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通过铑催化的N-磺酰基酮亚胺与噻吩或呋喃的交叉脱氢偶联反应合成螺环磺内酰胺和杂芳基化合物。

Spirocyclic Sultam and Heterobiaryl Synthesis through Rh-Catalyzed Cross-Dehydrogenative Coupling of N-Sulfonyl Ketimines and Thiophenes or Furans.

作者信息

Mei Shu-Tao, Liang Hong-Wen, Teng Bin, Wang Nan-Jin, Shuai Li, Yuan Yi, Chen Ying-Chun, Wei Ye

机构信息

College of Pharmacy, Third Military Medical University , Chongqing 400038, China.

出版信息

Org Lett. 2016 Mar 4;18(5):1088-91. doi: 10.1021/acs.orglett.6b00197. Epub 2016 Feb 23.

Abstract

A useful approach is developed for the synthesis of various structurally interesting spirocyclic sultams and heterobiaryls using a cross-dehydrogenative coupling strategy that features high atom and step economy. This method employs [Cp*RhCl2]2 as a catalyst and N-sulfonylimine, a weak coordinating group, as an efficient directing group to assist C-H activation. A number of the coupled products were converted into interesting molecules through further synthetic transformations.

摘要

利用具有高原子经济性和步骤经济性的交叉脱氢偶联策略,开发了一种用于合成各种结构有趣的螺环磺内酰胺和杂联芳基的有效方法。该方法采用[Cp*RhCl₂]₂作为催化剂,以及弱配位基团N-磺酰亚胺作为有效的导向基团来辅助C-H活化。通过进一步的合成转化,许多偶联产物被转化为有趣的分子。

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