作者:Lars Kyhn Rasmussen、Brant C. Boren、Valery V. Fokin
DOI:10.1021/ol701912s
日期:2007.12.1
The formation of 1,5-disubstituted 1,2,3-triazoles from aryl azides and alkynes was readily accomplished using [Cp*RuCl]4 catalyst in dimethylformamide. It was also demonstrated that the reaction provided higher yields, cleaner product, and shorter reaction times when carried out under microwave irradiation.
使用在二甲基甲酰胺中的[Cp * RuCl] 4催化剂,很容易完成由芳基叠氮化物和炔烃形成的1,5-二取代的1,2,3-三唑。还证明了当在微波辐射下进行时,该反应提供更高的产率,更清洁的产物和更短的反应时间。