Chennat‐Type Synthesis of 1,4‐Dihydropyridine Derivatives in Water: Role of a Hydrogen‐Bonding Network
Author:
Affiliation:
1. Department of Medicinal Chemistry Yokohama University of Pharmacy 601 Matano-cho, Totsuka-ku Yokohama 245-0066 Japan
2. Graduate School of Pharmaceutical Sciences The University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-8654 Japan
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/slct.201904144
Reference21 articles.
1. NAD+/NADH and NADP+/NADPH in Cellular Functions and Cell Death: Regulation and Biological Consequences
2. The biochemistry and molecular biology of the dihydropyridine-sensitive calcium channel
3. Calcium channel antagonists: Clinical uses—Past, present and future
4. Ueber die Synthese pyridinartiger Verbindungen aus Acetessigäther und Aldehydammoniak
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1. Effect of Water in the Trimer‐Cyclisation of Alkynyl Ketone;ChemistrySelect;2024-02-27
2. Recent developments in the Hantzsch synthesis of dihydropyridines;Advances in Heterocyclic Chemistry;2023
3. Selective Synthesis of the Aminobutadiene Intermediate and Mechanistic Analysis of 1,4-Dihydropyridine Formation Reaction in Water;Chemical and Pharmaceutical Bulletin;2022-03-01
4. A review on recent trends in synthesis and applications of 1,4-dihydropyridines;Materials Today: Proceedings;2022
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