Synthetic Communications p. 1949 - 1952 (1992)
Update date:2022-08-23
Topics:
Ciattini
Morera
Ortar
The title compound has been prepared in 47% overall yield from androst-4-ene-3,17-dione (1) by a two-step sequence comprising hydroxylation of 1 with OsO4/H2O2, followed by dehydration of the resultant diols 3 in alkaline medium.
View MoreContact:+86-20-32051076
Address:1105,Building A, International Business Incubator,Science City
Shanghai Chemchallenger Biotech Co., Ltd.
Contact:0086-21-68110815
Address:Room 2056, Building 1, No. 1065, Jiaxin Road Shanghai China (Mainland) 201800
Hangzhou Mole's Science & Technology Co.,Ltd.
Contact:+86-571-56880228
Address:15F Guodu development Building, NO.182 Zhaohui Road
Contact:+86-10-83993285
Address:Rm.1708, Haobai Tower, Building 6, No.50, North Road, West Third Ring, Haidian District, Beijing, China
XI'AN CHUKANG BIOTECHNOLOGY CO.,LTD
Contact:29-63685658 63685359
Address:Room 3-1202,Building 1,Oriental oasis,East of Xianning Road,Xi'an,Shaanxi 710043 P.R.China
Doi:10.1021/om4008218
(2013)Doi:10.1016/j.cplett.2011.02.046
(2011)Doi:10.1080/00397919608003803
(1996)Doi:10.1021/ja01590a031
(1956)Doi:10.1021/acs.joc.8b02220
(2018)Doi:10.1039/c9cc04533c
(2019)