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Synthetic Communications
An International Journal for Rapid Communication of Synthetic Organic Chemistry
Volume 20, 1990 - Issue 5
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Original Articles

A Highly Regioselective Iodoenoletherification of α-Allyl-β-ketoesters. A Convenient Route to 2-Alkyl-5-iodomethyl-3-methoxycarbonyl-4, 5-Dihydrofurans

Javed Iqbal Department of Chemistry, Indian Institute of Technology, Kanpur, 208 016, India
&
Anu Pandey Department of Chemistry, Indian Institute of Technology, Kanpur, 208 016, India
Pages 665-670 | Received 31 Oct 1989, Published online: 24 Oct 2006
 
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Abstract

A variety of α-allyl-β-ketoesters (1) containing two different double bonds, undergo highly regioselective iodoenoletherification to give the titled compound (2) in excellent yields.

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