Amine-Catalyzed Addition of Azide Ion to α,β-Unsaturated Carbonyl Compounds
- 9 September 1999
- journal article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 1 (7), 1107-1109
- https://doi.org/10.1021/ol9909076
Abstract
[formula: see text] A new protocol for the beta-azidation of alpha,beta-unsaturated carbonyl compounds is described. The method employs tertiary amines as catalysts for azide addition. The azide source is a 1:1 mixture of TMSN3 and AcOH. Tertiary amines, either in solution or bound to a solid support, are efficient catalysts for the reaction.Keywords
This publication has 1 reference indexed in Scilit:
- Efficient Conjugate Addition of Hydrogen Azide to EnoatesTetrahedron Letters, 1997