RAS PresidiumДоклады Российской академии наук. Химия, науки о материалах Doklady Chemistry

  • ISSN (Print) 2686-9535
  • ISSN (Online) 3034-5111

ENANTIOSELECTIVE BIOREDUCTION OF PROCHIRAL AROMATIC AND HETEROAROMATIC KETONES CATALYZED BY AND CELLS

PII
S3034511125050032-1
DOI
10.7868/S3034511125050032
Publication type
Article
Status
Published
Authors
Volume/ Edition
Volume 524 / Issue number 1
Pages
18-24
Abstract
A convenient method for the synthesis of optically pure secondary heteroaromatic -alcohols by asymmetric reduction of prochiral heteroaromatic ketones catalyzed by or cells has been developed. Using -bromophenylethanone as an example, we studied the effect of the substituent position in the aromatic ring of acetophenone on the efficiency and stereoselectivity of carbonyl group bioreduction by and catalysts.
Keywords
биокатализатор биотрансформация оптически чистые гетероароматические спирты S-спирты энантиоселективное биовосстановление
Date of publication
01.01.2025
Year of publication
2025
Number of purchasers
0
Views
43

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