Iodine-mediated cyclization of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols and their subsequent condensation leading to the formation of novel bis(1-imidazo[1,5-a]pyridyl)arylmethanes

被引：29

作者：

Tahara, Shinsuke ^{[1
]}

Shibahara, Fumitoshi ^{[1
]}

Maruyama, Toshifumi ^{[1
]}

Murai, Toshiaki ^{[1
]}

机构：

[1] Gifu Univ, Dept Chem, Fac Engn, Gifu 5011193, Japan

来源：

CHEMICAL COMMUNICATIONS | 2009年 / 45期

关键词：

AROMATIC-ALDEHYDES; DERIVATIVES; TRIARYLMETHANES; RECYCLIZATION; ALKYLATION; THIOAMIDES; RADICALS; REAGENT; ACCESS; ARENES;

D O I：

10.1039/b910172a

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The treatment of N-thioacyl-1-(2-pyridyl)-1,2-aminoalcohols with iodine and pyridine in THF at room temperature for 30 min leads to the formation of bis(1-imidazo[1,5-a] pyridyl)arylmethanes as green solids in good to high yields.

引用

页码：7009 / 7011

页数：3

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