Beckmann Henning S G, Wittmann Valentin
Fachbereich Chemie, Universität Konstanz, D-78457 Konstanz, Germany.
Org Lett. 2007 Jan 4;9(1):1-4. doi: 10.1021/ol0621506.
[reaction: see text] A one-pot reaction for Cu(II)-catalyzed diazo transfer and Cu(I)-catalyzed azide-alkyne 1,3-dipolar cycloaddition (sometimes called click reaction) is reported. 1,4-Disubstituted 1,2,3-triazoles are obtained in excellent yields from a variety of readily available amines without the need for isolation of the azide intermediates. The reaction has a broad scope and is especially practical for the synthesis of multivalent structures because compounds substituted with multiple azides are potentially unstable.
[反应:见正文] 报道了一种一锅法反应,该反应包括铜(II)催化的重氮转移以及铜(I)催化的叠氮化物-炔烃1,3-偶极环加成反应(有时称为点击反应)。从各种容易获得的胺出发,无需分离叠氮化物中间体,就能以优异的产率得到1,4-二取代的1,2,3-三唑。该反应适用范围广泛,对于多价结构的合成尤其实用,因为被多个叠氮化物取代的化合物可能不稳定。