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钴催化的以吡啶甲酰胺为无痕迹导向基团的异喹啉的选择性合成。

Cobalt-Catalyzed Selective Synthesis of Isoquinolines Using Picolinamide as a Traceless Directing Group.

机构信息

Engineering Research Center of Molecular Medicine of Ministry of Education, Key Laboratory of Fujian Molecular Medicine, Key Laboratory of Xiamen Marine and Gene Drugs, School of Biomedical Sciences, Huaqiao University , Xiamen 361021, P. R. China.

出版信息

Org Lett. 2017 Apr 21;19(8):2102-2105. doi: 10.1021/acs.orglett.7b00702. Epub 2017 Apr 13.

Abstract

Picolinamide has first been employed as a traceless directing group for the cobalt-catalyzed oxidative annulation of benzylamides with alkynes to synthesize isoquinolines through C-H/N-H bonds activation. Oxygen is used as a terminal oxidant. This protocol exhibits good functional group tolerance and excellent regioselectivity. Both terminal and internal alkynes can be efficiently applied to this catalytic system as substrates.

摘要

吡啶甲酰胺最初被用作无痕迹导向基团,用于钴催化的苯甲酰胺与炔烃的氧化环化反应,通过 C-H/N-H 键的活化合成异喹啉。氧气被用作末端氧化剂。该方案表现出良好的官能团容忍度和优异的区域选择性。末端和内部炔烃都可以作为底物有效地应用于这个催化体系。

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