SYNTHESIS OF HANTZSCH 1,4-DIHYDROPYRIDINES UNDER MICROWAVE IRRADIATION
- 1 January 2002
- journal article
- Published by Taylor & Francis in Synthetic Communications
- Vol. 32 (4) , 659-663
- https://doi.org/10.1081/scc-120002415
Abstract
Biologically active substituted 1,4-dihydropyridines have been synthesized in excellent yields by the reaction of aldehydes, ethyl or methyl acetoacetic ester and ammonium acetate under microwave irradiation (MWI) within 0.75–3 min.This publication has 15 references indexed in Scilit:
- Microwave Assisted One Pot Synthesis of Substituted 3-Formyl Benzoates Using Vilsmeier ReagentSynthetic Communications, 2000
- Identification of a Dihydropyridine as a Potent α1a Adrenoceptor-Selective Antagonist That Inhibits Phenylephrine-Induced Contraction of the Human ProstateJournal of Medicinal Chemistry, 1998
- Convenient Synthesis of α,α1-bis(Substituted Furfurylidene) Cycloalkanones and Chalcones Under Microwave Irradiation.Synthetic Communications, 1997
- Minute Synthesis of Electrophilic Alkenes under Microwave IrradiationSynthesis, 1994
- Synthesis of 1,4-Dihydropyridines under Microwave IrradiationSynlett, 1992
- Dry Reaction Under Microwave: Condensation of Sulfones with Aldehydes on KF-AluminaSynthetic Communications, 1991
- Highly Accelerated Reactions in a Microwave Ovem: Synthesis of HeterocyclesHETEROCYCLES, 1990
- New developments in calcium ion channel antagonistsJournal of Medicinal Chemistry, 1983
- A Study of the Primary Acid Reaction on Model Compounds of Reduced Diphosphopyridine Nucleotide1,2Journal of the American Chemical Society, 1958
- Hantzsch's Pyridine SynthesisJournal of the American Chemical Society, 1949