Volume 27, Issue 16
Preparative Organic Chemistry
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ChemInform Abstract: Iodine in Methanol: A Simple Selective Method for the Cleavage of p- Methoxybenzyl Ethers.

A. R. VAINO

A. R. VAINO

Dep. Chem., Queen′s Univ., Kingston, Ont. K7L 3N6, Can.

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W. A. SZAREK

W. A. SZAREK

Dep. Chem., Queen′s Univ., Kingston, Ont. K7L 3N6, Can.

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First published: April 16, 1996

Abstract

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ChemInform Abstract

Catalytic iodine in methanol is a well-known reagent for the deprotection of acetals. During a preparation in which the removal of an isopropylidene group in the presence of a Pmb ether is required, a simultaneous cleavage of the Pmb ether is discovered. The finding is evaluated to a simple selective method for the deprotection of a variety of Pmb ethers, even in the presence of benzyl ethers.

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