Issue 5, 2014

The synthesis of new calix[n]arene quaternary ammonium salts and investigation of their catalytic affinities for three component Mannich-type reactions in water

Abstract

Two new calix[n]arenes and a non-cyclic analogue substituted with 1-(2-furoyl)piperazine have been synthesized. Moreover, their quaternary ammonium salts have been prepared by treatment with methyl iodide. All of the new quaternary ammonium salts have been employed as catalysts in one-pot Mannich reactions to afford β-aminocarbonyl compounds. The combination of good to excellent yields, the need for a small amount of catalyst and simple work-up, mean that this route can be considered to be green chemistry.

Graphical abstract: The synthesis of new calix[n]arene quaternary ammonium salts and investigation of their catalytic affinities for three component Mannich-type reactions in water

Article information

Article type
Paper
Submitted
25 Jul 2013
Accepted
14 Oct 2013
First published
04 Dec 2013

RSC Adv., 2014,4, 2219-2225

The synthesis of new calix[n]arene quaternary ammonium salts and investigation of their catalytic affinities for three component Mannich-type reactions in water

S. Sayin and M. Yilmaz, RSC Adv., 2014, 4, 2219 DOI: 10.1039/C3RA43881C

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