Potassium tert-butoxide mediated Heck-type cyclization/isomerization-benzofurans from organocatalytic radical cross-coupling reactions

被引：114

作者：

Rueping, Magnus ^{[1
]}

Leiendecker, Matthias ^{[1
]}

Das, Arindam ^{[1
]}

Poisson, Thomas ^{[1
]}

Bui, Lan ^{[1
]}

机构：

[1] Rhein Westfal TH Aachen, D-52074 Aachen, Germany

来源：

CHEMICAL COMMUNICATIONS | 2011年 / 47卷 / 38期

关键词：

C-H ACTIVATION; ARYL HALIDES; INTRAMOLECULAR ARYLATION; CATALYZED ADDITION; DERIVATIVES; CYCLIZATION; AMINATION; CHLORIDES; STYRENES; PHENOLS;

D O I：

10.1039/c1cc14297f

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A transition metal-free Heck-type cyclization/isomerization reaction has been developed. Mediated by potassium tertbutoxide and phenanthroline a variety of benzofuran derivatives have been synthesized.

引用

页码：10629 / 10631

页数：3

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