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Nickel‐Catalyzed Carbon‐Sulfur Bond Formation through Couplings of Aryl Iodides and Aryl Ethanethioates
Author(s) -
Mao Pu,
Sui HongDa,
Yuan JinWei,
Xiao YongMei,
Yang LiangRu,
Mai WenPeng
Publication year - 2020
Publication title -
chemistryselect
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.437
H-Index - 34
ISSN - 2365-6549
DOI - 10.1002/slct.202002787
Subject(s) - aryl , nickel , catalysis , palladium , sulfur , chemistry , ruthenium , combinatorial chemistry , organic chemistry , alkyl
A nickel‐catalyzed reductive coupling between aryl iodides and aryl ethanethioates has been developed to afford diaryl sulfides. This method provides a novel and practical route to aryl thioetherification and can be effectively applied to electronically diverse aryl iodides without expensive metals such as palladium and ruthenium.