Synthesis of biaryls via nickel-catalyzed cross-coupling reaction of arylboronic acids and aryl mesylates

被引：79

作者：

Ueda, M ^{[1
]}

Saitoh, A ^{[1
]}

Oh-tani, S ^{[1
]}

Miyaura, N ^{[1
]}

机构：

[1] Hokkaido Univ, Grad Sch Engn, Div Mol Chem, Sapporo, Hokkaido 0608628, Japan

来源：

TETRAHEDRON | 1998年 / 54卷 / 43期

关键词：

D O I：

10.1016/S0040-4020(98)00809-6

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The cross-coupling reaction of arylboronic acids (1.3 equivs) with aryl methane-sulfonates was carried out in the presence of a nickel(0) catalyst (3 mol%) and K3PO4. nH(2)O (3 equivs). The use of toluene or the solvent and the nickel(0)-dppf catalyst prepared fram NiCl2(dppf) plus dppf with BuLi were recognized to be the most efficient to achieve both high yields and high selectivity. The reaction can be applied to various electron-deficient and -rich aryl methanesulfonates to give high yields. (C) 1998 Elsevier Science Ltd. All rights reserved.

引用

页码：13079 / 13086

页数：8

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