Unexpected enantioselectivity and activity of penicillin acylase in the resolution of methyl 2,2-dimethyl-1,3-dioxane-4-carboxylate-Reference-Cited by-同舟云学术

Unexpected enantioselectivity and activity of penicillin acylase in the resolution of methyl 2,2-dimethyl-1,3-dioxane-4-carboxylate

Published:2003-04 Issue:1-2 Volume:22 Page:55-59
ISSN:1381-1177
Container-title:Journal of Molecular Catalysis B: Enzymatic
language:en
Short-container-title:Journal of Molecular Catalysis B: Enzymatic

Author:

Yao Yiming,Lalonde Jim J

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,Biochemistry,Bioengineering,Catalysis

Reference22 articles.

1. K. Matsumoto, in: A. Tanaka, T. Tosa, T. Knobayashi (Ed.), Industrial Application of Immobilized Biocatalysts, Marcel Dekker, New York, 1993, p. 67.

2. Enzymatic synthesis of β-lactam antibiotics using penicillin-G acylase in frozen media

3. Penicillin acylase-catalyzed peptide synthesis: a chemo-enzymatic route to stereoisomers of 3,6-diphenylpiperazine-2,5-dione

4. Deacylation of acylamino compounds other than penicillins by the cell-bound penicillin acylase of Escherichia coli

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