Article ID Journal Published Year Pages File Type
5279006 Tetrahedron Letters 2009 4 Pages PDF
Abstract

The nucleophilic addition of amines to Baylis-Hillman acetates has been efficiently carried out in water at room temperature in the absence of any base, acid, or metal catalyst to produce α-dehydro-β-amino esters and nitriles. This procedure addresses a variety of aliphatic open-chain and cyclic amines and anilines. All the reactions are highly regio- and stereoselective, fast and high yielding.

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Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
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