
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.
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Doi:10.1016/S0040-4020(01)88649-X
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