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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(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)