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铑催化喹喔啉酮在水相中的硒化和亚磺酰化反应

Rhodium-catalyzed selenylation and sulfenylation of quinoxalinones 'on water'.

作者信息

Lalji Ram Sunil Kumar, Gupta Mohit, Kumar Sandeep, Kumar Amit, Singh Brajendra Kumar

机构信息

Bio-Organic Research Laboratory, Department of Chemistry, University of Delhi Delhi 110007 India

Department of Chemistry, Kirori Mal College, University of Delhi Delhi 110007 India.

出版信息

RSC Adv. 2023 Feb 20;13(9):6191-6198. doi: 10.1039/d2ra07400a. eCollection 2023 Feb 14.

Abstract

A rhodium-catalysed, regioselective synthetic methodology for selenylation and sulfenylation of 3-phenyl quinoxolinones has been developed through N-directed C-H activation in the presence of silver triflimide, and silver carbonate using dichalcogenides 'on water'. The methodology has been proven to be efficient, regioselective and green. Using this method, a range of selenylations and sulfenylations of the substrates has been carried out in good to excellent yields. Further, late-stage functionalisation produced potential anti-tumour, anti-fungal and anti-bacterial agents making these compounds potential drug candidates.

摘要

通过在三氟甲磺酸银和碳酸银存在下,利用二硫属化物在水相中进行N-导向的C-H活化,开发了一种铑催化的3-苯基喹喔啉酮硒化和亚磺酰化的区域选择性合成方法。该方法已被证明是高效、区域选择性和绿色的。使用该方法,已以良好至优异的产率对一系列底物进行了硒化和亚磺酰化反应。此外,后期功能化产生了潜在的抗肿瘤、抗真菌和抗菌剂,使这些化合物成为潜在的药物候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4f7b/9940630/07acbc48e422/d2ra07400a-f1.jpg

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