Department of Chemistry and Materials Engineering, Faculty of Chemistry, Materials and Bioengineering, Kansai University, Suita, Osaka, Japan.
Org Lett. 2011 May 20;13(10):2568-71. doi: 10.1021/ol200662e. Epub 2011 Apr 14.
Three-component [2 + 2 + 2] cycloaddition of terminal alkynes, internal alkynes, and terminal alkenes is achieved using an NbCl(3)(DME) catalyst, leading to 1,3,4,5-substituted 1,3-cyclohexadienes in excellent yields with high chemo- and regioselectivity.
三组分[2 + 2 + 2]环加成反应,使用 NbCl(3)(DME)催化剂,使末端炔烃、内部炔烃和末端烯烃反应,以高产率和高化学选择性和区域选择性得到 1,3,4,5-取代的 1,3-环己二烯。