
Journal of Organic Chemistry p. 792 - 798 (1982)
Update date:2022-09-26
Topics:
Kergomard, A.
Renard, M. F.
Veschambre, H.
Microbiological reduction of α,β-unsaturated ketones was studied.Variously substituted cyclopentenones, cyclohexenones, and methylalkenones were reduced by Beauveria sulfurescens under low-aeration conditions.The reaction takes place only with a small substituent in the α-position and hydrogen in the β-position.The saturated ketone is always obtained, sometimes accompanied by saturated alcohol.Yields and optical purities of the products are excellent.
View MoreContact:+86-731-84427351
Address:154 JIANXIANG SOUTH ROAD
Buffett (China) Holding Co.,Ltd
Contact:4006570891
Address:
Contact:+86-22-26358246
Address:601-4-20, Fujiayuan, Tiantai Road, Hebei District, Tianjin, China
shanghai tuomiao chemicial co.,ltd.
website:https://www.tuomiaochem.com/
Contact:021 - 59853336
Address:shanghai
website:http://www.fwdchem.com
Contact:86-21-54450828
Address:Room 802,Lotus Tower ,159 Tianzhou Road,Xuhui District,Shanghai
Doi:10.1016/S0040-4020(01)88649-X
(1983)Doi:10.1055/s-2004-831163
(2004)Doi:10.1248/cpb.29.2691
(1981)Doi:10.1039/P19810002764
(1981)Doi:10.1246/bcsj.54.3088
(1981)Doi:10.1039/c39810000992
(1981)