A MODIFICATION TO THE HANTZSCH METHOD TO OBTAIN PYRIDINES IN A ONE POT REACTION: USE OF A BENTONITIC CLAY IN A DRY MEDIUM
Author:
Publisher
Walter de Gruyter GmbH
Subject
Organic Chemistry
Link
https://www.degruyter.com/document/doi/10.1515/HC.1996.2.4.359/pdf
Reference6 articles.
1. Ueber die Synthese pyridinartiger Verbindungen aus Acetessigäther und Aldehydammoniak
2. MnO2/Bentonite: A New Reactive for the Oxidation of Hantzsch'S Dihydropyridines Using Microwave Irradiation, in the Absence of Solvent (I)
3. Unusual Oxidative Dealkylation of Certain 4-Alkyl-1,4-Dihydropyridines With MnO2/Bentonite Using Microwave Irradiation, in the Absence of Solvent (II)
4. Oxydation d'esters de Hantzsch, par le nouveau système HNO3/bentonite, et irradiation aux micro-ondes
5. The Hantzsch Reaction. I. Oxidative Dealkylation of Certain Dihydropyridines
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1. A simple, efficient, one-pot three-component domino synthesis of Hantzsch pyridines under solvent-free condition;Journal of Heterocyclic Chemistry;2009-09
2. A revisit to the Hantzsch reaction: Unexpected products beyond 1,4-dihydropyridines;Green Chemistry;2009
3. Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview;Molecules;2003-04-30
4. Microwave assisted organic synthesis—a review;Tetrahedron;2001-11
5. Unusual nucleophilic versus electrophilic aromatic substitution on nitroanilines;Journal of Molecular Catalysis A: Chemical;2000-12
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