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Regio‐ and Chemoselective Formation of Spiroindolinone–Isoindolinone by a Palladium‐Catalyzed Buchwald–Hartwig Addition–Elimination Sequence
Author(s) -
Butani Himanshu H.,
Vachhani Dipak D.,
Bhoya Umed C.,
Shah Anamik K.,
Van der Eycken Erik V.
Publication year - 2014
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.201402909
Subject(s) - chemistry , combinatorial chemistry , palladium , catalysis , isatin , sequence (biology) , organic chemistry , biochemistry
The usual way to synthesize spiroindolinones is the application of isatin derivatives. Here, we report the first Pd‐catalyzed Buchwald–Hartwig addition–elimination strategy for the formation of the spiroindolinone–isoindolinone architecture. The application of the Ugi‐4‐component reaction (Ugi‐4CR) allows the facile introduction of diversity and increases the practicality of this protocol.