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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