FIELD OF INVENTION

The present invention relates to new taxoids possessing strong antitumor activities, the precursors of these antitumor taxoids, and pharmaceutical compositions thereof.

BACKGROUND OF THE INVENTION

Taxol (paciitaxel), a complex diterpene, is currently considered the most exciting lead in cancer chemotherapy. Paciitaxel possesses high cytotoxicity and strong antitumor activity against different cancers which have not been effectively treated by existing antitumor drugs. For example, paciitaxel has been approved by FDA in late 1992 for the treatment of advanced ovaπan cancer and for breast cancer in 1994. Paciitaxel is currently - in phase II and in clinical trial for lung cancer and other cancers.

Although paciitaxel is an extremely important "lead" in cancer chemotherapy, it is common that better drugs can be derived from naturally occurring lead compounds. In fact, French researchers have discovered that a modification ofthe C-13 side chain of paciitaxel brought about a new anticancer agent which seems to have antitumor activity superior to paciitaxel with better bioavailability. This unnatural compound was named "Taxotere (docetaxel)", which has t-butoxycarbonyl instead of benzoyl on the amino group of (2__,55)-phenylisoserine moiety at the C-13 position and a hydroxyl group instead of acetoxy group at C-10. Docetaxel is currently in phase II and III clinical trials in United States, Europe, and Japan, has shown excellent activity, especially against breast and lung cancers.

T- _t_f_ ( docataMi)

T_P_S» _>•_*-_*■»)

A recent report on clinical trials of paciitaxel and docetaxel has disclosed that paciitaxel causes, e.g., nerve damage, muscle pain or disturbances in heart rhythm, whereas docetaxel provokes, e.g., mouth sores and a plunge in white blood cells. Other less senous side effects also exist for these two drugs. Therefore, it is very important to develop new anti-cancer drugs different from these two drugs which have fewer undesirable side effects, better pharmacological properties, improved activity against drug-resistant tumors, and/or activity spectra against various tumor types.

It is an objective of the present invention to develop such new anti-tumor agents of paciitaxel class, i.e., taxoids, which have distinct structural differences from those of paciitaxel and docetaxel.

It is an object of the present invention to provide a series of new taxoids bearing a 1- prόpenyl, 2-methyl-l-propenyl, 2-methylpropyl, or tnfluromethyl radical at the C-3' position instead of a phenyl group, and which possess strong antitumor activities with better therapeutic profile, in particular against drug-resistant tumors. One of the serious drawbacks of both paciitaxel and docetaxel is the fact that these two drugs possess only a weak activity against drug-resistant tumors, e.g., adriamycin-resistant breast cancer. The new taxoids of the present invention have shown not only stronger antitumor activities against human ovarian, non-small ceil lung, colon, and breast cancers than those of the two drugs, but also exhibit more thin one order of magnitude better acuvity against adriamycin-resistant human breast cancer ceils than those of the two drugs. Multi-drag-resistance (MDR) is a senous issue in clinical oncology, and thus the new taxoid anutumor agents of this invention will serve as important drugs to overcome this problem.

SUMMARY OF THE INVENTION

A taxoid of the formula (I)

in which

R ¹ is a C ₃ -Cj alkyl or alkenyl or trifluoromethyl radical;

R ¹ is a C,-C, branched alkyl radical;

R ¹ and R ⁴ are independently selected from hydrogen and hydroxyl protecting groups including functional groups which increase the water solubility of the taxoid antitumor agent;

R ^s represents a hydrogen or hydroxyl-protecting an acyl or alkoxycarbonyl or carbamoyl group;

R ⁶ represents an acyl radical, which are useful as antitumor agents or their precursors.

Preferably, R ^l is selected from propy I, 2-methyl-l-propenyl, 1 -methyl- 1 -propeny I, 2- methylpropyl. l-rnerhylpropyl, tert-butyl. cyclopropyl. cyclopropylmethyl, I -methyl- 1 -butenyl. 2-methyl- 1 -butenyl, 3-methyl-l -butenyl, 1-methylbutyl. 2-methylbutyl. isobutyl. 2-methylethyl. 3-methylbutyl, 2-butenyl, or trifluoromethyl radicals:

- 4 -

R ² is selected from isopropyl, cyclopropyl, isobutyl, sec-butyl, 2-methylpropyl, 3- methylpropyl, tert-butyl, cyclobutyl. cyclopentyl, 1 -ethyl propy I. or 1, 1-dimethylprop l radicals;

R ⁵ is selected from hydrogen, C ₂ -C ₆ acyl, C _r C ₆ alkoxylcarbonyl, C,-C ₆ N- alkylcarbamoyl, or C,-C ₆ V.iV-dialkylcarbamoyl radicals; and

R* is selected from benzoyl, fluorobenzoyl, chlorobenzoyl, azidobenzoyl, cyclohexanecarbonyl, acryloyl, crotonoyl, 1-methylacryloyl, 2-methyl-2-butenoyl, or 3-methyl- 3-butenoyl radical.

More preferably, R ³ is selected from acetyl, propanoyl, cyclopropanecarbonyl, acryloyl, crotonoyl, 3,3-dimethylacryloyl. /V-methylcarbamoyl, /V-ethylcarbamoyl, N.N- dimethylcarbamoyl, tV.iV-diethylcarbamoyl, pyrroiidine-/V-carbonyl, piperidine-iV-carbonyl, morpholine-iV-carbonyl, methoxycarbonyl, ethoxylcarbonyl, propoxylcarbonyl, butoxy carbonyl. cyclopentanecarbonyl, or cyclohexanecarbonyl radicals.

These new taxoids (I) are synthesized by the processes which comprise the coupling reactions of the baccatin of the formula (II)

(II)

wherein G, represents a hydroxyl protecting group, and R ⁵ and R ⁴ have been defined above _, with the β-lactams of the formula (III)

wherein G is a hydroxyl protecting group such as ethoxyethyl (EE), triethylsilyl (TES), (tert- buty dimethylsilyl (TBS), and triisopropylsilyl (TIPS), and R' and R ^: have been defined above, in the presence of a base.

DETAILED DESCRIPTION OF THE INVENTION

New taxoids of the formula (I) hereinabove are useful as antitumor agents or their precursors. These taxoids possess strong antitumor activities against human breast, non-small cell lung, ovarian, and colon cancers including drug-resistant cancer ceils, as well as leukemia and melanoma.

The new taxoids of the formula (I) are synthesized by modifying the baccatins of the formula (II)

wherein G, , R*, and R* have been defined above.

The baccatins (II) are coupled with the β-lactams of the formula (HI)

GO.

wherein G, R ¹ , and R ² have been defined hereinabove, to yield the new taxoids (I) .

The β-lactams (III) are readily prepared via the β-lactams (IV) which are easily obtained through the chiral enolate-imine cyclocondensation method that has been developed in the present inventor's laboratory as shown in Scheme 1 (Ojima et al., Bioorg. Med. Chem. Lett., 1993, 3, 2479, Ojima et al.. Tetrahedron Lett., 1993. 34, 4149, Ojima et al.. Tetrahedron Lett. 1992. 33, 5739, Ojima et al.. Tetrahedron, 1992, 48, 6985. Ojima. I. et al., J. Org. Chem., 1 91. 56, 1681, the disclosures of which are incorporated herein by reference). In this preparation, the β-lactams (IV) with extremely high enantiomeric purities are obtained in high yields. In Scheme 1, R* is a chiral auxiliary moiety which is (-)-trans-2-phenyl-l- cyclohexyl or (-)-lO-dicyclohexylsulfamoyl-D-isobomyl, TMS is a trimethylsilyl radical, and the base is lithium diisopropylamide or lithium hexamethyldisilazide and G and W have been defined hereinabove. Scheme 1:

G-O-CHrCOOR*

CAN

The β-lactams (IV) can be converted to the corresponding N-alkoxycarbonyl-β-lactams (HI) in excellent yields by reacting with alkyl chloroformates in the presence of a base (Scheme 2). This transformation is known to those skilled in the art.

The β-lactams (HI) are readily used for the coupling with the baccatins (II) in the presence of a base, followed by deprotection to give the new taxoids (I) in high yields (Scheme 3). Scheme 2:

Scheme 3:

In Schemes 1-3, R ¹ through R ⁶ have been defined above, M is an alkali metal _, and the hydroxyl protecting group G, is independently selected from methoxylmethyl (MOM), methoxyethyl (MEM), 1 -ethoxyethyl (EE). benzyloxymethyl, (β-trimethylsilylethoxyl)-methyl _, tetrahydropyranyl, 2,2,2-trichloroethoxylcarbonyl (Troc), benzyloxycarbonyl (CBZ) _, tert- butoxycarbonyl (t-BOC), 9-fluorenylmethoxycarbonyl (Fmoc), 2,2.2-trichloroethoxymethyl _, trimethylsilyl. triethylsilyl, tripropylsilyl, dimethylethylsilyl. dimethyl(t-butyl)silyl. diethylmethylsilyl, dimethylphenylsilyl, diphenylmethylsilyl, acetyl, chloroacetyl. dichloroacetyl, trichloroacetyl and trifluoroacetyl.

The coupling reaction of the baccatin (H) and the β-lactams (VI) is carried out via an alkali metal alkoxide of the baccatin (II) at the C-13 hydroxyl group. The alkoxide can readily be generated by reacting the baccatin with an alkali metal base such as sodium hexamethyldisilazide, potassium hexamethyldisiiazide, lithium hexamethyldisilazide, sodium diisopropylamide, potassium diisopropylamide, lithium diisopropylamide, sodium hydride, in a dry nonprotic organic solvent such as tetrahydrofuran (THF), dioxane, ether, dimethoxyethane (DME), diglyme, dimethylformamide (DMF), mixtures of these solvents with hexane. toluene, and xylene, in a preferred temperature range from about -100°C to about 50°C, more preferably at about -78*0 to about 25°C. This reaction is preferably carried out under inert atmosphere such as nitrogen and argon. The amount of the base used for the reaction is preferably approximately equivalent to the amount of the baccatin when soluble bases such as sodium hexamethyldisilazide, potassium hexamethyldisilazide, lithium hexamethyldisilazide. sodium diisopropylamide. potassium diisopropylaπude. lithium diisopropylamide are used. The use of a slight excess of the- base does not adversely affect the reaction. When heterogeneous bases such as sodium hydride and potassium hydride are used, 5-10 equivalents of die base (to the amount of the baccatin) are preferably employed.

The coupling reaction of the metal alkoxide of the baccatin thus generated with the β- lactam is typically carried out by adding the solution of the β-lactam in a dry organic solvent exemplified above in a preferred temperature range from about -100°C to 50°C, more preferably at about -35°C to 25°C. The mixture of reactants is stirred for 15 minutes to 24 hours and the progress and the completion of the reaction is monitored by thin layer chromatography (TLC), for example. When the limiting reactant is completely consumed, the reaction is quenched by addition of a cold brine solution. The crude reaction mixture is worked up using the standard isolation procedures which are generally known to those skilled in the art to give the corresponding taxoid. The proportion of the β-lactam and the baccatin is in a range from 2:1 to 1:2, more preferably approximately 1:1 for purposes of economy and efficiency, but the ratio is not critical for the reaction.

The hydroxyl protecting groups can then be removed by using the standard procedures which are generally known to those skilled in die art to give the desired taxoid derivatives. For example, EE and TES groups can be removed with 0.5 N HCl at room temperature for 36 h, TIPS and TBS groups can be removed by treating with fluoride ion or HF in a non-prottc organic solvent, and Tre group can be removed with zinc and acetic acid in methanol at 60°C for 1 hour without disturbing the other functional groups and the skeleton of the taxoid.

It has been shown that the introduction of 2-methyl-l-propenyl group to the C-3' position of paciitaxel appears to increase the cytotoxicity, especially against drug-resistant cancer cells: Holton and Nadizadeh disclosed in U.S. Patent 5.284.864 (1994) that 3 - desphenyl-3'-isobutenylpaciitaxel (RAH-1 ) exhibited 4 times better activity than paciitaxel and 7 times better activity than docetaxel against human colon carcinoma ceils HCT-1 16. and also about 20 times better activity than paciitaxel and 9 times better activity than docetaxel against multi-drug resistant phenotype human colon carcinoma cells HCT-1 16 VM.

We have found that the structural requirements for taxoid antitumor agents to express strong potency are rather strict and unpredictable. For example, 3'-desphenyl-3'-(2- phenyiethenyDdocetaxel, bearing 2-phenyiethenyl group instead of the isobutenyl group of RAH-1, has dramatically decreased cytotoxicity (>20 times) and 3'-desphenyl-3'- neopentyldocetaxel, bearing neopentyl group which has just one more methyl than isobutenyl group, is virtually not cytotoxic against A121 human ovarian, A549 human non-small cell lung, HT-29 human colon and MCF7 human breast cancer cells. While looking at the structure-activity relationships (SAR) of new taxoids that have different substituents at the C- 3' and C-10, we discovered that there are optimum combinations of these two substituents which achieve extraordinarily high activity against drug-resistant cancer cells.

After searching for the best substituent for die C-3' and the C-10 positions by employing many alkyl groups and alkenyl groups by trial and error, we have identified 1- propenyl, 2-methyl-l-propenyl, 2-methylpropyl, and trifluoromethyl groups to be the optimum substituents for the C-3' position, and acyl groups, alkoxycarbonyl groups, and N,N- dialkylcarbamoyl groups to be the optimum substituents for the C-10 position.

For example, 3 ^, -desphenyl-3 ^, -(l-propenyl)-l0-acetyldocetaxel (Taxoid Ia) showed a substantially better activity spectrum than that of paciitaxel and docetaxel against human ovaian, human non-small cell lung, human colon, and human breast cancer ceils mentioned above (see TABLE 1 in EXAMPLE 32). Moreover, this agent possesses 21 times better activity than paciitaxel and 17 times better activity than docetaxel against the drug-resistant human breast cells MCF7-R. which are mammary carcinoma ceils 180 fold resistant to a widely used anticancer drug, adriamycin. In the same assay, Hoiton's compound RAH- 1 showed only marginal activity that was one order of magnitude weaker than that of Taxoid Ia (see TABLE 1 in EXAMPLE 32).

- -

3'-Desphenyl-3'-(2-methyl- 1 -propenyl)- 10-cyclopropanecarbonyldocetaxel (Taxoid IX) showed one order of magnitude better activity than that of paciitaxel and docetaxel against human human breast cancer cells mentioned above (see TABLE 2 in Example 32), and possesses two order of magnitude ( 142 times) better activity against the drug-resistant human breast ceils mentioned above. These extraordinarily high activities are totally unpredictable from the exsisting SAR studies of paciitaxel and docetaxel, and thus demonstrate the exceptional importance of our discovery.

The taxoids of the formula (I) of this invention are useful for inhibiting tumor growth or regression of tumors in animals including humans and are preferably administered in the form of a pharmaceutical composition including effective amounts of the antitumor agent of this invention in combination with a pharmaceutically acceptable vehicle or diluent

The pharmaceutical compositions of the antitumor agents of the present invention may be made in any form suitable for desired use, e.g., oral, parenteral or topical administration. Examples of parenteral administration are intramuscular, iπtraveneous, intraperitoneal. rectal, and subcutaneous administration. The vehicle or diluent ingredients should not reduce the therapeutic effects of the antitumor agents of this invention.

Suitable dosage forms for oral use include tablets, dispersible powders, granules, capsules, suspension, syrups, and elixirs. Examples of inert diluents and vehicles for tablets include calcium carbonate, sodium carbonate, lactose and talc. Examples of inert diluents and vehicles for capsules include calcium carbonate, calcium phosphate, and kaolin. Dosage forms appropriate for parenteral administration include solutions, suspensions, dispersions, and emulsions.

The water solubility of the antitumor agents of the formula (I) may be improved by modifying the C-2' and /or C-7 substituents to incorporate suitable functional groups, such as

R ³ and R ⁴ . In order to increase the water solubility, R ³ and R ⁴ can be independently selected from hydrogen and -CO-X-Y, wherein X is selected from -(CH ₂ ),,- (n = 1-3). -CH=CH-, cyclohexanediyl, and benzenediyl and Y is selected from -COOH and its pharmaceutically acceptable salts, -S0 ₃ H and its pharmaceutically acceptable salts. -NR'R ⁸ and its pharmaceutically acceptable salts, the pharmaceutically acceptable ammonium salt -NR'R'R',

-CONR'R ⁹ , or -COOR', in which

-NR ⁷ R* includes cyclic amine radicals selected from pyrrolidinyl, piperidinyl, morphorino, piperazinyl, and N-methylpiperazinyl;

R ⁷ and R* are independently selected from hydrogen, allyl, C,-C _β alkyl, and -(CH ₂ ),-Z

(n = 1-3);

R' is selected from C,-C ₆ alkyl, allyl, and -(CH ₂ )„-Z (n = 1-3), and

Z is selected from -COOH and its pharmaceutically acceptable salts, -SO,H and its pharmaceutically acceptable salts, -NR ⁷ R* and its pharmaceutically acceptable salts, and pharmaceutically acceptable ammonium salt -NR'R'R ¹⁰ , in which R'° is selected from hydrogen, allyl, and C,-C ₆ alkyl.

The preparation of the water-soluble analogs of paciitaxel bearing the functionalized acyl groups described above has been disclosed in Kingston et al., U.S. Patent 5.059,699

(1991); Stella et aL. U.S. Patent, 4,960,790 (1990), the disclosures of which are incorporated herein by reference, and thus it is not difficult for the people in the ait to carry out such modifications.

The following non-limiting examples are iliustxanve of the present invenuon. It should be noted that various changes could be made in the examples and processes therein without departing from the scope of the present invenuon. For this reason, it is intended that

the illustrative embodiments of the present application should be interpreted as being illustrative and not limiting in any sense.

EXAMPLE I (-)-(lR__S)-2-phenyl-l-cyclohexyl triisopropylsilyloxyacetate:

A solution of (-)-(lR,2S)-2-phenyl- 1 -cyclohexyl hydroxyacetate (851 mg, 3.63 mmol) was prepared through esterification of benzyloxyacetyl chloride with (-)-( 1 R.2S)-2-pheny 1- 1 - cyclohexanol followed by hydrogenolysis. Then, triisopropylsilyl chloride (840 mg, 4.36 mmol) and imidazole (618 mg, 9.08 mmol) in dimethylformamide (DMF) (1.7 mL) was added and stirred at room temperature for 12-20 hours. The mixture was poured into pentane (25 mL), and washed with water and brine. The combined organic layers were dried over anhydrous MgSO, and concentrated in vacuo. The crude product was subjected to a purification on a short silica gel column using hexane chloroform (3/1) as the eluant to give pure (-)-(lR,2S)-2-phenyl-l-cyclohexyl triisopropylsilyloxyacetate (1.35 g, 95% yield) as a colorless oil: [α] _D ^ω -17.1° (c 3.15, CHC1,); IR (neat) 1759. 1730 ("CO) cm ¹ ; 'H NMR (CDC1 ₃ ) δ 0.93-0.99 (m, 21H). 1.30-1.62 (m, 4H), 1.72-2.0 (m. 3H), 2.10-2.19 (m, IH). 2.66 (dt, J = 1 1.5, 4.0 Hz, IH). 3.90 (d, J » 16.6 Hz, IH), 4.07 (d, J = 16.6Hz, IH). 5.07 (dt, J = 10.6, 4.0 Hz, IHX 7.16-7.30 (m, 5H). Anal. Calcd for C^H^Si: C, 70.72; H, 9.81. Found: C, 70.79; ft 9.85.

EXAMPLES 2-3 N-(4-Methoxyphenyl)-2-alkenytaldimine:

To a solution of 0.360 g. (2.9 mmol) of p-anisidine (recrystallized twice from ethanol) in 12 mL of CH_C1 ₂ over anhydrous Na-SOj was added 0.24 g (3.5 mmol) of 2-butenal

(crotonaldehyde) (distilled immediately pπor to use) under nitrogen. After 4 hours. Na,S0 ₄ was filtered off and the solvent removed under vacuum to give N-(4-methoxyphenyl)-2- butenaldimine in quantitative yield, which was used for the synthesis of β-lactam without further purification.

In the same manner, N-(4-methoxyphenyl)-3-methyl-22-butenaldimιne was obtained in quantitative yield.

EXAMPLES 4-5 (3R,4S)-l-(4-Methoxyphenyl)-3-triisopropylsilyloxy-4-<l.a lkenyl)azetidin-2-one (V):

To a solution of 0.27 mL (1.9 mmol) of diisopropylamine in 10 mL of THF was added 0.76 mL (1.9 mmol) of 2.5M n-butyllithium in hexanes at -10 ^e C. After stirring for 45 minutes, die solution was cooled to -85°C. A solution of (-)-(lR,2S)-2-phenyl-l -cyclohexyl triisopropylsilyioxy-acetate (0.575 g 1.47 mmol) in 10 mL of THF was added via cannula over a period of 1.5 hours. After stirring for an additional hour, a solution of N-(4- methoxyphenyl)-2-butenaldimine (336 mg, 2.2 mmol) in 10 mL of THF was added via cannula over a period of approximately I hour. The mixture was stirred for 2 hours and allowed to warm up to room temperature overnight while stirring. The reaction was then quenched with saturated NH_C1. The aqueous layer was extracted with ethyl acetate (EtOAc) and die combined organic layers were washed with saturated NH.CI solution, and bπne. and then dried over MgS0 ₄ . After the removal of solvent under vacuum, the crude product was obtained, which was purified by flash chromatography on silica gel (hexane:EtOAc = 10: 1 to 6:1) to afford pure PMP-β-lactam Va (399 mg, 70% yield) as a rust-colored oil. The enantiomeric purity of the PMP-β-lactam Va was determined to 97% ee on the basts of chiral HPLC analysis: [α] ₀ = +33.1° (c 0.27. CHCI,); H NMR (CDC1„ 250 MHz) δ 1.04-1.16 ( .

21H). 1.76 (dd, J = 6.5. 1.3 Hz, 3H). 3.74 (s, 3H). 4.51 (dd, J = 8.6. 5.0 Hz, IH). 5.04 (d. J =

5.0 Hz. IH), 5.59 (ddd, J = 15.4. 8.6. 1.3 Hz, IH). 5.92 (dq, J = 15.4, 6.5 Hz, IH). 6.83 (d, J

= 9.0. 2H). 7.36 (d, J = 9.0 Hz. 2H); "C NMR (63 MHz, CDCl,) d 1 1.89. 17.63, 17.68,

55.38, 61.89, 77.57, 1 14.18, 1 18.48. 126.65, 127.48, 128.34, 128.55. 132.59, 156.03. 165.43.

In the same manner, PMP-β-lactam Vb (R' » 2-methyl-l-propenyl) was obtained in

73% yield (93% ee): [α] _D = +65.7° (c 1.00, CHCl,); Η NMR (CDCl,, 300 MHz) δ 1.08-1.12

(m, 21 H), 1.81 (s, 3 H), 1.86 (s, 3 H), 3.78 (s. 3 H). 4.79-4.84 (dd, J = 5.1, 9.9 Hz, 1 H),

5.05-5.07 (d, J = 5.1 Hz, I H), 5.33-5.36 (bd, J = 9.9 Hz, 1 H); ^l3 C NMR (CDCl,. 63 MHz) d

11.92, 17.61, 18.33, 26.11, 55.44, 57.56, 76.51, 77.015, 77.52, 114.25, 118.34. 120.15.

128.73, 131.52, 139.14, 156.00, 165.61.

EXAMPLES 6-7 (3R,4S)-3-Triisopropylsilylox7-4-(l-alkenyl)azetidln-2-one (IV):

To a solution of 260 mg. (0.67 mmol) of N-PMP-β-lactam Va in 20 ml. of acetonitrile at -10°C, was added dropwise a solution of 1.13 g (2.07 mmol) of cerium ammonium nitrate (CAN) in 25 mL of water. The mixture was allowed to stir for 1 hour and then diluted with 50 mL of water. The aqueous layer was extracted with ethyl acetate (2 x 35 mL) and the combined organic layers were washed with water, 5% NaHSO,, 5% Na-CO,, and brine. After drying over MgS0 ₄ and concentrating under vacuum, the organic layers afforded the crude product, which was purified on a silica gel column using hexane-ethyl acetate as the eluant (hexane:EtOAc = 3:1) to give the pure β-lactam IVa (R' = 1-propenyi) (124 mg. 65% yield) as a pale yellow viscous oil: Η NMR (CDCl,, 250 MHz) δ 1.04-1.16 (m, 21H), 1.70 (dd, J » 6.5, 1.2 Hz, 3H), 4.13 (dd. J = 8.7, 4.9, IH). 4.94 (d, J » 4.9 Hz, IH). 5.51 (ddd. J

= 14.1, 8.7. 1.2 Hz, IH), 5.67 (m. I H), 6.68 (br s, IH); ⁿ C NMR (63 MHz. CDCl,) d 1 1.80. 17.57, 17.62, 58.14, 79.18, 127.97, 130.64, 170.36.

In the same manner, β-lactam IVb (R ¹ = 2-methyl- 1 -propeny!) was obtained in 94% yield: Η NMR (CDCl,, 300 MHz) δ 1.02-1.10 (m. 21 H). 1.65 (s. 3 H). 1.72 (s, 3 H). 4.36- 4.40 (dd, J = 4.5. 9.6 Hz. 1 H). 4.91-4.93 (dd, J = 2.1, 4.5 Hz, 1 H), 5.23-5.26 (bd. J = 9.6 Hz. 1 H), 6.28 (bs, I H. NH).

EXAMPLES 8-9 (3R,4S)-l-tert-Butoxycarbonyl-3-triisopropylsilyloxy-4-(l-al kenyl)azetidin-2-one (III):

To a solution of 100 mg (0.35 mmol) of the β-lactam IVa, 0.24 mL (1.75 mmol) of triethylamine, and a catalytic amount of dimethylaminopyridine (DMAP) in 1 1 mL of CH ₂ C1 ₂ , was added dropwise at room temperature, 85 mg. (0.38 mmol) of di(tert-butyl) dicarbonate in 2 mL of CH ₂ C1 ₂ . The mixture was stirred for 1 hour and quenched with saturated NH ₄ Cl solution. The mixture was diluted with 60 mL of ethyl acetate and the organic layer was washed with brine, dried over MgS0 ₄ , and concentrated. The crude product was purified by flash chromatography on silica gel (hexane:EtOAc = 4: 1) to yield pure N-'BOC-β-lactam Lϋa (R' = 1-propenyl) as colorless oil (105 mg. 87% yield): 'H NMR (CDCl,, 250 MHz) δ 1.02- 1.08 (m, 21H) _. 1.48 (« 9H), 1.74 (dd, J = 6.4, 1.3 Hz, 3H). 4.44 (dd, J - 8.6, 5.8 Hz, IH). 4.94 (d _. J - 5.8 Hz, IH). 5.54 (ddd, J * 15.4. 8.6, 1.3 Hz). 5.83 (dq, J _■ 15.4, 6.4 Hz, IH); ^l3 C NMR (63 MHz. CDCl,) δ 11.76, 17.52. 17.95. 27.97, 61.04, 83.06. 124.80, 132.72, 148.0. 166.07. Anal. Calcd for C^NO^i: C. 62.62. H. 9.72. N. 3.65. Foun± C. 62.62: H. 9.63; N, 3.61.

In die same manner, N-UOC-β-lactam mb (R ¹ = 2-methyl-l-propenyl) was obtained as a colorless oil in 82% yield: Η NMR (CDCl,. 300 MHz) δ 0.97-1.06 (m. 21 H), 1.48 (s.

H). 1.75 (s. 3 H). 1.78 (s. 3 H). 4.72-4.77 (dd, J = 5.7, 9.9 Hz, 1 H). 4.94^.96 (dd, J = 5.7 Hz. 1 H), 5.25-5.28 (bd, J = 9.9 Hz . 1 H).

EXAMPLES 10-15 7-Tr-ethylsilyl-lO-O-substituted 10-deacetylbaccatin III (Ilb-g).

To a solution of 1.0 g (1.84 mmol) of 10-deacetylbaccatin in and 375 mg (5.52 mmol) of imidazole in 10 mL DMF was added dropwise 0.9 L (5.52 mmol) of chlorotriethylsilane (TESC1). The reaction mixture was stirred for 5 hours at room temperature and quenched with water, then diluted with EtOAc. The aqueous layer was extracted with EtOAc and d e combined organic layers were washed with water, dried over MgS0 ₄ , and concentrated. The crude product was purified by flash chromatography on silica gel (hexane EtOAc, 1:1) to give 774 mg (64%) of 7-triethylsilyl- 10-deacetylbaccatin IH (7-TES-DAB) as a white solid: 'H NMR (CDCl,. 250 MHz) δ 0.50 (m, 6 H), 0.97 (m, 9 H), 1.21 (s, 3 H), 1.58 (s, 3 H), 1.73 (s, 3 H). 1.85 (dt, I H), 1.99 (s, 3 H). 2.23 (s. 3 H), 2.24 (s, 2 H), 2.47 (ddd, 1 H). 3.94 (d. J = 7.2 Hz. I H), 4.14 (AB, J^ = 8.4 Hz, I H), 4.32 (AB, J _AB « 8.1 Hz, 1 H . 4.41 (d, J = 6.3 Hz, 1 H), 4.84 (t, 1 H), 4.94 (d, J = 8.4 Hz, I H), 5.14 (s, 1 H), 5.19 (s, 1 H), 5.58 (d. J __ 7.2 Hz. 1 H), 7.40 (t, 2 H), 7.54 (t, 1 H), 8.10 (d, 2 H).

To 77 mg ( i 17 mmol) of 7-TES-DAB in 5 mL THF was added 0.12 mL of LiHMDS (IM in THF). The reaction mixture was stirred at -40°C for 5 minutes, then 0.010 mL (0.117 mmol) of propanoyl chloride (previously distilled) was added. The solution was allowed to warm up at 0 ^β C over a 30 min period. Then the solvent was removed in vacuo and the crude product was purified by flash chromatography on silica gel (hexane then hexane EtOAc, 4:1, then 2:1 and 1:1) to afford 60 mg (72%) of 7-triethylsilyl- 10-propanoyl- 10-deacetylbaccatin m (lib) as a white solid: [α] ₀ ^:ι -68.57° (c 1.75. CHC1,); ^l H NMR

(CDCl,, 250 MHz) δ 0.52 (q, 6 H). 0.87 (t, 9 H). 1.02 (s, 3 H). 1.16-1.22 (m, 6 H). 1.55 (s _,

9 H), 1.67 (s, 3 H), 1.86 (m, I H), 2.19 (s. 3 H), 2.25 (s, 2 H), 2.27 (s. 3 H), 2.42 (m, 3 H).

3.86 (d, J = 6.9 Hz, 1 H), 4.12 (AB. J _AB = 8.0 Hz. I H), 4.27 (AB. J _AB __ 8.0 Hz. 1 H), 4.49

(dd, I H). 4.83 (t, I H), 4.93 (d, J = 9.2 Hz, I H). 5.61 (d, J = 6.9 Hz. 1 H). 6.46 (s. I H).

7.43 (t, 2 H), 7.56 (t, 1 H), 8.08 (d, 2 H); "C NMR (CDCl,, 63 MHz) δ 5.2, 6.7, 9.2. 9.9,

14.9, 20.1. 22.6. 26.7. 27.6, 37.2, 38.3. 42.7, 58.6. 67.8. 72.3, 74.7, 75.5. 76.5. 77.0. 77.5,

78.7, 80.8. 84.2. 128.5, 129.4, 130.0, 132.6, 133.5. 143.9, 167.8, 170.7, 174.5. 202.3. IR

(neat, cm" ¹ ) 2953, 2913, 1789. 1738. 1715, 1681, 1454. 1434, 1392, 1362, 1315. 1175. 1108.

HRMS (FAB, DCM/NBA) m z: Calcd. for C„H, ₄ θ _H SiH ^* , 715.3513. Found, 715.3552.

In the same manner, the following 7-triethylsilyl- 1-O-substituted-lO-deacetylbaccatin

His were prepared.

7-Triethylsilyl-lO-cyclopropanecarbonyl-lO-deacetylbaccat ln HI (Oc).

White solid; _α] ₀ ¹ ' -61.42° (c 7.00. CHC1,); 'H NMR (CDCl,. 250 MHz) δ 0.46 (m. 6 H). 0.82 (m, 9 H), 0.97 (s, 3 H), 1.12 (s, 3 H), 1.18 (m. 2 H), 1.60 (s, 3 H), 1.68 (m. 2 H). 1.79 (m, 1 H), 2.12 (s, 3 H). 2.16 (s. 2 H), 2.20 (s, 3 H). 2.40 (m, 1 H , 2.50 (d, 1 H). 3.79 (d, J = 6.9 Hz, I H). 4.03 (AB. J _A , » 8.1 Hz, 1 H), 4.24 (AB. J _Aβ = 8.1 Hz, I H), 4.38 (dd. J = 6.6 Hz_ 10.1 Hz. 1 H). 4.75 (t, 1 H). 4.87 (d, J « 9.0 Hz, 1 H), 5.55 (d, J = 6.6 Hz. I H), 6.39 (s, I H).7.37 (t, 2 H), 7.51 (t, 1 H). 8.02 (d, 2 H); IR (neat, cm ¹ ) 2958. 2356. 1771, 1732. 1716. 1699. 1652. 1558, 1456. 1393, 1268. 1169. 1107. 1070, 1026, 738. Anal. Calcd. for C„H, ₄ 0 _M Si: C. 64.44: H. 7.49. Found: C. 64.52. H. 7.49.

-Triethylsilyl-10-crotonoyl-10-deacetylbaccatin III (Hd).

White solid; (__]„" -68.57° (c 7.00, CHC1,); Η NMR (CDCl,, 250 MHz) δ 0.51 (q, 6

H), 0.86 (t, 9 H). 1.00 (s, 3 H), 1.20 (s, 3 H). 1.66 (s, 3 H), 1.80 (m, 1 H). 1.88 (d. 3 H). 2.19

(s. 2 H), 2.20 (s, 3 H), 2.26 (s, 3 H). 2.51 (m, 3 H), 3.87 (d, J = 6.8 Hz. 1 H). 4.08 (AB, J _AB

= 8.2 Hz, I H), 4.26 (AB. J _AB = 8.2 Hz, I H). 4.45 (dd, J = 6.7 Hz, 9.9 Hz, 1 H), 4.80 (t, l

H), 4.92 (d, J = 9.7 Hz, I H), 5.61 (d, J = 6.8 Hz. 1 H). 5.92 (d, J * 15 Hz. 1 H). 6.48 (s,

1 H), 7.02 (m , I H). 7.42 (t, 2 H), 7.55 (t, 1 H). 8.07 (d, 2 H); "C (CDCl,. 63 MHz) δ 5.2.

6.7, 9.9, 14.9, 18.1, 20.1, 22.6, 26.7. 37.2, 38.2. 42.7, 47.3, 58.6. 67.9, 72.3, 74.7. 75.5, 76.5,

77.0, 77.5, 78.7. 80.8, 84.2. 122.3, 128.5, 129.4, 130.0, 132.7, 133.6, 143.9, 145.6, 164.7,

167.1, 170.7, 202.3; IR (neat, cm ^"1 ) 2953, 2356.1716, 1558, 1455, 1267.1173, 1106, 1001,

822.

7-Triethylsilyl-10- V,iV.d_methylcarbamoyl-10-deace_ylbaccatin HI (lie).

White solid; [__]„*' -30° (c 2.00, CHCU); Η NMR (CDCl,, 300 MHz) δ 0.57 (m. 6 H). 0.91 ( , 9 H), 1.21 (s, 3 H), 1.27 (s, 3 H), 1.69 (s, 3 H), 1.84 (dt, I H). 2.21 (s. 2 H), 2.26 (s, 3 H), 2.29 (s, 2 H). 2.49 (m, I H). 2.95 (s, 3 H). 3.09 (s, 3 H), 3.91 (d, J = 6.9 Hz. I H), 4.12 (AB, J^ = 8.4 Hz, I H). 4.30 (AB, J _AB = 8.4 Hz. 1 H), 4.48 (dd, J = 6.7 Hz. 10.2 Hz, I H), 4.84 (t, 1 H), 4.97 (d, J = 9.0 Hz, 1 H), 5.64 (d, J = 6.9 Hz, 1 H), 6.40 (s. ! H). 7.46 (t, 2 H), 7_59 (t, 1 H), 8.1 1 (d, 2 H). HRMS (FAB, DCM/NBA/NaCI) m/z: Calcd. for CnH _jj OuNSiNa ^* , 752.3442. Found. 752.3483.

7.Triethy_silyH0-mβthoxycarbon I- 10-deacetylbaccatin III (IH).

White solid; [α} ₀ ° -72.50° (c 4.00. CHC1,); 'H NMR (CDCl,, 300 MHz) δ 0.54 (m, 6 H). 0.89 (m, 9 H), 1.03 (s, 3 H), 1.15 (s. 3 H). 1.67 (s, 3 H), 1.82 (dt. I H), 2.18 (s. 3 H).

2.25 (s, 2 H), 2.27 (s, 3 H), 2.47 (ddd, I H). 3.82 (s, 3 H). 3.84 (d, 1 H). 4.1 1 (AB, J _Aβ = 8.1

Hz, 1 H), 4.27 (AB, J _AB = 8.1 Hz. I H), 4.44 (dd, J = 6.6 Hz. 10.2 Hz. 1 H), 4.83 (t, 1 H) _,

4.93 (d, J = 9.0 Hz, I H). 5.59 (d, J = 6.9 Hz. 1 K). 6.27 (s. 1 H). 7.43 (t. 2 H), 7.56 (t. 1 H) _,

8.07 (d, 2 H). IR (neat, cm ¹ ) 3524.2957, 1715, 1442, 1371, 1266, 1108, 1025, 912.820,

732.

7-Triethylsilyl-10-acryloyl-10-deacetylbaccatin III dig).

White solid; (α] _D ^a -77.5° (c 4.00, CHCl,); 'H NMR (CDCl,, 250 MHz) δ 0.51 (q, 6 H), 0.87 (t. 9 H), 1.01 (s, 3 H), 1.21 (s, 3 H), 1.68 (s, 3 H), 1.81 (m, I H). 2.15 (d, 2 H). 2.22 (s, 3 H), 2.27 (s, 3 H), 2.46 (m. I H), 3.87 (d, J » 6.9 Hz, 1 H), 4.12 (AB, J _AB = 8.3 Hz, 1 H), 4.28 (AB, J _A , m 8.3 Hz, 1 H), 4.47 (dd, J = 6.7 Hz, 10.2 Hz, 1 H), 4.81 (t, 1 H). 4.94 (d, J » 8.7 Hz, 1 H). 5.62 (d, J « 6.9 Hz, 1 H), 5.88 (d, J « 10.7 Hz, 1 H), 6.18 (m. I H). 6.47 (m, 1 H), 6.51 (s, I H), 7.02 (m , 1 H), 7.43 (t, 2 H), 7.56 (t, 1 H), 8.08 (d, 2 H); C NMR (CDCl,, 63 MHz) δ 5.2, 6,7, 9.9. 14.9, 20.1, 22.6, 26.7, 37.2, 38.2, 42.7, 47.3. 58.6. 67.9. 72.3. 74.7, 75.8, 76.5, 77.0, 77.5, 78.7, 80.8. 84.2, 128.1. 128.5, 129.3, 130.0. 131.5. 132.5. 133.6. 144.2, 164.5, 167.0, 170.7, 202.0; IR (neat, cm ¹ ) 2950, 2250, 1734, 1717. 1653. 1635. 1506, 1457, 1362, 1269.

EXAMPLES 16-21 7-Triethy- _S -lyl-lO-ø-βubst-tnted 2'-triisopropylsUyl-3Ml-prop«nyl)doceuuel (I-P):

To a solution of 68 mg (0.097 mmol) of 7-triediylsilylbaccarin HI (Ha) and 58 mg 0.15 mmol) of the N-ΕOC-β-lactam (Via) in 4 mL of THF at -30°C was added 0.12 mL 0.12 mmol) of LiHMDS. The mixture was allowed to warm to -10°C and stirred for 1 hour

and was then quenched with NH ₄ C1. The aqueous layer was extracted with 75 L of EtOAc and the combined organics were washed with NH ₄ C1 and brine. The organics were then dried over MgS0 ₄ and concentrated under vacuum. Upon purification by flash column chromatography on silica gel (hexane:EtOAc = 4: 1 ). 83 mg (79% yield) of pure protected taxoid 7-Triethylsilyl-10-acetyl-2'-triisopropylsilyl-3 ^' -desphenyl-3'-( l-propenyl)docetaxel (la-P) was collected (90% conversion, 88% conversion yield) as a white solid: Mp. 131.0- 132.5 °C; Η NMR (CDCl,, 250 MHz) δ 0.57 (q. J - 7.7 Hz, 6H), 0.92 (t. J __ 7.7 Hz. 9H), 1.05-1.1 1 (m, 21H), 1.20 (s, 3H), 1.23 (s, 3H), 1.32 (s, 9H), 1.69 (s. 3H). 1.73 (d, J = 6.2 Hz, 3H). 1.76-1.95 (m. IH), 2.01 (s, 3H), 2.18 (s. 3H), 2.22-2.35 (m, 2H). 2.41 (s. 3H). 2.43-2.60 (m. IH), 3.83 (d, J = 6.8 Hz, IH). 4.17 (d, J = 8.3 Hz, IH). 4.31 (d, J - 8.3 Hz, IH), 4.42-4.55 (m, 2H). 4.62 (br m, IH). 4.85-4.98 (m, 2H), 5.46 (dd, J ■ 14.3, 6.2 Hz, IH). 5.62-5.75 (m, 2H), 6.18 (t, J = 9.1 Hz, IH), 6.47 (s, IH), 7.49 (t, J . 7.2 Hz, 2H). 7.59 (t, J = 7.2 Hz. IH), 8.1 1 (d, J = 7.2 Hz, 2H); ^,J C NMR (63 MHz, CDCl,) δ 5.29, 6.71, 10.04, 12.50, 14.41. 17.71. 17.94, 20.85. 21.24, 22.75, 26.39. 28.18, 35.36, 37.21. 43.28. 46.73. 55.0. 58.21, 71.23. 72.24, 74.89, 75.06, 78.05, 79.5. 81.12, 84.24, 127.67. 128.64, 129.25. 130.19. 133.40, 133.53. 140.74, 155.0, 167.0, 169.25, 169.89. 171.64. 203.72.

In a similar manner, the following 7-triethylsilyl- 10-0-substituted 2'-triisopropylsilyl- 3'-(l -propeny Ddocetaxels (I-P) were obtained in high yields:

7-Triethy_s_lyl-10-propanoyl-2 ^, -triisopropy-silyl-3 ^, -desphenyl-3'-(2-methyl-l- propenyDdocetaxei (Ib-P):

Η NMR (CDCl,. 250 MHz) δ 0.53 (q, 6 H), 0.86 (t, 9 H), 1.09 (s. 21 H). 1.15 (s. 3 H). 1.19-1.20 (m, 6 H), 1.31 (s, 9 H). 1.66 (s. 3 H). 1.73 (s, 3 H). 1.77 (s. 3 H). 1.86 (m. 1 H). 1.91 (s, 3 H), 2.34 (s, 3 H), 2.38 (s. 2 H). 2.41 (m. 1 H). 3.81 (d, J = 6.6 Hz. I H). 4.15

(AB. J^ _B = 8.1 Hz, I H), 4.26 (AB, J _AB = 8.1 Hz. 1 H), 4.41 (s, 1 H). 4.45 (m. I H). 4.79 (nr.. 1 H + NH), 4.89 (d, J __ 8.9 Hz, 1 H), 5.30 (d, J = 7.7 Hz. I H). 5.65 (d, J = 6.6 Hz, 1 H) _, 6.06 (t. I H). 6.47 (s. I H). 7.40 (t, 2 H), 7.54 (t, 1 H). 8.06 (d, 2 H).

7-Triethylsilyl-10-cyclopropanecarbonyl-2'-triisopropylsi lyl-3'-desphenyl-3 ^, -(2.methyl-l- propenyl) docetaxel (Ic-P):

'H NMR (CDCl, 300 MHz) δ 0.42 (m. 6 H), 0.82 (m. 9 H). 1.04 (s, 21 H). 1.12 (s, 3 H), I. 16 (s, 3 H), 1.18 (m. 2 H), 1.27 (s. 6 H), 1.62 (s, 3 H). 1.68 (bs, 5 H), 1.72 (s, 3 H). 1.84 (dt, I H), 1.94 (s, 3 H), 2.28 (s, 3 H). 2.32 (s. 2 H), 2.88 (ddd, I H), 2.50 (d, 1 H). 3.74 (d. J = 6.9 Hz. 1 H). 4.1 1 (AB, J _AB = 8.4 Hz. 1 H). 4.22 (AB. J _AB » 8.4 Hz. 1 H). 4.36 (bs, 1 H), 4.39 (m, 1 H), 4.69 (m, 1 H + NH). 4.85 (d, J = 9.0 Hz, I H), 5.25 (d, J = 8.1 Hz. 1 H). 5.61 (d, J « 6.6 Hz, I H). 5.99 (t, 1 H). 6.41 (s. 1 H). 7.37 (t, 2 H), 7.51 (t. I H). 8.02 (d, 2 H).

7-Triethy_sUyI-10-crotonoyl-2 ^, -trllsopropy_silyl-3'-desphenyl-3'- (2-methyl-l- propenyl)docetaxel (Id-P):

'H NMR (CDCl,. 250 MHz) δ 0.51 (q, 6 H), 0.87 (t, 9 H). 1.10 (s, 21 H), 1.17 (s. 3 H), 1.24 (s, 3 H), 1.32 (s, 9 H). 1.68 (s. 3 H). 1.74 (s, 3 H), 1.78 (s, 3 H). 1.86 (m. I H). 1.9*0 (d, 3 H 2.03 (s _. 3 H), 2.35 (s, 3 H). 2.39 (s. 2 H). 2.45 (ra, I H). 3.84 (d, J . 7.1 Hz. I H). 4.17 (AB, J^ » 8.3 Hz. I H), 4.28 (AB. J _AB = 8.3 Hz. 1 H), 4.42 (d, 1 H), 4.45 (dd. J = 6.4 Hz. 10.2 Hz, 1 H), 4.75 (m, 1 H + NH). 4.91 (d. J = 8.5 Hz, 1 H). 5.31 ⁽ d, J = 8.2 Hz. 1 H:. 5.67 (d, J » 7.1 Hz. 1 H), 5.92 (d, 1 H). 6.04 (t, 1 H), 6.51 (s, I H). 6.99 (m, 1 H). 7.42 ⁽ t. 1 H). 7.56 (t, I H). 8.08 (d, 2 H).

7-Triethylsilyl-10-iV,N.dimethylcarbamoyl-2'-triisopropylsil yl-3'-desphenyl-3 ^, .(2-methy|.l- propenyDdocetaxel (Ie-P):

Η NMR (CDCl,. 250 MHz) δ 0.52 (m, 6 H), 0.86 (m. 9 H). 1.09 (s, 21 H). 1.17 (s. 3 H), I . 19 (s. 3 H), 1.31 (s. 6 H), 1.66 (s. 3 H). 1.72 (s. 3 H). 1.76 (s, 3 H), 1.85 (dt. 1 H). 2.03 (s, 3 H), 2.33 (s, 3 H), 2.38 (s, 3 H), 2.48 (ddd. I H). 2.91 (s, 3 H). 3.03 (s. 3 H), 3.82 (d, J = 6.9 Hz. 1 H), 4.15 (AB. J _AB = 8.2 Hz. I H). 4.25 (AB, J _AB = 8.2 Hz. 1 H), 4.39 (m, 1 H). 4.41 (bs. 1 H). 4.73 (m, 1 H + NH). 4.89 (d. J = 8.8 Hz. 1 H), 5.30 (d. J __ 8.0 Hz. 1 H), 5.65 (d, J = 6.9 Hz. I H), 6.04 (t, I H). 6.38 (s, I H). 7.39 (t, 2 H). 7.54 (t, 1 H). 8.06 (d. 2 H).

7-Trlethylsllyl-10-methoxycarbonyl-2'-triisopropylsUyl-3' -desphenyl-3'-(2-methyl-l- propenyl) docetaxel (If-P):

Η NMR (CDCl,. 250 MHz) δ 0.52 (m, 6 H), 0.88 (m, 9 H). 1.10 (s, 21 H). 1.18 (s, 6 H). 1.32 (s. 9 H), 1.68 (s, 3 H). 1.73 (s, 3 H), 1.77 (s, 3 H), 1.83 (dt, 1 H), 2.00 (s, 3 H). 2.34 (s, 3 H), 2.38 (s, 2 H), 2.44 (ddd, 1 H), 3.79 (d, I H), 3.80 (s, 3 H), 4.15 (AB. J _AB = 8.3 Hz. 1 H). 4.27 (AB, J _AB = 8.3 Hz. I H), 4.41 (d, J = 2.3 Hz, I H), 4.44 (m, 1 H), 4.74 (m. 1 H + NH), 4.90 (d, J » 8.3 Hz, 1 H). 5.30 (d, J * 8.2 Hz. I H). 5.64 (d, J = 7.0 Hz. 1 H), 6.04 (t, 1 H). 6.26 (s, 1 H). 7.40 (t, 2 H). 7.55 (t, I H), 8.06 (d, 2 H).

7.Trie_hyl _f __yl 0.ac-7loy_-2^triisopropy-silyl-3 ^, -d__phenyl-3 ^, -(2-_oethyl-l- propenyl)docetaxel (Ig-P):

Η NMR (CDCl,. 250 MHz) δ 0.51 (m, 6 H). 0.86 (m. 9 H), 1.10 (s, 21 H). 1.16 (s. 3 H). 1.24 (s. 3 H). 1.32 (s, 9 H). 1.62 (s. 3 H). 1.68 (s. 3 H), 1.74 (s, 3 H). 1.78 (s. 3 H). 1.83 (tn, 1 H). 2.35 (s, 2 H), 2.39 (s, 3 H). 2.42 (m. 1 H). 3.83 (d, J » 7.3 Hz. I H). 4.16 (AB. J _AB

= 8.3 Hz, I H), 4.28 (AB, J _AB = 8.3 Hz, I H). 4.41 (d, J = 2.1 Hz. I H), 4.45 (m, 1 H) _, 4.74 (m, 1 H + NH). 4.90 (d, J = 9.4 Hz, 1 H), 5.30 (d, J = 7.8 Hz, 1 H), 5.62 (d, J = 7.3 Hz, 1 H), 5.88 (d, J * 10.3 Hz. I H). 6.04 (t, 1 H), 6.17 ( , 1 H). 6.46 (m. I H). 6.52 (s. 1 H), 7.41 (t, 2 H), 7.56 (t, I H). 8.07 (d, 2 H).

EXAMPLES 22-28 3'-Desphenyl-3'-(l-alkenyl)-10-O-substituted docetaxel (I):

To a solution of 46 mg. (0.042 mmol) of the protected taxoid la-P in 3 mL of 1 : 1 mixture of acetonitrile and pyridine was added 0.5 mL of HF/pyridine (70:30). The reaction mixture was stirred at 35-40°C for 2 hours. The reaction was quenched with 2N HCl. The mixture was extracted with EtOAc and the organic layer washed with 2N HCl and brine. After drying over MgSO., the crude product was purified by flash chromatography on silica gel (hexane:EtOAc * 1:2) to yield 24 mg (70% yield) of the pure taxoid 3'-desphenyl-3'-(l - propenyD-lO-acetyldocetaxel (Ia) as a white solid: Mp. 152.0-155.0 °C; [α] _D -86.7° (c, 0.15, CHC1,); 'H NMR (CDCl,, 250 MHz) δ 1.15 (s, 3H), 1.25 (s. 3H), 1.32 (s, 9H), 1.67 (s, 3H). 1.75 (d, J = 6.3 Hz, 3H), 1.86 (br s, 4H). 2.23 (s, 3H). 2.30-2.39 (m, 2H). 2.40 (s. 3H), 2.45- 2.60 (m, IH), 3.38 (br s, IH). 3.81 (d. J » 6.9 Hz, IH), 4.17 (d, J « 8.4 Hz, IH), 4.30-4.33 (m, 2H). 4.42 (dd, J » 10J. 6.9 Hz. IH). 4.60 (br m. IH), 4.90-4.98 (m, 2H), 5.53 (dd. J = 16.2, 63 Has, IH), 5.67 (d, J * 6.9 Hz. IH). 5.72-5.82 (m. IH), 6.21 (t, J = 8.8 Hz. IH). 6.30 (s, IH). 7_52 (t, J - 7.2 Hz, 2H), 7.61 (t, J = 7.2 Hz, IH). 8.11 (d. J = 7.1 Hz. 2H): "C NMR (63 MHz, CDCl,) δ 9.53, 14.95. 17.87. 20.84. 21.82. 22.54, 26.69. 28.18. 35.45. 35.60. 54.90. 58.62, 72.19, 73.12, 74.98, 75.61. 79.03. 79.55. 81.10, 84.41, 127.37, 128.71. 129.1. 130.19, 133.1, 133.68, 142.50, 155.50. 167.20. 170.13, 171.5. 173.40, 203.73. Anal. Calcd. for C„H„O _ls N: C, 61.98; H, 6.81; N, 1.72. Found: C. 62.12; H, 6.59; N, 1.67.

In a similar manner the following 3'-Desphenyl-3'-(l-al enyl)-l0- -substιtuted docetaxel (Ib-g) were obtained in high yields:

3'-Desphenyl-3'-(2-methyl-l-propenyl)-10-propanoyldocetax el (lb):

White solid; (α] ₀ ^il -40° (c 1.00, CHC1,); 'H NMR (CDCl,, 300 MHz) δ 1.08 (s. 3 H), 1.13-1.18 (m, 6 H), 1.28 (s. 9 H). 1.60 (s, 3 H), 1.69 (s. 6 H), 1.72 ( . 1 H). 1.83 (s, 3 H), 2.29 (s. 3 H), 2.31 (s, 2 H), 2.44 (m, 3 H), 3.38 (bs, OH), 3.74 (d, J = 6.9 Hz. 1 H). 4.10 (AB. J _AB = 8.1 Hz, I H), 4.13 (bs. 1 H), 4.22 (AB. J _AB = 8.1 Hz, 1 H), 4.33 (dd, J = 7.5 Hz, 10.1 Hz, I H), 4.67 (m, 1 H + NH). 4.88 (d, J = 9.3 Hz, 1 H), 5.23 (d, J = 8.4 Hz, 1 H), 5.59 (d, J = 6.9 Hz, 1 H), 6.06 (t, I H). 6.24 (s, I H). 7.37 (t, 2 H). 7.51 (t, 1 H). 8.01 (d, 2 H); ^l3 C NMR (CDCl,, 63 MHz) δ 9.0, 9.5. 14.9, 18.5, 21.8, 22.3, 25.7. 26.6, 27.5, 28.2, 35.5, 43.1, 45.6, 51.6. 55.5. 58.5, 72.1, 72.3, 73.7, 75.0, 75.4, 76.4, 76.5, 77.0, 77.5. 79.1, 79.9, 81.0. 84.3. 120.6, 128.6, 129.2, 130.1, 132.9, 133.6, 137.8, 142.4, 155.4, 166.9. 170.1, 173.0, 174.6, 203.8. HRMS (FAB, DCM/NBA), /z: Calcd. for C^O^M. ^* . 842.3962. Found, 842.4007.

3'-Despheny 3 2-metlιyl«l-pπ>penylV10-€yclopropanecarbonyldocetaxe l (lc):

White solid; [o] ₀ ²¹ -160° (c 1.00, CHCI,); 'H NMR (CDCl,. 250 MHz) δ 1.10 (m, 2 H), 1.14 (s, 3 Hλ 1.25 (s. 3 H). 1.34 (s, 9 H), 1.65 (s, 3 H), 1.71 (s, 2 H), 1.75 (s. 6 H). 1.84 (dt, t H). 1.88 (s. 3 H), 2.34 (s. 3 H). 2.37 (s. 2 H), 2.46 (ddd, I H). 2.56 (d. J = 3.3 Hz. I H). 3.36 (d. OH), 3.78 (d. J « 6.9 Hz. I H). 4.13 id. J =» 8.4 Hz. I H), 4.18 ⁽ bs. 1 H ⁾ . 4.27 (AB. J^- 8.4 Hz, 1 H). 4.40 (m, 1 H). 4.72 (m. I H + NH). 4.93 (AB. J _AB = 8.6 Hz. 1 H ⁾ . 5.28 (d, J « 7.6 Hz. 1 H), 5.64 (d, J « 6.9 Hz, 1 H), 6.16 (t, 1 H). 6.28 (s, 1 H), 7.43 (t. 2 H). 7.56 (t, 1 H), 8.07 (d, 2 H); ^l3 C NMR (CDCl,. 63 MHz) δ 9.1, 9.4. 9.5. 13.0, 14.9. 18.5.

- 26 - 21.9, 22.4, 25.7, 26.7. 28.2, 35.5. 35.6. 43.2. 45.6, 51.6. 58.5, 72.2, 72.3, 73.7, 75.0, 75.4 _, 76.5. 77.0. 77.5, 79.2, 79.7. 81.0, 84.4, 120.6. 128.6. 129.2. 130.1, 132.9, 133.6, 137.9, 142.6. 155.4. 166.9, 170.1. 175.1, 203.9; IR (neat, cm '): 3368. 2989. 2915, 1786. 1754. 1725, 1709. 1641, 1630, 1355, 1315, 1 109. HRMS (FAB. DCM NBA/NaCl), m/z: Calcd. for C ₄₅ H ₅₉ 0 _ls NNa ^* . 876.3784. Found 876.3782.

3'-Desphenyl-3'-(2-methyl-l-ρropenyl)-lO-crotonoyidoceta xel (Id):

White solid; [α] _D ²¹ -30° (c 1.00, CHC1,); 'H NMR (CDCl,, 250 MHz) δ 1.16 (s. 3 H). 1.26 (s. 3 H), 1.35 (s. 9 H), 1.67 (s, 3 H). 1.76 (s, 6 H), 1.22 (m, 1 H), 1.90 (s, 3 H). 1.92 (dd, 3 H). 2.35 (s, 3 H), 2.39 (s, 2 H). 2.49 (m, I H), 3.38 (bs, OH). 3.82 (d, J = 6.9 Hz, I H), 4.10 (AB, J _A , = 8.3 Hz, 1 H), 4.20 (bs, 1 H), 4.29 (AB. J _Aβ « 8.3 Hz, I H), 4.45 (m, I H). 4.73 (m, I H + NH), 4.95 (d, J • 7.9 Hz, 1 H), 5.30 (d, I H), 5.66 (d, J » 6.9 Hz, 1 H), 5.95 (dd, 1 H). 6.14 (t, 1 H), 6.36 (s, 1 H), 7.03 ( . 1 H), 7.44 (t, 2 H). 7.57 (t, 1 H). 8.08 (d, 2 H); ^l3 C NMR (CDCl,, 63 MHz) δ 9.5, 14.9. 18.2, 18.5. 21.9, 22.4. 25.7, 26.7. 28.2. 29.6. 35.5, 35.6, 43.2. 45.6. 51.6, 58.6, 72.2. 72.3. 73.7, 75.1, 75.3, 76.5, 77.0, 77.5. 79.2, 79.9, 81.0, 84.4, 120.6, 121.6, 128.6, 129.2. 130.1, 132.9, 133.6. 137.9. 142.6. 147.2. 155.4, 166.2. 166.9, 170.0, 173.0, 174.6, 203.8. HRMS (FAB. DCN NBA/NaCl) m/r. Calcd. for CwH^O _H Na* _. 876.3782. Found. 876.3749.

3'.De_phenyl-3'-<2-methyH-propenyl)-10-/V,N-d_methylca rbamoyldoce xel (le):

White solid: [α] ₀ ^:ι -50" (c 2.00. CHC ); 'H NMR (CDCl,, 250 MHz) δ 1.13 ⁽ s. 3 H). 1.23 (s. 3 H), 1.33 (s, 9 H), 1.64 (s, 3 H), 1.74 (s. 6 H). 1.85 (dt, I H). 1.89 (s. 3 H). 2.33 (s. 3 H), 2.36 (s, 2 H), 2.45 (ddd, I H), 2.93 (s. 3 H). 3.02 (s. 3 H), 3.20 (bs, OH), 3.45 (d. OH). 3.78 (d, J = 6.9 Hz, 1 H). 4.14 (AB, _ _AB = 8.4 Hz. 1 H), 4.18 (bs. 1 H), 4.26 (AB. J _AB = 8.4

Hz, I H), 4.40 (dd, J = 6.7 Hz, 10.2 Hz, I H). 4.69 (d, I H). 4.80 (s. NH), 4.93 (d. J = 8.6 Hz, 1 H), 5.27 (d, J = 7.6 Hz, 1 H), 5.62 (d, J = 6.9 Hz. I H), 6.12 (t, 1 H). 6.23 (s, I H). 7.41 (t, 2 H), 7.55 (t, I H), 8.06 (d, 2 H); ^π C NMR (CDCl,, 63 MHz) δ 9.3. 15.0, 18.5, 22.2. 22.3. 25.7, 26.8, 28.2. 35.3, 35.6, 36.0, 36.6. 43.1. 45.6, 51.6, 58.4, 72.3. 72.4. 73.7, 75.2. 76.2, 76.4. 76.5, 77.0, 77.5. 79.2, 81.0, 84.6, 128.6. 129.2, 130.1, 133.1. 133.6. 137.8. 142.9. 155.4, 156.1. 166.9, 170.0, 173.0. 205.6. HRMS (FAB, DCM/NBA) m/z: Calcd. for C^H^O N-Na ^* . 879.3891. Found, 879.3870.

3'-Desphenyl-3'-(2-methyl-l-propenyi)-10-me_hoxycarbonyld ocetaxel (If):

White solid; [o] _D ²¹ -15.0° (c 2.00, CHCl,); 'H NMR (CDCl,, 250 MHz) δ 1.14 (s, 3 H). 1.23 (s, 3 H). 1.33 (s, 9 H), 1.68 (s, 3 H), 1.71 (s, 6 H). 1.87 (m, 1 H). 1.92 (s. 3 H). 2.34 (s, 3 H), 2.47 (d, 2 H), 2.55 (m. 1 H), 3.40 (bs, OH), 3.76 (d, J » 6.9 Hz. 1 H), 3.85 (s. 3 H), 4.15 (AB, J^ = 8.3 Hz, 1 H), 4.19 (bs. 1 H), 4.28 (AB, J _AB = 8.3 Hz, 1 H). 4.38 (m, 1 H), 4.72 (m, I H + NH). 4.93 (d, J = 8.6 Hz. I H), 5.29 (d. J » 7.8 Hz, 1 H), 5.64 (d. J = 6.9 Hz, 1 H), 6.11 (s, I H), 6.15 (s, 1 H), 7.43 (t, 2 H), 7.56 (t, 1 H), 8.07 (d. 2 H); ¹³ C NMR (CDCl,, 75 MHz) δ 9.4. 15.0, 18.5. 21.7, 22.3. 25.7. 26.5, 28.2. 35.5, 43.1. 45.6. 51.6. 55.5. 58.6, 72.0, 72.2, 73.7, 75.0, 76.4, 76.5. 77.0, 77.2. 77.4. 78.3, 79.1, 79.9, 81.0, 84.3, 120.6. 128.6, 129.2, 130.1, 132.5. 133.6. 137.9. 143.4. 155.4. 155.7. 166.9. 170.1. 172.9, 203.9. HRMS (FAB, DCM/NBA PPG) m/z: Calcd. for CHj βNH ^* . 844.3710. Found, 844.3755.

3'-Desphtnτl-3'-_r__luoπ)-πetlιyl-10-acetyldoce_axel (Ig):

White solid; Η NMR (250 MHz CDCl,): δ 1.14 (s, 3 H), 1.24 (s, 3 H), 1.30 (s. 9 H). 1.67 (s, 3 H), 1.75 (br s, 1 H), 1.92 (s. 3 H), 2.24 (s. 3 H), 2.28-2.37 (m, 5 H), 2.48-2.61 (m. I H), 3.46 (br d, 1 H), 3.79 (d, J = 7.0 Hz. 1 H). 4.16 (d. J = 8.3 Hz, I H). 4.30 (d, J =

8.3 Hz, 1 H), 4.39 (br t, 1 H), 4.71-4.84 (m, 2 H), 4.93 (d, J = 8.1 Hz, 1 H), 5.24 (d _, J =

10.6 Hz, I H), 5.65 (d, J = 7.0 Hz, 1 H), 6.21-6.28 (m. 2 H), 7.49 (t. J = 7.4 Hz, 2 H), 7.61

(t, J = 7.4 Hz, I H), 8.1 1 (d, J = 7.4 Hz. 2 H). "C NMR (63 MHz, CDCl,) S 9.57. 14.82.

20.86, 21.92. 22.35, 26.72. 27.94, 35.39, 35.58. 43.25. 45.65. 53.54. 54.03. 58.59. 68.08 _,

73.15, 73.32, 74.94. 75.48. 76.51. 79.01. 81.18. 81.37. 84.43, 126.24. 128.77, 129.01, 130.23.

133.38, 133.74, 141.60. 154.67, 167.16, 170.28, 171.25. 171.76. 203.54. Anal. Calc. for

C ₄ oHsoF _. NO _l3 :C, 57.07; H, 5.99; N, 1.66. Found: C, 56:33; H. 6.02; N. 1.69.

EXAMPLES 29-32 3'-Desphenyl-3 ^, -(2-methylpropyl)-10-O-substituted docetaxel (lb ¹ ):

A solution of 14 mg (0.016 mmol) of lb in 2.0 mL of ethyl acetate was stirred under one atmosphere of hydrogen at room temperature, in the presence of palladium ( 10%) on activated carbon (23 mg). After 24 hours the suspension was purified by chromatography on silica gel (EtOAc) to afford 14 mg (100%) of 3'-desphenyl-3'-(2-meιhylpropyl)-l0- propanoyldocetaxel (lb') as a white solid: [α] ₀ ^:ι -30° (c 1.00, CHC1,); Η NMR (CDCl,, 250 MHz) δ 0.96 (d, 6 H). 1.13 (s. 3 H), 1.22-1.27 (m, 6 H), 1.30 (s, 9 H). 1.63 (s, 3 H).

1.73 (s, 2 H), 1.82 (m, I H). 1.88 (s. 3 H), 2.36 (s, 3 H), 2.40 (s, 2 H). 2.46 (m. 1 H). 2.49 (m. 2 H), 3.25 (bs, OH), 3.79 (d, J * 7.0 Hz. 1 H). 4.09 (AB, J _AB = 8.3 Hz, I H). 4.16 (bs. 1

H), 4.27 (AB, J _Λ , - 8 J Hz, 1 H), 4.38 (dd, J = 6.7 Hz, 10.2 Hz, I H). 4.57 (d, J = 9.5 Hz.

NH). 4.94 (d, J - 8.0 Hz, I H). 5.64 (d, J = 7.0 Hz. 1 H). 6.13 (t. I H), 6.30 (s. 1 H). 7.43 (t.

2 H), 7.56 (t, 1 H). 8.08 (d. 2 H); ^l3 C NMR (CDCl,. 63 MHz) δ 9.0. 9.5. 14.9. 21.8. 21.9.

22.5. 23.2. 24.6, 26.5. 27.5. 28.1. 29.6. 35.5, 41.2. 43.1. 45.6. 51.3, 58.5. 72.1. 72.6. 73.0.

75.1, 75.4. 76.4. 76.5, 77.0, 77.5, 79.1. 79.7. 81.0, 84.4. 128.6. 129.2, 130.1, 132.9, 133.6.

142.4, 155.5. 166.9, 169.9. 173.9, 174.6, 203.8. HRMS (FAB. DCM/NBA) m z Calcd. for C ₁₄ H ₆₁ 0 ₁₃ NH*. 844.41 19. Found, 844.4157.

In the same manner, the following 3 ^' -desphenyl-3 ^' -(2-methylpropyl)-l0-O-substιtuted docetaxel (Ic'-f) were obtained in quantitative yields:

3'-Desphenyl-3'-(2-methylpropyl)-10-cyclopropanecarbonyld ocetaxel (lc ¹ ):

White solid; (α] ₀ ² ' -30° (c 1.00. CHCl,); Η NMR (CDCl,, 250 MHz) δ 0.96 (d. 6 H), 1.09 (m, 2 H), 1.14 (s, 3 H), 1.24 (s, 3 H), 1.30 (s, 9 H), 1.62-1.70 (m, 4 H), 1.66 (s, 3 H), 1.73 (m, I H), 1.88 (s, 3 H), 2.36 (s, 3 H), 2.39 (s, I H). 2.48 (ddd, I H). 2.50 (d, I H), 3.20 (d, OH), 3.78 (d, J = 6.9 Hz, 1 H), 4.16 (AB. J _AB = 8.3 Hz, I H). 4.20 (bs. I H). 4.27 (AB, J _AB = 8.3 Hz, 1 H), 4.40 (m, 1 H), 4.55 (d, NH), 4.93 (d, J = 8.1 Hz, 1 H), 5.64 (d, J = 7.0 Hz, 1 H), 6.14 (t, 1 H), 6.29 (s, I H). 7.43 (t, 2 H), 7.56 (t, 1 H), 8.09 (d, 2 H); ^l3 C NMR (CDCl,, 63 MHz) δ 9.1, 9.4, 9.5, 13.0, 14.9, 21.9, 22.0. 22.5, 23.2. 24.7, 26.6. 28.1, 35.4, 35.5, 41.2, 43.1. 45.6, 51.3. 58.5, 72.2, 72.7, 72.9. 75.1. 75.4. 76.5, 77.0, 77.5, 79.2, 79.7. 81.0. 84.4, 128.6, 129.2, 130.2, 132.9, 133.6, 142.6. 155.5, 166.9. 169.9. 173.9, 175.1. 203.9. HRMS (FAB, DCM/NBC/NaCl), /z: Calcd. for C _w H _βl O _ls NNaΛ 878.3938. Found, 878.3926.

3'-Desph«ιyl-3*-<2-πι_thylpπ)pyl)-10- V, V-dimethylcarbamoyldoce-axel (Ie ¹ ):

White solid; [α] ₀ ²¹ -80° (c 2.00, CHCl,): 'H NMR (CDCl,. 250 MHz) δ 0.95 (d. 6 H).

1.14 (s. 3 H). 1.23 (s, 3 H), 1.29 (s. 9 H). 1.66 (s. 3 H). 1.68 (m. 2 H), 1.82 (m. 1 H). 1.90 (s, 3 H). 2.36 (s, 3 H), 2.39 (s, 2 H), 2.50 (m. 1 H). 2.95 (s, 3 H). 3.03 (s, 3 H). 3.22 (d. OH), 3.78 (d, J = 7.0 Hz. 1 H). 4.10 (AB. J _Aβ = 8.3 Hz. 1 H). 4.16 (bs. 1 H), 4.27 (AB. J _AB = 8.3 Hz, I H), 4.41 (dd, J * 6.5 Hz, 10.2 Hz. 1 H). 4.56 (d. NH). 4.95 (d, J = 8.1 Hz, 1 H).

5.63 (d, J = 7.0 Hz, 1 H), 6.14 (t. I H), 6.24 (s. 1 H), 7.42 (t, 2 H), 7.56 (t, I H), 8.08 (d _, 2 H); ^l3 C NMR (CDCl,, 75 MHz) δ 9.8. 15.3. 22.3. 22.7. 22.9. 23.6. 25.1. 27.2. 28.5, 35.8, 36.0, 36.4, 37.0, 41.6. 43.6. 46.0, 51.7, 58.9, 72.8. 73.1. 75.7, 76.6. 76.8. 76.9. 77.1, 77.4. 77.6, 77.8, 79.6, 80.0, 81.5, 85.0, 128.7, 129.0, 129.7, 130.6, 133.6, 133.9, 143.3, 155.9. 156.5, 167.3. 170.3. 174.3, 206.0. HRMS (FAB) m/z: Calcd. for C ^O.^N *. 881.4074. Found, 881.4047.

3'-Desphenyl-3'-(2-methylpropyl)-10-methoxycarbonyldoceta xel (ID:

White solid; (α] ₀ ²¹ -70° (c 1.00, CHCl,); Η NMR (CDCl,, 250 MHz) δ 0.96 (d, 6 H). 1.14 (s, 3 H), 1.23 (s, 3 H), 1.30 (s. 9 H), 1.66 (s. 2 H), 1.69 (s, 3 H). 1.84 (m, 1 H). 1.92 (s. 3 H), 2.37 (s. 3 H). 2.47 (s, 2 H), 2.55 (m, 1 H). 3.24 (d, OH). 3.77 (d, J = 6.8 Hz, I H). 3.86 (s. 3 H), 4.16 (AB, J*, - 8.2 Hz, I H). 4.17 (bs, I H), 4.28 (AB, J _AB = 8.2 Hz, I H), 4.40 (dd, I H), 4.56 (d, J - 9.3 Hz, NH), 4.94 (d, J = 8.0 Hz. 1 H). 5.65 (d, J = 7.0 Hz. 1 H). 6.11 (s, 1 H), 6.18 (t, 1 H), 7.43 (t. 2 H), 7.56 (t, I H), 8.09 (d, 2 H); ^l3 C NMR (CDCl,. 75 MHz) δ 9.5. 15.0. 21.8, 22.5. 23.2. 24.7. 26.5. 28.1. 35.5. 35.6, 41.2, 43.0. 45.5. 51.3, 55.5, 58.5. 72.0, 72.6. 73.0, 75.0, 76.5. 77.0, 77.5, 78.3, 79.1, 79.7, 81.0. 84.3. 128.6, 129.2, 130.2, 132.5, 133.6, 143.5, 155.5, 155.7, 166.9, 170.0, 173.9, 204.0. HRMS (FAB, DCM/NBA) m/fc Calcd. for C _4J H„0 ₁₄ NH\ 846.3912. Found, 846.3942.

EXAMPLE 33 Taxoid Ia and Ig were evaluated for tumor growth inhibitory activities against human tumor cell line, A121 (ovarian carcinoma). A549 (non-small cell lung carcinoma), HT-29 (colon carcinoma), MCF7 (mammary carcinoma) or MCF7-R (mammary carcinoma cells 180-

fold resistant to adriamycin), after 72 h drug exposure according to the literature method (see below). Results are shown in Table 1. Lower numbers indicate higher potency. Paciitaxel, docetaxel, and RAH- 1 (see above) were also used for comparison. The data represent the mean values of at least three separate experiments. Lower numbers indicate greater activity.

TABLE 1

The concentration of compound which inhibits 50% (IC _TO , nM) of the growth of human tumor ceil line.

Assessment of cell growth inhibition was determined according to the methods of S ehan et aL. /. Na Cancer Inst. 1990, 82, 1 107. Briefly, cells were plated between 400 and 1200 cells well in 96 well plates and incubated at 37°C for 15-18 h prior to drag addition to allow attachment of cells. Compounds tested were solubilized in 100% DMSO and further diluted in RPMI-1640 containing 10 mM HEPES. Each cell line was treated with 10 concentrations of compounds (5 log range). After a 72 h incubation. 100 mL of ice-cold 50% TCA was added to each well and incubated for I h at 4°C. Plates were then washed 5 times with tap water to remove TCA, low-molecular- weight metabolites and serum proteins. Sulforhodamine B (SRB) (0.4%, 50 mL) was added to each well. Following a 5 mm

incubation at room temperature, plates were rinsed 5 times with 0.1 % acetic acid and air dried. Bound dye was solubilized with 10 mM Tris Base (pH 10.5) for 5 mm on a gyratory shaker. Optical density was measured at 570 nm.

Data were fit with the Sigmoid-Emax concentration-effect model (see Holford, N. H. G.; Scheiner, L. B., "Understanding the dose-effect relationship: Clinical applications of pharmaco-kinetic-pharmacodynamic models.", Clin. Pharmacokin. 1981, 6, 429-453) with non-linear regression, weighted by the reciprocal of the square of the predicted response. The fitting software was developed by the Roswell Park Cancer Institute with Microsoft FORTRAN, and uses the Marquardt algorithm (see Marquardt, D. W., "An algoπthm for least squares estimation of nonlinear parameters", J. Soc. Ind. AppL Math. 1963, II, 431-441 ) as adopted by Nash (see Nash, J. C. "Compact numerical method for computers: Linear algebra and function minimization ", John Wiley & Sons, New York, 1979) for the non-linear regression. The concentration of drug which resulted in 50% growth inhibition (IC^) was calculated.

Since the new taxoids of this invention are unique in that these taxoids possess extremely high activities against drug-resistant human breast cancer cells MCF7-R (two orders of magnitude better than paciitaxel and docetaxel), the activities of these taxoids other than Ia and Ig were evaluated against human breast cancer cells (MCF7) (sensitive) and resistant cells (MCF7-R) (resistant) in the same manner as described above. Results are summarized in TABLE 2.

TABLE 2