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锰催化 C-H 活化合成 3-(吲哚-2-基)琥珀酰亚胺衍生物的方法。

An Approach to 3-(Indol-2-yl)succinimide Derivatives by Manganese-Catalyzed C-H Activation.

机构信息

College of Chemistry and Molecular Engineering, Henan Key Laboratory of Chemical Biology and Organic Chemistry, Zhengzhou University , Zhengzhou 450001, P. R. China.

出版信息

Org Lett. 2017 Aug 4;19(15):4042-4045. doi: 10.1021/acs.orglett.7b01795. Epub 2017 Jul 26.

Abstract

The manganese-catalyzed addition of C-2 position of indoles to maleimides has been achieved under additive-free conditions. The manganese catalyst exhibits excellent chemo- and regioselectivity, good functional group compatibility, and high catalytic efficiency. The substrate scope can also be extended to maleates, ethyl acrylate, 1,4-dihydro-1,4-epoxynaphthalene, pyrroles, and 2-phenylpyridine, which further demonstrates the universality of this straightforward approach.

摘要

锰催化吲哚 C-2 位与马来酰亚胺加成反应在无添加剂条件下实现。锰催化剂表现出优异的化学和区域选择性、良好的官能团相容性和高效的催化活性。底物范围还可以扩展到马来酸酐、丙烯酸乙酯、1,4-二氢-1,4-环氧萘、吡咯和 2-苯基吡啶,进一步证明了这种直接方法的普遍性。

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