Issue 10, 1990

An efficient method for the copper(II)-promoted stereoselective iodofunctionalization of alkenes

Abstract

A mixture of iodine and CuO·HBF4 reacts stereoselectively with alkenes in the presence of a wide variety of nucleophiles (water, MeOH, HCO2H, AcOH, EtCO2H, NaNO2, KSCN, NaSO2Ar, LiCl, LiBr, Nal, Et3SiH, and MeOPh) to give the corresponding 2-functionalized iodo compounds. A regio-chemistry study is also reported.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2807-2809

An efficient method for the copper(II)-promoted stereoselective iodofunctionalization of alkenes

J. Barluenga, M. A. Rodríguez and P. J. Campos, J. Chem. Soc., Perkin Trans. 1, 1990, 2807 DOI: 10.1039/P19900002807

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