Synthesis and Aromatization of Hantzsch 1,4-Dihydropyridines under Microwave Irradiation. An Overview
Domestic microwave ovens as well as laboratory reactors have been successfully employed to prepare dialkyl 1,4-dihydropyridine-3,5-dicarboxylates and to induce the synthesis of the corresponding aromatic derivatives. In that latter particular case, unexpected results have been reported.
Main Authors: | Annie Mayence, Jean Jacques Vanden Eynde |
---|---|
Format: | Article |
Language: | English |
Published: |
MDPI AG
2003-04-01
|
Series: | Molecules |
Subjects: | |
Online Access: | http://www.mdpi.com/1420-3049/8/4/381/ |
Similar Items
-
Oxidation of Hantzsch 1,4- Dihydropyridines to Pyridines with Thallium Triacetate
by: Mohammad Mahmoodi Hashemi, et al.
Published: (2003-12-01) -
Hydrogen Transfer from Hantzsch 1,4-Dihydropyridines to Carbon-Carbon Double Bonds under Microwave Irradiation
by: Jean Jacques Vanden Eynde, et al.
Published: (2002-07-01) -
Vitamin C-Catalyzed Hantzsch reaction under microwave condition: A greener access to 1,4-Dihydropyridines
by: Devalina Ray, et al.
Published: (2022-01-01) -
An efficient Hantzsch synthesis of 1,4-dihydropyridines using p-toluenesulfonic acid under solvent-free condition
by: Masoud Nasr-Esfahani, et al.
Published: (2014-03-01) -
An Efficient Method for The Synthesis of Dihydropyridine by Hantzsch Reaction with Fe/SiO2 Nano Heterogeneous Catalysts
by: Ateeq Rahman, et al.
Published: (2020-12-01)