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Direct Access to Isoindolin‐1‐one Scaffolds by Copper‐Catalyzed Divergent Cyclizations of 2‐Formylbenzonitrile and Diaryliodonium Salts
Author(s) -
Liu Li,
Qiang Jian,
Bai ShuHua,
Sung HuiLing,
Miao ChunBao,
Li Jian
Publication year - 2017
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201601403
Subject(s) - chemistry , copper , tandem , catalysis , cascade , combinatorial chemistry , cascade reaction , organic chemistry , materials science , chromatography , composite material
Copper‐catalyzed cascade transformations of 2‐formylbenzonitrile and diaryliodonium salts were carried out to efficiently afford isoindolin‐1‐one scaffolds. The process proceeds through a copper‐catalyzed tandem C–H/N–H arylation, producing two different isoindolin‐1‐one derivatives under different reaction conditions.
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