A Mild, Efficient, and Green Procedure for Michael Addition of Active Methylene Compounds to Chalcones Under Microwave Irradiation
Authors:
- 1 January 2005
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 35 (2) , 325-332
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Influence of ionic liquids on the phase transfer-catalysed enantioselective Michael reactionTetrahedron Letters, 2003
- Michael Addition Catalyzed by Potassium Hydroxide Under UltrasoundSynthetic Communications, 2003
- Enantioselective Michael reaction of malonates and chalcones by phase-transfer catalysis using chiral quaternary ammonium saltTetrahedron Letters, 2001
- Solvent-free Reactions1999
- A Novel Method for Michael Addition and Epoxidation of Chalcones in a Water Suspension Medium: A Completely Organic Solvent-Free Synthetic ProcedureHETEROCYCLES, 1998
- Highly diastereoselective Michael addition to 2-arylidene-1-tetralones complexed with Cr(CO)3Tetrahedron Letters, 1991
- Easy Michael Addition by Solid-Liquid Phase Transfer Catalysis Abnormal Reaction of N-AcetylaminomalonateSynthetic Communications, 1988
- An Improved Procedure for the Michael Reaction of ChalconesSynthesis, 1982
- The reactions of phenolic reagents with α-bromo Michael acceptors in the K2CO3-acetone system. A stereospecific AdSNE process.Tetrahedron Letters, 1981
- 197. Chalcones and related compounds. Part II. Addition of thiols and esters to the chalcone systemJournal of the Chemical Society (Resumed), 1957