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作 者:Xiao-Yue Chen Xin Kuang Yichen Wu Jian Zhou Peng Wang
机构地区:[1]Shonghai Key Laboratory of Green Chemistry and Chemica/Process,East China Norma/University,3663 N Zhongshan Rood,Shanghai 200062,China [2]State Key Laboratory of Organometallic Chemistry,Shanghoi Institute of Orgonic Chemistry,University of Chinese Acodemy of Sciences,CAS,345 Lingling Road,Shanghai 200032,China [3]CAS Key laboratony of Energy Regulation Moterials,Shanghai Istitute of Organic Chemistr,CAS,345 Lingling Rood,Shanghai 200320,China [4]School of Chemistry and Moterials Science,Hangzhou Institute for Advanced Study,University of Chinese Academy of Ssciences,1 Sub lane Xiangshan,Hangzhou,Zhejiang 310024,China
出 处:《Chinese Journal of Chemistry》2023年第16期1979-1986,共8页中国化学(英文版)
基 金:We gratefully acknowledge National Natural Science Foundation of China(22101291,22171277,21821002);National Key R&D Program of China(2021YFA1500200);Shanghai Rising-Star Program(20QA1411400);Shanghai Institute of Organic Chemistry,and State Key Laboratory of Organometallic Chemistry for finan cial support.
摘 要:Comprehensive Summary A novel transient SET mediator approach has been developed for the photoinduced radical-radical cross coupling reaction.Using the in-situ generated thianthrene radical cation as the transient SET mediator,the thiocyanation and selenocyanation of aryl thianthrenium salts have been realized under the mild conditions without the need for photocatalyst or single electron donor.In comparison with the photocatalyst enabled process,the protocol features mild conditions,simple manipulation,a broad substrate scope,excellent functional group and heterocycle tolerance.Due to the feasible accessibility of aryl thianthrenium salts,this method has also been applied in the efficient synthesis of a bioactive molecule,and the late-stage functionalization of complex arenes.
关 键 词:Transient SET mediator Thiocyanation and selenocyanation Arylthianthrenium salts Radical reaction Photosynthesis
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