Highly Regioselective Ring Opening of 2,3-Epoxy Alcohol Methanesulfonates

DOI: 10.1246/cl.1991.1787

Source and publish data:

Chemistry Letters p. 1787 - 1790 (1991)

Update date:2022-08-05

Topics:

Authors:

Gao, Lian-xun

Saitoh, Hitoshi

Feng, Fei

Murai, Akio

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Article abstract of DOI:10.1246/cl.1991.1787

Reaction of 2,3-epoxy-1-ol methanesulfonates with diethylaluminum chloride or with the mixture of diethylaluminum chloride and diethylamine hydrobromide in dichloromethane gave rise to regioselectively the corresponding 3-chloro- and 3-bromo-1,2-diol 1-methanesulfonates, respectively, in excellent yields.

Full text of DOI:10.1246/cl.1991.1787

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