Iron(III) trifluoroacetate and trifluoromethanesulfonate: 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-Reference-Cited by-同舟云学术

Iron(III) trifluoroacetate and trifluoromethanesulfonate: 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

Published:2007-12 Issue:12 Volume:8 Page:2119-2124
ISSN:1566-7367
Container-title:Catalysis Communications
language:en
Short-container-title:Catalysis Communications

Author:

Adibi Hadi,Samimi Heshmat Allah,Beygzadeh Mojtaba

Publisher

Elsevier BV

Subject

Process Chemistry and Technology,General Chemistry,Catalysis

Reference40 articles.

1. 100 years of the biginelli dihydropyrimidine synthesis

2. Indium(III) Chloride-Catalyzed One-Pot Synthesis of Dihydropyrimidinones by a Three-Component Coupling of 1,3-Dicarbonyl Compounds, Aldehydes, and Urea: An Improved Procedure for the Biginelli Reaction

3. Dihydropyrimidine calcium channel blockers: 2-heterosubstituted 4-aryl-1,4-dihydro-6-methyl-5-pyrimidinecarboxylic acid esters as potent mimics of dihydropyridines

4. One-pot synthesis of dihydropyrimidinones catalysed by lithium bromide: an improved procedure for the Biginelli reaction

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