The general formula I of the compounds that can be prepared according to the invention is where Rl is: an alkyl hydrocarbon chain containing 1-30 carbon atoms, an alkyl hydrocarbon chain containing 1-30 carbon atoms as well as 1-10 carboxylic acid groups attached to said chain, or alkali or earth alkali metal salt thereof, an alkyl hydrocarbon chain containing 1-30 carbon atoms and 1-10 carboxylic acid esters attached to said chain, a polyethoxylated hydrocarbon chain containing 1-20 ethoxyl groups, a carboxylic acid amide containing 1-30 carbon atoms, where N-Ri bond is an amide bond, or an N-alkyl-N-bis- [2- (1, 2-dicarboxy-ethoxy- (ethyl]-amine containing 1-20 carbon atoms in the alkyl chain, or an alkali or earth alkali metal salt thereof, and R2 and R3 are: hydrogen, an alkali metal ion or an earth alkali metal ion or an alkyl group containing 1-30 carbon atoms.

The compounds to be prepared find use especially as chelating agents.

Transition metal ions and earth-alkali metal ions are bound as water-soluble chelates, for example, in various washing processes. Chelates of metal ions are used in photography chemicals in the developing processes.

When oxygen or peroxide compounds are used in the total chlorine free (TCF) bleaching of pulp it is important to remove the transition metals from the fiber

before bleaching, since transition metal ions catalyze the decomposition of peroxy compounds, thus forming radical compounds. In consequence of these reactions the strength properties of the fiber are deteriorated.

Peroxy compounds such as hydrogen peroxide and peroxy acids can also be used in the so-called ECF-bleaching. Also in sequences which use chlorine dioxide or a combination of chlorine dioxide and peroxy acids, as described in the application FI-974221, a chelating agent can advantageously be used. Traditionally chelating agents are used in the alkaline peroxide bleaching of mechanical pulps such as SGW, TMP, PGW, CTMP etc. A chelating agent can be used directly in the bleaching or as a pretreatment before the bleaching proper. This is especially the case when a multistage peroxide bleaching is employd.

At present, the complexing agents most commonly used in the applications mentioned above are ethylenediaminetetraacetic acid (EDTA) and its salts and di- ethylenetriaminepentaacetic acid (DTPA) and its salts. These are excellent complexing agents, but their biodegradability is poor.

Patent applications FI-960758, FI-960757, FI-960756 and FI-960755 disclose the use of aspartic acid derivatives as chelators in the bleaching of pulp. Such chelators include ethylenediaminedisuccinic acid (EDDS) and its alkali and earth-alkali metal salts, as well as iminodisuccinic acid (ISA) and its alkali and earth-alkali metal salts.

EDDS and ISA are effective chelators of transition metals. In addition, they are biodegradable.

EDDS-type aspartic acid derivatives with longer hydrocarbon chain than in EDDS, are known from JP patent applications 7 261 355 and 6 282 044. One such substance is N, N'- (oxide-2, 1-ethanediyl)-bis-L-aspartic acid.

In most cases the chelators are disposed to waste waters after their use. In order to minimize the nitrogen load in waste waters the nitrogen contents of the chelator should as low as possible. Biodegradable chelators of the type of EDDS, wherein some of the nitrogen atoms have been replaced with oxygen atoms, are disclosed in JP patent applications 7 120899 and 7 120894. The applications disclose the use of various isomers of N- [2- (1, 2-dicarboxyethoxy)-ethyl]-aspartic acid (EDODS) in photographic chemicals. A method to prepare EDODS by La3+-catalyzed O-alkylation of maleic acid salts has been described in the literature (J. van Vestrenen et al., Recl. Trav. Chem. Pays. Bas., vol. 109,1990, p. 474-478).

However, in working tests performed by the applicants, EDODS did not prove to be a sufficiently effective chelator in pulp and paper applications. One possible explanation for the poor chelation result is the length of the carbon chain between the dicarboxyl ethoxy ethyl groups. If the carbon chain is not sufficiently long, strains are produced in the molecule during complexing and the metal complex will not be sufficiently stable.

In a previous application W097/45396 by the present applicant there were disclosed compounds according to the formula II. where Rl is: hydrogen, or and R2 and R3 are: hydrogen, an alkali metal ion or an earth alkali metal ion These compounds include N-bis- [2- (1, 2-dicarboxy-ethoxy)-ethyl]-amine (BCEEA), N-tris-[2-(1, 2-dicarboxy-ethoxy)-ethyl]-amine[2-(1, 2-dicarboxy-ethoxy)-ethyl]-amine (TCEEA) and N-bis- [2- (1,2-di- carboxy-ethoxy)-ethyl]-aspartic acid (BCEEAA), as well as the alkali metal and earth alkali metal salts of the said compounds, preferably Na+, K+, Ca2+ and Mg2+ salts.

In the molecular structure of said compounds, the central atom is a secondary or tertiary nitrogen atom and additionally, the molecule contains four or six carboxylic acid groups, which coordinate effectively with transition metal ions. The carbon chains are sufficiently long in terms of the formation of advantageous bond angles.

The object of the present invention is to provide methods for the preparation of effective chelating agents which would be biodegradable and contain a minimum amount of nitrogen.

According to the invention compounds of the formula (I) can be prepared according to the method as defined in claim 1 or its modification as defined in claim 6. With the exception of the compound referred to as BCEEAA in the above the compounds of the formula (I) are new compounds.

The invention thus comprises preparation of amine compounds according to the formula (I) by using alkali metal or earth-alkali metal salts of maleic acid and N- substituted diethanolamines as starting material in the presence of a lanthanide or earth alkali metal catalyst, in accordance with the following reaction. where Rl has a meaning as defined above in connection with the formula (I) and R2and R3= alkyl, alkali or earth alkali metal ions.

The preferred meanings of Ri are alkyl and (CH2)"COOR, where n = 1-20 and R = alkyl, alkali or earth alkali metal.

The maleic acid salt which is the intermediate stage in the synthesis can be prepared in an aqueous solution by preferably using, available initial substances such as maleic anhydride and alkali metal or earth alkali metal compounds. Alkali metal compounds suitable for the reaction include lithium hydroxide, sodium hydroxide, potassium hydroxide, sodium carbonate, potassium carbonate, and lithium carbonate. Earth alkali metal compounds suitable for the reaction include magnesium hydroxide, magnesium oxide, magnesium carbonate, calcium oxide, calcium hydroxide, and calcium carbonate.

The formation of maleate is an exothermal reaction. When maleic anhydride is added to water, maleic acid is formed. When an alkali is added to this solution at a

suitable rate, the temperature of the reaction mixture will increase to 80-90 °C, which is a temperature preferable for the performing of the alkylation reaction.

The amino alcohol, which is a diethanol amine derivative, and the lanthanum compound used as the catalyst can thereafter be added rapidly to the alkaline reaction mixture.

Alternatively, the amino alcohol can be added to the reaction mixture at pH 7 and the pH is adjusted alkaline thereafter.

Rare earth metal ions or their mixtures can be used as the catalyst. Rare earth metal compounds containing organic ligands, achiral or chiral, can be used as catalyst.

Likewise, suitable catalysts for 0-alkylation include earth-alkali metal compounds such as calcium oxide, calcium hydroxide, calcium carbonate, magnesium oxide, magnesium hydroxide and magnesium carbonate. Furthermore, nickel compounds can be used as the catalyst.

Rare earth metal catalyzed 0-alkylation of maleic acid salt with amino alcohols is a useful reaction, since the synthesis is a one-pot synthesis and the catalyst can be recycled. The catalyst can be separated from the reaction mixture after the reaction by rendering the reaction mixture acidic by means of mineral acids or organic acids followed by addition of oxalic acid to the reaction mixture. The rare earth metal oxalate precipitate formed can be separated from the reaction mixture by filtration.

The catalyst can also be precipitated from the reaction mixture by addition of a molar excess of oxalic acid. Furthermore, the catalyst can be precipitated from the reaction mixture by addition of sodium carbonate. The rare earth metal carbonate formed can be separated from the reaction mixture by filtration.

The pH of the reaction mixture before the precipitation of the catalyst can be adjusted by using hydrochloric acid, sulfuric acid, nitric acid, phosphoric acid, formic acid, acetic acid or oxalic acid, most preferably hydrochloric acid, formic acid, acetic acid or oxalic acid.

It is preferable to use as the catalyst lanthanum (III) compounds, such as lanthanum maleate, lanthanum (III) nitrate, lanthanum (III) chloride, lanthanum oxide or lanthanum octanoate. Likewise, lanthanum compounds which contain organic ligands, chiral ligands or achiral ligands, can be used as a catalyst in the reaction.

Also other metal salts belonging to the lanthanum group can advantageously be

used, especially such as praseodymium and neodymium salts depending on the availibility and price of the compounds.

The lanthanum (III) ion used as a catalyst can be separated from the oxalate precipitate by treating the precipitate with nitric acid or hydrochloric acid. After the treatment the catalyst can be reused. Moreover, the lanthanum ions can be recovered to lanthanum oxide (La203), lanthanum hydroxide or lanthanum carbonate by treating the precipitate at elevated temperatures (400-1000 °C).

When the lanthanum catalyst is precipitated from the reaction mixture as lanthanum carbonate, it can be either reused as is or converted to lanthanum oxide (La203) or lanthanum hydroxide by treating the precipitate at elevated temperatures (400- 1000 °C).

The invention further comprises a modification of the above described process in which an alkali metal or earth-alkali metal salt of maleic acid and diethanolamine are used as starting materials in the presence of a lanthanide or earth alkali metal catalyst. The synthesis starts with the following reaction: where R2and R3= alkyl, alkali or earth alkali metal ions.

N-bis-[2-(1, 2-dicarboxy-ethoxy)-ethyl]-aspartic[2-(1, 2-dicarboxy-ethoxy)-ethyl]-aspartic acid (BCEEAA) as obtained can be converted to N-bis- [2-(1, 2-dicarboxy-ethoxy)-ethyl]-amine by stirring the acidic reaction product containing N-bis- [2- (1, 2-dicarboxy-ethoxy)-ethyl]-aspartic acid BCEEAA at elevated temperature for 1-2 hours. The cyclic amide A formed in this reaction can be further converted to N-bis-[2-(1, 2-dicarboxy-ethoxy)-ethyl]-amine BCEEA in basic conditions. These reactions are as follows: At the last stage of the process the N-bis [2- (1, 2-dicarboxy-ethoxy)-ethyl]-amine as obtained is N-substituted by using a substitution agent replacing the hydrogen bound to the N atom with an organic group. The N-bis [2- (1, 2-dicarboxyethoxy)- ethyl amine can thus be N-substituted by using a carboxylic acid halide, a carboxylic acid anhydride, a methoxylalcoxyl halide or an alkyl halide. 2- chloroacetic acid and 2-bromoacetic acid may be cited as examples. If for instance an organic chloride is used as the substitution agent the reaction is as follows: Rl may have the meanings as defined before.

The invention specifically comprises the novel compounds according to formula (I) wherein Ri is a group selected from alkyl groups and groups comprising an alkyl chain with a single carboxylic acid group, and R2 and R3 represent hydrogen or alkali or earth alkali metal ions. N-methyl-N-bis- [2- (1, 2-dicarboxy-ethoxy)-ethyl]- amine or its alkali or earth alkali metal salt and N-carboxymethyl-N-bis- [2- (1,2- dicarboxy-ethoxy)-ethyl]-amine or its alkali or earth alkali metal salt are specific examples or the novel compounds.

The compounds obtained according to the invention are especially well suited for use in alkaline aqueous solutions, such as detergents and cleaning agents. Further- more, the compounds are suited for use in photography chemicals.

The compounds as obtained are useful chelators in, for example, alkaline aqueous solutions of hydrogen peroxide or in alkaline or acidic solutions of peroxy compounds such as peracetic acid. The compounds are particularly useful as chelators of transition metals in a pretreatment before the bleaching of cellulose with ozone, hydrogen peroxide or peroxy acids such as performic, peracetic, perpropionic or Caro's acid and combinations of the same.

The compounds are usable chelators of earth alkali metals from alkaline the water solutions. This ability makes them useful in detergent applications.

Since the compounds as obtained do not contain phosphorus and contain very little nitrogen, they load the environment considerably less than do the chelators currently used.

Specific uses covered by the invention are defined in claims 14-18.

The invention is described below with the help of examples. However, these examples do not limit the invention.

Example 1 A maleic acid solution was prepared by dissolving 56.0 g (0.571 mol) of maleic anhydride in 124.3 ml of water. 116.2 g of this solution was added to 71.3 g of a 48% lye solution (0.856 mol NaOH). During the addition the temperature of the reaction mixture was maintained at 70-90 °C. Lanthanum (III) oxide, La203, (15.5 g, 0,048 mol) was dissolved in remaining maleic acid solution (64. 1 g, 0. 192 mol) and

added to the reaction mixture together with diethanolamine (20.0 g, 0.190 mol). The reaction mixture was stirred at 95 °C under a reflux condenser for 24 hours. The reaction mixture was rendered acidic (pH 3.5) by addition of oxalic acid, C204H2-2H20 (47.96 g in 71.90 ml of water, 0.380 mol) and stirred at 80 °C for 1 hour. The reaction mixture was cooled and the formed La (III) oxalate precipitate was removed by filtration. From the remaining solution (194.1 g), which contained water 75.2%, the organic compounds were analyzed by means of 13C NMR spectra.

BCEEAA and BCEEA were identified from the 13C NMR spectra. Unreacted initial substances were identified on the basis of reference spectra: diethanolamine and maleic acid, as well as oxalic acid used for the precipitation of the catalyst. Malic acid and fumaric acid were formed as byproducts of the reaction; these were also identified on the basis of reference spectra.

On the basis of a quantitative 13C NMR analysis, the composition of the obtained reaction mixture containing BCEEAA and BCEEA, was as follows: BCEEAA 13.61 w-% BCEEA 3.99 w-% diethanolamine 2.39 w-% maleic acid 2.00 w-% malic acid 1.79 w-% water 75.20 w-% Since BCEEA and BCEEAA and the derivatives thereof are poorly soluble in organic solvents, the 1H-NMR technique cannot be used for the analysis of the reaction mixture. 13C NMR spectroscopy is therefore a useful method for the analysis of the reaction mixture. The 13C NMR spectrum data for BCEEAA and BCEEA are shown in Table 1, entries 1 and 2.

The NMR analysis was confirme by analyzing the same reaction mixture as silyl or methyl ester derivatives by gas chromatograph combined with mass spectrometer (GC-MS). The mass spectral data of the silyl derivatives of BCEEAA and BCEEA are shown in table 2, entries 1 and 2.

Example 2 The reaction product from reaction 1 was refluxed for 2 hours and the reaction mixture was cooled. A sample was withdrawn for analysis. The cyclic product A was identified by 13C NMR and by GC-MS analysis (table 1, entry 5 and table 2, entry 5, respectively). The reaction mixture was rendered basic (pH 13) by addition of 48% sodium hydroxide solution and stirred at 102 °C for 2 h and cooled to room temperature. Quantitative 13C analysis revealed the composition of the reaction mixture to be: BCEEA 6.23 w-% diethanolamine 0.95 w-% maleic acid 0.51 w-% malic acid 0.92 w-% fumaric acid 0.99 w-% oxydibutanedioate 0.64 w-% water 89.76 w-% Example 3 A disodium maleate solution was prepared by dissolving 19.6 g (0.2 mol) of maleic anhydride in 50 ml of water and by adding the resulting maleic acid solution to 33.3 g of a 48% lye solution (0.4 mol NaOH). During the addition the temperature of the reaction mixture was maintained at 70-90 °C. Lanthanum (III) oxide, La203, (8.15 g, 0.025 mol) was dissolved in 65% nitric acid (16.8 g, 0.173 mol) and in 12 ml of water and added to the reaction mixture together with N-methyl diethanol- amine (11.9 g, 0.1 mol). The reaction mixture was stirred at 85 °C under a reflux condenser for 70 hours. The reaction mixture was cooled and rendered acidic (pH 1-2) by addition of sulfuric acid. The formed La (III) sulfate precipitate was removed by filtration. The remaining sodium sulfate was precipitated by addition of acetone.

After filtration and concentration the remaining solution (7.2 g), which contained water 67.6 w-%, the organic compounds were analyzed as silyl or methyl ester derivatives by means of 13C NMR spectra and by GC-MS (table 1, entry 3, and table 2, entry 3, respectively).

On the basis of a quantitative 13C NMR analysis, the composition of the obtained reaction mixture was as follows: N-methyl-BCEEA 12.4 w-% N-methyl-diethanolamine 9.9 w-% maleic acid, fumaric acid 0.7 w-% malic acid 2.5 w-% oxydibutanedioate 6.9 w-% water 67.6 w-% Example 4 Diethanolamine (10 g, 0.095 mol) was treated with chloroacetic acid (9.44 g, 0.100 mol) in 10 g of water. During the addition the temperature raised to 57 °C.

Sodium hydroxide (49% solution in water, 8.15 g, 0.100 mol) was added to the reaction mixture and the temperature of the reaction mixture was elevated to 100 °C for 10 minutes and cooled to room temperature. The N-methylcarboxy diethanol- amine (MCDEA) was identified from 13C NMR and GC-MC spectra (table 1, entry 6, and table 2, entry 6, respectively).

Example 5 Lanthanum oxide (6.07 g, 0,09 mol), water (20 ml), and maleic anhydride (9.13 g, 0.093 mol) was added to the reaction vessel and the solution was heated to 85 °C.

Sodium hydroxide solution (49%, 7.60 g, 0.093 mol) and water (23 g) was added to the reaction mixture. MCDEA (38% solution in water, 20 g, 0.047 mol), the reaction product from the carboxymethylation reaction described in example 5, was added into the reaction mixture. The pH of the resulting suspension was adjusted to pH 8.5 by addition of sodium hydroxide solution. The resulting solution was stirred at 100 °C for 48 h. The lanthanum catalyst was precipitated by addition of oxalic acid. The reaction product was identified by using 13C NMR and GC-MS spectra (table 1, entry 4, and table 2, entry 4). 13C NMR analysis revealed the composition of the reaction mixture to be: N-carboxymethyl-BCEEA 23.86 w-% N-carboxymethyl-N-[2-(1, 2-dicarboxyethoxy)-ethyl]-N-ethanolamine[2-(1, 2-dicarboxyethoxy)-ethyl]-N-ethanolamine 6.42 w-% malic acid 2.09 w-%

Example 6 The reaction product described in example 2, containing BCEEA, was stirred with a magnesium salt of 2-bromoacetic acid with the excess of magnesium oxide at 35 °C for 3 days. The reaction product CMBCEEA was identified from 13C NMR spectra of the product by comparison with the previously obtained spectra (Table 1, entry 4).

Example 7 Stabilization of peracetic acid (PAA) is essential in pulp bleaching liquors and in detergent solutions. In the presence of metal ions (for example Mn, Fe, Cu), PAA is decomposed rapidly and the bleaching efficiency is decreased.

The efficiency of the novel chelating agents in stabilizing peracetic acid solutions were tested as follows: A water solution containing Mn ions 0.4 mg/1, was prepared by addition of Mn sulphate to water. An appropriate amount of DTPA, MeBCEEA and CMBCEEA, respectively, were added to the solution in order to adjust the concentration of the chelating agent to 140 mg/l. The pH of the solution was adjusted to 4,5 by using sodium hydroxide and the solution was warmed up to 50 °C. Peracetic acid concentration was adjusted to 2,0 g/1 by addition of distilled, 36% PAA solution.

The decomposition of PAA in the solutions was followed by iodometric titration.

The titration results are shown in table 3.

Table 3 Stability of peracetic acid solutions containing chelating agents as stabilizers at 50 °C in the presence of Fe and Mn ions.

Concentration of peracetic acid (9/1) Sample 1 2 3 Stabilizer DTPA MeBCEEA CMBCEEA Storage time mu 0 2.10 2.06 2.00 15 0.36 1.96 1.95 30 0.35 1.98 1.95 45 0.34 1.96 1.98 60 0.33 1.94 2.00 273 1. 90 300 1. 82 The results of the above mentioned example show clearly the usefullness of the novel complexing agents as stabilizers of peracetic acid solutions.

Example 8 The efficacy of the novel chelating agents to bind calcium ions was tested by using the method of Blay and Ryland (Analytical letters 4 (10), pp. 653-663 (1971). Thus, 0.002 M solution of calcium chloride (CaCl2) buffered to pH 9.5 was titrated by a buffered solution of the chelating agent. During the titration, the non-chelated calcium ions were determined by using a calcium selective electrode. Known chelating agents, DTPA, EDTA and nitrilotriacetic acid (NTA) were used as references.

Table 4 Non-chelated Ca mol-% 234Sample1 Chelating agent DTPA MeBCEEANTA Molar equivalents of chelating agent added 0.0 100.0 100.0 100.0 100.0 6.7 84.9 67.4 84.9 72.8 13.3 72.3 61.9 61.9 61.9 20.0 61.6 52.8 61.6 48.9 26.7 52.7 48.8 52.7 41.8 33.3 45.3 45.3 48.9 35.9 40.0 42.1 39.0 45.5 28.6 46.7 36.4 36.4 42.4 22.9 53.3 29.2 39.7 39.7 19.8 60.0 25.4 34.6 34.6 14.8 66.7 19.0 25.9 30.3 11.1 73.3 14.4 21.1 26.6 7.7 80.0 10.1 17.3 23.5 5.4 86.7 6.1 12.2 17.9 3.8 93.3 2.3 6.4 13.8 2.9 100.0 2.0 6.0 12.0 2.5

The results shown in table 4 show clearly that N-methyl BCEEA binds calcium ions more effectively than the reference chemicals.

Example 9 An O-Q-Op (oxygen delignification, chelation, peroxide reinforced oxygen) delignified softwood kraft pulp (kappa number 3.6, viscosity 718 dm3/kg) sample was taken from a Finnish pulp mill. 100 grams pulp samples were treated in laboratory with peracetic acid solutions and bleached with alkaline hydrogen peroxide. The bleaching conditions and chemical dosages are shown in table 5. The bleaching trials were conducted in plastic bags.

As can be seen from table 5, the concentration of residual peracetic acid (PAA) after treatment in the solution containing MeBCEEA or CMBCEEA is higher than in the PAA solution containing DTPA as chelating agent. This results in a lower consumption of peracetic acid in the bleaching. It is of importance especially if the liquor is recycled. The treatment of the pulp with the PAA solution containing MeBCEEA results in similar final viscosity than the treatment with the PAA solution containing DTPA. When no chelating agent was used, the final viscosity of the bleached pulp was unacceptable. In addition, the brightness of the pulp is much better after treatment with the PAA solution containing MeBCEEA. The treatment of the pulp with the PAA solution containing CMBCEEA gives an improved viscosity and a better viscosity than the treatment of the pulp with similar solution containing DTPA. According to these test results, it is clear that the use of the new chelating agents is advantageous in bleaching of pulp in sequences with comprises the use of peroxygen chemicals such as hydrogen peroxide, peroxy acids etc.

Table 5 Delignifying and bleaching of chemical pulp t, min T, °C Cs, % Start pH End pH PAA, kg/tm Chelating agent Dosage kg/tm Residual PAA, kg/tm Residual H202, kg/tm Kappa Viscosity, dm3/kg Brightness % ISO t, min T, C Cs, % Start pH End pH H202, kg/tm NaOH, kg/tm Residual H202, kg/tm H202 consumption, kg/tm Residual NaOH, kg/tm Kappa Viscosity, dm3/kg A-Viscosity, % Brightness % ISO A-brightness % ISO Yellowness QPAA QPAA QPAA QPAA 120 120 120 120 70 70 70 70 10 10 10 10 5.4 5. 5 5. 3 5.6 4.6 4. 3 4. 6 4.6 12 12 12 12 no DTPA MeBCEEA CMBCEEA 2 2 2 4.6 0. 6 4. 3 3.4 0.7 0. 9 1. 1 1.1 2.6 3. 1 2. 6 2.5 707 681 702 719 74.9 72.1 74.2 74.3 P P P P 180 180 180 180 90 90 90 90 10 10 10 10 10.4 10. 4 10. 4 10.4 10.4 10. 2 10. 3 10.3 20 20 20 20 15 10 12 10 4 9. 1 9. 8 12.8 16.0 10. 9 10. 2 7.2 5.1 5. 2 6. 3 6.3 1.3 1. 9 1. 5 1.5 489 570 577 643 31.9 20. 6 19. 6 10.4 87.2 84. 6 86. 6 86.4 22.8 20. 2 22. 2 22.0 6. 7 11.3 9. 3 9.7 Table 1 Formula 13C NMR PPM (xplanation) a a 175 (a), 176 (b), 37.9 (c), HOOCcH e e HzC-75.8 (d), 66. 4 (e), 47. 8 (f) I CH2 NH CH2 H b/a'oi \ y OOC f f d COOH BCEEA 175 (a), 176 (b), 37.9 (c), COOL 75.8 (d), 65.5 (e), 54.4 (f), cooH 62. 0, 32. 6 h a cCH HOOCcH, e e H-00011 170.3 (I), 173.9 (j) 1 CH2 N CH2 b° CH \o-CH. b HOOC f f d COOH BCEEAA 175. 9 (a), 176.0 (b), e CH3 HOOCCHZ I e HZCCOOH 3'7, 5 (C), 75.5 (d), 63.7 (e), b Ao-cHrS-Vkb 55"2 (f) ? CH H HOOC f z COOH MeBCEEA COOH 176.8 (a), 177.3 (b), a c gCH h C_COOH 39. 9 (c), 77. 8 (d), 66 9 (e), CHZ e 56. 7. 58. 1 HC/Hz\/Iw/CHZ bl-11 d.-O CH2 CH2/"0--CH b 172.2 (h) HOOC f f dCOOH CMBCEEA Formula 13C NMR PPM (xplanation) b g h 177.6 (a), 178.1 (b), COOH d e/\ 40.3 (c), 77.9 (d), 65.3 (e), HOOC N 0 50.3 (f), 49.6 (g), 70.8 (h), ou 0< k 76. 3 (i), (k), 100H 177. 0 (1) COOH Compound A COOH 62. 6 (e), 57. 5 (f), 58. 8 (g), CHX 175.3 (h) I e CH2 N CH2 CH2 fCH \OH f I Table 2 Mass spectra of the silyl derivatives of the novel compounds Compound MS-spectra of the silylated compounds m/z (relative intensity) a a HOOC-CTI2 e e H0011 406 (100%), 73 (96%), IC CH2 NH/CH2 l 333 (50%), 407 (34%), HOOC d f f d sCOOH 147 (17%), 171 (16%), BCEEA 422 (10%), 245 (8%) Compound MS-spectra of the silylated compounds m/z (relative intensi COOH CH 73 (100%), 594 (61%), a C CH e a 147 (32%), 245 (18%), HOOC CH gN CHIZC-COOH 610 (15%), 678 (12%), bocnr'"CHCH b 608 (9%), 520 (5%) HOOC f f d COOH BCEEAA a a CH c HOOC-CH2 e CH3 e H CCOOH 348 (100%), 73 (54%), 2 b o,-ou, CH2 o d b 349 (28%), 364 (18%), HOOC fCH2 XCOOH 147 (15%), 245 (10%), 624 (2%), 522 (1%) MeBCEEA COOH CH/h a ? 3 (100%), 464 (94%), HOOCCHZ e g I e H CCOOH I (36%), 465 (35%), CL2 N CH2 bHd WcH \CH/vH b 147 (31%), 245 (18%), HOOC- d f f u d COOH Hooc f f ° acooH 638 (15%), 117 (12%) CMBCEEA COOH h HOOC d 73 (100%), 258 (65%), d e HOOC o 75 (63%), 184 (38%), a w, 147 (30%), 245 (26%), a 140 (24%), 274 (24%) COOH Compound A