Melamine trisulfonic acid as an efficient catalyst for the synthesis of 2,6-dimethyl-4-substituted-1,4-dihydropyridine-3,5-diethyl/dimethylcarboxylate derivatives via Hantzsch reaction in solvent free condition-Reference-Cited by-同舟云学术

Melamine trisulfonic acid as an efficient catalyst for the synthesis of 2,6-dimethyl-4-substituted-1,4-dihydropyridine-3,5-diethyl/dimethylcarboxylate derivatives via Hantzsch reaction in solvent free condition

Published:2013-07 Issue:3 Volume:25 Page:191-199
ISSN:1018-3647
Container-title:Journal of King Saud University - Science
language:en
Short-container-title:Journal of King Saud University - Science

Author:

Mansoor S. Sheik,Aswin K.,Logaiya K.,Sudhan S.P.N.

Funder

University Grants Commission, Government of India, New Delhi

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference46 articles.

1. Iron (III) trifluoroacetate and trifluoromethane sulfonate: recyclable Lewis acid catalysts for one-pot synthesis of 3,4-dihydropyrimidinones or their sulfur analogues and 1,4-dihydropyridines via solvent-free Biginelli and Hantzsch condensation protocols;Adibi;Catal. Commun.,2007

2. Melamine trisulfonic acid catalyzed regioselevtive nitration of aromatic compounds with sodium nitrate under solvent-free conditions;Albadi;Arab. J. Chem.,2012

3. One-step, synthesis of Hantzsch esters and polyhydroquinoline derivatives using new organocatalyst;Baghbanian;Chin. Chem. Lett.,2010

4. A microwave-assisted bismuth nitrate-catalyzed unique route toward 1,4-dihydropyridines;Bandyopadhyay;Molecules,2012

5. An efficient one-step synthesis of 1,4-dihydropyridines via a triphenylphosphine-catalyzed three-component Hantzsch reaction under mild conditions;Debache;Tetrahedron Lett.,2009

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