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典型文献
Boron-promoted reductive deoxygenation coupling reaction of sulfonyl chlorides for the C(sp3)-S bond construction
文献摘要:
Herein,we report a borane-promoted reductive deoxygenation coupling reaction to synthesize sulfides.This reaction features excellent functional group compatibility,high efficiency,broad substrate scope,and application in late-stage functionalization of biomolecules.Preliminary mechanistic studies suggest di-aryl sulfides are the intermediates of this reaction.Moreover,the real active aryl sulfide anions may be generated in situ with the aid of B2pin2 and react with alkyl tosylates through a concerted SN2 pathway.
文献关键词:
作者姓名:
Shuo Chen;Qingru Wen;Yanqing Zhu;Yanru Ji;Yu Pu;Zhengli Liu;Yun He;Zhang Feng
作者机构:
Chongqing Key Laboratory of Natural Product Synthesis and Drug Research,School of Pharmaceutical Sciences,Chongqing University,Chongqing 401331,China;Medical Imaging Key Laboratory of Sichuan Province,North Sichuan Medical College,Nanchong 637000,China
引用格式:
[1]Shuo Chen;Qingru Wen;Yanqing Zhu;Yanru Ji;Yu Pu;Zhengli Liu;Yun He;Zhang Feng-.Boron-promoted reductive deoxygenation coupling reaction of sulfonyl chlorides for the C(sp3)-S bond construction)[J].中国化学快报(英文版),2022(12):5101-5105
A类:
B2pin2,tosylates
B类:
Boron,promoted,reductive,deoxygenation,coupling,reaction,sulfonyl,chlorides,sp3,bond,construction,Herein,we,report,borane,synthesize,sulfides,This,features,excellent,group,compatibility,high,efficiency,broad,substrate,scope,application,stage,functionalization,biomolecules,Preliminary,mechanistic,studies,suggest,aryl,are,intermediates,this,Moreover,real,active,anions,may,be,generated,situ,aid,alkyl,through,concerted,SN2,pathway
AB值:
0.685584
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