Process for preparing L-.alpha.-methylphenyl alanines

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a process for preparing L-.alpha.-methylphenyl alanines by biochemical asymmetric hydrolysis of DL-.alpha.-methylphenyl alanine amides, in which a microbial enzyme catalyzing a hydrolysis of L-isomer of DL-.alpha.-methylphenyl alanine amides is utilized.
2. Description of the Prior Art
It is known in the art that pharmacological activities are possessed by L-.alpha.-methylphenyl alanines, but not D-.alpha.-methylphenyl alanines. For instance, L-3,4-dihydroxy-.alpha.-methylphenyl alanine, usually referred to as "methyl dopa", is a well-known excellent hypotensor, while D-3,4-dihydroxy-.alpha.-methylphenyl alanine has no hypotensor activity. Accordingly, effective optical resolution of chemically synthesized DL-.alpha.-methylphenyl alanines is an extremely important problem to be solved in the art.
Various optical resolution methods of the racemic mixture of .alpha.-methylphenyl alanines have been heretofore proposed, including physical methods, such as diastereomer methods or fractional crystallization methods, and biochemical methods, utilizing microorganisms.
Diastereomer methods are disadvantageous in that the yield of the desired product is low, the recovery of the desired product is troublesome, the resolution agent used is expensive, and the recovery of the resolution agent is not easy.
Fractional crystallization methods are disadvantageous in that the racemic mixture is often crystallized prior to crystallization of the desired optically active product even if crystals of the desired optically active product are seeded and that both the resolution rate (%) and the crystallization reproducibility of the desired optically active product are low.
In known biochemical resolution methods, N-succinyl or N-benzoyl derivatives of DL-.alpha.-methylphenyl alanines are used as substrates for asymmetric hydrolysis by microbial enzymes. These methods are, however, disadvantageous in that the synthesis of the substrates is troublesome, the reuse of the remaining substrates (i.e., D-derivatives) is difficult, and the yield of the desired product is low.
SUMMARY OF THE INVENTION
Accordingly, an object of the present invention is to provide a biochemical method for resolution of DL-.alpha.-methylphenyl alanines eliminating the above-mentioned disadvantages in the prior arts, thereby effectively producing L-.alpha.-methylphenyl alanines.
Other objects and advantages of the present invention will be apparent from the description set forth hereinbelow.
In accordance with the present invention, there is provided a process for preparing an L-.alpha.-methylphenyl alanine having the general formula [I]: ##STR3## wherein R.sub.1 and R.sub.2 may be independently a hydrogen atom or lower alkyl group, or R.sub.1 and R.sub.2 may be alkylene groups combined together to form 5-through 8-membered rings, comprising the steps of:
(a) making a DL-.alpha.-methylphenyl alanine amide having the general formula [II]: ##STR4## wherein R.sub.1 and R.sub.2 are the same as defined above, interact with the culture product of a microorganism capable of producing enzyme catalyzing the hydrolysis of L-isomer of DL-.alpha.-methylphenyl alanine amide or the treated product thereof, whereby asymmetric hydrolysis of an L-.alpha.-methylphenyl alanine amide is effected; and
(b) separating the resultant L-.alpha.-methylphenyl alanines from the hydrolysis mixture.
DETAILED DESCRIPTION OF THE INVENTION
The term "the treated product" used herein means that the cells or broth separated from the cultivation mixture, or enzyme preparations including cell-free extract, crude enzyme and purified enzyme prepared from the cultivation mixture, the cells or broth, or the immobilized preparations derived from all of them.
Typical examples of the DL-.alpha.-methylphenyl alanine amides having the above-mentioned general formula [II] and usable as substrates in the present invention are as follows. It should be noted, however, that these substrates are not restrictive, but illustrative. ##STR5## DL-3,4-dihydroxy-.alpha.-methylphenyl alanine amide ##STR6## DL-4-hydroxy-3-methoxy-.alpha.-methylphenyl alanine amide ##STR7## DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide ##STR8## DL-3,4-methylenedioxy-.alpha.-methylphenyl alanine amide
These substrates may be readily prepared by, for example, reacting ammonium cyanide to phenylacetones to form the amino nitrile derivatives and hydrolyzing the nitrile group of the resultant amino nitrile derivatives in the presence of an acid.
The microorganisms usable in the present invention include any microorganisms which can produce enzyme catalyzing the hydrolysis of only L-isomer in a racemic mixture of DL-.alpha.-methylphenyl alanine amides, regardless of their taxonomical groups. Examples of the genus names of these microorganisms are listed in the following table, in which the typical species name of the microorganism belonging to each genus is also listed. However, it should be noted that the microorganisms which can be employed in the practice of the present invention are not limited to these specific examples. All the exemplified microorganisms are known and also readily available from the depositories of JFCC (Japanese Federation of Culture Collections of Microorganisms) such as IFO (Institute for Fermentation, Osaka, Japan) and IAM (Institute of Applied Microbiology, University of Tokyo, Tokyo, Japan), and NIHJ (National Institute of Health, Japan).
______________________________________ (1) Genus Rhizopus IFO-4768 Rhizopus chinensis (2) Genus Absidia IFO-4011 Absidia orchidis (3) Genus Aspergillus IFO-4068 Aspergillus niger var fermentarius (4) Genus Penicillium IFO-5692 Penicillium frequentans (5) Genus pullularia IFO-4464 Pullularia pullulans (6) Genus Fusarium IFO-5421 Fusarium roseum (7) Genus Gibberella IFO-5268 Gibberella fujikuroi (8) Genus Trichoderma IFO-4847 Trichoderma viride (9) Genus Gliocladium IFO-5422 Gliocladium roseum(10) Genus Cunninghamella IFO-4441 Cunninghamella elegans(11) Genus Actinomucor IFO-4022 Actinomucor repens(12) Genus Geotrichum IFO-6454 Geotrichum candidum(13) Genus Saccharomyces IFO-0505 Saccharomyces rouxii(14) Genus Shizosaccharomyces IFO-0346 Shizosaccharomyces pombe(15) Genus Pichia IFO-0195 Pichia polimorpha(16) Genus Hansenula IFO-0117 Hansenula anomala(17) Genus Debariomyces IFO-0023 Debariomyces hansenii(18) Genus Nadsonia IFO-0665 Nadsonia elongata(19) Genus Sporobolomyces IFO-0376 Sporobolomyces pararoseus(20) Genus Cryptococcus IFO-0378 Cryptococcus albidus(21) Genus Torulopsis IFO-0768 Torulopsis candida(22) Genus Brettanomyces IFO-0642 Brettanomyces anomalus(23) Genus Candida IFO-0396 Candida utilis(24) Genus Tricosporon IFO-0598 Tricosporon beigelii(25) Genus Rhodotorula IFO-0412 Rhodotorula minuta var texensis(26) Genus Mycobacterium Mycobacterium smegmatis NIHJ-1628 Mycobacterium avium chester IFO-3154 Mycobacterium phlei IFO-3158(27) Genus Nocardia IFO-3424 Nocardia asteroides(28) Genus Streptomyces IFO-3356 Streptomyces griseus(29) Genus Aerobacter IFO-3320 Aerobacter aerogenes(30) Genus Alcaligenes IAM-1517 Alcaligenes viscolactis(31) Genus Flvobacterium IAM-1100 Flavobacterium arborescens(32) Genus Bacillus IFO-3026 Bacillus subtilis(33) Genus Agrobacterium IFO-13262 Agrobacterium tumefaciens(34) Genus Micrococcus IFO-3242 Micrococcus flavus(35) Genus Sarcina IFO-3064 Sarcina aurantiaca(36) Genus Arthrobacter IFO-3530 Arthrobacter simplex(37) Genus Brevibacterium IFO-12071 Brevibacterium ammoniagenes(38) Genus Pseudomonas Pseudomonas iodinum IFO-3558 Pseudomonas fluorescens IFO-3081(39) Genus Lactobacillus IFO-3322 Lactobacillus casei(40) Genus Streptococcus IFO-3434 Streptococcus lactis(41) Genus Clostridium IFO-3346 Clostridium acetobutyricum(42) Genus Enterobacter IFO-3317 Enterobacter aerogenes(43) Genus Ustilago IFO-5346 Ustilago zeae______________________________________
Among these microorganisms, microorganisms belonging to genera Trichoderma, Nocardia, Mycobacterium, Bacillus, Rhizopus, Candida, Hansenula, Streptomyces, Aerobacter, Arthrobacter, Pseudomonas, Gibberella, Torulopsis, Enterobacter, and Ustilago are especially useful in the practice of the present invention,
In the practice of the present invention, the above-mentioned microorganisms can be made to interact with the DL-.alpha.-methylphenyl alanine amides in the form of the cultivation mixture thereof, the cells or broth separated from the mixture, or enzyme preparations including cell-free extract, crude enzyme, and purified enzyme prepared from the cultivation mixture, the cells or the broth according to conventional methods. The cells, or enzyme may be immobilized on carriers in the practice of the present invention.
The enzyme which can catalyze the hydrolysis of L-isomer of DL-.alpha.-methylphenyl alanine amides is not clearly understood, but it would seem amidase, without prejudice to the invention.
Examples of the carriers usable in the present invention are natural products such as alginic acid, carrageenan, collagen, cellulose, acetylcellulose, agar, cellophane, and collodion and synthetic polymer substances such as polyacrylamide, polystyrene, polyethylene glycol, polypropylene glycol, polyurethane, and polybutadiene. The immobilization of the cells or enzyme on the carrier can be carried out in a conventional methods under moderate conditions so that the activity of the enzyme is not impaired.
The suitable reaction temperature of the asymmetric hydrolysis according to the present invention can be within the range of from 20.degree. C. through 50.degree. C. However, in order to minimize the decrease in the enzymatic activity, the use of the reaction temperature of from 25.degree. C. through 40.degree. C. is economically advantageous. The suitable reaction time of the asymmetric hydrolysis according to the present invention can be within the range of from 5 through 50 hours. However, the reaction time can be shortened by raising the reaction temperature or by increasing the amount of the enzymes used. Furthermore, the reaction can be generally carried out under a pH of 5 through 10, more preferably 7 through 9.
The amount of the microorganisms employed in the practice of the present invention is desirably in a weight ratio of from 0.01 through 2, in terms of the freeze dried cells, based on the weight of the DL-.alpha.-methylphenyl alanine amides. In the case where the cultivation mixtures of the microorganisms, enzyme preparations prepared from the mixtures or cells, or the immobilized products thereof are employed, the amount thereof can be determined in terms of the amount of the freeze dried cells. The suitable concentration of the substrate, i.e., DL-.alpha.-methylphenyl alanine amides in the reaction mixture is generally within the range of from 1% through 40% by weight, desirably 5% through 30% by weight.
According to the present invention, the asymmetric hydrolysis reaction is stopped after the hydrolysis of L-.alpha.-methylphenyl alanine amides proceeds at the conversion rate of almost 100%, and then, L-.alpha.-methylphenyl alanines and D-.alpha.-methylphenyl alanine amides are separately isolated from the reaction mixture. This separation can be readily carried out by using any conventional separation techniques, such as fractional crystallization and solvent extraction, D-.alpha.-methylphenyl alanine amides are not affected by the action of the microorganisms in the above-mentioned asymmetric hydrolysis and, therefore, almost all D-.alpha.-methylphenyl alanine amides can be recovered from the racemic mixture. The D-.alpha.-methylphenyl alanine amides thus recovered can be readily hydrolyzed by using any conventional techniques, for example, by heating in the presence of an aqueous acid or alkaline solution. The resultant D-.alpha.-methylphenyl alanines are treated by sodium hypochlorite to form phenyl acetones, which, in turn, are again usable as starting material for the synthesis of the above-mentioned substrate.
The present invention has the advantages in that, as compared with known biochemical processes, (1) the substrates to be used can be readily prepared at a low cost, (2) the separation of the desired product from the remaining substrate (i.e., D-isomer) in the reaction mixture is not difficult and the recovered D-isomer can be used again as the starting material for the synthesis of the substrate, and (3) the optical purity and yield of the desired product are high.

EXAMPLES
The present invention will now be further illustrated by, but is by no means limited to, the following examples wherein the yield of L-.alpha.-methylphenyl alanines is calculated from the following equation. ##EQU1##
EXAMPLES 1 THROUGH 15
One hundred ml of a culture medium having a pH of 7.0 and containing 5% by weight of glycerol, 5% by weight of corn steep liquor, 0.5% by weight of ammonium sulfate, and 1 ml of a mixture of inorganic salts was charged into a shaking flask. The inorganic salts mixture was prepared by dissolving 20 g of MgSO.sub.4.7H.sub.2 O, 5 g of FeSO.sub.4.7H.sub.2 O, 2 g of CaCl.sub.2, 0.2 g of MnCl.sub.2.4H.sub.2 O, 0.1 g of NaMoO.sub.4.2H.sub.2 O, and 0.1 g of NaCl in 1,000 ml of distilled water. After sterilizing the content of the flask, 2 loopfuls each of the microorganisms listed in Table 1 below were inoculated from an agar slant and, then, the reciprocal shaking culture (or incubation) was carried out at a temperature of 30.degree. C. for 65 hours.
Thereafter, 2 g of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide was added to the flask and, then, the reciprocal shaking culture was carried out at a temperature of 30.degree. C. for 48 hours. The cells were removed from the reaction mixture by centrifugation or filtration. The filtrate was analyzed with a high speed liquid chromatograph. Thus, the yield of 3.4-dimethoxy-.alpha.-methylphenyl alanine thus obtained was determined.
No specific optical rotation data of L- or D-3,4-dimethoxy-.alpha.-methylphenyl alanine were available in literatures. Accordingly, the resultant 3,4-dimethoxy-.alpha.-methylphenyl alanine was converted to N-acetyl-3,4-dimethoxy-.alpha.-methylphenyl alanine according to a method described in the following Example 16. From the specific optical rotation data of the N-acetyl derivatives available in literatures, it was confirmed that the 3,4-dimethoxy-.alpha.-methylphenyl alanine obtained in each Example was L-isomer.
The results obtained in Examples 1 through 15 are shown in the following Table 1.
TABLE 1______________________________________ Formed L-3,4-dimethoxy- .alpha.-methylphenyl alanine Specific optical rotation [.alpha.].sub.DExample Microorganism used yield (%) (C = 1, H.sub.2 O)*______________________________________1 Enterobacter aerogenes 42 -50.degree. IFO-33172 Bacillus subtilis 74 -49.degree. IFO-30263 Candida utilis 36 -51.degree. IFO-03964 Rhizopus chinensis 30 -47.degree. IFO-47685 Trichoderma viride 28 -46.degree. IFO-48476 Nocardia asteroides 49 -48.degree. IFO-34247 Mycobacterium smegmatis 86 -52.degree. NIHJ-16288 Streptomyces griseus 33 -49.degree. IFO-33569 Ustilago zeae 66 -51.degree. IFO-534610 Aerobacter aerogenes 51 -52.degree. IFO-332011 Arthrobacter simplex 23 -49.degree. IFO-353012 Pseudomonas fluorescens 94 -53.degree. IFO-308113 Gibberella fujikuroi 31 -47.degree. IFO-526814 Torulopsis candida 17 -45.degree. IFO-076815 Hansenula anomala 30 -44.degree. IFO-0177______________________________________ *Specific optical rotation of N--acetyl compound
EXAMPLE 16
From the culture mixture of Mycobacterium avium chester (IFO-3154) prepared in the same manner as in Example 1, the cells were collected by centrifugation and, then, washed twice with distilled water.
The washed cells were added to 100 ml of a 0.1 M phosphate buffer solution having a pH of 7.0 and containing 2 g of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide. The resultant mixture was incubated at a temperature of 30.degree. C. for 20 hours.
After completing the reaction, the cells were removed from the reaction mixture by centrifugation. The resultant reaction mixture thus obtained was analyzed by a high speed liquid chromatography. As a result, the resultant reaction mixture contained 950 mg of L-3,4-dimethoxy-.alpha.-methylphenyl alanine (yield=95%) and 1030 mg of D-3,4-dimethoxy-.alpha.-methylphenyl alanine amide.
The reaction mixture was extracted by 200 ml of benzene. Thus, 970 mg of the unreacted oily D-3,4-dimethoxy-.alpha.-methylphenyl alanine amide having a specific optical rotation [.alpha.].sub.D of +20.5.degree. (c=1, methanol) was recovered.
On the other hand, the water layer after the extraction was adjusted to a pH of 2.0 by using hydrochloric acid. The resultant solution was vaporized to dryness. Thus, 980 mg of L-3,4-dimethoxy-.alpha.-methylphenyl alanine hydrochloride crystal having a specific optical rotation [.alpha.].sub.D of +5.4.degree. (c=1, methanol) was obtained. Thereafter, the resultant crystal was dissolved in 20 ml of iso-propanol, and 2.0 ml of triethylamine and 2.0 l of acetic anhydride were added. The resultant solution was allowed to stand overnight and was concentrated under reduced pressure. The residue was dissolved in 2.0 ml of water, and the pH of the resultant solution was adjusted to 2.0 by using concentrated hydrochloric acid. The resultant solution was extracted with ethyl acetate, and the extracted ethyl acetate layer was dried and distillated under reduced pressure. Thus, 800 mg of L-N-acetyl-3,4-dimethoxy-.alpha.-methylphenyl alanine crystal having a melting point of 182.degree. C. through 185.degree. C. and a specific optical rotation [.alpha.].sub.D of -53.0.degree. (c=1, methanol) was obtained.
The above-obtained specific optical rotation value is identical to that of L-N-acetyl-3,4-dimethoxy-.alpha.-methylphenyl alanine in literatures. Accordingly, it was confirmed that the resultant acetyl compound was L-acetyl compound and the 3,4-dimethoxy-.alpha.-methylphenyl alanine obtained above was also the L-isomer having an optical purity of 96.4%. Furthermore, the 3,4-dimethoxy-.alpha.-methylphenyl alanine amide recovered above was the D-isomer.
EXAMPLE 17
The washed cells of Mycobacterium avium chester (IFO-3154) prepared in the same manner as in Example 16 were washed with cold acetone. Thus, acetone dried cells were obtained.
DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide was dissolved in distilled water and substrate solutions having various concentrations listed in Table 2 below and having a pH of 7.0 were prepared.
The above-mentioned acetone dried cells were added to 10 ml of the substrate solutions in such an amount that the weight ratio of the dried cells to the substrate were 0.2. Then, the reaction was carried out at a temperature of 30.degree. C. for 20 hours. The resultant reaction mixture was analyzed to determine the yield of L-3,4-dimethoxy-.alpha.-methylphenyl alanine by using a high speed liquid chromatograph.
The results are shown in Table 2 below.
TABLE 2______________________________________Concentration of substrate(DL-3,4-dimethoxy-.alpha.-methylphenyl Yield of L-3,4-dimethoxy-.alpha.-alanine amide) methylphenyl alanine(% by weight) (%)______________________________________1 1002 1005 10010 10020 8630 7240 49______________________________________
EXAMPLE 18
The washed cells of Mycobacterium avium chester (IFO-3154) prepared in the same manner as described in Example 16 were freeze dried.
The freeze dried cells were added to 10 ml of distilled water containing 10% by weight of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide and having a pH of 7.5 in a weight ratio of the cells to the substrate listed in Table 3 below. The resultant mixture was incubated at a temperature of 30.degree. C. for 20 hours. The reaction mixture was analyzed to determine the yield of L-3,4-dimethoxy-.alpha.-methylphenyl alanine by a high speed liquid chromatograph.
The results are shown in Table 3 below.
TABLE 3______________________________________Freeze dried cells Yield of L-3,4-dimethoxy-.alpha.-Substrate methylphenyl alanine(Weight ratio) (%)______________________________________0.01 680.05 890.1 970.5 1001.0 100______________________________________
EXAMPLE 19
Fifty mg of the freeze dried cells of Mycobacterium avium chester (IFO-3154) prepared in the same manner as described in Example 18 were suspended in 5 ml of 0.2 M phosphate buffer solution having a pH of 7.0 and, then, the cells were disrupted under cooling by using a French press (20,000 psi). The resultant mixture was centrifuged under 20,000.times.g for 30 minutes. To 5 ml of the supernatant solution thus obtained, 100 mg of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide was added, and the pH of the mixture was adjusted to 7.5. Thereafter, the mixture was incubated at a temperature of 30.degree. C. for 20 hours.
The reaction mixture thus obtained was analyzed by a high speed liquid chromatograph. L-3,4-dimethoxy-.alpha.-methylphenyl alanine was obtained at a yield of 85%.
EXAMPLE 20
To 5 ml of the cell-free extract of Mycobacterium avium chester (IFO-3154) prepared in the same manner as described in Example 19, ammonium sulfate was added. The ammonium sulfate precipitate obtained at a saturation of 25% through 75% of ammonium sulfate was collected by centrifugation. Then, 5 ml of 0.2 M phosphate buffer solution containing 100 mg of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide and having a pH of 7.5 was added thereto. The mixture was incubated at a temperature of 30.degree. C. for 20 hours.
The reaction mixture thus obtained was analyzed by a high speed liquid chromatograph. As a result, L-3,4-dimethoxy-.alpha.-methylphenyl alanine was obtained at a yield of 58%.
EXAMPLE 21
Ten ml of the cell-free extract of Mycobacterium avium chester (IFO-3154) prepared in the same manner as in Example 19 was passed through a column having a diameter of 1.5 cm and a height of 65 cm and packed with Sephadex G-75. Thus, fractions having the enzyme activity were collected. These fractions were concentrated by using a semipermeable membrane method to a volume of 5 ml.
Thereafter, 100 mg of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide was added thereto. The mixture was incubated at a temperature of 30.degree. C. for 20 hours.
The reaction mixture was analyzed by a high speed liquid chromatograph. As a result, L-3,4-dimethoxy-.alpha.-methylphenyl alanine was obtained at a yield of 48%.
EXAMPLE 22
The washed cells (corresponding to 1.0 g of the freeze dried cells) of Mycobacterium avium chester (IFO-3154) prepared in the same manner as in Example 16 were suspended in 15 ml of 0.1 M phosphate buffer solution having a pH of 7.0 and, then, 3.75 g of acrylamide monomer, 0.2 g of N,N'-methylene bisacrylamide (i.e., crosslinking agent), 2.5 ml of a 5% aqueous 3-dimethylamino propionitrile solution (i.e., polymerization promotor), and 2.5 ml of aqueous potassium persulfate solution (i.e., polymerization initiator) were added and mixed with one another. The mixture was allowed to stand at a temperature of 25.degree. C. for 1 hour. Thus, the gellation of the mixture was completed.
The gel thus obtained was crushed and washed with water. The resultant immobilized product (i.e., gel particles having a particle diameter of 0.2 through 0.5 mm) was packed into a column having a diameter of 2 cm and a height of 50 cm. Thereafter, distilled water containing 10% by weight of DL-3,4-dimethoxy-.alpha.-methylphenyl alanine amide and having a pH of 7.5 was passed through the column at a temperature of 30.degree. C. from the top of the column at a space velocity (SV) of 0.2/hr.
In this continuous reaction, the yield of L-3,4-dimethoxy-.alpha.-methylphenyl alanine was maintained at 85% or more until the reaction time became 200 hours.
EXAMPLES 23 THROUGH 25
One hundred mg of the freeze dried cells of Pseudomonas iodinum (IFO-3558) prepared in the same manner as described in Example 18 were suspended in 50 ml of 0.1 M phosphate buffer solution having a pH of 7.5. Various DL-3,4-dihydroxy-.alpha.-methylphenyl alanine amides were added to the resultant suspension and the incubation was carried out at a temperature of 30.degree. C. for 20 hours. After removing the cells, the yields of the resultant L-3,4-dihydroxy-.alpha.-methylphenyl alanines were determined by means of a high speed liquid chromatograph.
The unreacted D-3,4-dihydroxy-.alpha.-methylphenyl alanine amides were recovered from the reaction mixtures according to the same method as described in Example 16. The L-3,4-dihydroxy-.alpha.-methylphenyl alanines thus obtained were isolated.
The results thus obtained are shown in Table 4 below.
TABLE 4__________________________________________________________________________Example ProductNo. Substrate Chemical name Yield % Specific optical rotation__________________________________________________________________________23 DL-3,4-dihydroxy- L-3,4-dihydroxy- 83 [.alpha.].sub.D -4.5.degree. .alpha.-methyl- .alpha.-methylphenyl (c = 2, 0.1 N HCl) phenyl alanine alanine amide24 DL-4-hydroxy- L-4-hydroxy-3- 92 [.alpha.].sub.D +159.degree. 3-methoxy- methoxy-.alpha.- (c = 0.5, 0.25 M CuSO.sub.4) .alpha.-methyl- methylphenyl phenyl alanine alanine amide25 DL-3,4-methylene- L-3,4-methylene- 94 [.alpha.].sub.D +22.0.degree. dioxy-.alpha.-methyl- dioxy-.alpha.-methyl- (c = 1, 0.1 N HCl) phenyl alanine phenyl alanine amide__________________________________________________________________________

Number	Name	Date	Kind
4260684	Schutt	Apr 1981
4366250	Jallageas et al.	Dec 1982

Process for preparing L-.alpha.-methylphenyl alanines

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Entry
Derwent Abstract 77260A/43 of Japanese Patent 53-107,481 (9/19/78).
Methods in Enzymology vol. XVII B pp. 652-656 (1971).
Chemical Abstracts vol. 62: 15998e (1965).