Literature DB >> 12882300

Applying slow-release biocatalysis to the asymmetric reduction of ethyl 4-chloroacetoacetate.

Jer-Yiing Houng1, Jia-Sheng Liau.   

Abstract

Amberlite XAD 2 resin enhanced the asymmetric reduction of ethyl 4-chloroacetoacetate (ECA) to S-4-chloro-3-hydroxybutyric acid ethyl ester as catalyzed by Saccharomyces cerevisiae. The absorbed ECA was released slowly to the solution during the reaction so that the substrate inhibition and the spontaneous chemical hydrolysis of ECA were considerably lessened. With 75 g resin l(-1) and ECA at 74 mM, the reaction yield and the product's optical purity increased from 75% to 84% and from 88% to 93%, respectively.

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Year:  2003        PMID: 12882300     DOI: 10.1023/a:1021761627090

Source DB:  PubMed          Journal:  Biotechnol Lett        ISSN: 0141-5492            Impact factor:   2.461


  2 in total

1.  Asymmetric synthesis of (S)-ethyl-4-chloro-3-hydroxybutanoate using Candida parapsilosis ATCC 7330.

Authors:  Tarjan Kaliaperumal; S Kumar; Sathyanarayana N Gummadi; Anju Chadha
Journal:  J Ind Microbiol Biotechnol       Date:  2009-11-08       Impact factor: 3.346

2.  Self-sufficient asymmetric reduction of β-ketoesters catalysed by a novel and robust thermophilic alcohol dehydrogenase co-immobilised with NADH.

Authors:  Alejandro H Orrego; Daniel Andrés-Sanz; Susana Velasco-Lozano; Mercedes Sanchez-Costa; José Berenguer; José M Guisan; Javier Rocha-Martin; Fernando López-Gallego
Journal:  Catal Sci Technol       Date:  2021-03-12       Impact factor: 6.119

  2 in total

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