NbCl5-mediated amidation of olefins with nitriles to secondary amides

被引：17

作者：

Yasuda, Kaoru ^{[1
]}

Obora, Yasushi ^{[1
]}

机构：

[1] Kansai Univ, Dept Chem & Mat Engn, Fac Chem Mat & Bioengn, Suita, Osaka 5648680, Japan

来源：

JOURNAL OF ORGANOMETALLIC CHEMISTRY | 2015年 / 775卷

关键词：

Niobium; Amidation; Nitrile; Olefin; CATALYZED INTERMOLECULAR HYDROAMINATION; LIQUID-HYDROGEN FLUORIDE; ONE-POT SYNTHESIS; RITTER REACTION; ORGANIC-REACTIONS; MOLECULAR-IODINE; N-FORMYLATION; AMINES; ALDEHYDES; ALCOHOLS;

D O I：

10.1016/j.jorganchem.2014.10.017

中图分类号：

O61 [无机化学];

学科分类号：

070301 ; 081704 ;

摘要：

NbCl5-mediated amidation of olefins with nitriles was successfully achieved. Various aliphatic, cyclic, and aromatic olefins, and various aliphatic and aromatic nitriles were used in this reaction to give secondary amides in high yields. (C) 2014 Elsevier B.V. All rights reserved.

引用

页码：33 / 38

页数：6

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