期刊文献+

Straightforward Sulfonamidation via Metabisulfite-Mediated CrossCoupling of Nitroarenes and Boronic Acids under Transition-Metal-Free Conditionst 被引量:2

原文传递
导出
摘要 of main observation and conclusion A straightforward multicomponent sufonamidation of nitroarenes,sodium metabisulfite and boronicacids was established under transition-mnetal-free conditions to access diverse sulfonamides from readily avilable and low-cost materials modularv.Inorganic salt sodium metabisulfite not only served as a sulfur dioxide source,but also played a key role for both activator and reductant duringsulfonamidation.Notably,naturlly occuring biomolecules and pharmaceuticals with multiple heteroatorms and sensitive functional groups were intensivly investigated in this transformtion providing versatile sulionamides collectively,further mechanistic studies demonstrated that nitrosoarene is thekey intermediate,and the activation of boronic acid is the rate-determining step in the transformation.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2020年第12期1521-1525,共5页 中国化学(英文版)
基金 The authors are grateful for the financial support provided by The National Key Research and Development Program of China(No.2017YFDO200500),NSFC(Nos.21971065,21722202,21672069 and 21871089 for M.W.) S&TCSM of Shanghai(GrantNo.18JC1415600) Professor of Special Appointment(EasternScholar)at Shanghai lnstitutions of Higher Learning,the NationalProgram for Support of Top-notch Young Professionals,andInnovative Research Team of High-Level lLocal Universities inShanghai.
  • 相关文献

参考文献1

二级参考文献1

共引文献4

同被引文献11

引证文献2

二级引证文献3

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部