Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer

Hiroyuki Akita, Hiroko Matsukura, Takeshi Oishi, Atsuo Tanaka, Kenji Sonomoto

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Asymmetric reduction of a-methyl β-keto esters using microbial cells immobilized by the prepolymer method was examined. It was found that by a proper selection of the prepolymer in the stage of immobilization, the chemical and optical yields were both improved appreciably in some cases compared to those obtained by reduction with the native microorganisms.

Original languageEnglish
Pages (from-to)4985-4987
Number of pages3
JournalChemical and Pharmaceutical Bulletin
Volume35
Issue number12
DOIs
Publication statusPublished - Jan 1 1987
Externally publishedYes

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Immobilized Cells
Immobilization
Esters
Microorganisms

All Science Journal Classification (ASJC) codes

  • Chemistry(all)
  • Drug Discovery

Cite this

Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer. / Akita, Hiroyuki; Matsukura, Hiroko; Oishi, Takeshi; Tanaka, Atsuo; Sonomoto, Kenji.

In: Chemical and Pharmaceutical Bulletin, Vol. 35, No. 12, 01.01.1987, p. 4985-4987.

Research output: Contribution to journalArticle

Akita, Hiroyuki ; Matsukura, Hiroko ; Oishi, Takeshi ; Tanaka, Atsuo ; Sonomoto, Kenji. / Asymmetric Reduction of α-Methyl β-Keto Esters by Microbial Cells Immobilized with Prepolymer. In: Chemical and Pharmaceutical Bulletin. 1987 ; Vol. 35, No. 12. pp. 4985-4987.
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