 1 .96 (1 H, m), 2.00 (1 H, td), 2.29 (1 H, dd), 2.37 - 2.45 (1 H, m), 3.18 (1 H, d), 3.28 (1 H, dd), 3.59 (1 H, dd), 4.36 - 4.49 (1 H, m) ; m/z (ES ⁺) [M+H] ⁺ = 330. Example 11 : (2ff.4ff)-4-((S)-2-amino-3.3-dimethylbutanamido)-2-(4- boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 30 Intermediate 33

Intermediate 34 Example 11

Intermediate 33: (2R.4R)-2-benzv! 1-tert-butyl 4-((S)-2-(tert-butoxycarbonylamino)-3.3- dimethylbutanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxabor olan-2-yl)butyl)Dyrrolidine-1 ,2- dicarboxylate

A/,/V-Diisopropylethylamine (0.165 ml_, 0.95 mmol) was added slowly to a stirred solution of HATU (158 mg, 0.42 mmol) and Boc-Tle-OH (92 mg, 0.40 mmol) in DMF (1 .5 mL) at room temperature. The solution was stirred for 15 min and then a solution of (2F?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 190 mg, 0.38 mmol) in DMF (1 .5 mL) was added. The reaction was stirred for 3 h, diluted with EtOAc (30 mL) and washed sequentially with water (3 x 25 mL), saturated aqueous NaHCC> ₃ (30 mL) and saturated aqueous sodium chloride (30 mL). The organic layer was dried over MgSC , filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (5 to 65% EtOAc in hexanes) to afford (2R,4H)-2.- benzyl 1 -terf-butyl 4-((S)-2-(terf-butoxycarbonylamino)-3,3-dimethylbutanamido)- 2-(4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 33, 261 mg, 96% yield) as a white solid and as a mixture of rotamers. ¹ H NMR (500MHz, DMSO-de) d 0.69 (2H, q), 0.87 (9H, s), 1 .17 (12H, s), 1 .26 (5H, s), 1 .29 - 1 .32 (1 H, m), 1 .34 (5H, s), 1 .38 (9H, s), 1 .72 - 1 .85 (1 H, m), 1 .90 - 2.08 (2H, m), 2.06 - 2.18 (1 H, m), 2.22 - 2.35 (2H, m), 3.1 1 - 3.22 (1 H, m), 3.68 - 3.81 (2H, m), 4.23 - 4.37 (1 H, m), 5.06 - 5.19 (2H, m), 6.40 (1 H, t), 7.31 - 7.40 (5H, m), 8.1 1 (1 H, d); m/z (ES ⁺) [M+Na] ⁺ = 738.

Intermediate 34: (2R,4R)-1-(tert-butoxycarbonyl)-4-((S)-2-(tert-butoxycarbony lamino)-3,3- dimethylbutanamido)-2-(4-(4, 4, 5, 5-tetramethyl- 1 , 3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid

Pd/C (10% wt, 25 mg, 0.23 mmol) was added to a solution of (2fl,4fl)-2-benzyl 1 -tert- butyl 4-((S)-2-(terf-butoxycarbonylamino)-3,3-dimethylbutanamido)- 2-(4-(4, 4, 5, 5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 33, 260 mg, 0.36 mmol) in EtOAc (4 mL). The suspension was stirred under a hydrogen atmosphere (balloon, flask evacuated and back-filled with hydrogen x3) at room temperature for 15 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and the filtrate was concentrated to dryness. The crude material was purified by silica gel chromatography (2 to 10% MeOH in DCM) to afford (2P?,4/ ^:?)-1 -(te/f-butoxycarbonyl)-4-((S)-2-(te/f- butoxycarbonylamino)-3,3-dimethylbutanamido)-2-(4-(4,4,5,5-t etramethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 34, 207 mg, 91 % yield) as a white solid and as a mixture of rotamers. ¹H NMR (500MHz, DMSO-de) d 0.63 - 0.72 (2H, m), 0.86 (9H, s), 1 .09 - 1 .20 (14H, m), 1 .21 - 1 .30 (2H, m), 1 .33 (5H, s), 1 .35 - 1 .38 (13H, m), 1 .61 - 1 .73 (1 H, m), 1 .89 - 2.1 1 (2H, m), 2.14 - 2.27 (1 H, m), 3.06 - 3.14 (1 H, m), 3.59 - 3.72 (1 H, m), 3.72 - 3.80 (1 H, m), 4.20 - 4.30 (1 H, m), 6.35 (1 H, d), 8.08 (1 H, br s), 12.47 (0.4H, br s), 12.63 (0.6H, br s); m/z (ES ⁺) [M+H] ⁺ = 626.

Example 11: (2R,4R)-4-((S)-2-amino-3,3-dimethylbutanamido)-2-(4-boronobu tyl)pyrrolidine-2- carboxylic acid

Trifluoroacetic acid (0.38 mL, 4.9 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-3 ,3-dimethylbutanamido)-2- (4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 34, 206 mg, 0.33 mmol) in DCM (2 mL). The reaction was stirred at room temperature for 15 h and was then concentrated under reduced pressure. The crude amino acid was dissolved in 1 M HCI aq (4 mL) and Et ₂0 (4 mL). Phenylboronic acid (120 mg, 0.99 mmol) was added and the clear biphasic solution stirred at room temperature for 3 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL), and the layers were separated. The aqueous layer was washed with Et ₂0 and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and purified by ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 2 to 50% acetonitrile in water) to afford (2F?,4/ ^:?)-4-((S)-2-amino-3,3-dimethylbutanamido)- 2-(4-boronobutyl)pyrrolidine-2-carboxylic acid (Example 11 , 40 mg, 35% yield) as a white solid. ¹H NMR (500MHz, D ₂0) d 0.72 (2H, td), 0.89 (9H, s), 1 .10 - 1 .21 (1 H, m), 1 .22 - 1 .30 (1 H, m),

1 .35 (2H, quin), 1 .64 - 1 .75 (1 H, m), 1 .90 - 2.02 (1 H, m), 2.22 - 2.34 (2H, m), 3.04 (1 H, s), 3.22 (1 H, dd), 3.56 (1 H, dd), 4.41 (1 H, quin); m/z (ES ⁺) [M+H] ⁺ = 344.

Example 12: (2ff.4ff)-2-(4-boronobutyl -((S)-pyrrolidine-2-carboxamido)pyrrolidine-2- carboxylic acid

Intermediate 30 Intermediate 35

Intermediate 36 Example 12

Intermediate 35: (2R.4R)-2-benzv! 1 -tert-butyl 4-((S)-1 -(tert-butoxycarbonyl)Dyrrolidine-2- carboxamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)Dyrrolidine-1 ,2- dicarboxylate

A/,/V-Diisopropylethylamine (0.182 mL, 1 .04 mmol) was added slowly to a stirred solution of HATU (175 mg, 0.46 mmol) and Boc-Pro-OH (94 mg, 0.44 mmol) in DMF (1 .5 mL) at room temperature. The solution was stirred for 20 min and then a solution of (2P?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 210 mg, 0.42 mmol) in DMF (1 .5 mL) was added. The reaction was stirred for 2 h, diluted with EtOAc (30 ml.) and washed sequentially with water (3 x 25 mL), saturated aqueous NaHCC>3 and saturated aqueous sodium chloride (30 mL). The organic layer was dried over MgSC , filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (5 to 100% EtOAc in hexanes) to afford (2fl,4fl)-2-benzyl 1 -terf-butyl 4-((S)-1 -(terf-butoxycarbonyl)pyrrolidine-2-carboxamido)-2-(4-(4,4,5 ,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 35, 249 mg, 85% yield) as a colorless film and as a mixture of rotamers. ¹H NMR (500MHz, CD2CI2) d 0.68 - 0.79 (2H, m), 1 .20 (12H, s), 1 .31 (5H, s), 1 .36 - 1 .48 (16H, m), 1 .74 - 1 .87 (3H, m), 1 .89 - 2.10 (3H, m), 2.13 - 2.46 (2H, m), 3.27 - 3.40 (1 H, m), 3.44 (2H, br s), 3.50 - 3.64 (2H, m), 3.78 - 4.05 (1 H, m), 4.49 (1 H, br s), 5.10 - 5.27 (2H, m), 7.10 (1 H, br s), 7.30 - 7.42 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 700.

Pd/C (10% wt, 25 mg, 0.23 mmol) was added to a solution of (2P?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-((S)-1 -(terf-butoxycarbonyl)pyrrolidine-2-carboxamido)-2-(4-(4,4,5 ,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 35, 249 mg, 0.36 mmol) in EtOAc (4 mL). The suspension was stirred under a hydrogen atmosphere (balloon, flask evacuated and back-filled with hydrogen x3) at room temperature for 5 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and the filtrate was concentrated under reduced pressure to afford (2P?,4/ ^:?)-1 -(te/f-butoxycarbonyl)-4-((S)-1 -(fe/f- butoxycarbonyl)pyrrolidine-2-carboxamido)-2-(4-(4,4,5,5-tetr amethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 36, 207 mg, 87% yield) as a colorless film and as a mixture of rotamers which was used without further purification. ¹H NMR (500MHz, CD2CI2) d 0.66 - 0.83 (2H, m), 1 .21 (12H, s), 1 .34 - 1 .51 (21 H, m), 1 .63 - 1 .97 (4H, m), 2.06 (1 H, m), 2.1 1 - 2.29 (2H, m), 2.33 - 2.67 (1 H, m), 3.24 - 3.52 (3H, m), 3.53 - 3.67 (1 H, m), 4.15 - 4.34 (1 H, m), 4.47 - 4.74 (1 H, m), 6.76 - 7.23 (1 H, m), 7.17 - 7.69 (1 H, m), 9.74 (1 H, br s); m/z (ES ⁺) [M+H] ⁺ = 610.

Trifluoroacetic acid (0.518 mL, 6.73 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((S)-1 -(te/f-butoxycarbonyl)pyrrolidine-2-carboxamido)-2-(4- (4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 36, 205 mg, 0.34 mmol) in DCM (2 mL). The reaction was stirred at room temperature for 2 h and was then concentrated under reduced pressure. The crude amino acid was dissolved in 1 M HCI aq (4 mL) and Et ₂0 (4 mL). Phenylboronic acid (123 mg, 1 .01 mmol) was added and the clear biphasic solution stirred at room temperature for 2 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL), and the layers were separated. The aqueous layer was washed with

Et ₂0 and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and purified by ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 0 to 50% acetonitrile in water) to afford (2P?,4/ ^:?)-2-(4-boronobutyl)-4-((S)-pyrrolidine-2- carboxamido)pyrrolidine-2-carboxylic acid (Example 12, 89 mg, 81 % yield) as a white solid. ¹ H NMR (500MHz, D ₂0) d 0.70 - 0.79 (2H, m), 1 .1 1 - 1 .23 (1 H, m), 1 .24 - 1 .33 (1 H, m), 1 .34 - 1 .42 (2H, m), 1 .60 - 1 .71 (1 H, m), 1 .81 - 1 .91 (3H, m), 1 .91 - 1 .99 (1 H, m), 2.18 (1 H, dd), 2.22 - 2.29 (1 H, m), 2.40 (1 H, dd), 3.08 - 3.16 (1 H, m), 3.16 - 3.22 (1 H, m), 3.25 (1 H, dd), 3.48 (1 H, dd), 3.99 (1 H, dd), 4.29 - 4.38 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 328.

Example 13: (2ff.4ff)-4-(2-aminoacetamido)-2-(4-boronobutyl)pyrrolidine- 2-carboxylic acid

Intermediate 30 Intermediate 37

Intermediate 38 Example 13

Intermediate 37: (2R,4R)-2-benzyl 1-tert-butyl 4-(2-(tert-butoxycarbonylamino)acetamido)-2-(4- ( 4,4.5.5-tetramethyl-1,3.2-dioxaborolan-2-yl)butyl)Dyrrolidin e-1,2-dicarboxylate

A/,/V-Diisopropylethylamine (0.182 mL, 1 .04 mmol) was added slowly to a stirred solution of HATU (175 mg, 0.46 mmol) and Boc-Gly-OH (77 mg, 0.44 mmol) in DMF (1 .5 mL) at room temperature. The solution was stirred for 20 min and then a solution of (2F?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 210 mg, 0.42 mmol) in DMF (1 .5 mL) was added. The reaction solution was stirred for 2 h, diluted with EtOAc (30 mL) and washed sequentially with water (3 x 25 mL), saturated aqueous NaHCC>3 and saturated aqueous sodium chloride (30 mL). The organic layer was dried over MgSC , filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (10 to 100% EtOAc in hexanes) to afford (2R,AH)-2.- benzyl 1 -terf-butyl 4-(2-(terf-butoxycarbonylamino)acetamido)-2-(4-(4,4,5,5-tetr amethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 37, 235 mg, 85% yield) as a colorless film and as a mixture of rotamers. ¹H NMR (500MHz, CD2CI2) d 0.70 - 0.78 (2H, m),

1 .12 - 1 .18 (1 H, m), 1 .20 (12H, s), 1 .25 - 1 .30 (1 H, m), 1 .33 (5H, s), 1 .43 (15H, s), 1 .74 - 1 .86 (1 H, m), 1 .95 (0.5H, br d), 2.03 (0.5H, br d), 2.15 - 2.26 (1 H, m), 2.26 - 2.37 (1 H, m), 2.40 (1 H, dd), 3.43 - 3.57 (3H, m), 3.57 - 3.64 (1 H, m), 4.50 (1 H, br s), 5.03 (0.5H, br s), 5.10 (0.5H, br s),

5.13 - 5.25 (1 H, m), 7.01 (1 H, dd), 7.32 - 7.37 (1 H, m), 7.36 - 7.41 (4H, m); m/z (ES ⁺) [M+H] ⁺ = 660.

Intermediate 38: (2R,4R)-1-(tert-butoxYcarbonyl)-4-(2-(tert-butoxYcarbonylami no)acetamido)-2-

-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-vl)butyl)pyrro lidine-2-carboxylic acid

Pd/C (10% wt, 25 mg, 0.23 mmol) was added to a solution of (2fl,4fl)-2-benzyl 1 -tert- butyl 4-(2-(te/f-butoxycarbonylamino)acetamido)-2-(4-(4,4,5,5-tetr amethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 37, 233 mg, 0.35 mmol) in EtOAc (4 mL). The suspension was stirred under a hydrogen atmosphere (balloon, flask evacuated and back filled with hydrogen x3) at room temperature for 6 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and the filtrate was concentrated to dryness to afford (2R?,4R?)-1 -(tert-butoxycarbonyl)-4-(2-(fert-butoxycarbonylamino)acetam ido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 38, 176 mg, 87% yield) as a colorless film and as a mixture of rotamers which was used without further purification. ¹H NMR (500MHz, CD2CI2) d 0.65 - 0.80 (2H, m), 1 .1 1 - 1 .18 (1 H, m), 1 .18 - 1 .23 (12H, m), 1 .25 - 1 .32 (1 H, m), 1 .36 - 1 .45 (13H, m), 1 .47 (7H, s), 1 .70 - 1 .83 (0.4H, m), 1 .84 - 1 .95 (0.6H, m), 2.06 - 2.27 (2H, m), 2.33 - 2.47 (0.4H, m), 2.63 (0.6H, br d), 3.44 - 3.62 (2H, m), 3.63 - 3.82 (2H, m), 4.28 (0.6H, br s), 4.36 - 4.60 (0.4H, m), 5.26 (0.6H, br s), 5.58 - 5.90 (0.3H, m), 6.83 (0.6H, br s), 6.97 - 7.44 (0.4H, m); m/z (ES ⁺) [M+H] ⁺ = 570. Example 13: (2R,4R)-4-(2-aminoacetamido)-2-(4-boronobutyl)Dyrrolidine-2- carboxylic acid

Trifluoroacetic acid (0.476 ml_, 6.18 mmol) was added dropwise to a stirred solution of (2f?,4/ ^:?)-1 -(fert-butoxycarbonyl)-4-(2-(fert-butoxycarbonylamino)acetam ido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 38, 176 mg, 0.31 mmol) in DCM (2 mL). The reaction solution was stirred at room temperature for 2 h and was then concentrated under reduced pressure. The crude amino acid was dissolved in 1 M HCI aq (4 mL) and Et ₂0 (4 mL). Phenylboronic acid (1 13 mg, 0.93 mmol) was added and the clear biphasic solution stirred at room temperature for 2 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL), and the layers were separated. The aqueous layer was washed with Et ₂0 and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and purified by ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 0 to 40% acetonitrile in water) to afford (2fl,4fl)-4-(2-aminoacetamido)-2-(4- boronobutyl)pyrrolidine-2-carboxylic acid (Example 13, 62 mg, 70% yield) as a white solid. ¹ H NMR (500MHz, D ₂0) d 0.76 (2H, td), 1 .15 - 1 .25 (1 H, m), 1 .26 - 1 .34 (1 H, m), 1 .36 - 1 .46 (2H, m), 1 .69 - 1 .79 (1 H, m), 2.00 (1 H, ddd), 2.27 (1 H, dd), 2.44 (1 H, dd), 3.33 (1 H, dd), 3.42 (2H, s), 3.59 (1 H, dd), 4.36 - 4.45 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 288.

Example 14: (2ff,4ff)-4-((S)-2-aminobutanamido)-2-(4-boronobutyl)pyrroli dine-2- carboxylic acid

Intermediate 30 Intermediate 39

Intermediate 40 Example 14

Intermediate 39: (2R.4R)-2-benzv! 1-tert-butyl 4-((S)-2-(tert-butoxycarbonylamino)butanamido)-

2-(4-(4,4.5,5-tetramethyl- 1,3,2-dioxaborolan-2-yl)butyl)Dyrrolidine- 1 ,2-dicarboxylate HATU (804 mg, 2.1 1 mmol) was added to a solution of Boc-Abu-OH (430 mg, 2.1 1 mmol) in DMF (4 mL) and the reaction stirred at room temperature for 10 min. (2F?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 885 mg, 1 .76 mmol) was added to the reaction mixture as a solution in DMF (3 mL). A/,/V-Diisopropylethylamine (0.75 mL, 4.3 mmol) was added and the reaction stirred at room temperature overnight. The reaction was then diluted with water (15 mL) and Et ₂0 (10 mL). The layers were separated and the aqueous layer was extracted with Et ₂0 (2 x 10 mL). The combined organics were washed with 5% aqueous lithium chloride (10 mL), dried over MgSC , filtered, and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (2fl,4fl)-2-benzyl 1 -terf-butyl 4-((S)-2- (terf-butoxycarbonylamino)butanamido)-2-(4-(4,4,5,5-tetramet hyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 39, 766 mg, 63% yield) as a white solid. ¹ H NMR (500MHz, CDCIs) d 0.70 - 0.84 (5H, m), 1 .09 - 1 .19 (1 H, m), 1 .21 (12H, s), 1 .36 - 1 .46 (18H, m), 1 .46 - 1 .97 (7H, m), 2.12 - 2.45 (2H, m), 3.45 - 3.60 (1 H, m), 3.68 (1 H, br d), 3.78 - 3.94 (1 H, m), 4.42 - 4.64 (1 H, m), 4.73 - 5.03 (1 H, m), 5.07 - 5.33 (2H, m), 7.09 (1 H, br d), 7.28 - 7.40 (5H, m). m/z (ES ⁺) [M+H] ⁺ = 688.

Intermediate 40: (2R,4R)-1-(tert-butoxycarbonyl)-4-((S)-2-(tert - butoxycarbonylamino)butanamido)-2-(4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2- yl)butyl)pyrrolidine-2-carboxylic acid

(2F?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-((S)-2-(terf-butoxycarbonylamino)butanamido)-2-(4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 39, 766 mg, 1 .1 1 mmol) was dissolved in EtOAc (1 1 mL) and treated with Pd/C (10 wt%, 1 19 mg, 0.1 1 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with EtOAc and methanol. The filtrate was concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (2R,4R)- -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)butanamid o)-2-(4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 40, 470 mg, 70% yield) as a white foam. ¹ H NMR (500MHz, CDCI ₃) d 0.67 - 0.82 (2H, m), 0.89 (3H, br t), 1 .1 1 - 1 .28 (14H, m), 1 .37 - 1 .51 (20H, m), 1 .53 - 1 .65 (1 H, m), 1 .65 - 1 .94 (2H, m), 2.02 - 2.12 (1 H, m),

2.13 - 2.31 (1 H, m), 2.70 (1 H, br d), 3.40 - 3.62 (2H, m), 3.88 - 4.04 (1 H, m), 4.26 (1 H, br s),

5.01 (1 H, br s), 6.73 (1 H, br d); m/z (ES ⁺) [M+H] ⁺ = 598. Example 14: (2R,4R)-4-((S)-2-aminobutanamido)-2-(4-boronobutyl)Dyrrolidi ne-2-carboxylic acid Phenylboronic acid (192 mg, 1 .57 mmol) was added to a solution of (2R,4R)- -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)butanamid o)-2-(4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 40, 470 mg, 0.79 mmol) in 2 M HCI aq (5 mL) and the reaction stirred at room temperature for 16 h. The reaction was diluted with water (10 mL) and Et ₂0 (10 mL) and the layers were separated. The aqueous layer was washed with Et ₂0 (3 x 5 mL) and then lyophilized to a foam. The organic layer was concentrated under vacuum. The resulting residue was diluted in 4 M HCI in dioxane (4 mL, 16 mmol) and the resulting solution stirred at room temperature for 20 h. The reaction was diluted with water (10 mL) and Et ₂0 (10 mL) and the layers were separated. The aqueous layer was washed with Et2<D (3 x 5 mL) and then lyophilized to a foam. The foams from these two operations were combined and the resulting crude amino acid was purified by ion exchange chromatography (Silicycle SiliaSep SPE-R51230B-20X 5g column). The desired product was eluted from the column using a 5% ammonia in MeOH solution. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 25% acetonitrile in water) to afford (2P?,4/ ^:?)-4-((S)-2-aminobutanamido)-2-(4-boronobutyl)pyrrolid ine- 2-carboxylic acid (Example 14, 96 mg, 39% yield) as a white solid. ¹H NMR (500MHz, D ₂0) d 0.55 - 0.82 (2H, m), 0.88 (3H, t), 1 .12 - 1 .48 (4H, m), 1 .56 - 1 .81 (3H, m), 1 .86 - 2.10 (1 H, m),

2.12 - 2.53 (2H, m), 3.15 - 3.37 (1 H, m), 3.41 - 3.53 (1 H, m), 3.62 (1 H, dd), 4.35 - 4.52 (1 H, m); m/z (ES ⁺) [M-H ₂0+H] ⁺ = 298.

Example 15: (2ff.4ff)-4-((2S.3S)-2-amino-3-methylpentanamido)-2-(4- boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 30 Intermediate 41

Intermediate 42 Example 15 mol) in DMF (4 ml.) and the reaction stirred at room temperature for 10 min. (2F?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 30, 885 mg, 1 .76 mmol) was added to the reaction mixture as a solution in DMF (3 mL). A/,/V-Diisopropylethylamine (0.75 mL, 4.3 mmol) was added and the reaction stirred at room temperature overnight. The reaction was then diluted with water (15 mL) and Et ₂0 (10 mL). The layers were separated and the aqueous layer was extracted with Et ₂0 (2 x 10 mL). The combined organic layers were washed with 5% aqueous lithium chloride (10 mL), dried over MgSC , filtered, and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (2fl,4fl)-2-benzyl 1 -tert-butyl 4- ((2S,3S)-2-(tert-butoxycarbonylamino)-3-methylpentanamido)-2 -(4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 41 , 707 mg, 56% yield) as a white solid. ¹H NMR (500MHz, CDCI ₃) d 0.79 (2H, br t), 0.83 - 1 .05 (8H, m), 1 .12 - 1 .21 (1 H, m), 1 .24 (12H, s), 1 .32 - 1 .61 (20H, m), 1 .62 - 2.02 (4H, m), 2.18 - 2.55 (2H, m), 3.49 - 3.65 (1 H, m), 3.65 - 3.78 (1 H, m), 3.90 (1 H, br s), 4.53 - 4.72 (1 H, m), 4.95 (1 H, br s), 5.07 - 5.43 (2H, m),

7.16 (1 H, br d), 7.30 - 7.44 (5H, m). m/z (ES ⁺) [M+H] ⁺ = 716.

Intermediate 42: (2R,4R)-1-(tert-butcxycarbcnyl)-4-((2S,3S)-2-(tert-butcxycar bcnylaminc)-3- methylpentanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaboro lan-2-yl)butyl)pyrrolidine-2- carboxylic acid

(2F?,4/ ^:?)-2-benzyl 1 -tert-butyl 4-((2S,3S)-2-(tert-butoxycarbonylamino)-3- methylpentanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 41 , 707 mg, 0.99 mmol) was dissolved in EtOAc (10 mL) and treated with Pd/C (10 wt%, 105 mg, 0.10 mmol). The flask was equipped with a balloon of FL and the suspension stirred overnight at room temperature. The reaction mixture was filtered through diatomaceous earth and rinsed with EtOAc and methanol. The filtrate was

concentrated to dryness to afford (2F?,4/ ^:?)-1 -(tert-butoxycarbonyl)-4-((2S,3S)-2-(tert- butoxycarbonylamino)-3-methylpentanamido)-2-(4-(4,4,5,5-tetr amethyl-1 ,3,2-dioxaborolan-2- yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 42, 603 mg, 98% yield) which was used without further purification. ¹H NMR (500MHz, CDCI ₃) d 0.68 - 0.80 (2H, m), 0.83 - 0.93 (6H, m), 1 .05 - 1 .14 (1 H, m), 1 .21 (12H, s), 1 .28 - 1 .36 (1 H, m), 1 .37 - 1 .55 (22H, m), 1 .71 - 1 .96 (2H, m), 2.18 - 2.31 (1 H, m), 2.72 (1 H, br d), 3.42 - 3.51 (2H, m), 3.52 - 3.63 (1 H, m), 3.86 - 4.04 (1 H, m), 4.16 - 4.34 (1 H, m), 4.98 (1 H, br d), 6.69 (1 H, br s); m/z (ES ⁺) [M+H] ⁺ = 626.

Example 15: (2R,4R)-4-((2S,3S)-2-amino-3-methylpentanamido)-2-(4-boronob utyl)pyrrolidine-2- carboxylic acid

Trifluoroacetic acid (1 .10 ml_, 14.3 mmol) was added to a solution of (2R,4H)-^ -(tert- butoxycarbonyl)-4-((2S,3S)-2-(terf-butoxycarbonylamino)-3-me thylpentanamido)-2-(4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 42, 603 mg, 0.96 mmol) in DCM (6 mL). The resulting solution stirred at room temperature for 16 h and was then concentrated under vacuum. The crude amino acid was dissolved in Et ₂0 (10 mL) and reconcentrated under vacuum. This redissolution and reconcentration process was repeated twice more. The crude amino acid was then dissolved in Et ₂0 (6 mL) and 1 M HCI aq (6 mL). Phenylboronic acid (235 mg, 1 .93 mmol) was added and the clear biphasic solution stirred at room temperature for 3 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (Silicycle SiliaSep SPE-R51230B-20X 5g column). The desired product was eluted from the column using a 5% ammonia in MeOH solution. The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18Aq, 0 to 25% acetonitrile in water) to afford (2P?,4/ ^:?)-4-((2S,3S)-2-amino-3-methylpentanamido)-2-(4-borono butyl)pyrrolidine-2- carboxylic acid (Example 15, 136 mg, 41 % yield) as a white solid. ¹ H NMR (500MHz, D ₂0) d 0.55 - 0.81 (2H, m), 0.89 (6H, dd), 1 .07 - 1 .52 (6H, m), 1 .63 - 1 .83 (2H, m), 1 .86 - 2.09 (1 H, m), 2.13 - 2.51 (2H, m), 3.1 1 - 3.40 (2H, m), 3.45 - 3.67 (1 H, m), 4.39 - 4.54 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 344.

Example 16: (2ff,4ff)-4-((S)-2-amino-4-methylpentanamido)-2-(4-boronobut yl)pyrrolidine- 2-carboxylic acid

Intermediate 30 Intermediate 43

Intermediate 44 Example 16

Intermediate 43: (2R.4R)-2-benzv! 1-tert-butyl 4-((S)-2-(tert-butoxycarbonylamino)-4- methylDentanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaboro lan-2-yl)butyl)Dyrrolidine-1,2- dicarboxylate

HATU (247 mg, 0.65 mmol) was added to a solution of Boc-Leu-OH (125 mg, 0.54 mmol) in DCM (2 mL) and the reaction stirred at room temperature for 10 min. (2f?,4f?)-2- benzyl 1 -terf-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-

1 .2-dicarboxylate (Intermediate 30, 272 mg, 0.54 mmol) was added to the reaction mixture as a solution in DCM (2 mL). A/,/V-Diisopropylethylamine (0.19 mL, 1 .1 mmol) was added and the reaction stirred at room temperature for 1 h. The reaction was then diluted with DCM (20 mL) and washed sequentially with water (25 mL) and saturated aqueous sodium chloride (30 mL). The organic layer was dried over MgSC , filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (2fl,4fl)-2-benzyl 1 -terf-butyl 4-((S)-2-(terf-butoxycarbonylamino)-4-methylpentanamido)-2-( 4-(4,4,5,5-tetramethyl-

1 .3.2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 43, 210 mg, 54% yield) as a colorless foam and as a mixture of rotamers. ¹H NMR (500MHz, CDCL) d 0.77 (2H, t), 0.91 (6H, d), 1 .06 - 1 .19 (1 H, m), 1 .19 - 1 .24 (12H, m), 1 .31 - 1 .51 (20H, m), 1 .50 - 1 .63 (2H, m), 1 .73 - 2.02 (2H, m), 2.17 - 2.55 (2H, m), 3.35 - 3.75 (2H, m), 3.84 - 4.06 (1 H, m), 4.35 - 4.75 (2H, m), 5.00 - 5.46 (2H, m), 7.08 - 7.22 (1 H, m), 7.28 - 7.42 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 716. Intermediate 44: (2R,4R)-1-tert-butoxycarbonyl)-4-((S)-2-(tert-butoxycarbonyl amino)-4- methylpentanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaboro lan-2-yl)butyl)pyrrolidine-2- carboxylic acid

(2f?,4/ ^:?)-2-benzyl 1 -tert- butyl 4-((S)-2-(terf-butoxycarbonylamino)-4-methylpentanamido)- 2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate

(Intermediate 43, 201 mg, 0.28 mmol) was dissolved in EtOAc (4 mL) and treated with Pd/C (10 wt%, 100 mg, 0.094 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 2 h. The reaction mixture was filtered through diatomaceous earth and rinsed with EtOAc and methanol. The filtrate was concentrated to dryness to afford (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((S)-2-(fert-butoxycarbonylamino)-4 - methylpentanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2- carboxylic acid (Intermediate 44, 170 mg, 97% yield) as a white solid and as a mixture of rotamers. ¹ H NMR (500MHz, CDCI ₃) d 0.78 (2H, t), 0.93 (6H, d), 1 .15 - 1 .25 (12H, m), 1 .25 - 1 .31 (2H, m), 1 .39 - 1 .51 (19H, m), 1 .55 - 1 .72 (2H, m), 1 .73 - 1 .89 (1 H, m), 2.01 - 2.1 1 (1 H, m), 2.18 - 2.36 (1 H, m), 2.47 - 2.83 (1 H, m), 3.37 - 3.74 (2H, m), 3.96 - 4.10 (1 H, m), 4.17 - 4.32 (1 H, m), 4.82 - 5.31 (1 H, m), 6.62 - 7.12 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 626.

Example 16: (2R,4R)-4-((S)-2-aminc-4-methylpentanamidc)-2-(4-bcrcncbutyl )pyrrclidine-2- carboxylic acid

Trifluoroacetic acid (1 .00 mL, 13.0 mmol) was added to a solution of (2R,4H)-^ -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-4-methyl pentanamido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 44, 170 mg, 0.27 mmol) in DCM (2 mL). The resulting solution stirred at room temperature for 2 h and was then concentrated under vacuum. The crude amino acid was then dissolved in Et ₂0 (5 mL) and water (4 mL). Phenylboronic acid (66 mg, 0.54 mmol) was added and the clear biphasic solution stirred at room temperature for 2 h. The reaction mixture was diluted with water (5 mL) and Et ₂0 (20 mL) and the layers were separated. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 2g column) to afford (2R,4H)-4- ((S)-2-amino-4-methylpentanamido)-2-(4-boronobutyl)pyrrolidi ne-2-carboxylic acid (Example 16, 88 mg, 94% yield) as a white solid. ¹ H NMR (500MHz, D ₂0) d 0.46 - 0.68 (2H, m), 0.73 - 0.82 (6H, m), 1 .03 - 1 .13 (1 H, m), 1 .13 - 1 .23 (1 H, m), 1 .23 - 1 .42 (4H, m), 1 .42 - 1 .52 (1 H, m), 1 .54 - 1 .66 (1 H, m), 1 .76 - 1 .93 (1 H, m), 2.07 - 2.19 (1 H, m), 2.29 (1 H, dd), 3.13 (1 H, q), 3.34 (1 H, t), 3.48 (1 H, q), 4.23 - 4.40 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 344. Example 17: (2ff,4ff)-4-((S)-2-amino-3-hvdroxypropanamido)-2-(4- boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 30 Intermediate 45

Intermediate 46 Example 17

Intermediate 45: (2R.4R)-2-benzv! 1-tert-butyl 4-((S)-2-(tert-butoxycarbonylamino)-3- hydroxyDroDanamido)-2-{4-{4,4,5,5Jetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)Dyrrolidine-1 ,2- dicarboxylate

A/,/V-Diisopropylethylamine (0.108 ml_, 0.62 mmol) was added to a stirred solution of COMU (292 mg, 0.68 mmol), (2f?,4f?)-2-benzyl 1 -terf-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 30, 31 1 mg, 0.62 mmol) and Boc-Ser-OH (133 mg, 0.65 mmol) in DMF (5 mL) at room temperature. The reaction was stirred for 3 h, diluted with water (80 mL) and EtOAc (15 mL). The phases were separated and the aqueous phase was further diluted with saturated aqueous NaHCC>3 then extracted with EtOAc (2 x 20 mL). The combined organics were washed with saturated aqueous NaCI (2 x 10 mL), dried over MgS04, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford (2fl,4fl)-2-benzyl 1 -terf-butyl 4-((S)-2- (terf-butoxycarbonylamino)-3-hydroxypropanamido)-2-(4-(4,4,5 ,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 45, 358 mg, 84% yield) as colorless dry film and as a mixture of rotamers. ¹H NMR (500MHz, CDCI3) d 0.76 (2H, t), 1 .16 (1 H, m), 1 .21 (12H, s), 1 .31 (6H, s), 1 .35 - 1 .42 (5H, m), 1 .43 (1 1 H, s), 1 .73 - 1 .87 (1 H, m), 1 .87 - 2.02 (2H, m), 2.14 - 2.24 (1 H, m), 2.29 - 2.41 (1 H, m), 3.43 - 3.52 (0.4H, m), 3.52 - 3.61 (2H, m), 3.66 (0.6H, d), 3.79 - 3.92 (1 H, m), 3.92 - 4.04 (1 H, m), 4.51 (1 H, br s), 5.06 - 5.26 (2H, m), 5.36 (1 H, br s), 7.30 - 7.40 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 690. Intermediate 46: (2R,4R)-1-tert-butoxycarbonyl)-4-((S)-2-(tert-butoxycarbonyl amino)-3- hydrcxyprcpanamidc)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dicxabcr clan-2-yl)butyl)pyrrclidine-2- carboxylic acid

(2f?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-((S)-2-(terf-butoxycarbonylamino)-3- hydroxypropanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 45, 358 mg, 0.52 mmol) was dissolved in EtOAc (4 mL) and treated with Pd/C (10 wt%, 50 mg, 0.047 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 3.5 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth concentrated to dryness to afford (2R,4H)-^ -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-3-hydrox ypropanamido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 46, 303 mg, 97% yield) as a white solid and as a mixture of rotamers, which was used without further purification. ¹H NMR (500MHz, CD ₂CI ₂) d 0.67 - 0.91 (2H, m), 1 .25 (14H, s), 1 .41 - 1 .47 (3H, m), 1 .48 (9H, s), 1 .53 (10H, s), 1 .82 - 1 .90 (2H, m), 2.06 - 2.14 (1 H, m), 2.24 - 2.33 (1 H, m),

2.76 - 2.91 (1 H, m), 3.48 - 3.54 (1 H, m), 3.59 (1 H, dd), 3.70 (1 H, dd), 3.93 (1 H, d), 4.03 - 4.17 (1 H, m), 4.29 (1 H, d), 6.79 - 6.98 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 600.

Example 17: (2R,4R)-4-((S)-2-amino-3-hydroxypropanamido)-2-(4-boronobuty l)pyrrolidine-2- carboxylic acid

Trifluoroacetic acid (0.771 mL, 10.01 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-3 -hydroxypropanamido)-2- (4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 46, 300 mg, 0.50 mmol) in DCM (4 mL) at room temperature. After 1 .5 h the solution was concentrated under reduced pressure and the resultant residue was dissolved in 1 M HCI aq (4 mL, 4.00 mmol) and Et ₂0 (4 mL). Phenylboronic acid (183 mg, 1 .50 mmol) was added and the clear biphasic solution stirred at room temperature for 3 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL) and the layers were separated. The aqueous layer was washed with Et ₂0, the layers were separated and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and subject to ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 0 to 30% acetonitrile in water) to afford (2fl,4fl)-4-((S)-2-amino-3- hydroxypropanamido)-2-(4-boronobutyl)pyrrolidine-2-carboxyli c acid (Example 17, 94 mg, 59% yield) as a white solid. ¹H NMR (500MHz, D ₂0) d 0.77 (2H, td), 1 .16 - 1 .26 (1 H, m), 1 .26 - 1 .35 (1 H, m), 1 .35 - 1 .45 (2H, m), 1 .76 (1 H, ddd), 2.02 (1 H, ddd), 2.29 (1 H, dd), 2.46 (1 H, dd), 3.35 (1 H, dd), 3.48 (1 H, t), 3.62 (1 H, dd), 3.66 - 3.77 (2H, m), 4.40 - 4.50 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 318. Example 18: (2ff,4ff)-4-((S)-2-amino-3-methoxypropanamido)-2-(4- boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 30 Intermediate 47

Intermediate 48 Example 18

Intermediate 47: (2R.4R)-2-benzv! 1-tert-butyl 4-((S)-2-(tert-butoxycarbonylamino)-3- methoxyDroDanamido)-2-(4-(4,4,5,5-tetramethyl-1,3,2-dioxabor olan-2-yl)butyl)Dyrrolidine-1 ,2- dicarboxylate

A/,/V-Diisopropylethylamine (0.082 ml_, 0.47 mmol) was added to a stirred solution of COMU (220 mg, 0.51 mmol), (2f?,4f?)-2-benzyl 1 -terf-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 30, 235 mg, 0.47 mmol) and N-Boc-O-methyl-L-serine (108 mg, 0.49 mmol) in DMF (3 mL) at room temperature. The reaction was stirred for 2 h then diluted with water (60 mL) and DCM (15 mL). The phases were separated and the aqueous phase was extracted with DCM (2 x 20 mL). The combined organics were washed with saturated aqueous NaHCC> ₃ (30 mL), saturated aqueous NaCI (2 x 10 mL), dried over MgSC , filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel chromatography (hexanes/EtOAc) to afford (2fl,4fl)-2-benzyl 1 -tert- butyl 4-((S)-2-(fert-butoxycarbonylamino)-3-methoxypropanamido)-2- (4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 47, 145 mg, 44% yield) as colorless dry film and as a mixture of rotamers. ¹ H NMR (500MHz, CDCI ₃) d 0.78 (2H, t), 1 .18 (1 H, br dd), 1 .22 - 1 .26 (13H, m), 1 .33 (6H, s), 1 .44 (5H, br s), 1 .46 (9H, s),

1 .57 - 1 .74 (1 H, m), 1 .74 - 1 .85 (1 H, m), 1 .94 (0.4H, d), 2.01 (0.6H, d), 2.18 - 2.27 (0.6H, m), 2.32 - 2.47 (1 AH, m), 3.32 (3H, s), 3.39 - 3.46 (1 H, m), 3.49 - 3.55 (0.4H, m), 3.60 (1 H, dd), 3.65 - 3.76 (1 .6H, m), 4.15 (1 H, br d), 4.51 - 4.64 (1 H, m), 5.06 - 5.22 (2H, m), 5.23 - 5.34 (1 H, m), 7.32 - 7.39 (5H, m); m/z (ES ⁺) [M+H] ⁺ = 704.

Intermediate 48: (2R,4R)-1-(tert-butoxycarbonyl)-4-((S)-2-(tert-butoxycarbony lamino)-3- methoxypropanamido)-2-(4-(4,4, 5, 5-tetramethyl- 1 , 3,2-diexaberelan-2-yl)butyl)pyrrelidine-2- carbexylic acid

(2f?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-((S)-2-(terf-butoxycarbonylamino)-3- methoxypropanamido)-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2- dicarboxylate (Intermediate 47, 145 mg, 0.21 mmol) was dissolved in EtOAc (2 mL) and treated with Pd/C (10 wt%, 22 mg, 0.021 mmol). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 4 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth concentrated to dryness to afford (2R,4R)-1 -(tert- butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-3-methox ypropanamido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 48, 126 mg, 100% yield) as a white solid and as a mixture of rotamers, which was used without further purification. ¹H NMR (500MHz, CD ₂CI ₂) d 0.65 - 0.80 (2H, m), 1 .14 - 1 .29 (14H, m), 1 .35 - 1 .43 (5H, m), 1 .44 (7H, s), 1 .46 - 1 .60 (8H, m), 1 .77 - 1 .95 (1 H, m), 2.03 - 2.14 (1 H, m), 2.14 - 2.26 (1 H, m), 2.68 (1 H, br d), 3.33 (3H, s), 3.38 - 3.47 (1 H, m), 3.47 - 3.60 (2H, m), 3.65 - 3.76 (1 H, m), 4.02 - 4.15 (1 H, m), 4.24 (1 H, br s), 5.38 (1 H, br s), 7.06 (1 H, br s); m/z (ES ⁺) [M+H] ⁺ = 614.

Example 18: (2RAR)-4-((S)-2-aminc-3-methcxyprcpanamidc)-2-(4-bcrcncbutyl )pyrrclidine-2- carbcxylic acid

Trifluoroacetic acid (0.25 mL, 3.26 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -(fe/f-butoxycarbonyl)-4-((S)-2-(te/f-butoxycarbonylamino)-3 -methoxypropanamido)-2- (4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-2-carboxylic acid (Intermediate 48, 100 mg, 0.16 mmol) in DCM (2 mL) at ambient temperature. After 1 h the solution was concentrated under reduced pressure and the resultant residue was dissolved in 1 M HCI aq (2 mL, 2.00 mmol) and Et ₂0 (2 mL). Phenylboronic acid (60 mg, 0.49 mmol) was added and the clear biphasic solution stirred at room temperature for 3 h. The mixture was diluted with Et ₂0 (20 mL) and water (5 mL) and the layers were separated. The aqueous layer was washed with Et ₂0, the layers were separated and the aqueous layer was lyophilized. The resulting solid was dissolved in MeOH (3 mL) and subject to ion exchange chromatography (PoraPak Rxn CX 20 cc column). The desired product was eluted from the column using a 5% ammonia in MeOH solution (20 mL). The obtained material was further purified by reverse phase chromatography (RediSep Rf Gold® C18, 0 to 20% acetonitrile in water). The product fractions were lyophilized and the resultant material was again subject to reverse phase flash chromatography (RediSep Rf Gold® C18, 0 to 2% acetonitrile in water). The product fractions were lyophilized and the resultant material was again re-purified by reverse phase flash chromatography (RediSep Rf Gold® C18, 0 to 5% acetonitrile in water) to afford (2fl,4fl)-4-((S)-2-amino-3- methoxypropanamido)-2-(4-boronobutyl)pyrrolidine-2-carboxyli c acid (Example 18, 18 mg, 35% yield) as a white solid. ¹H NMR (500MHz, D ₂0) d 0.77 (2H, td), 1 .14 - 1 .27 (1 H, m), 1 .27 - 1 .35 (1 H, m), 1 .35 - 1 .45 (2H, m), 1 .72 - 1 .81 (1 H, m), 2.02 (1 H, ddd), 2.30 (1 H, dd), 2.41 (1 H, dd), 3.31 - 3.38 (4H, m), 3.55 - 3.60 (3H, m), 3.63 (1 H, dd), 4.42 - 4.51 (1 H, m); m/z (ES ⁺) [M+H] ⁺ = 332.

Example 19: (S)-2-amino-N-((3R,5R)-8-hvdroxy-6-oxo-7-oxa-1 -aza-8- boraspiror4.71dodecan-3-yl)-3-methylbutanamide - Compound B

Compound A Compound B

Compound B (Example 19) was obtained by the intramolecular cyclization of Example 9 (Compound A) via an interconversion process. Furthermore, interconversions between Compound A (Example 9) and Compound B were observed under various conditions. For example, Compound B was converted to Compound A in the presence of water and such conversion was proportional to the concentration of water in the solvent. This is demonstrated in Figure 1 where the NMR spectra of compound B prepared in 100% d6-DMSO (labeled A), 75% D ₂0 in d6-DMSO (labeled B), 50% D ₂0 in d6-DMSO (labeled C), 25% D ₂0 in d6-DMSO (labeled E) and 100% D ₂0 (labeled F) are shown. In d6-DMSO, compound B predominates, while there is a proportional increase in compound A with increase in D ₂0 concentration. The proportion of compound A relative to compound B in 100% D ₂0 reaches approximately 90%. Furthermore, Compound B was converted to Compound A under acidic condition. In Figure 2, the NMR spectrum of compound B in 0.1 M DCI (in D ₂0) demonstrates that acidification yields almost complete conversion to compound A. In addition, it was determined that crystalline Compound B and amorphous Compound B have the same structural form. In Figure 3, the NMR spectra (obtained in d6-DMSO) demonstrate that both crystalline Compound B and the amorphous Compound B have the same cyclic structure.

Intermediate 30 Intermediate 52 Example 20

A/,/V-Diisopropylethylamine (0.13 mL, 0.76 mmol) was added to a solution of (S)-N- alpha-f-Butyloxycarbonyl-3, 3-dimethyl-serine (106 mg, 0.454 mmol) and HATU (0.173 g, 0.454 mmol) in DMF (2.6 mL) at 0 C and the reaction stirred for 15 min. A solution of (2R,4H)-2- benzyl 1 -tert-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine- 1 ,2-dicarboxylate (Intermediate 30, 190 mg, 0.38 mmol) in DMF (1 mL) was added and the reaction stirred for 2 h while slowly warming to room temperature. The reaction mixture was diluted with EtOAc (40 mL) and washed with saturated aqueous NFUCI (2 x 20 mL), saturated aqueous NaHCC>3 (2 x 20 mL) and brine (20 mL). The organic layer was dried over Na ₂S0 ₄, filtered and concentrated to dryness. The crude material was purified by silica gel

chromatography (0-50% EtOAc in hexanes) to afford 2-benzyl l -(terf-butyl) (2R,4H)-4-((S)-2- ((tert-butoxycarbonyl)amino)-3-hydroxy-3-methylbutanamido)-2 -(4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 52, 223 mg, 82% yield) as a white foam and as a mixture of rotamers. ¹ H NMR (500 MHz, MeOH-d _t) d 0.70 - 0.83 (m, 2 H) 1 .14 - 1 .27 (m, 19 H) 1 .31 (s, 6 H) 1 .36 - 1 .42 (m, 5 H) 1 .44 (s, 10 H) 1 .81 - 1 .93 (m, 1 H) 2.02 - 2.14 (m, 1 H) 2.14 - 2.30 (m, 1 H) 2.36 - 2.49 (m, 1 H) 3.39 - 3.48 (m, 1 H) 3.73 - 3.83 (m, 1 H) 3.87 - 3.97 (m, 1 H) 4.43 - 4.53 (m, 1 H) 5.09 - 5.25 (m, 2 H) 7.28 - 7.45 (m, 5 H); m/z (ES ⁺) [M+H] ⁺ = 718. Example 20: (2R,4R)-4J[(2S)-2-amino-3-hydroxy-3-methyl-butanoyl]amino]-2 -(4- boronobutyl)pyrrolidine-2-carboxylic acid

Pd/C (10% wt, 100 mg, 0.09 mmol) was added to a solution of 2-benzyl 1 -(terf-butyl) (2P?,4/ ^:?)-4-((S)-2-((te/i-butoxycarbonyl)amino)-3-hydroxy-3-m ethylbutanamido)-2-(4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 52, 220 mg, 0.31 mmol) in EtOAc (3 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 3 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and concentrated to dryness. The white solid was dissolved in DCM (1 mL) and trifluoroacetic acid (0.50 mL, 6.5 mmol) and the reaction stirred at room temperature for 2 h. The solution was concentrated, and the resulting residue was dissolved in Et ₂0 (2 mL) and 1 M HCI aq (2 mL). Phenylboronic acid (100 mg, 0.82 mmol) was added and the clear biphasic solution stirred at room temperature for 2 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2R,4H)-4-[[(2S)-2- amino-3-hydroxy-3-methyl-butanoyl]amino]-2-(4-boronobutyl)py rrolidine-2-carboxylic acid

(Example 20, 92 mg, 87% yield) as a white solid. ¹ H NMR (500 MHz, D ₂0) d 0.70 (2H, t), 1 .20 (4H, s), 1 .28 (4H, s), 1 .31 - 1 .40 (2H, m), 1 .77 - 1 .88 (1 H, m), 2.04 - 2.14 (1 H, m), 2.40 - 2.47 (1 H, m), 2.48 - 2.54 (1 H, m), 3.40 (1 H, dd), 3.74 (1 H, s), 3.75 - 3.80 (1 H, m), 4.47 - 4.55 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 346.

Example 21 : (2i?,4/7)-4-IT(2S)-2-amino-2,3-dimethyl-butanoyllaminol-2-(4 - boronobutvDpyrrolidine-2-carboxylic acid

Intermediate 30 Intermediate 53 Example 21

Intermediate 53: 2-benzyl 1-tert-butyl (2R.4R)-4-ll(2S)-2-(tert-butoxycarbonylamino)-2.3- dimethyl-butanoyllaminol-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine- 2- dicarboxylate A/,/V-Diisopropylethylamine (0.14 ml_, 0.82 mmol) was added to a solution of (S)-2-((tert- butoxycarbonyl)amino)-2,3-dimethylbutanoic acid (0.1 13 g, 0.489 mmol) and HATU (0.186 g, 0.489 mmol) in DMF (3 mL) at 0 ^"C and the reaction stirred for 15 min. A solution of (2R,4H)-2- benzyl 1 -terf-butyl 4-amino-2-(4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine- 1 ,2-dicarboxylate (Intermediate 30, 205 mg, 0.408 mmol) in DMF (1 mL) was added and the reaction stirred for 3 h while slowly warming to room temperature. The reaction mixture was diluted with EtOAc (50 mL) and washed with saturated aqueous NFUCI (2 x 25 mL), saturated aqueous NaHCC>3 (2 x 25 mL) and brine (20 mL). The organic layer was dried over Na ₂S0 ₄, filtered and concentrated to dryness. The crude material was purified by silica gel

chromatography (0-50% EtOAc in hexanes) to afford 2-benzyl 1 -terf-butyl ( 2R,4H)-4-[[(2S)-2 - (terf-butoxycarbonylamino)-2,3-dimethyl-butanoyl]amino]-2-[4 -(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 53, 21 1 mg, 72% yield) as a white foam and as a mixture of rotamers. ¹ H NMR (500 MHz, MeOH-d _t) d 0.72 - 0.79 (2H, m), 0.80 - 0.93 (6H, m), 1 .17 - 1 .25 (13H, m), 1 .31 (9H, d), 1 .36 - 1 .47 (16H, m), 1 .82 - 1 .92 (2H, m), 1 .97 - 2.09 (1 H, m), 2.15 - 2.30 (1 H, m), 2.34 - 2.51 (1 H, m), 3.61 - 3.75 (1 H, m), 4.42 - 4.56 (1 H, m), 5.08 - 5.31 (2H, m), 7.29 - 7.46 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 716.

Pd/C (10% wt, 90 mg, 0.08 mmol) was added to a solution of 2-benzyl 1 -fed-butyl (2F?,4/ ^:?)-4-[[(2S)-2-(fed-butoxycarbonylamino)-2,3-dimethyl-b utanoyl]amino]-2-[4-(4,4,5,5- tetramethyl-1 ,3, 2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 53, 210 mg, 0.29 mmol) in EtOAc (4 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 3 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and concentrated to dryness. The white solid was dissolved in DCM (1 mL) and trifluoroacetic acid (0.50 mL, 6.5 mmol) and the reaction stirred at room temperature for 2 h. The solution was concentrated, and the resulting residue was dissolved in Et ₂0 (2 mL) and 1 M HCI aq (2 mL). Phenylboronic acid (100 mg, 0.82 mmol) was added and the clear biphasic solution stirred at room temperature for 2 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2R,4H)-4-[[(2S)-2- amino-2,3-dimethyl-butanoyl]amino]-2-(4-boronobutyl)pyrrolid ine-2-carboxylic acid (Example 21 , 90 mg, 89% yield) as a white solid. ¹ H NMR (500 MHz, D ₂0) d 0.74 - 0.78 (2H, m), 0.79 (3H, d), 0.89 (3H, d), 1 .17 - 1 .27 (4H, m), 1 .28 - 1 .35 (1 H, m), 1 .36 - 1 .47 (2H, m), 1 .70 - 1 .81 (1 H, m), 1 .93 - 2.07 (2H, m), 2.27 (1 H, dd), 2.43 (1 H, dd), 3.27 - 3.39 (1 H, m), 3.60 (1 H, dd), 4.39 - 4.48 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 344.

Example 22: (2fl.4ff)-2-(4-boronobutyl -rr(2S)-2.3-diaminopropanoyl1amino1pyrrolidine-

2-carboxylic acid

Intermediate 30 Intermediate 54 Example 22

Intermediate 54: 2-benzyl 1-tert-butyl (2RAR)-4-[[(2S)-2.3-bis(tert- butoxycarbonylamino)propanoyllaminol-2-f4-(4,4,5,5-tetrameth yl-1 ,3,2-dioxaborolan-2- yDbutvIlpyrrolidine- 1 ,2-dicarboxylate

A/,/V-Diisopropylethylamine (0.14 mL, 0.82 mmol) was added to a solution of Boc- Dap(Boc)-OH*DCHA (0.238 g, 0.489 mmol) and HATU (0.186 g, 0.489 mmol) in DMF (3 mL) at 0 ^"C and the reaction stirred for 15 min. A solution of (2F?,4/ ^:?)-2-benzyl 1 -terf-butyl 4-amino-2-(4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl)pyrrolidine-1 ,2-dicarboxylate (Intermediate 30, 205 mg, 0.408 mmol) in DMF (1 mL) was added and the reaction stirred for 16 h while slowly warming to room temperature. The reaction mixture was diluted with EtOAc (50 mL) and washed with saturated aqueous NFUCI (2 x 25 mL), saturated aqueous NaHCC>3 (2 x 25 mL) and brine (20 mL). The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (0-50% EtOAc in hexanes) to afford 2-benzyl 1 -tert-butyl (2R,4R)-4-[[(2S)-2,3-b\s(tert- butoxycarbonylamino)propanoyl]amino]-2-[4-(4,4,5,5-tetrameth yl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 54, 214 mg, 66% yield) as a white foam and as a mixture of rotamers. ¹H NMR (500 MHz, MeOH-d _t) d 0.76 (2H, q), 1 .19 - 1 .26 (14H, m),

1 .27 - 1 .34 (6H, m), 1 .37 - 1 .52 (24H, m), 1 .76 - 1 .93 (1 H, m), 2.06 - 2.31 (2H, m), 2.50 (1 H, s), 3.19 - 3.27 (2H, m), 3.66 - 3.84 (1 H, m), 4.00 - 4.13 (1 H, m), 4.35 - 4.50 (1 H, m), 5.04 - 5.25 (2H, m), 7.26 - 7.50 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 789. Pd/C (10% wt, 57 mg, 0.053 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2P?,4/ ^:?)-4-[[(2S)-2,3-bis(te/i-butoxycarbonylamino)propanoyl ]amino]-2-[4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 54, 210 mg, 0.27 mmol) in EtOAc (4 mL). The flask was equipped with a balloon of H2 and the suspension stirred at room temperature for 3 h. The reaction mixture was diluted with MeOH, filtered through diatomaceous earth and concentrated to dryness. The white solid was dissolved in DCM (1 mL) and trifluoroacetic acid (0.50 mL, 6.5 mmol) and the reaction stirred at room temperature for 2 h. The solution was concentrated, and the resulting residue was dissolved in Et ₂0 (2 mL) and 1 M HCI aq (2 mL). Phenylboronic acid (100 mg, 0.82 mmol) was added and the clear biphasic solution stirred at room temperature for 3 h. The reaction mixture was diluted with water and washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange

chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2P?,4/ ^:?)-2-(4-boronobutyl)-4-[[(2S)-2,3- diaminopropanoyl]amino]pyrrolidine-2-carboxylic acid (Example 22, 74 mg, 88% yield) as a white solid. ¹ H NMR (500 MHz, D ₂0) d 0.71 (2H, t), 1 .1 1 - 1 .24 (1 H, m), 1 .26 - 1 .41 (3H, m),

1 .75 - 1 .89 (1 H, m), 2.00 - 2.13 (1 H, m), 2.31 - 2.48 (1 H, m), 2.51 - 2.67 (1 H, m), 3.39 - 3.53 (3H, m), 3.68 - 3.80 (1 H, m), 4.27 (1 H, t), 4.41 - 4.52 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 317.

Example 23: (2ff.4ff)-2-(4-boronobutyl)-4-(methylamino)pyrrolidine-2-car boxylic acid

Intermediate 55 Intermediate 56

Intermediate 62 Example 23

Intermediate 55: 1-tert-butyl 2-methyl (2S.4R)-4-(tert-butoxycarbonylamino)Dyrrolidine-1.2- dicarboxylate

Di-terf-butyl dicarbonate (4.41 g, 20.2 mmol) was added to a solution of l -(terf-butyl) 2- methyl (2S,4f?)-4-aminopyrrolidine-1 ,2-dicarboxylate oxalic acid salt (4.50 g, 13.5 mmol) and triethylamine (5.63 mL, 40.4 mmol) in DCM (57 mL) and the reaction stirred at room

temperature overnight under an atmosphere of N ₂. The crude reaction mixture was diluted with DCM (200 mL) and washed sequentially with 0.5 M HCI (aq), saturated sodium bicarbonate and brine. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (DCM/MeOH) to afford 1 -terf-butyl 2- methyl (2S,4f?)-4-(terf-butoxycarbonylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 55, 3.66 g, 79% yield) as a white solid. ¹H NMR (500MHz, DMSO-d ₆) d 1 .29 - 1 .42 (18H, m), 1 .96 2.17 (2H, m), 3.12 - 3.17 (1 H, m), 3.45 - 3.56 (1 H, m), 3.62 - 3.69 (3H, m), 3.96 - 4.06 (1 H, m), 4.24 - 4.34 (1 H, m), 7.17 - 7.26 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 345.

Sodium hydride (60% dispersion in mineral oil) (0.491 g, 12.3 mmol) was added portion- wise to a solution of 1 -terf-butyl 2-methyl (2S,4F?)-4-(terf-butoxycarbonylamino)pyrrolidine-1 ,2- dicarboxylate (Intermediate 55, 3.66 g, 10.7 mmol) in DMF (35 mL). Following addition, the reaction stirred for 10 min then methyl iodide (0.715 ml, 1 1 .4 mmol) was added and the reaction stirred for an additional 3 h. The reaction mixture was cooled to 0 °C and quenched with water. The mixture was diluted with EtOAc (200 mL) and the layers were separated. The organic layer was washed sequentially with water and brine, dried over Na2S0 ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford 1 -terf-butyl 2-methyl (2S,4F?)-4-[terf-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 56, 3.13 g, 82% yield) as a colorless oil. ¹ H NMR (500MHz, DMSO-de) d 1 .28 - 1 .41 (18H, m), 1 .87 - 2.02 (1 H, m), 2.29 - 2.44 (1 H, m), 2.69 (3H, s), 3.13 - 3.25 (1 H, m), 3.44 - 3.57 (1 H, m), 3.60 - 3.68 (3H, m), 4.23 - 4.32 (1 H, m), 4.62 (1 H, br s); m/z: (ES ⁺) [M+H] ⁺ = 359.

A solution of sodium hydroxide (2.10 g, 52.4 mmol) in water (1 1 mL) was added to a solution of 1 -terf-butyl 2-methyl (2S,4F?)-4-[fe/f-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 56, 3.13 g, 8.73 mmol) in THF (22 mL) and MeOH (1 1 mL) at 0 °C. The reaction mixture stirred for 3 hrs while slowly warming to room temperature. The volatiles were removed under reduced pressure and the aqueous layer was acidified to pH ~3 with 5 M HCI (aq) and extracted with DCM. The combined organics were dried over Na ₂S0 ₄, filtered and concentrated in dryness to afford the crude carboxylic acid as a white solid which was used without further purification.

Benzyl bromide (1 .24 mL, 10.5 mmol) was added to a solution of the crude carboxylic acid, sodium iodide (1 .737 g, 1 1 .59 mmol) and K ₂CO ₃ (3.01 g, 21 .8 mmol) in DMF (28 mL) and the reaction stirred at room temperature for 17 h. The reaction mixture was filtered, and the solids were rinsed with EtOAc. The filtrate was concentrated and purified by silica gel chromatography (hexanes/EtOAc) to afford 2-benzyl 1 -tert-butyl (2S,4F?)-4-[tert- butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 57, 3.05 g, 81 % yield) as a colorless oil. ¹H NMR (500MHz, DMSO-d ₆) d 1 .20 - 1 .42 (18H, m), 1 .91 - 2.07 (1 H, m),

2.33 - 2.46 (1 H, m), 2.69 (3H, s), 3.12 - 3.26 (1 H, m), 3.44 - 3.57 (1 H, m), 4.20 - 4.38 (1 H, m), 4.66 (1 H, br s), 5.07 - 5.20 (2H, m), 7.25 - 7.41 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 435.

Intermediate 58: 2-benzyl 1-tert-butyl ( 4R)-2-(but-2-enyl)-4-[tert - butoxycarbonyl(methyl)aminolpyrrolidine-1,2-dicarboxylate

2-Benzyl 1 -fert-butyl (2S,4F?)-4-[tert-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 57, 3.05 g, 7.02 mmol) and crotyl bromide (1 .08 mL, 10.5 mmol) were dissolved in THF (25 mL) and the solution was cooled to -78 °C under an atmosphere of N ₂. A solution of KHMDS (0.5M in toluene, 21 .0 mL, 10.5 mmol) was added dropwise to the reaction mixture and the reaction stirred for 17 h while slowly warming to room temperature.

The crude reaction mixture was quenched with water and the volatiles were removed under reduced pressure. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel purification (hexanes/EtOAc) to afford 2-benzyl 1 - tert-butyl (4F?)-2-(but-2-enyl)-4-[tert-butoxycarbonyl(methyl)amino]pyr rolidine-1 ,2-dicarboxylate (Intermediate 58, 1 .26 g, 37% yield) as a yellow oil and as a mixture of diastereomers, E/Z olefin isomers and rotamers. ¹ H NMR (500MHz, DMSO-afe) d 1 .23 - 1 .44 (18H, m), 1 .51 - 1 .70 (3H, m), 2.00 - 2.26 (2H, m), 2.38 - 2.47 (1 H, m), 2.57 - 2.68 (3H, m), 2.71 - 3.00 (1 H, m), 3.00 - 3.25 (1 H, m), 3.40 - 3.74 (1 H, m), 4.54 - 4.80 (1 H, m), 5.01 - 5.27 (2H, m), 5.28 - 5.47 (1 H, m), 5.49 - 5.72 (1 H, m), 7.25 - 7.42 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 489.

Intermediate 59: 2-benzyl 1-tert-butyl (4R)-4-[tert-butoxycarbonyl(methyl)amino]-2-[4-(4, 4,5,5- tetramethyl- 1,3,2-dioxaborolan-2-yl)butynpyrrolidine- 1 ,2-dicarboxylate

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (269 mg, 0.400 mmol) and

bis(diphenylphosphino)methane (308 mg, 0.801 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (1 1 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (1 .28 mL, 8.82 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. 2-Benzyl 1 -tert-butyl (4F?)-2- (but-2-enyl)-4-[tert-butoxycarbonyl(methyl)amino]pyrrolidine -1 ,2-dicarboxylate (Intermediate 58, 1 .96 g, 4.01 mmol) was added to the reaction as a solution in DCM (7.5 mL) and the reaction mixture stirred for 16 h at room temperature. The reaction mixture was cooled to 0 °C and carefully quenched with MeOH and water. The layers were separated, and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The resulting residue was purified by flash silica chromatography (hexanes/EtOAc) to afford 2-benzyl 1 -terf-butyl (4f?)-4-[terf-butoxycarbonyl(methyl)amino]-2-[4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 59, 2.5 g, 100% yield) as a yellow oil and as a mixture of diastereomers and rotamers. The purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 30 mm x 250 mm, 5 pm, Temperature = 20 °C, Mobile phase = 0-30% MeOH:CC>2, UV detection @ 220 nm, loading = 31 mg/inj, cone = 125 mg/mL in MeOH, flow rate = 75 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry of each diastereomer was assigned retrospectively based on the enzyme potency of Example 23 and Example 24 to be congruent with other exemplified compounds.

Intermediate 60 (Isomer 2, 637 mg): 2-benzyl 1 -terf-butyl (2R,4H)-4-[tert- butoxycarbonyl(methyl)amino]-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹H NMR (500MHz, DMSO-afe) d 0.58 - 0.76 (2H, m), 1 .15 (12H, d), 1 .21 - 1 .47 (22H, m), 1 .69 - 1 .82 (1 H, m), 1 .94 - 2.23 (3H, m), 2.56 - 2.62 (3H, m), 3.19 - 3.28 (1 H, m), 3.45 - 3.57 (1 H, m), 4.58 - 4.79 (1 H, m), 5.01 - 5.26 (2H, m), 7.26 - 7.41 (5H, m).

Intermediate 61 (Isomer 1 , 860 mg): 2-benzyl 1 -terf-butyl (2S,4H)-4-[tert- butoxycarbonyl(methyl)amino]-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹H NMR (500MHz, DMSO-afe) d 0.62 - 0.71 (2H, m), 1 .15 (12H, s), 1 .20 - 1 .42 (22H, m), 1 .67 - 1 .84 (1 H, m), 1 .92 - 2.32 (3H, m), 2.69 (3H, s), 3.04 - 3.15 (1 H, m), 3.57 - 3.71 (1 H, m), 4.52 - 4.73 (1 H, m), 4.98 - 5.25 (2H, m), 7.24 - 7.40 (5H, m).

Intermediate 62: (2R,4R)-1Jert-butoxycarbonyl-4-itert-butoxycarbonyl(methyl)a mino]-2-f4 -

4,5,5Jetramethvl-1,3,2-dioxaborolan-2-vl)butvllPvrrolidin e-2-carboxvlic acid

Pd/C (10% wt, 165 mg, 0.155 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2P?,4/ ^:?)-4-[te/f-butoxycarbonyl(methyl)amino]-2-[4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 60, 637 mg, 1 .03 mmol) in EtOAc (7 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness and purified by silica gel chromatography (hexanes/EtOAc) to afford (2P?,4/ ^:?)-1 -fe/f-butoxycarbonyl-4-[te/f-butoxycarbonyl(methyl)amino]- 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid

(Intermediate 62, 350 mg, 64% yield) as a white solid. ¹H NMR (500MHz, DMSO-afe) d 0.63 - 0.73 (2H, m), 1 .14 - 1 .19 (12H, m), 1 .22 - 1 .42 (21 H, m), 1 .63 - 1 .77 (1 H, m), 1 .99 - 2.18 (3H, m), 2.63 - 2.67 (3H, m), 3.21 - 3.27 (2H, m), 3.41 - 3.55 (1 H, m), 4.57 - 4.80 (1 H, m), 12.32 - 12.75 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 527.

Trifluoroacetic acid (0.51 mL, 6.7 mmol) was added dropwise to a stirred solution of (2f?,4/ ^:?)-1 -fert-butoxycarbonyl-4-[fe/f-butoxycarbonyl(methyl)amino]-2- [4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 62, 350 mg, 0.66 mmol) in DCM (4 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (162 mg, 1 .33 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 60cc column). The desired product was eluted from the column using 5% ammonia in MeOH (60 mL) to afford (2R?,4R?)-2-(4- boronobutyl)-4-(methylamino)pyrrolidine-2-carboxylic acid (Example 23, 140 mg, 86% yield) as a white solid. ¹H NMR (500 MHz, D ₂0) d 0.72 - 0.82 (2H, m), 1 .09 - 1 .43 (4H, m), 1 .62 - 1 .77 (1 H, m), 1 .83 - 1 .95 (1 H, m), 2.23 (2H, d), 2.46 (3H, s), 3.02 - 3.1 1 (1 H, m), 3.37 - 3.49 (1 H, m), 3.49 - 3.61 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 245.

Pd/C (10% wt, 223 mg, 0.209 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2S,4f?)-4-[terf-butoxycarbonyl(methyl)amino]-2-[4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 61 , 860 mg, 1 .39 mmol) in EtOAc (9.3 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness and purified by silica gel chromatography (hexanes/EtOAc) to afford (2S,4P?)-1 -te/f-butoxycarbonyl-4-[fe/f-butoxycarbonyl(methyl)amino]- 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 63, 520 mg, 71 % yield) as a white solid. ¹H NMR (500MHz, DMSO-afe) d 0.60 - 0.75 (2H, m), 1 .16 (12H, s), 1 .28 - 1 .45 (22H, m), 1 .56 - 1 .74 (1 H, m), 1 .84 - 1 .95 (1 H, m), 2.01 - 2.22 (2H, m), 2.69 (3H, s), 3.01 - 3.17 (1 H, m), 3.56 - 3.70 (1 H, m), 4.52 - 4.73 (1 H, m), 12.35 - 12.77 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 527.

Example 24: (2S,4R)-2-{4-boronobutyl)-4-{methylamino)Dyrrolidine-2-carbo xylic acid

Trifluoroacetic acid (1 .23 mL, 16.0 mmol) was added dropwise to a stirred solution of (2S,4f?)-1 -terf-butoxycarbonyl-4-[terf-butoxycarbonyl(methyl)amino]-2- [4-(4,4,5,5-tetramethyl- 1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 63, 520 mg, 0.80 mmol) in DCM (8.5 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (196 mg, 1 .60 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 60cc column). The desired product was eluted from the column using 5% ammonia in MeOH (60 mL) to afford (2S,4f?)-2-(4- boronobutyl)-4-(methylamino)pyrrolidine-2-carboxylic acid (Example 24, 163 mg, 83% yield) as a white solid. ¹H NMR (500 MHz, D ₂0) d 0.70 - 0.90 (2H, m), 1 .10 - 1 .46 (4H, m), 1 .65 - 1 .77 (2H, m), 1 .96 - 2.07 (1 H, m), 2.43 (3H, s), 2.68 - 2.77 (1 H, m), 2.96 - 3.10 (1 H, m), 3.37 - 3.50 (1 H, m), 3.50 - 3.60 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 245.

Example 25: (2ff,4ff)-2-(4-boronobutyl)-4-(dimethylamino)pyrrolidine-2-c arboxylic acid

Intermediate 64 Intermediate 65 Intermediate 66

Intermediate 67 Intermediate 68 Intermediate 69

Intermediate 70 Example 25

Intermediate 64: 2-benzyl 1 -tert-butyl (2R.4R)-4-aminoDyrrolidine-1 ,2-dicarboxylate

Triphenylphosphine (7.87 g, 30.0 mmol) and water (0.54 mL, 30.0 mmol) were added to a solution of 2-benzyl 1 -(terf-butyl) (2f?,4/ ^:?)-4-azidopyrrolidine-1 ,2-dicarboxylate (5.20 g, 15.0 mmol) in THF (68 mL) at room temperature. The reaction was heated to 60 °C and stirred for 6 h. The reaction mixture was cooled to room temperature, diluted with EtOAc, and washed sequentially with water (2 x 100 mL) and saturated aqueous sodium chloride (100 mL). The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (DCM/MeOH) to afford 2-benzyl 1 -terf-butyl (2R,4H)- 4-aminopyrrolidine-1 ,2-dicarboxylate (Intermediate 64, 3.2 g, 67% yield) as a colorless oil. ¹H NMR (500MHz, DMSO-d ₆) d 1 .20 - 1 .49 (9H, m), 1 .53 - 1 .64 (1 H, m), 1 .65 - 1 .79 (2H, m), 2.26 - 2.40 (1 H, m), 2.85 - 3.01 (1 H, m), 3.31 - 3.42 (1 H, m), 3.45 - 3.56 (1 H, m), 4.13 - 4.24 (1 H, m), 4.99 - 5.25 (2H, m), 7.36 (5H, s) ; m/z: (ES ⁺) [M+H] ⁺ = 321 .

Sodium triacetoxyborohydride (6.35 g, 29.9 mmol) was added portion-wise to a solution of 2-benzyl 1 -tert-butyl (2f?,4/ ^:?)-4-aminopyrrolidine-1 ,2-dicarboxylate (Intermediate 64, 3.20 g, 9.99 mmol) and formaldehyde (37 wt% in H2O, 4.46 mL, 59.9 mmol) in MeOH (79 mL).

Following addition, the reaction stirred at room temperature for 17 h. The volatiles were removed under reduced pressure and the resulting residue was diluted with DCM. The solids were removed by filtration and the filtrate was concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc with NH ₄OH) to afford 2-benzyl 1 -tert- butyl (2F?,4/ ^:?)-4-(dimethylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 65, 3.00 g , 86% yield). ¹ H NMR (500MHz, DMSO-d ₆) d 1 .24 (9H, s), 1 .53 - 1 .67 (1 H, m), 2.10 (6H, s), 2.40 - 2.48 (1 H, m) , 2.53 - 2.73 (1 H, m), 2.83 - 3.06 (1 H, m), 3.59 - 3.69 (1 H, m), 4.1 5 - 4.29 (1 H, m), 5.02 - 5.21 (2H, m), 7.26 - 7.42 (5H, m) ; m/z: (ES ⁺) [M+H] ⁺ = 350.

Intermediate 66: 2-benzyl 1-tert-butyl (4R)-2-(but-2-enyl)-4-(dimethylamino)pyrrolidine-1 ,2-

2-Benzyl 1 -tert-butyl (2F?,4/ ^:?)-4-(dimethylamino)pyrrolidine-1 ,2-dicarboxylate

(Intermediate 65, 3.00 g, 8.61 mmol) and crotyl bromide (1 .33 mL, 1 2.9 mmol) were dissolved in THF (1 8 mL) and the solution was cooled to -78 °C under an atmosphere of N ₂. A solution of KHMDS (0.5M in toluene, 25.8 mL, 1 2.9 mmol) was added dropwise to the reaction mixture and the reaction stirred for 1 7 h while slowly warming to room temperature. The crude reaction mixture was quenched with water and the volatiles were removed under reduced pressure. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel purification (hexanes/EtOAc) to afford 2-benzyl 1 -fert-butyl (4F?)-2-(but-2-enyl)-4-(dimethylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 66, 1 .55 g, 45% yield) as a yellow oil and as a mixture of diastereomers, E/Z olefin isomers and rotamers.

¹ H NMR (500MHz, DMSO-d ₆) d 1 .21 - 1 .44 (9H, m), 1 .51 - 1 .70 (3H, m), 1 .79 - 1 .96 (1 H, m), 2.05 (6H, s), 2.08 - 2.24 (1 H, m), 2.31 - 2.43 (1 H, m), 2.54 - 2.74 (1 H, m), 2.75 - 3.08 (2H, m), 3.56 - 3.86 (1 H, m), 5.00 - 5.23 (2H, m), 5.23 - 5.42 (1 H, m), 5.43 - 5.73 (1 H, m), 7.23 - 7.41 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 403.

Intermediate 67: 2-benzyl 1-tert-butyl (4R)-4-(dimethylamino)-2-[4-(4,4,5,5-tetramethyl-1,3,2- dioxaborolan-2-yl)butynpyrrolidine- 1,2-dicarboxylate

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (240 mg, 0.36 mmol) and

bis(diphenylphosphino)methane (275 mg , 0.715 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (10 ml.) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (1 .14 mL, 7.87 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. 2-benzyl 1 -terf-butyl (4f?)-2- (but-2-enyl)-4-(dimethylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 66, 1 .44 g, 3.58 mmol) was added to the reaction as a solution in DCM (6.7 mL) and the reaction mixture stirred for 16 h at room temperature. The reaction mixture was cooled to 0 °C and carefully quenched with MeOH and water. The layers were separated, and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The resulting residue was purified by flash silica chromatography (hexanes/EtOAc) to afford 2- benzyl 1 -terf-butyl (4f?)-4-(dimethylamino)-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 67, 1 .5 g, 79% yield) as a yellow oil and as a mixture of diastereomers and rotamers. The purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 30 mm x 250 mm, 5 pm, Temperature = 20 °C, Mobile phase = 0-15% MeOH:C0 ₂, UV detection @ 220 nm, loading = 32 mg/inj, cone = 80 mg/mL in MeOH, flow rate = 120 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry of each diastereomer was assigned retrospectively based on the enzyme potency of Example 25 and Example 26 to be congruent with other exemplified compounds.

Intermediate 68 (Isomer 2, 190 mg): 2-benzyl 1 -terf-butyl (2P?,4/ ^:?)-4-(dimethylamino)-2- [4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹H NMR (500MHz, DMSO-de) d 0.64 - 0.71 (2H, m), 0.97 - 1 .12 (1 H, m), 1 .13 - 1 .17 (12H, m), 1 .24 (13H, s), 1 .57 - 1 .81 (1 H, m), 1 .81 - 1 .99 (1 H, m), 2.06 (6H, s), 2.09 - 2.21 (1 H, m), 2.55 - 2.74 (1 H, m), 3.02 - 3.12 (1 H, m), 3.59 - 3.70 (1 H, m), 5.00 - 5.20 (2H, m), 7.27 - 7.41 (5H, m).

Intermediate 69 (Isomer 1 , 491 mg): 2-benzyl 1 -terf-butyl (2S,4P?)-4-(dimethylamino)-2- [4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹H NMR (500MHz, DMSO-de) d 0.52 - 0.72 (2H, m), 0.93 - 1 .12 (1 H, m), 1 .12 - 1 .20 (12H, m), 1 .20 - 1 .39 (13H, m), 1 .59 - 1 .74 (1 H, m), 1 .77 - 1 .93 (1 H, m), 2.06 (6H, s), 2.08 - 2.15 (1 H, m), 2.53 - 2.65 (1 H, m), 2.78 - 2.96 (1 H, m), 3.67 - 3.82 (1 H, m), 5.00 - 5.21 (2H, m), 7.27 - 7.42 (5H, m).

Intermediate 70: (2R,4R)- 1 -tert-butoxycarbonyl-4-(dimethylamino)-2-[4-(4,4,5,5-tetrame thyl-

1.3.2-dioxaborolan-2- yl)butyl]p yrrolidine-2-carboxylic acid

Pd/C (10% wt, 57 mg, 0.054 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2P?,4/ ^:?)-4-(dimethylamino)-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-

1 .2-dicarboxylate (Intermediate 68, 189 mg, 0.356 mmol) in EtOAc (2.4 mL). The flask was equipped with a balloon of H2 and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness to afford (2P?,4/ ^:?)-1 -te/f-butoxycarbonyl-4-(dimethylamino)-2-[4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 70, 150 mg, 96% yield) as a white solid which was used without further purification. ¹H NMR (500MHz, DMSO-de) d 0.53 - 0.70 (2H, m), 1 .1 1 - 1 .20 (12H, m), 1 .21 - 1 .41 (14H, m), 1 .56 - 1 .71 (1 H, m), 1 .92 - 2.06 (2H, m), 2.20 (7H, s), 2.69 - 2.78 (1 H, m), 3.37 - 3.51 (1 H, m), 3.67 - 4.21 (1 H, m) ; m/z: (ES ⁺) [M+H] ⁺ = 441 .

Example 25: (2R,4R)-2-(4-boronobutyl)-4-(dimethylamino)pyrrolidine-2-car boxylic acid

Trifluoroacetic acid (0.26 mL, 3.4 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -fert-butoxycarbonyl-4-(dimethylamino)-2-[4-(4,4,5,5-tetrame thyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 70, 150 mg, 0.34 mmol) in DCM (2 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (83 mg, 0.68 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2P?,4/ ^:?)-2-(4-boronobutyl)-4- (dimethylamino)pyrrolidine-2-carboxylic acid (Example 25, 73 mg, 83% yield) as a white solid.

¹H NMR (500 MHz, D ₂0) d 0.62 - 0.73 (2H, m), 1 .14 - 1 .36 (4H, m), 1 .79 - 1 .90 (1 H, m), 1 .99 - 2.10 (1 H, m), 2.57 - 2.73 (2H, m), 2.82 - 2.90 (6H, m), 3.48 - 3.56 (1 H, m), 3.89 - 3.98 (1 H, m), 4.12 - 4.20 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 259.

Example 26: (2S.4fl)-2-(4-boronobutyl -(dimethylamino)pyrrolidine-2-carboxylic acid

Intermediate 69 Intermediate 71 Example 26

Intermediate 71: (2S.4R)-1-tert-butoxycarbonyl-4-idimethylamino)-2-i4-{4.4.5. 5-tetramethyl -

1 , 3, 2-dioxaborolan-2- yDbutvilo yrrolidine-2-carboxylic acid

Pd/C (10% wt, 148 mg, 0.139 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2S,4f?)-4-(dimethylamino)-2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine- 1 ,2-dicarboxylate (Intermediate 69, 490 mg, 0.93 mmol) in EtOAc (6.7 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness to afford (2S,4f?)-1 -terf-butoxycarbonyl-4-(dimethylamino)-2-[4- (4,4,5,5-tetramethyM ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 71 , 405 mg, 99% yield) as a white solid which was used without further purification. ¹H NMR (500MHz, DMSO-de) d 0.52 - 0.71 (2H, m), 0.83 - 1 .06 (1 H, m), 1 .16 (12H, s), 1 .32 (12H, s), 1 .53 - 1 .67 (1 H, m), 1 .75 - 1 .88 (1 H, m), 2.01 - 2.13 (7H, m), 2.54 - 2.69 (1 H, m), 2.79 - 2.95 (1 H, m), 3.66 - 3.83 (1 H, m), 7.24 - 7.46 (1 H, m), 1 1 .86 - 12.88 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 441 .

Example 26: (2S,4R)-2-(4-boronobutyl)-4-(dimethylamino)pyrrolidine-2-car boxylic acid

Trifluoroacetic acid (1 .0 mL, 13 mmol) was added dropwise to a stirred solution of (2S,4f?)-1 -terf-butoxycarbonyl-4-(dimethylamino)-2-[4-(4,4,5,5-tetrame thyl-1 ,3,2-dioxaborolan-2- yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 71 , 405 mg, 0.919 mmol) in DCM (5.1 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (224 mg, 1 .84 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 60cc column). The desired product was eluted from the column using 5% ammonia in MeOH (60 mL) to afford (2S,4f?)-2-(4-boronobutyl)-4- (dimethylamino)pyrrolidine-2-carboxylic acid (Example 26, 206 mg, 87% yield) as a white solid. ¹H NMR (500 MHz, D ₂0) d 0.71 - 0.89 (2H, m), 1 .12 - 1 .44 (4H, m), 1 .70 - 1 .82 (2H, m), 1 .97 - 2.1 1 (1 H, m), 2.29 (6H, s), 2.62 - 2.71 (1 H, m), 2.95 - 3.10 (2H, m), 3.61 - 3.68 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 259.

Example 27: (2ff,4ff)-4-(2-aminoethylamino)-2-(4-boronobutyl)pyrrolidine -2-carboxylic acid

Intermed iate 72 Intermed iate 73

Intermediate 74 Intermediate 75 Intermediate 76

Intermediate 77 Intermediate 78

Intermediate 79 Example 27

Intermediate 72: 1-tert-butyl 2-methyl (2SAR)-4-[2-(tert- butoxycarbonylamino)ethylaminolDyrrolidine-1,2-dicarboxylate

Acetic acid (42 mI_, 0.73 mmol) was added to a solution of 1 -(terf-butyl) 2-methyl (2S,4f?)-4-aminopyrrolidine-1 ,2-dicarboxylate (7.48 g, 30.6 mmol) and terf-butyl (2- oxoethyl)carbamate (4.64 g, 29.2 mmol) in MeOH (194 mL) and the reaction stirred at room temperature for 3 h. The solution was cooled to 0 °C and sodium triacetoxyborohydride (9.27 g, 43.7 mmol) was added portion-wise. The reaction stirred overnight while slowly warming to room temperature. The reaction mixture was concentrated under reduced pressure and the resulting residue was diluted with DCM washed sequentially with saturated sodium

bicarbonate, water and saturated sodium chloride. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel

chromatography (DCM/EtOAc/MeOH) to afford 1 -terf-butyl 2-methyl (2S,4R)-4-[2-(tert- butoxycarbonylamino)ethylamino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 72, 4.77 g, 42% yield) as a colorless oil. ¹ H NMR (500MHz, DMSO-de) d 1 .25 - 1 .48 (20H, m), 1 .84 - 2.07 (3H, m), 2.88 - 2.98 (2H, m), 3.02 - 3.17 (1 H, m), 3.17 - 3.27 (1 H, m), 3.40 - 3.51 (1 H, m), 3.64 (3H, s), 4.14 - 4.24 (1 H, m), 6.63 - 6.74 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 388.

Intermediate 73: 1 -tert-butyl 2-methyl (2S,4R)-4Jtert-butexycarbenyl-[2-(tert- butoxycarbonylamino)ethvnamino]pyrrolidine-1,2-dicarboxylate

Di-terf-butyl dicarbonate (4.29 mL, 18.5 mmol) was added to a solution of 1 -terf-butyl 2- methyl (2S,4f?)-4-[2-(terf-butoxycarbonylamino)ethylamino]pyrrolidi ne-1 ,2-dicarboxylate

(Intermediate 72, 4.77 g, 12.3 mmol) and A/,/V-diisopropylethylamine (4.30 mL, 24.6 mmol) in DCM (53 mL) at room temperature and the reaction stirred for 17 h. The reaction mixture was diluted with DCM and washed sequentially with water and saturated aqueous sodium chloride. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (hexanes/EtOAc) to afford 1 -terf-butyl 2- methyl (2S,4f?)-4-[te/f-butoxycarbonyl-[2-(te/f-butoxycarbonylamino )ethyl]amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 73, 4.25 mg, 71 % yield). ¹H NMR (500MHz, DMSO-afe) d 1 .21 - 1 .27 (1 H, m), 1 .27 - 1 .42 (27H, m), 1 .99 - 2.07 (1 H, m), 2.33 - 2.46 (1 H, m), 2.93 - 3.14 (3H, m), 3.17 - 3.24 (1 H, m), 3.48 - 3.61 (1 H, m), 3.61 - 3.69 (3H, m), 4.20 - 4.44 (2H, m), 6.79 - 6.94 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 488.

Intermediate 74: 2-benzyl 1 -tert-butyl (2S,4R)-4-[tert-butexycarbenyl-[2-(tert- butoxycarbonylamino)ethyl]amino]pyrrolidine-1,2-dicarboxylat e

A solution of sodium hydroxide (2.09 g, 52.3 mmol) in water (1 1 mL) was added to a solution of 1 -terf-butyl 2-methyl (2S,4R)-4-[tert-butoxycarbor\y\-[2-(tert- butoxycarbonylamino)ethyl]amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 73, 4.25 g, 8.72 mmol) in THF (22 mL) and MeOH (1 1 mL) at 0 °C. The reaction mixture stirred for 6 hrs while slowly warming to room temperature. The volatiles were removed under reduced pressure and the aqueous layer was acidified to pH ~3 with 5 M HCI (aq) and extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated in dryness to afford the crude carboxylic acid as a white solid which was used without further purification.

Benzyl bromide (1 .24 mL, 10.5 mmol) was added to a solution of the crude carboxylic acid, sodium iodide (1 .96 g, 13.1 mmol) and K ₂CO ₃ (3.62 g, 26.2 mmol) in DMF (28 mL) and the reaction stirred at room temperature for 17 h. The reaction mixture was filtered, and the solids were rinsed with EtOAc. The filtrate was concentrated and purified by silica gel chromatography (hexanes/EtOAc) to afford 2-benzyl 1 -tert-butyl (2S,4F?)-4-[tert-butoxycarbonyl-[2-(tert- butoxycarbonylamino)ethyl]amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 74, 3.91 g, 80% yield) as a white solid. ¹H NMR (500MHz, DMSO-d ₆) d 1 .20 - 1 .47 (27H, m), 2.00 - 2.13 (1 H, m), 2.36 - 2.45 (1 H, m), 2.93 - 3.01 (2H, m), 3.02 - 3.26 (3H, m), 3.48 - 3.64 (1 H, m), 4.26 - 4.43 (2H, m), 5.05 - 5.22 (2H, m), 6.78 - 6.93 (1 H, m), 7.25 - 7.41 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 564. Intermediate 75: 2-benzyl 1-tert-butyl (4R)-2-(but-2-enyl)-4-[tert-butoxycarbonyl-[2-(tert- butoxycarbonylamino)ethyl]aminolpyrrolidine-1,2-dicarboxylat e

2-Benzyl 1 -fert-butyl (2S,4F?)-4-[tert-butoxycarbonyl-[2-(tert- butoxycarbonylamino)ethyl]amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 74, 3.91 g, 6.94 mmol) and crotyl bromide (0.93 mL, 9.0 mmol) were dissolved in THF (10.6 mL) and the solution was cooled to -78 °C under an atmosphere of N ₂. A solution of KHMDS (0.5M in toluene, 34.7 mL, 17.3 mmol) was added dropwise to the reaction mixture and the reaction stirred for 17 h while slowly warming to room temperature. The crude reaction mixture was quenched with water and the volatiles were removed under reduced pressure. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel purification (hexanes/EtOAc) to afford 2-benzyl 1 -tert-butyl (4F?)-2-(but-2-enyl)-4- [tert-butoxycarbonyl-[2-(tert-butoxycarbonylamino)ethyl]amin o]pyrrolidine-1 ,2-dicarboxylate (Intermediate 75, 1 .34 g, 31 % yield) as a yellow oil and as a mixture of diastereomers, E/Z olefin isomers and rotamers. ¹ H NMR (500MHz, DMSO-afe) d 1 .21 - 1 .45 (27H, m), 1 .53 - 1 .71 (3H, m), 1 .91 - 2.32 (2H, m), 2.37 - 2.47 (1 H, m), 2.69 - 2.86 (1 H, m), 2.86 - 3.1 1 (4H, m), 3.46 - 3.58 (1 H, m), 3.58 - 3.77 (1 H, m), 4.29 - 4.57 (1 H, m), 5.00 - 5.20 (2H, m), 5.28 - 5.46 (1 H, m), 5.46 - 5.71 (1 H, m), 6.83 - 7.00 (1 H, m), 7.19 - 7.43 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 618.

Intermediate 76: 2-benzyl 1 -tert-butyl (4R)-4-[tert-butoxycarbonyl-[2-(tert- butoxycarbonylamino)ethynamino]-2-[4-(4,4,5,5-tetramethyl-1, 3,2-dioxaborolan-2- yDbutyllpyrrolidine- 1 ,2-dicarboxylate

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (222 mg, 0.331 mmol) and

bis(diphenylphosphino)methane (254 mg, 0.661 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (9 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (1 .05 mL, 7.26 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. 2-Benzyl 1 -terf-butyl (4f?)-2- (but-2-enyl)-4-[terf-butoxycarbonyl-[2-(terf-butoxycarbonyla mino)ethyl]amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 75, 2.04 g, 3.30 mmol) was added to the reaction as a solution in DCM (6.1 mL) and the reaction mixture stirred for 16 h at room temperature. The reaction mixture was cooled to 0 °C and carefully quenched with MeOH and water. The layers were separated, and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The resulting residue was purified by flash silica chromatography (hexanes/EtOAc) to afford 2-benzyl 1 -terf-butyl (4R)-4-[tert- butoxycarbonyl-[2-(terf-butoxycarbonylamino)ethyl]amino]-2-[ 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 76, 1 .14 g, 46% yield) as a yellow oil and as a mixture of diastereomers and rotamers. The purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 30 x 250 mm, 5 pm, Temperature = 20 °C, Mobile phase = 0-20% IPA with 0.2% NH ₄0H:C0 ₂, UV detection @ 220 nm, loading = 18 mg/inj, cone = 46 mg/mL in MeOH, flow rate = 120 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The stereochemistry of each diastereomer was assigned retrospectively based on the enzyme potency of Example 27 and Example 28 to be congruent with other exemplified compounds.

Intermediate 77 (Isomer 2, 347 mg): 2-benzyl 1 -terf-butyl {2R,4R)-4-[tert- butoxycarbonyl-[2-(terf-butoxycarbonylamino)ethyl]amino]-2-[ 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (500MHz, DMSO-afe) d 0.60 - 0.76 (2H, m), 1 .15 (12H, s), 1 .21 - 1 .52 (31 H, m), 1 .66 - 1 .82 (1 H, m), 1 .96 - 2.19 (2H, m), 2.19 -

2.33 (1 H, m), 2.83 - 3.10 (4H, m), 3.48 - 3.66 (1 H, m), 4.34 - 4.53 (1 H, m), 5.00 - 5.23 (2H, m),

6.83 - 6.93 (1 H, m), 7.25 - 7.43 (5H, m).

Intermediate 78 (Isomer 1 , 540 mg): 2-benzyl 1 -terf-butyl (2S,4H)-4-[tert- butoxycarbonyl-[2-(terf-butoxycarbonylamino)ethyl]amino]-2-[ 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (500MHz, DMSO-afe) d 0.61 - 0.76 (2H, m), 1 .15 (12H, s), 1 .21 - 1 .47 (31 H, m), 1 .61 - 1 .80 (1 H, m), 1 .93 - 2.24 (2H, m), 2.26 -

2.43 (1 H, m), 2.89 - 3.13 (5H, m), 3.60 - 3.81 (1 H, m), 4.33 - 4.49 (1 H, m), 5.00 - 5.20 (2H, m),

6.86 - 6.94 (1 H, m), 7.27 - 7.39 (5H, m).

Intermediate 79: (2R,4R)-1Jert-butoxycarbonyl-4-[tert-butoxycarbonyl-[2-(tert - butoxycarbonylamino)ethyl]aminol-2-f4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2- yl)butynpyrrolidine-2-carboxylic acid Pd/C (10% wt, 99 mg, 0.093 mmol) was added to a solution of 2-benzyl 1 -terf-butyl (2P?,4/ ^:?)-4-[te/i-butoxycarbonyl-[2-(te/i-butoxycarbonylamino )ethyl]amino]-2-[4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 77, 347 mg, 0.465 mmol) in EtOAc (2.3 mL). The flask was equipped with a balloon of hk and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness to afford (2P?,4/ ^:?)-1 -fert-butoxycarbonyl-4-[fe/f-butoxycarbonyl-[2-(te/f-butoxyc arbonylamino)ethyl]amino]- 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid

(Intermediate 79, 287 mg, 94% yield) as a white solid which was used without further purification. ¹H NMR (500MHz, DMSO-de) d 0.65 - 0.74 (2H, m), 1 .14 - 1 .21 (12H, m), 1 .31 - 1 .43 (31 H, m), 1 .66 - 1 .76 (1 H, m), 2.00 - 2.27 (3H, m), 2.96 - 3.12 (5H, m), 3.37 - 3.42 (1 H, m), 3.49 - 3.61 (1 H, m), 4.34 - 4.49 (1 H, m), 6.84 - 6.93 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 656.

Example 27: (2R,4R)-4-(2-aminoethylamino)-2-(4-boronobutyl)pyrrolidine-2 -carboxylic acid

Trifluoroacetic acid (0.67 mL, 8.8 mmol) was added dropwise to a stirred solution of (2P?,4/ ^:?)-1 -fert-butoxycarbonyl-4-[fe/f-butoxycarbonyl-[2-(te/f-butoxyc arbonylamino)ethyl]amino]- 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid

(Intermediate 79, 287 mg, 0.438 mmol) in DCM (3.7 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (107 mg, 0.878 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2P?,4/ ^:?)-4-(2-aminoethylamino)-2-(4-boronobutyl)pyrrolidine- 2-carboxylic acid (Example 27, 106 mg, 89% yield) as a white solid. ¹H NMR (500 MHz, D ₂0) d 0.63 - 0.77 (2H, m), 1 .13 - 1 .23 (1 H, m), 1 .37 (3H, br d), 1 .63 - 1 .76 (1 H, m), 1 .92 - 2.02 (1 H, m), 2.06 - 2.14 (1 H, m), 2.24 - 2.33 (1 H, m), 2.78 (2H, s), 2.96 (2H, s), 3.08 - 3.19 (1 H, m), 3.28 - 3.43 (1 H, m), 3.43 - 3.51 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 274. Example 28: i-4-(2-ami -2-carboxyl ic acid

Intermediate 78 Intermediate 80 Example 28

Intermediate 80: (2S.4R)- 1 -tert-butoxycarbonyl-4-[tert-butoxycarbonylJ2-(tert- butoxycarbonylamino)ethvnaminol-2-[4-(4,4.5,5-tetramethyl-1, 3.2-dioxaborolan-2- yl)butvnDyrrolidine-2-carboxylic acid

Pd/C (10% wt, 137 mg, 0.129 mmol) was added to a solution of 2-benzyl 1 -ferf-butyl (2S,4P?)-4-[ie/i-butoxycarbonyl-[2-(iert-butoxycarbonylamino )ethyl]amino]-2-[4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 78, 480 mg, 0.64 mmol) in EtOAc (7.2 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness and purified by silica gel chromatography (hexanes/EtOAc) to afford (2S,4f?)-1 -terf-butoxycarbonyl-4-[terf- butoxycarbonyl-[2-(terf-butoxycarbonylamino)ethyl]amino]-2-[ 4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 80, 170 mg, 40% yield) as a white solid. ¹ H NMR (500MHz, DMSO-de) d 0.58 - 0.73 (2H, m), 1 .15 (12H, s), 1 .37 (31 H, br d), 1 .58 - 1 .74 (2H, m), 2.18 - 2.33 (2H, m), 2.92 - 3.16 (6H, m), 3.59 - 3.73 (1 H, m), 4.31 - 4.50 (1 H, m), 6.84 - 6.95 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 656.

Example 28: (2S.4R)-4-{2-aminoethylamino)-2-{4-boronobutyl)Dyrrolidine-2 -carboxylic acid

Trifluoroacetic acid (1 .00 mL, 13.0 mmol) was added dropwise to a stirred solution of (2S,4P?)-1 -te/f-butoxycarbonyl-4-[fert-butoxycarbonyl-[2-(fert-butoxyc arbonylamino)ethyl]amino]- 2-[4-(4,4,5,5-tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid

(Intermediate 80, 170 mg, 0.26 mmol) in DCM (5 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (63 mg, 0.52 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 20cc column). The desired product was eluted from the column using 5% ammonia in MeOH (20 mL) to afford (2S,4f?)-4-(2-aminoethylamino)-2-(4-boronobutyl)pyrrolidine- 2-carboxylic acid (Example 28, 67 mg, 95% yield) as a white solid. ¹ H NMR (500 MHz, D ₂0) d 0.65 - 0.77 (2H, m), 1 .1 1 - 1 .24 (1 H, m), 1 .25 - 1 .34 (1 H, m), 1 .34 - 1 .42 (2H, m), 1 .62 - 1 .79 (2H, m), 1 .97 - 2.06 (1 H, m), 2.61 - 2.70 (1 H, m), 2.72 - 2.84 (2H, m), 2.93 (3H, s), 3.30 - 3.41 (1 H, m), 3.47 - 3.55

(1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 274.

Example 29: (2ff,4ff)-4-IT(2S)-2-amino-3-methyl-butanovn-methyl-amino1-2 -(4- boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 81 Intermediate 82 Intermediate 83

Intermediate 84 Intermediate 85 te 86

Intermediate 87 Intermediate 88 Intermediate 89

Intermediate 90 Example 29

Di-terf-butyl dicarbonate (6.27 g, 28.8 mmol) was added to a solution of 1 -benzyl 2- methyl (2S,4F?)-4-aminopyrrolidine-1 ,2-dicarboxylate (5.00 g, 18.0 mmol) and triethylamine (5.00 mL, 35.9 mmol) in DCM (78 ml) and the reaction stirred at room temperature for 16 h.

The reaction mixture was diluted with DCM and washed sequentially with 0.5 M HCI (aq), saturated sodium bicarbonate and saturated sodium chloride. The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel chromatography (DCM/MeOH) to afford 1 -benzyl 2-methyl (2S,4R)-4-(tert- butoxycarbonylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 81 , 5.4 g, 79% yield) as a white solid. ¹ H NMR (500MHz, DMSO-d ₆) d 1 .31 - 1 .42 (9H, m), 1 .99 - 2.23 (2H, m), 3.22 - 3.28 (1 H, m), 3.52 - 3.65 (4H, m), 3.96 - 4.10 (1 H, m), 4.30 - 4.48 (1 H, m), 4.92 - 5.13 (2H, m), 7.18 - 7.41 (5H, m) ; m/z: (ES ⁺) [M+H] ⁺ = 379.

Sodium hydride (60% dispersion in mineral oil) (0.423 g, 12.3 mmol) was added portion- wise to a solution 1 -benzyl 2-methyl (2S,4f?)-4-(fert-butoxycarbonylamino)pyrrolidine-1 ,2- dicarboxylate (Intermediate 81 , 3.20 g, 8.46 mmol) in DMF (33 mL) at 0 °C. The reaction mixture stirred at 0 °C for 1 h before warming to room temperature with stirring for an additional 1 h. Methyl iodide (0.63 ml, 10.2 mmol) was added and the reaction stirred at room temperature for 16 h. The reaction mixture was cooled to 0 °C and quenched with water. The volatiles were removed under reduced pressure and the suspension was diluted with DCM (200 mL). The layers were separated, and the organic layer was washed sequentially with water (4 x 50 mL) and saturated aqueous sodium chloride (2 x 50 mL). The organic layer was dried over Na ₂SC> ₄, filtered and concentrated to dryness to afford 1 -benzyl 2-methyl ( 2S,4R)-4-[tert - butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 82, 2.33 g, 70% yield) as a colorless oil which was used without further purification. ¹ H NMR (500MHz, DMSO-afe) d 1 .25 - 1 .47 (9H, m), 1 .89 - 2.08 (1 H, m), 2.31 - 2.46 (1 H, m), 2.69 (3H, d), 3.22 - 3.39 (2H, m), 3.65 (4H, s), 4.22 - 4.49 (1 H, m), 4.87 - 5.17 (2H, m), 7.18 - 7.46 (5H, m); m/z: (ES ⁺) [M+H] ⁺ = 393.

Intermediate 83: dibenzyl (2S,4R)-4-[tert-butoxycarbonyl(methyl)amino]pyrrolidine-1,2-

A solution of sodium hydroxide (1 .425 g, 35.62 mmol) in water (7.5 mL) was added to a solution of 1 -benzyl 2-methyl (2S,4F?)-4-[te/f-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 82, 2.33 g, 5.94 mmol) in THF (15 mL) and MeOH (7.5 mL) at 0 °C. The reaction mixture stirred for 6 hrs while slowly warming to room temperature. The volatiles were removed under reduced pressure and the aqueous layer was acidified to pH ~3 with 5 M HCI (aq) and extracted with DCM (4 x 50 mL). The combined organics were dried over Na ₂SC> ₄, filtered and concentrated in dryness to afford the crude carboxylic acid as a white solid which was used without further purification.

Benzyl bromide (0.66 mL, 5.6 mmol) was added to a solution of the crude carboxylic acid, sodium iodide (1 .1 1 g, 7.38 mmol) and K ₂CO ₃ (1 .92 g, 13.9 mmol) in DMF (28 mL) and the reaction stirred at room temperature for 17 h. The reaction mixture was filtered, and the solids were rinsed with EtOAc. The filtrate was concentrated and purified by silica gel chromatography (hexanes/EtOAc) to afford dibenzyl (2S,4F?)-4-[terf-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 83, 2.45 g, 94% yield) as a pale-yellow oil. ¹ H NMR (500MHz, DMSO-de) d 1 .28 - 1 .45 (9H, m), 1 .98 (1 H, s), 2.30 - 2.46 (1 H, m), 2.64 - 2.71 (3H, m), 3.30 (1 H, s), 3.51 - 3.76 (1 H, m), 4.48 (1 H, d), 4.53 - 4.75 (1 H, m), 4.88 - 5.21 (4H, m), 7.18 - 7.42 (1 OH, m); m/z: (ES ⁺) [M+H] ⁺ = 469.

Intermediate 84: dibenzyl ( 4R)-2-(but-2-enyl)-4-[tert-butoxycarbonyl(methyl)amino]pyrro lidine -

1 ,2-dicarboxvlate

Dibenzyl (2S,4F?)-4-[terf-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2-dicarboxylate

(Intermediate 83, 2.45 g, 5.23 mmol) and crotyl bromide (0.81 mL, 7.8 mmol) were dissolved in THF (18 mL) and the solution was cooled to -78 °C under an atmosphere of N ₂. A solution of KHMDS (0.5M in toluene, 15.7 mL, 7.85 mmol) was added dropwise to the reaction mixture and the reaction stirred for 17 h while slowly warming to room temperature. The crude reaction mixture was quenched with water and the volatiles were removed under reduced pressure. The crude mixture was diluted in DCM and the layers were separated. The organic layer was washed with water, dried over Na ₂SC> ₄, filtered and concentrated to dryness. The crude material was purified by silica gel purification (hexanes/EtOAc) to afford dibenzyl (4F?)-2-(but-2- enyl)-4-[te/7-butoxycarbonyl(methyl)amino]pyrrolidine-1 ,2-dicarboxylate (Intermediate 84, 2.10 g, 86% yield) as a yellow oil and as a mixture of diastereomers, E/Z olefin isomers and rotamers. ¹ H NMR (500MHz, DMSO-d ₆) d 1 .31 - 1 .40 (9H, m), 1 .46 - 1 .68 (3H, m), 1 .99 - 2.31 (2H, m), 2.40 - 2.47 (1 H, m), 2.55 - 2.68 (3H, m), 2.69 - 3.00 (1 H, m), 3.30 (1 H, s), 3.51 - 3.77 (1 H, m), 4.55 - 4.74 (1 H, m), 4.79 - 5.21 (4H, m), 5.26 - 5.41 (1 H, m), 5.42 - 5.71 (1 H, m), 7.16 - 7.42 (1 OH, m); m/z: (ES ⁺) [M+H] ⁺ = 523.

Intermediate 85: dibenzyl ( 4R)-2-(but-2-enyl)-4-(methylamino)pyrrolidine - 1 ,2-dicarboxylate Trifluoroacetic acid (3.84 ml_, 50.2 mmol) was added dropwise to a solution of dibenzyl (4F?)-2-(but-2-enyl)-4-[terf-butoxycarbonyl(methyl)amino]pyr rolidine-1 ,2-dicarboxylate

(Intermediate 84, 2.10 g, 4.02 mmol) in DCM (32 mL) and the reaction stirred at room temperature for 2 h. The reaction mixture was concentrated to dryness to afford the TFA salt of dibenzyl (4F?)-2-(but-2-enyl)-4-(methylamino)pyrrolidine-1 ,2-dicarboxylate (Intermediate 85,

2.55 g, 100% yield) as a colorless oil which was used without purification. ¹H NMR (500MHz, DMSO-de) d 1 .45 - 1 .74 (3H, m), 2.14 - 2.33 (1 H, m), 2.34 - 2.46 (1 H, m), 2.57 - 2.65 (3H, m), 2.66 - 3.07 (1 H, m), 3.15 - 3.56 (1 H, m), 3.66 - 3.77 (1 H, m), 3.81 - 4.13 (1 H, m), 4.79 - 5.22 (4H, m), 5.26 - 5.73 (2H, m), 7.20 - 7.41 (1 OH, m), 8.62 - 8.87 (2H, m); m/z: (ES ⁺) [M+H] ⁺ = 423. Intermediate 86: dibenzyl (4R)-2-(but-2-enyl)-4-[[(2S)-2-(tert-butoxycarbonylamino)-3- methyl- butanoyll-methyl-aminolpyrrolidine- 1 ,2-dicarboxylate

A/,/V-Diisopropylethylamine (0.70 mL, 4.0 mmol) was added to a solution of HATU (1 .52, 4.02 mmol) and Boc-Val-OH (873 mg, 4.02 mmol) in DMF (15 mL) and the reaction stirred at room temperature for 30 min. A solution of dibenzyl (4F?)-2-(but-2-enyl)-4- (methylamino)pyrrolidine-l ,2-dicarboxylate TFA salt (Intermediate 85, 2.16 g, 4.02 mmol) in DMF (15 mL) and A/,/V-Diisopropylethylamine (0.70 mL, 4.0 mmol) were added and the reaction stirred at room temperature for an additional 17 h. The reaction mixture was concentrated and directly purified by silica gel chromatography (hexanes/EtOAc) to afford dibenzyl (4F?)-2-(but-2- enyl)-4-[[(2S)-2-(terf-butoxycarbonylamino)-3-methyl-butanoy l]-methyl-amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 86, 1 .97 g, 79% yield) as a mixture of rotamers. ¹ H NMR (500MHz, DMSO-de) d ¹ H NMR (500MHz, DMSO-d ₆) 0.61 - 0.92 (6H, m), 1 .35 (9H, br s), 1 .62 (3H, br d),

1 .79 - 1 .92 (1 H, m), 2.03 - 2.33 (2H, m), 2.57 - 2.76 (2H, m), 2.76 - 3.00 (3H, m), 3.30 (1 H, s), 3.49 - 3.77 (1 H, m), 4.04 - 4.16 (1 H, m), 4.78 - 5.20 (5H, m), 5.26 - 5.72 (2H, m), 6.72 - 7.03 (1 H, m), 7.17 - 7.38 (1 OH, m); m/z: (ES ⁺) [M+H] ⁺ = 622.

Intermediate 87: dibenzyl (4R)-4-[[(2S)-2-(tert-butoxycarbonylamino)-3-methyl-butanoyl ]-methyl- amino]-2-f4-(4, 4, 5, 5-tetramethyl-1, 3, 2-dioxaborolan-2-yl)butylloyrrolidine-1 ,2-dicarboxylate

Bis(1 ,5-cyclooctadiene)diiridium(l) dichloride (213 mg, 0.317 mmol) and

bis(diphenylphosphino)methane (244 mg, 0.635 mmol) were added to an oven-dried round- bottom flask. The flask was sealed and purged with N ₂. The solids were dissolved in DCM (8.9 mL) and 4,4,5,5-tetramethyM ,3,2-dioxaborolane (1 .01 mL, 6.97 mmol) was slowly added to the solution. The reaction was stirred at room temperature for 10 min. Dibenzyl (4F?)-2-(but-2-enyl)- 4-[[(2S)-2-(terf-butoxycarbonylamino)-3-methyl-butanoyl]-met hyl-amino]pyrrolidine-1 ,2- dicarboxylate (Intermediate 86, 1 .97 g, 3.17 mmol) was added to the reaction as a solution in DCM (5.9 mL) and the reaction mixture stirred for 16 h at room temperature. The reaction mixture was cooled to 0 °C and carefully quenched with MeOH and water. The layers were separated, and the aqueous layer was extracted with DCM. The combined organics were dried over Na ₂SC> ₄, filtered and concentrated to dryness. The resulting residue was purified by flash silica chromatography (hexanes/EtOAc) to afford dibenzyl (4f?)-4-[[(2S)-2-(terf- butoxycarbonylamino)-3-methyl-butanoyl]-methyl-amino]-2-[4-( 4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 87, 1 .5 g, 63% yield) as a yellow oil and as a mixture of diastereomers and rotamers. The purified material was subjected to chiral SFC [(S,S)Whelk-01 column, 30 x 250 mm, 5 pm, Temperature = 20 °C, Mobile phase = 0-30% MeOH:C0 ₂, UV detection @ 220 nm, loading = 31 mg/inj, cone = 125 mg/mL in MeOH, flow rate = 75 mL/min, Outlet Pressure = 100 bar] to give two diastereomers. The

stereochemistry of each diastereomer was assigned retrospectively based on the enzyme potency of Example 29 and Example 30 to be congruent with other exemplified compounds.

Intermediate 88 (Isomer 2, 280 mg): dibenzyl (2R,4R)-4-[[(2S)-2-(tert- butoxycarbonylamino)-3-methyl-butanoyl]-methyl-amino]-2-[4-( 4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (500MHz, DMSO-afe) d 0.51 - 0.70 (2H, m), 0.72 - 0.93 (6H, m), 1 .14 (12H, s), 1 .20 - 1 .52 (13H, m), 1 .67 - 2.31 (5H, m), 2.54 - 2.90 (3H, m), 3.33 - 3.48 (1 H, m), 3.49 - 3.85 (1 H, m), 4.01 - 4.18 (1 H, m), 4.71 - 5.23 (5H, m), 6.71 - 7.07 (1 H, m), 7.19 - 7.33 (1 OH, m).

Intermediate 89 (Isomer 1 , 590 mg): dibenzyl (2S,4F?)-4-[[(2S)-2-(terf- butoxycarbonylamino)-3-methyl-butanoyl]-methyl-amino]-2-[4-( 4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate. ¹ H NMR (500MHz, DMSO-afe) d 0.49 - 0.72 (2H, m), 0.73 - 0.90 (6H, m), 1 .15 (12H, s), 1 .34 (13H, br s), 1 .59 - 2.34 (5H, m), 2.94 (3H, br s), 3.30 (1 H, s), 3.63 - 3.76 (1 H, m), 3.96 - 4.17 (1 H, m), 4.75 - 5.18 (5H, m), 6.71 - 7.05 (1 H, m), 7.17 - 7.41 (10H, m).

Intermediate 90: (2R,4R)-4-[[(2S)-2-(tert-butoxycarbonylamino)-3-methyl-butan ovn-methyl- amino]-2-[4-(4,4,5,5-tetramethvl-1,3,2-dioxaborolan-2-vl)but vllpvrrolidine-2-carboxvlic acid

Pd/C (10% wt, 99 mg, 0.093 mmol) was added to a solution of dibenzyl (2R,4R)-4-[[(2S)- 2-(terf-butoxycarbonylamino)-3-methyl-butanoyl]-methyl-amino ]-2-[4-(4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 88, 280 mg, 0.37 mmol) in EtOAc (1 .8 mL). The flask was equipped with a balloon of H ₂ and the suspension stirred at room temperature for 4 h. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness to afford (2R,4H)-4-[[(2S)-2-(tert- butoxycarbonylamino)-3-methyl-butanoyl]-methyl-amino]-2-[4-( 4,4,5,5-tetramethyl-1 ,3,2- dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 90, 180 mg, 92% yield) as a white solid which was used without further purification. ¹H NMR (500MHz, DMSO-afe) d 0.59 - 0.69 (2H, m), 0.74 - 0.87 (6H, m), 1 .16 (12H, s), 1 .22 - 1 .30 (3H, m), 1 .35 (9H, s), 1 .49 - 1 .65 (1 H, m), 1 .65 - 1 .82 (1 H, m), 1 .82 - 1 .95 (2H, m), 2.15 - 2.26 (1 H, m), 2.63 - 2.91 (3H, m), 2.92 - 3.21 (3H, m), 4.05 - 4.22 (1 H, m), 4.80 - 5.16 (1 H, m), 6.76 (1 H, s), 7.56 - 8.05 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 526.

Example 29: (2R,4R)-4-[[(2S)-2-amino-3-methyl-butanoyll-methyl-aminol-2- (4- boronobutyl)pyrrolidine-2-carboxylic acid

Trifluoroacetic acid (0.53 mL, 6.9 mmol) was added dropwise to a stirred solution of (2f?, 4f?)-4-[[(2S)-2-(tert-butoxycarbonylamino)-3-methyl-butanoyl ]-methyl-amino]-2-[4-(4, 4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 90, 180 mg, 0.34 mmol) in DCM (10 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (84 mg, 0.69 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 60cc column). The desired product was eluted from the column using 5% ammonia in MeOH (60 mL) to afford (2R?,4R?)-4- [[(2S)-2-amino-3-methyl-butanoyl]-methyl-amino]-2-(4-boronob utyl)pyrrolidine-2-carboxylic acid (Example 29, 98 mg, 86% yield) as a white solid. ¹ H NMR (500 MHz, D ₂0) d 0.72 - 0.83 (2H, m), 0.85 - 1 .01 (6H, m), 1 .10 - 1 .45 (4H, m), 1 .61 - 1 .84 (1 H, m), 1 .85 - 2.03 (2H, m), 2.19 - 2.34 (1 H, m), 2.34 - 2.49 (1 H, m), 3.00 (3H, s), 3.16 - 3.51 (2H, m), 3.76 - 3.96 (1 H, m), 4.95 - 5.10 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 344.

Example 30: (2S.4flM-IT(2S)-2-amino-3-methyl-butanovn-methyl-amino1-2-(4 - boronobutvhpyrrolidine-2-carboxylic acid

Intermediate 89 Intermediate 91 Example 30

Intermediate 91 : (2S,4R)-4-[[(2S)-2-(tert-butoxycarbonylamino)-3-methyl-butan oyll-methyl- aminol-2-[4-{4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but yllpyrrolidine-2-carboxylic acid Pd/C (10% wt, 209 mg, 0.196 mmol) was added to a solution of dibenzyl (2S,4f?)-4- [[(2S)-2-(terf-butoxycarbonylamino)-3-methyl-butanoyl]-methy l-amino]-2-[4-(4,4,5,5-tetramethyl-

1 .3.2-dioxaborolan-2-yl)butyl]pyrrolidine-1 ,2-dicarboxylate (Intermediate 89, 590 mg, 0.79 mmol) in EtOAc (4 mL). The flask was equipped with a balloon of hk and the suspension stirred overnight at room temperature. The reaction mixture was diluted with MeOH and filtered through diatomaceous earth. The filtrate was concentrated to dryness to afford (2S,4f?)-4- [[(2S)-2-(terf-butoxycarbonylamino)-3-methyl-butanoyl]-methy l-amino]-2-[4-(4,4,5,5-tetramethyl-

1 .3.2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 91 , 397 mg, 96% yield) as a white solid which was used without further purification. ¹H NMR (500MHz, DMSO-afe) d 0.58 - 0.67 (2H, m), 0.73 - 0.87 (6H, m), 1.16 (12H, s), 1 .22 - 1 .31 (3H, m), 1 .35 (9H, s), 1 .51 -

1 .67 (1 H, m), 1 .68 - 1 .95 (3H, m), 2.28 - 2.37 (2H, m), 2.95 (4H, s), 4.05 - 4.20 (1 H, m), 4.66 - 4.79 (1 H, m), 6.65 - 6.90 (1 H, m), 7.85 - 8.15 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 526.

Example 30: (2S,4E)-4-[[(2S)-2-amino-3-methyl-butanoyl]-methyl-amino]-2- (4- boronobutyl)pyrrolidine-2-carboxylic acid

Trifluoroacetic acid (1 .17 mL, 15.2 mmol) was added dropwise to a stirred solution of (2S,4f?)-4-[[(2S)-2-(terf-butoxycarbonylamino)-3-methyl-buta noyl]-methyl-amino]-2-[4-(4,4,5,5- tetramethyl-1 ,3,2-dioxaborolan-2-yl)butyl]pyrrolidine-2-carboxylic acid (Intermediate 91 , 397 mg, 0.755 mmol) in DCM (10 mL) at room temperature. After 1 h the solution was concentrated under reduced pressure and the resulting residue was dissolved in 1 M HCI aq (5 mL) and Et ₂0 (5 mL). Phenylboronic acid (186 mg, 1 .52 mmol) was added and the clear biphasic solution stirred at room temperature for 1 h. The mixture was diluted with Et ₂0 and water and the layers were separated. The aqueous layer was washed with Et ₂0. The aqueous layer was lyophilized and purified by ion exchange chromatography (PoraPak Rxn CX 60cc column). The desired product was eluted from the column using 5% ammonia in MeOH (60 mL) to afford (2S,4f?)-4- [[(2S)-2-amino-3-methyl-butanoyl]-methyl-amino]-2-(4-boronob utyl)pyrrolidine-2-carboxylic acid (Example 30, 163 mg, 92% yield) as a white solid. ¹H NMR (500 MHz, D ₂0) d 0.68 - 0.78 (2H, m), 0.83 - 0.94 (6H, m), 1 .10 - 1 .41 (4H, m), 1 .66 - 2.13 (4H, m), 2.49 - 2.68 (1 H, m), 3.02 (3H, s), 3.22 - 3.30 (1 H, m), 3.43 - 3.60 (1 H, m), 3.70 - 3.88 (1 H, m), 4.53 - 4.66 (1 H, m); m/z: (ES ⁺) [M+H] ⁺ = 344.

Example 31 : Bioloaical Activity of Examples 1 to 30

The inhibitory effects of Examples 1 to 30 on the activity of Human Arginase 1 and Arginase 2 activity were quantified by measuring the formation of the thiol group from thioarginine using recombinant Arginase 1 or Arginase 2 produced from E. coli. The thiol group was detected with Ellman’s reagent, 5,5' -dithiobis(2-nitrobenzoic acid) (DTNB). DTNB reacts with the thiol to give the mixed disulfide and 2-nitro-5-thiobenzoic acid (TNB) which is quantified by the absorbance of the anion (TNB ² ) at 412 nm.

The assays were run in clear 384 well plates (Greiner cat no: 781 101 ). Various concentrations of Examples 1 to 30 in 300 nl_ DMSO were dispensed to assay plates using an Echo acoustic dispenser immediately followed by plate sealing and centrifugation.

Two pre-mixes were prepared from reagents thawed immediately before addition to assay plates. Pre-mix one comprised human Arginase 1 or human Arginase 2, at a final concentration of 5 nM and 0.5mM DTNB in assay buffer, 45mM HEPES pH7.5, brij 35, 0.045% (w/v) and 100 mM MnCl2. Pre-mix two comprised freshly thawed 0.5mM thioarginine in assay buffer. Fifteen microlitres of pre-mix one was dispensed to assay plates containing Examples 1 to 30, centrifuged and incubated for 30 minutes at room temperature prior to adding fifteen microlitres of pre-mix two.

Assay plates were centrifuged prior to reading absorbance at 412nm in a Pherastar multi-mode plate reader to collect data at time point 0 (TO). The plates were incubated at room temperature for 60 min prior to reading again to collect data at time point 1 (T1 ). Data is derived by subtracting the A412 signal measured at TO (time point 0) from that measured at T1 (time point 1 ). The data was transformed to % effect using the equation:

Compound % effect = 100 ^*[(X-min)/(max-min)], where X represents the normalized value for the compound based on the Min (vehicle) and Max (reference compound) inhibition control.

The concentration of Examples 1 to 30 that inhibited the activity by 50% (i.e. the IC50) was calculated by plotting the % effect versus test compound concentration and fitting the data using the Genedata Screener Smart fit algorithm. The results of these assays are found in Table 2:

Table 2

Example 32: Bioavailabilitv Studies

Examples 8, 9, and 13 to 20 are prodrug forms of Example 7. The following

pharmacokinetic study was performed to demonstrate bioavailability of Example 7 from

Example 8. Example 8 was formulated in 0.9% w/v saline pH 4 (adjusted with 1 M HCI) for IV dosing. The formulation was dosed at 2 mg/kg by femoral catheter to two male rats each (170— 250 g). Jugular vein catheter serial blood samples were taken at 0.033, 0.083, 0.167, 0.5, 1 , 2,

4, 8, and 24 hrs post-dose. For PO dosing, Example 8 was formulated in deionized water pH 4 (adjusted with 1 M HCI) and dosed at 5 mg/kg by oral gavage to two male rats each (170-250 g). Serial blood samples were taken by jugular vein catheter at 0.25, 0.5, 1 , 1 .5, 2, 3, 4, 8, and 24 hrs post dose. Plasma samples were generated from blood using low speed centrifugation. A single set of calibration standards containing Example 7 and Example 8 were prepared by spiking blank plasma. The samples and standards were extracted by precipitation with two volumes of acetonitrile followed by centrifugation. The results obtained were used to determine the Cl (mL/min/kg), Vdss ( L/kg ) , Cmax (mM), AUC (mM h), tmax (h), and %F for both Example 7 and Example 8. Absolute bioavailability was determined by comparing the PO dose normalized AUC of Example 7 when dosed as Example 8, versus the dose normalized IV AUC of Example 7 when dosed as Example 7. Where appropriate, measured and not nominal doses were used to calculate bioavalability. In an analogous fashion, the same procedure was repeated for Examples 9 and 13 to 20. The results are shown in Tables 3 to 12. These results indicate that bioavailability may be increased by incorporating certain amino acid moieties as prodrugs.