Muniraj Nachimuthu, Prabhu Kandikere Ramaiah
Department of Organic Chemistry, Indian Institute of Science, Bangalore 560012, Karnataka, India.
ACS Omega. 2017 Aug 11;2(8):4470-4479. doi: 10.1021/acsomega.7b00870. eCollection 2017 Aug 31.
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.
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。