VCl3 Catalysed Efficient Synthesis of β-enamine Esters and Ketones from β-keto Esters
Author:
Affiliation:
1. Department of Chemistry, National Institute of Technology, Warangal, India
Abstract
Publisher
SAGE Publications
Subject
General Chemistry
Link
http://journals.sagepub.com/doi/pdf/10.3184/030823405774663237
Reference32 articles.
1. Enaminones
2. Long-acting dihydropyridine calcium antagonists. 1. 2-Alkoxymethyl derivatives incorporating basic substituents
3. Long-acting dihydropyridine calcium antagonists. 5. Synthesis and structure-activity relationships for a series of 2-[[(N-substituted-heterocyclyl)ethoxy]methyl]-1,4-dihydropyridine calcium antagonists
4. Studies on novel and chiral 1,4-dihydropyridines. V. Hantzsch-type 1,4-dihydropyridines having a chiral sulfinyl group: Syntheses, structures, and biological activity as a calcium channel antagonist
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1. Stereoselective Chlorination and Bromination of Enamides and Enamines via an Electrostatic Attraction Effect Using (1,1-Diacetoxyiodo)benzene and a Halide Source;The Journal of Organic Chemistry;2015-10-07
2. An efficient and modified biginelli one-pot synthesis of new isoxazole substitted 3,4-dihydropyrimidin-2(1H)-ones and thiones catalyzed by VCl3;Journal of Heterocyclic Chemistry;2007-03
3. VCl3-Catalyzed Efficient Synthesis of β-Enamine Esters and Ketones from β-Keto Esters.;ChemInform;2006-01-10
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