Biocatalytic preparation of a chiral synthon for a vasopeptidase inhibitor: enzymatic conversion of N2-[N-Phenylmethoxy)carbonyl] L-homocysteinyl]- L-lysine (1- > 1′)-disulfide to [4S-(4I,7I,10aJ)] 1-octahydro-5-oxo-4-[phenylmethoxy)carbonyl]amino]-7H-pyrido-[2,1-b] [1,3]thiazepine-7-carboxylic acid methyl ester by a novel L-lysine ϵ-aminotransferase

Author:

Patel Ramesh N,Banerjee Amit,Nanduri Venkata B,Goldberg Steven L,Johnston Robert M,Hanson Ronald L,McNamee Clyde G,Brzozowski David B,Tully Thomas P,Ko Raphael Y,LaPorte Thomas L,Cazzulino Dana L,Swaminathan Shankar,Chen Chien-Kuang,Parker Larry W,Venit John J

Publisher

Elsevier BV

Subject

Applied Microbiology and Biotechnology,Biochemistry,Biotechnology,Bioengineering

Reference32 articles.

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3. The biocatalytic approach to the preparation of enantiomerically pure chiral building blocks;Santaneillo;Chem Rev,1992

4. Enzymes in the synthesis of chiral drugs;Margolin;Enzym Microbiol Technol,1993

5. “Enzymes in synthetic organic chemistry” tetrahedron organic chemistry series, Vol. 12;Wong,1994

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