Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu 610064, P. R. China.
Beilstein J Org Chem. 2010 Jun 28;6:70. doi: 10.3762/bjoc.6.70.
The Suzuki-Miyaura cross-coupling reaction of 1-aryltriazenes with arylboronic acids catalyzed by a recyclable polymer-supported Pd-NHC complex catalyst has been realized for the first time. The polymer-supported catalyst can be re-used several times still retaining high activity for this transformation. Various aryltriazenes were investigated as electrophilic substrates at room temperature to give biaryls in good to excellent yields and showed good chemoselectivity over aryl halides in the reactions.
首次实现了由可回收聚合物负载的 Pd-NHC 配合物催化剂催化 1-芳基三氮唑与芳基硼酸的铃木-宫浦交叉偶联反应。该聚合物负载的催化剂在多次重复使用后仍然保持对该转化的高活性。研究了各种芳基三氮唑作为亲电底物在室温下进行反应,以良好至优秀的收率得到联芳基产物,并在反应中对芳基卤化物表现出良好的化学选择性。