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钴(III)催化的C-H活化:马来酰亚胺在吲哚C-2位的位点选择性共轭加成反应

Co(III)-Catalyzed C-H Activation: A Site-Selective Conjugate Addition of Maleimide to Indole at the C-2 Position.

作者信息

Muniraj Nachimuthu, Prabhu Kandikere Ramaiah

机构信息

Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, Karnataka, India.

出版信息

ACS Omega. 2017 Aug 11;2(8):4470-4479. doi: 10.1021/acsomega.7b00870. eCollection 2017 Aug 31.

Abstract

The cobalt(III)-catalyzed site-selective C-2 functionalization of indole has been developed using the pyrimidinyl group as a directing group. This reaction furnishes 3-arylated succinimide derivatives in excellent yields in a shorter duration using an inexpensive Co catalyst. Highly selective C-2 functionalization of indoles was achieved in the presence of the highly reactive C-3 position. This protocol is compatible with a variety of -pyrimidinyl indole and maleimide derivatives, and it can be easily scaled-up. This method is also applicable for maleic ester and heteroarenes.

摘要

已开发出以嘧啶基作为导向基团的钴(III)催化吲哚的位点选择性C-2官能化反应。该反应使用廉价的钴催化剂,能在较短时间内以优异的产率提供3-芳基化琥珀酰亚胺衍生物。在高活性的C-3位存在的情况下,实现了吲哚的高度选择性C-2官能化。该方案与多种嘧啶基吲哚和马来酰亚胺衍生物兼容,并且易于放大规模。该方法也适用于马来酸酯和杂芳烃。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3b58/6641948/beedaf9a76a6/ao-2017-008703_0009.jpg

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