Enviar artigo por via de e-mail ENANTIOSELECTIVE BIOREDUCTION OF PROCHIRAL AROMATIC AND HETEROAROMATIC KETONES CATALYZED BY DAUCUS CAROTA AND PETROSELINUM CRISPUM CELLS
- Autores: Chanysheva A.R1, Privalov N.V1, Peperva V.V1, Zorin V.V1
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Afiliações:
- Ufa State Petroleum Technological University
- Edição: Volume 524, Nº 1 (2025)
- Páginas: 18–24
- Seção: CHEMISTRY
- URL: https://ogarev-online.ru/2686-9535/article/view/375934
- DOI: https://doi.org/10.7868/S3034511125050032
- ID: 375934
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Resumo
A convenient method for the synthesis of optically pure secondary heteroaromatic S-alcohols by asymmetric reduction of prochiral heteroaromatic ketones catalyzed by D. carota or P. crispum cells has been developed. Using o-, m-, p-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 D. carota and P. crispum catalysts.
Sobre autores
A. Chanysheva
Ufa State Petroleum Technological University
Email: aliyach@mail.ru
450062 Ufa, Russian Federation
N. Privalov
Ufa State Petroleum Technological University450062 Ufa, Russian Federation
V. Peperva
Ufa State Petroleum Technological University450062 Ufa, Russian Federation
V. Zorin
Ufa State Petroleum Technological University450062 Ufa, Russian Federation
Bibliografia
- Kochetkov K.A., Bystrova N.A., Pavlov P.A., Oshehepkov M.S., Oshehepkov A.S. // J. Ind. Eng. Chem. 2022. V. 115. P. 62–91. https://doi.org/10.1016/j.jiec.2022.08.025
- Кочетков К.А., Ощепков М.С. Стерехимия биологически активных веществ. Учебник для Вузов. М.: Лаборатория Знаний, 2025. 189 с.
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