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二苯并噻吩亚磺酰亚胺:一种方便的分子间铑催化 C-H 酰胺化方法。

Dibenzothiophenesulfilimines: A Convenient Approach to Intermolecular Rhodium-Catalysed C-H Amidation.

机构信息

Organisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.

Chemistry Department, Faculty of Science, King Abdulaziz University, Jeddah, 21589, Saudi Arabia.

出版信息

Chemistry. 2020 Jul 2;26(37):8235-8238. doi: 10.1002/chem.202002371. Epub 2020 Jun 9.

Abstract

A sulfilimine-based Group 9 transition-metal-catalysed C-H amidation procedure is reported. Dibenzothiophene-based sulfilimines were shown to constitute a class of novel amidation reagents which enable the transfer of a wide range of N-sulfonyl and N-acyl moieties. It was demonstrated that sulfilimines, which are easily accessible from cheap reagents, are safe-to-handle and represent broadly applicable amidation reagents. The dibenzothiophene can be recycled after use. The C-H amidation was shown to proceed with high selectivity and gave the mono-amidated products, mostly in good to excellent yields.

摘要

本文报道了一种基于亚磺酰胺的 Group 9 过渡金属催化的 C-H 酰胺化方法。基于二苯并噻吩的亚磺酰胺被证明是一类新型的酰胺化试剂,能够实现广泛的 N-磺酰基和 N-酰基的转移。实验表明,亚磺酰胺很容易从廉价试剂中获得,操作安全,是一种广泛适用的酰胺化试剂。使用后的二苯并噻吩可以回收利用。C-H 酰胺化具有很高的选择性,主要生成单酰胺化产物,产率良好到优秀。

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