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Palladium‐Catalyzed Suzuki Coupling of N ‐Acyloxazolidinones via Selective Cleavage of C–N Bonds
Author(s) -
Jian Junsheng,
He Zhanyu,
Zhang Yuqi,
Liu Tingting,
Liu Lizhen,
Wang Zijia,
Wang Hui,
Wang Sanyong,
Zeng Zhuo
Publication year - 2020
Publication title -
european journal of organic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.825
H-Index - 155
eISSN - 1099-0690
pISSN - 1434-193X
DOI - 10.1002/ejoc.202000575
Subject(s) - chemistry , palladium , catalysis , suzuki reaction , cleavage (geology) , bond cleavage , coupling reaction , functional group , combinatorial chemistry , medicinal chemistry , organic chemistry , polymer chemistry , polymer , geotechnical engineering , fracture (geology) , engineering
By implementing a palladium‐catalyzed Suzuki coupling reaction of N ‐acyloxazolidinones with arylboronic acid, we herein report on the preparation of substituted diaryl ketones via selective cleavage of exocyclic C–N Bonds. The reaction was carried out under mild reaction conditions with excellent functional group compatibility in good yields (up to 93 %).