Abstract
An efficient aza-Michael addition of amines to a series of α,β-unsaturated ketones, carboxylic esters, nitriles and chalcones has been carried out using perchloric acid supported over silica gel (HClO4-SiO2) at room temperature in high yields under solvent-free reaction conditions.
Keywords: Aza-Michael addition, amines, synthetic methods, electron-deficient alkenes, HClO4-SiO2, solvent-free
Letters in Organic Chemistry
Title: Aza-Michael Addition of Amines to Activated Alkenes Catalyzed by Silica Supported Perchloric Acid Under a Solvent-Free Condition
Volume: 4 Issue: 1
Author(s): Chinmoy Mukherjee and Anup Kumar Misra
Affiliation:
Keywords: Aza-Michael addition, amines, synthetic methods, electron-deficient alkenes, HClO4-SiO2, solvent-free
Abstract: An efficient aza-Michael addition of amines to a series of α,β-unsaturated ketones, carboxylic esters, nitriles and chalcones has been carried out using perchloric acid supported over silica gel (HClO4-SiO2) at room temperature in high yields under solvent-free reaction conditions.
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Cite this article as:
Mukherjee Chinmoy and Misra Anup Kumar, Aza-Michael Addition of Amines to Activated Alkenes Catalyzed by Silica Supported Perchloric Acid Under a Solvent-Free Condition, Letters in Organic Chemistry 2007; 4 (1) . https://dx.doi.org/10.2174/157017807780037414
DOI https://dx.doi.org/10.2174/157017807780037414 |
Print ISSN 1570-1786 |
Publisher Name Bentham Science Publisher |
Online ISSN 1875-6255 |
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