share
Acta Chimica Sinica ›› 1982, Vol. 40 ›› Issue (7): 648-656. Previous Articles Next Articles
周维善1, 黄大中1, 董纪昌2, 王锺麒1
投稿日期:
发布日期:
通讯作者:
ZHOU WEI-SHAN1, HUANG DA-ZHONG1, DONG QI-CHANG2, WANG ZHONG-QI1
Received:
Published:
Share
The optically active intermediates 6(R=CH3, C2H5) for total syntheses of steroidal oral contraceptives was prepared from symmetrical diketones 2 (R=CH3,C2H5 by microbial asymmetrical reduction.Thus 2a and 2b were cultivated with Saccharomyces cerevisirie (2.346) to give optically active products 6a and 6b in 73% and 71% yields respectively.
ZHOU WEI-SHAN, HUANG DA-ZHONG, DONG QI-CHANG, WANG ZHONG-QI. ASYMMETRICAL REDUCTION OF THE SYMMETRICAL DIKETONES BY MICRO-ORGANISM——Ⅰ. ASYMMETRICAL REDUCTION OF 2-ALKYL-2-(3’-OXOBUTYL)-1, 3-CYCLOPENTANEDIONE[J]. Acta Chimica Sinica, 1982, 40(7): 648-656.
Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks