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Copper-catalyzed cyclization of 2-cyanobenzaldehydes and 2-isocyanoacetates: an efficient strategy for the synthesis of substituted 1-aminoisoquinolines†‡
Wen Bao,Jun-Qi Wang,Xue-Tao Xu,Bang-Hong Zhang,Wei-Ting Liu,Lin-Sheng Lei,Huan Liang,Kun Zhang
Chemical Communications Pub Date : 06/29/2018 00:00:00 , DOI:10.1039/C8CC04733B
Abstract

A Cu(acac)2-catalyzed cyclization reaction of 2-cyanobenzaldehydes with 2-isocyanoacetates has been successfully developed providing an efficient strategy for the synthesis of substituted 1-aminoisoquinolines. The reaction proceeds smoothly under mild conditions with high efficiency, and might provide an alternative strategy for the synthesis of 1-aminoisoquinoline containing molecules.

Graphical abstract: Copper-catalyzed cyclization of 2-cyanobenzaldehydes and 2-isocyanoacetates: an efficient strategy for the synthesis of substituted 1-aminoisoquinolines
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