Selective esterifications of alcohols and phenols through carbodiimide couplings

R Shelkov, M Nahmany, A Melman

Index: Shelkov, Rimma; Nahmany, Moshe; Melman, Artem Organic and Biomolecular Chemistry, 2004 , vol. 2, # 3 p. 397 - 401

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Citation Number: 47

Abstract

Esterification of carboxylic acids capable of forming ketene intermediates upon treatment with carbodiimides permits the selective acylation of alcohols in the presence of phenols lacking strong electron-withdrawing groups. The selectivity of acylations involving highly acidic phenols could be reversed through the addition of catalytic amount of acid. Esterification of other carboxylic acids was found to proceed through the formation of ...