Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5219524 | Tetrahedron | 2011 | 9 Pages |
Abstract
The optimization, substrate scope, and mechanism of esterification and amidation of carboxylic acids mediated by imidazole-based reagents are discussed. The innate reactivity of carbonylimidazole reagents with a range of nucleophiles is also explored. New reagents developed for the synthesis of α,β-unsaturated esters are described, as are reagents for the preparation of tertiary amides directly from carboxylic acids.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Stephen T. Heller, Richmond Sarpong,