Tetrahedron Asymmetry p. 573 - 580 (1992)
Update date:2022-08-05
Topics:
Martin, Victor S.
Ode, Jesus M.
Palazon, Jose M.
Soler, Marcos A.
The regioselective opening with benzoic acid of 2,3-epoxy alcohols obtained from the asymmetric epoxidation of 2,3-allylic alcohols, and deoxygenation of the resulting diol benzoates provides an effective, general and simple method to convert chiral 2,3-epoxy alcohols, into vinyl carbinols without the loss of any optical purity.
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Doi:10.1016/j.tet.2013.01.008
(2013)Doi:10.1016/S0040-4020(01)92271-9
(1992)Doi:10.1021/jo01036a532
(1963)Doi:10.1016/j.tet.2012.12.067
(2013)Doi:10.1021/co3001204
(2013)Doi:10.1016/0223-5234(91)90031-H
(1991)
