Facile access to -acyloxyamides via epoxide rearrangement/three-component domino reaction catalyzed by indium(III) chloride

被引：12

作者：

Lingaswamy, Kadari ^{[1
]}

Krishna, Palakodety Radha ^{[1
]}

Prapurna, Y. Lakshmi ^{[1
]}

机构：

[1] Indian Inst Chem Technol, CSIR, Organ & Biomol Chem Div, Discovery Lab, D-207, Hyderabad 500007, Andhra Pradesh, India

来源：

SYNTHETIC COMMUNICATIONS | 2016年 / 46卷 / 15期

关键词：

Epoxides; highly regioselective; indium(III) chloride; tandem rearrangement; Passerini condensation; TosMIC; PASSERINI REACTION; MULTICOMPONENT REACTIONS; 3-COMPONENT REACTION; ISOCYANIDES; CHEMISTRY; ALDEHYDES; KETONES; ACID; ISONITRILES; DIVERSITY;

D O I：

10.1080/00397911.2016.1201511

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

A simple and efficient Passerini reaction of epoxides involving highly regioselective rearrangement of epoxide to aldehyde/three-component Passerini reaction catalyzed by indium(III) chloride is described. In the present protocol, epoxides served as wonderful substrates to furnish a library of -acyloxyamides under mild reaction conditions in shorter reaction times and in good yields. [GRAPHICS]

引用

页码：1275 / 1282

页数：8

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