PALLADIUM-CATALYZED COUPLING OF TETRAORGANOTIN COMPOUNDS WITH ARYL AND BENZYL HALIDES - SYNTHETIC UTILITY AND MECHANISM

被引：495

作者：

MILSTEIN, D ^{[1
]}

STILLE, JK ^{[1
]}

机构：

[1] COLORADO STATE UNIV,DEPT CHEM,FT COLLINS,CO 80523

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1979年 / 101卷 / 17期

关键词：

D O I：

10.1021/ja00511a032

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Palladium complexes catalyze the coupling of tetraorganotin compounds with benzyl and aryl halides, benzylchlorobis(triphenylphosphine)palladium(II) (1) being the catalyst of choice. Various functional groups are tolerated by this reaction and generally high yields of the cross-coupled products are obtained. Oxygen has a considerable accelerating effect on the reaction, whereas triphenylphosphine has little effect. The reaction of substituted bromobenzenes with tetramethyltin catalyzed by 1 is accelerated by electron-withdrawing groups; however, a simple Hammett correlation is not observed. Optically active α-deuteriobenzyl bromide reacts with tetramethyltin to afford optically active α-deuterioethylbenzene with inversion of configuration. Homocoupling is the main reaction observed when lithium or Grignard reagents react with benzyl chloride under the influence of various palladium catalysts. © 1979, American Chemical Society. All rights reserved.

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页码：4992 / 4998

页数：7

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