Aryl Diazonium versus Iodonium Salts: Preparation, Applications and Mechanisms for the Suzuki-Miyaura Cross-Coupling Reaction

被引：129

作者：

Bonin, Helene ^{[1
]}

Fouquet, Eric ^{[2
]}

Felpin, Francois-Xavier ^{[2
]}

机构：

[1] Univ Lille, CNRS, USTL ENSCL, Unite Catalyse & Chim Solide,UMR 8181, F-59652 Villeneuve Dascq, France

[2] Univ Bordeaux, Inst Mol Sci, CNRS, UMR 5255, F-33405 Talence, France

来源：

ADVANCED SYNTHESIS & CATALYSIS | 2011年 / 353卷 / 17期

关键词：

aryl diazonium salts; C-C coupling; cross-coupling; iodonium salts; palladium; Suzuki-Miyaura reaction; ARENEDIAZONIUM TETRAFLUOROBORATE SALTS; ONE-POT SYNTHESIS; HYPERVALENT IODINE; BORONIC ACIDS; SODIUM TETRAPHENYLBORATE; CATALYST-FREE; PALLADIUM(0)-CATALYZED ARYLATION; STEREOSELECTIVE-SYNTHESIS; DIARYLIODONIUM SALTS; PALLADIUM CATALYSTS;

D O I：

10.1002/adsc.201100531

中图分类号：

O69 [应用化学];

学科分类号：

081704 ;

摘要：

This review gives an overview of the use of unusual diazonium and iodonium salts as electrophiles for the Suzuki-Miyaura reaction. The discussion mainly focuses, with a critical view, on catalytic systems developed with these electrophiles. The review also discusses their general properties and preparation as well as mechanistic aspects. A last and brief comparison of diazonium versus iodonium salts, by highlighting advantages and drawbacks of both, gives the reader an understandable resume.

引用

页码：3063 / 3084

页数：22

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