4.5 Review

An Overview of Recent Advances in Hantzsch's Multicomponent Synthesis of 1,4-Dihydropyridines: A Class of Prominent Calcium Channel Blockers

期刊

CURRENT ORGANIC CHEMISTRY
卷 27, 期 2, 页码 119-129

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BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/1385272827666230403112419

关键词

Calcium channel blockers; multicomponent reactions; dihydropyridine; hypertension; one-pot synthesis; hantzsch synthesis

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1,4-Dihydropyridine is an important class of nitrogen-containing heterocyclic compounds with significant therapeutic effects in pharmaceutical chemistry. Multicomponent reactions have been discovered as valuable tools for the synthesis of 1,4-dihydropyridine. The efficient synthesis of 1,4-dihydropyridine via multicomponent reactions provides structural diversity crucial for the discovery of new compounds and therapeutics. This review focuses on the recent developments in the multicomponent synthesis of 1,4-dihydropyridines and their fused analogs as potent antihypertensive drugs, offering valuable insights for researchers in heterocyclic chemistry, medicinal chemistry, and drug design.
Among all the heterocyclic scaffolds, 1,4-dihydropyridine (1,4-DHPs) is an important class of nitrogen-containing heterocyclic compounds possessing prominent therapeutic effects, which play an essential role in pharmaceutical chemistry. Multicomponent reactions (MCRs) have proven to be an invaluable tool for swiftly synthesizing large and structurally diverse molecules from simple starting materials. The chemists have discovered a large number of new MCRs for the synthesis of 1,4-dihydropyridine. The synthesis of 1,4-Dihydropyridine via multicomponent reaction is an efficient procedure in terms of delivering adequate structural diversity, which is essential for the process of discovering new 1,4-DHPs compounds and their therapeutics.1,4-dihydropyridines are well-known L-type calcium channel blockers. This review aims to study and summarize the recent developments in the multicomponent synthesis of 1,4-dihydropyridines and their fused analogs that act as potent antihypertensive drugs. The findings of this study will prove to be an invaluable resource for researchers in the areas of heterocyclic chemistry, medicinal chemistry, and drug design.

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