State Key Laboratory of Natural and Biomimetic Drugs, School of Pharmaceutical Sciences, Peking University, Xue Yuan Rd. 38, Beijing 100191, China.
Angew Chem Int Ed Engl. 2013 Jul 22;52(30):7850-4. doi: 10.1002/anie.201303376. Epub 2013 Jun 26.
Breakthrough: A novel catalyzed direct highly selective C(sp2)-C(sp) bond functionalization of alkynes to amides has been developed. Nitrogenation is achieved by the highly selective C(sp2)-C(sp) bond cleavage of aryl-substituted alkynes. The oxidant-free and mild conditions and wide substrate scope make this method very practical.
开发了一种新型催化的炔烃到酰胺的直接高选择性 C(sp2)-C(sp)键官能化方法。氮化为芳基取代的炔烃的高选择性 C(sp2)-C(sp)键断裂来实现。无氧化剂且温和的条件以及广泛的底物范围使得该方法非常实用。