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A convenient and practical heterogeneous palladium‐catalyzed carbonylative Suzuki coupling of aryl iodides with formic acid as carbon monoxide source
Author(s) -
You Shengyong,
Yan Chenyu,
Zhang Rongli,
Cai Mingzhong
Publication year - 2019
Publication title -
applied organometallic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.53
H-Index - 71
eISSN - 1099-0739
pISSN - 0268-2605
DOI - 10.1002/aoc.4650
Subject(s) - chemistry , palladium , carbon monoxide , aryl , catalysis , formic acid , carbonylation , suzuki reaction , denticity , monoxide , heterogeneous catalysis , inorganic chemistry , organic chemistry , crystal structure , alkyl
A practical heterogeneous palladium‐catalyzed carbonylative Suzuki coupling of aryl iodides with arylboronic acids under carbon monoxide gas‐free conditions has been developed using a bidentate phosphino‐functionalized magnetic nanoparticle‐immobilized palladium(II) complex as catalyst. Formic acid was utilized as the carbon monoxide source with dicyclohexylcarbodiimide as the activator, and a wide variety of biaryl ketones were generated in moderate to high yields. The new heterogeneous palladium catalyst can be prepared via a simple procedure and can easily be separated from a reaction mixture by simply applying an external magnet and recycled up to 10 times without any loss of activity.