Method for preparing optically active homophenylalanine and este

Chemistry: molecular biology and microbiology – Process of utilizing an enzyme or micro-organism to destroy... – Resolution of optical isomers or purification of organic...

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C12P 4100

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055523170

ABSTRACT:
A process for the preparation of optically active D-homophenylalanine and its esters, comprising the steps of: (a) preparing a reaction mixture containing an DL-homophenylalanine ester and a lipase or an acylase in an aqueous solution; (b) reacting the reaction mixture at temperatures between 4.degree. and 60.degree. C.; and (c) using an organic extractant to separate the reaction mixture into an upper layer, which contains an optically active D-homophenylalanine ester, and a lower layer, which contains L-homophenylalanine. The optically active D-homophenylalanine ester can be chemically hydrolyzed to obtain an optically active D-homophenylalanine. The lipase can be selected from the group consisting of Aspergillus niger lipase, Pseudomonas sp. lipase, Rhizopus sp. lipase, porvine pancreas lipase, wheat germ lipase, and hog pancreas lipase, and the acylase can be porcine kidney acylase. Many of these lipases or acylase provide an enantiometric excess of more than 95%. The optically active D-homophenylalanine is an important starting material for many anti-hypertensive drugs, such as Enalapril, Lisinopril, and Quinapril.

REFERENCES:
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