Bulletin of the Chemical Society of Japan p. 3532 - 3533 (1993)
Update date:2022-08-03
Topics:
Tada, Masahiro
Chiba, Kazuhiro
Izumiya, Koji
Tamura, Mihoko
Reduction of tosylhydrazones by hydride reagents in wet alcohol gave predominantly alcohols whose stereochemistries are opposite to those of the major reduction products of the corresponding ketones with sodium borohydride.
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Doi:10.1016/0040-4020(78)89018-8
(1978)Doi:10.1246/bcsj.52.524
(1979)Doi:10.1002/jhet.5570150813
(1978)Doi:10.1002/ardp.19793120213
(1979)Doi:10.1016/0040-4020(78)89019-X
(1978)Doi:10.1007/s00706-014-1223-8
(2014)
