Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported N-heterocyclic carbene-palladium complex catalyst

被引：45

作者：

Nan, Guangming ^{[1
,2
]}

Ren, Fang ^{[1
]}

Luo, Meiming ^{[1
]}

机构：

[1] Sichuan Univ, Key Lab Green Chem & Technol, Minist Educ, Coll Chem, Chengdu 610064, Peoples R China

[2] Ili Teachers Coll, Dept Chem, Yining 835000, Xinjiang, Peoples R China

来源：

BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY | 2010年 / 6卷

关键词：

1-aryltriazenes; N-heterocyclic carbene-palladium complex; polymer-supported catalyst; recyclable catalyst; Suzuki-Miyaura reaction; ARENEDIAZONIUM SALTS; ARYL CHLORIDES; BORONIC ACIDS; LIGAND; BIARYLS;

D O I：

10.3762/bjoc.6.70

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

The Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported Pd-NHC complex catalyst has been realized for the first time. The polymer-supported catalyst can be re-used several times still retaining high activity for this transformation. Various aryltriazenes were investigated as electrophilic substrates at room temperature to give biaryls in good to excellent yields and showed good chemoselectivity over aryl halides in the reactions.

引用

页数：6

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