Biotechnology Letters 2003-07-01

Enhanced enzymatic synthesis of a semi-synthetic cephalosprin, cefaclor, with in situ product removal.

Liu Yang, Dong-Zhi Wei

Index: Biotechnol. Lett. 25(14) , 1195-8, (2003)

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Abstract

In the enzymatic synthesis of cefaclor, 3-chloro-7-d-(2-phenylglycinamide)-3-cephem-4-carboxylic acid, from phenylglycine methyl ester and 7-aminodesacetoxymethyl-3-chlorocephalosporanic acid, the in situ product could influence both the overall conversion and hydrolysis of the ester. Optimization of the parameters, such as pH 6.2, 5 degrees C and substrate molar ratio of 2:1, made in situ product removal improve the overall conversion from 64% to 85% (mol/mol).

Related Compounds

  • H-D-Phg-OMe．HC...
  • 7-Aminodeacetoxyce...

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