Efficient synthesis of N-arylsulfonyl-1,2,3-triazoles from 1,1-dibromo-2-arylethylenes

被引：4

作者：

Xu, Wenjing ^{[1
]}

Zhang, Wensheng ^{[1
]}

Zhang, Fei ^{[2
]}

机构：

[1] Jiaozuo Teachers Coll, Sch Sci, Jiaozuo 454100, Peoples R China

[2] Jiaozuo Vocat Tech Sch, Jiaozuo 454100, Peoples R China

来源：

HETEROCYCLIC COMMUNICATIONS | 2016年 / 22卷 / 03期

关键词：

1,2-dibromoethylene; Cs2CO3; CuI; gem-dibromoethylene; N-arylsulfonyl-1,2,3-triazole; synthesis; TsN3; ONE-POT; STEREOSELECTIVE-SYNTHESIS; CONTROLLING SELECTIVITY; TERMINAL ALKYNES; SULFONYL AZIDES; SUZUKI-MIYAURA; CYCLOADDITION; 1,1-DIBROMOALKENES; 1,2,3-TRIAZOLES; CONVERSION;

D O I：

10.1515/hc-2016-0051

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

N-arylsulfonyl-1,2,3-triazoles were synthesized from 1,1-dibromo-2-arylethylenes via a one-pot reaction involving the Cs2CO3-mediated dehydrobromination process of the dibromoalkenes to produce alkynes followed by the Cu(I)-catalyzed Huisgen cycloaddition of the alkyne intermediates with tosyl azide.

引用

页码：165 / 167

页数：3

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