
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.
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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)