Reactions of 1,2-& 1,4-dihydropyridines

被引：15

作者：

Singh, Sunil K. ^{[1
]}

Sharma, Vivek K. ^{[2
]}

机构：

[1] Univ Delhi, Kirori Mal Coll, Dept Chem, Delhi 110007, India

[2] Univ Delhi, Dept Chem, Delhi 110007, India

来源：

CURRENT ORGANIC CHEMISTRY | 2014年 / 18卷 / 09期

关键词：

1,2-1,4-Dihydropyridines; aromatization; cycloaddition; diamination; oxidation; oxyselenation; photodimerisation; rearrangement; DIELS-ALDER REACTION; ORGANOCATALYTIC TRANSFER HYDROGENATION; ASYMMETRIC TRANSFER HYDROGENATION; ROOM-TEMPERATURE AROMATIZATION; CONVENIENT OXIDIZING-AGENT; HIGH-YIELD OXIDATION; ONE-POT SYNTHESIS; HANTZSCH 1,4-DIHYDROPYRIDINES; EFFICIENT OXIDATION; ORGANIC AZIDES;

D O I：

10.2174/1385272819666140201003050

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

This review provides a comprehensive compilation of available literature concerning the reactions of 1,2- & 1,4-dihydropyridines, which have opened new frontiers in the area of synthetic and medicinal chemistry. These reactions mainly include cycloaddition, 1,3-Dipolar cycloaddition, alkoxy halogenation, diamination, hydroxyamination, oxidation, hydroxylation, photooxygenation reaction, nucleophilic addition, cyclization, electrophilic substitution, multicomponent reactions (MCRs) and rearrangement reactions. 1,4-Dihydropyridine has also been used in hydrogen transfer reactions as a synthetic NADH model for the reduction of several important molecules in excellent yields.

引用

页码：1159 / 1207

页数：49

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