Issue 4, 2002

EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

Abstract

An efficient method for the regioselective synthesis of β-iodo ethers and iodohydrines from styrene, indene and dihydronaphthalene in presence of EPZ-10R has been presented wherein only 0.5 equivalent iodine (I2) has been used. Similarly, o-allylphenols are converted to 2-iodomethyl-2,3-dihydrobenzofurans in high yields. This demonstrates a clean green chemical transformation with significant atom economy.

Graphical abstract: EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

Article information

Article type
Paper
Submitted
18 Mar 2002
First published
05 Jun 2002

Green Chem., 2002,4, 325-327

EPZ-10 catalyzed regioselective transformation of alkenes into β-iodo ethers, iodohydrins and 2-iodomethyl-2,3-dihydrobenzofurans

V. A. Mahajan, P. D. Shinde, A. S. Gajare, M. Karthikeyan and R. D. Wakharkar, Green Chem., 2002, 4, 325 DOI: 10.1039/B202725A

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