Oxidative dual C-H thiolation of imidazopyridines with ethers or alkanes using elemental sulphur

被引：80

作者：

Zhang, Jun-Rong ^{[1
]}

Liao, Yan-Yan ^{[1
]}

Deng, Jian-Chao ^{[1
]}

Feng, Kai-Ying ^{[1
]}

Zhang, Min ^{[1
]}

Ning, Yun-Yun ^{[1
]}

Lin, Zi-Wei ^{[1
]}

Tang, Ri-Yuan ^{[1
,2
]}

机构：

[1] South China Agr Univ, Dept Appl Chem, Coll Mat & Energy, Guangzhou 510642, Guangdong, Peoples R China

[2] South China Agr Univ, Key Lab Nat Pesticide & Chem Biol, Minist Educ, Guangzhou 510642, Guangdong, Peoples R China

来源：

CHEMICAL COMMUNICATIONS | 2017年 / 53卷 / 55期

关键词：

S BOND FORMATION; ARYL BORONIC ACIDS; ONE-POT SYNTHESIS; REGIOSELECTIVE SULFENYLATION; CATALYZED SYNTHESIS; COUPLING REACTIONS; ROOM-TEMPERATURE; DIARYL SULFIDES; C(SP(3))-H BOND; IMIDAZOHETEROCYCLES;

D O I：

10.1039/c7cc03940a

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Dual C-H thiolation reactions using elemental sulphur remain a challenge. This communication discloses an oxidative radical dual sp(2)/sp(3) C-H thiolation strategy for the coupling of imidazopyridines with ethers or alkanes using elemental sulphur.

引用

页码：7784 / 7787

页数：4

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