Copper(I) Iodide-Catalyzed Synthesis of 4-Aryl-1H-1,2,3-triazoles from anti-3-Aryl-2,3-dibromopropanoic Acids and Sodium Azide

被引：19

作者：

Jiang, Yubo ^{[1
]}

Kuang, Chunxiang ^{[1
]}

Yang, Qing ^{[2
]}

机构：

[1] Tongji Univ, Dept Chem, Shanghai 200092, Peoples R China

[2] Fudan Univ, Sch Life Sci, Dept Biochem, Shanghai 200433, Peoples R China

来源：

SYNTHESIS-STUTTGART | 2010年 / 24期

关键词：

cyclizations; catalysis; heterocycles; azides; triazoles; ONE-POT SYNTHESIS; CLICK CHEMISTRY; UNSATURATED AZIDES; 1,4-DISUBSTITUTED 1,2,3-TRIAZOLES; 1,3-DIPOLAR CYCLOADDITION; STEREOSELECTIVE-SYNTHESIS; ALKYNE CYCLOADDITION; EFFICIENT SYNTHESIS; PROPARGYL AZIDES; HIGHLY EFFICIENT;

D O I：

10.1055/s-0030-1258312

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

4-Aryl-1H-1,2,3-triazoles were synthesized from anti-3-aryl-2,3-dibromopropanoic acids and sodium azide by using inexpensive copper(I) iodide as the catalyst in dimethyl sulfoxide.

引用

页码：4256 / 4260

页数：5

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