Journal of the Chemical Society. Perkin transactions I p. 1041 - 1045 (1981)
Update date:2022-08-02
Topics:
Crabb, Trevor A.
Saul, John A.
Williams, Roger O.
The microbiological transformation of 5α-androstan-17-one, and the 3β-acetoxy- and 3α-hydroxy-derivatives, by Cunninghamella elegans is dominated by 1β,7-dihydroxylation or 7-monohydroxylation. 3α-Acetoxy-5α-androstan-17-one undergoes predominant 6β,11β-dihydroxylation. 17a-Aza-D-homo-5α-androstan-17-one and the 3α-acetoxy-derivative undergo predominant monohydroxylation at 6β or 7α, in contrast to the 3β-acetoxy-derivative which, although undergoing similar monohydroxylation, gives good yield of 9α-monohydroxylated products.
View MoreWuhan Jadechem International Trade Co.,Ltd.
website:http://www.jadechem-intl.com
Contact:+86-27-83527060
Address:Room 502,Building C11,Software new city No.8,Huacheng Avenue,East Lake High-tech development zone,Wuhan,Hubei,China
Shanghai PotentPharm Science and Technology Co.,Ltd
Contact:86-021-51969655
Address:Unit B, Building 18, No.300, Chuantu Rd,Pudong District, Shanghai 201202, China
Contact:+86-29-88710656
Address:South Tai bai Road, High Tech Development Zone, Xi'an China
shijiazhuang baisheng chem co.; ltd
Contact:86-0311-80790826
Address:shijiazhuang hebei
Contact:0086-21-80264647
Address:RM 202, NO 1602 West Zhongshan Rd, Shanghai, China
Doi:10.1039/b203710f
(2002)Doi:10.1021/jacs.9b13753
(2020)Doi:10.1007/s11164-014-1782-7
(2015)Doi:10.1016/S0022-328X(01)01459-0
(2002)Doi:10.1002/jhet.5570390123
(2002)Doi:10.1021/jacs.5b10270
(2015)
