Issue 10, 1995
From the journal:

Journal of the Chemical Society, Perkin Transactions 1

Biocatalytic preparation of chiral alcohols by enantioselective reduction with immobilized cells of carrot

Yoshihiko Akakabe,   Mirai Takahashi,   Makoto Kamezawa,   Keiichi Kikuchi,   Hojun Tachibana,   Takehiko Ohtani  and  Yoshinobu Naoshima  

Abstract

The ability of immobilized cells of Daucus carota to reduce enantioselectively organic foreign substrates has been examined. The immobilized plant cells reduced, with excellent enantioselectivity, prochiral ketone substrates such as keto esters, aromatic ketones and heterocyclic aromatic ketones, leading to the corresponding chiral secondary alcohols with an enantiomeric purity of 52–99% ee in a chemical yield of 30–63%.

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Article information

DOI
https://doi.org/10.1039/P19950001295
Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 1295-1298

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Biocatalytic preparation of chiral alcohols by enantioselective reduction with immobilized cells of carrot

Y. Akakabe, M. Takahashi, M. Kamezawa, K. Kikuchi, H. Tachibana, T. Ohtani and Y. Naoshima, J. Chem. Soc., Perkin Trans. 1, 1995, 1295 DOI: 10.1039/P19950001295

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