Please use this identifier to cite or link to this item:
http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/2829
Title: | Sequential Copper-Catalyzed Sonogashira Coupling, Hydroamination and Palladium-Catalyzed Intramolecular Direct Arylation: Synthesis of Azepino-Fused Isoindolinones |
Authors: | Kumar, Anil |
Keywords: | Chemistry Copper-Catalyzed Sonogashira Coupling Azepino-Fused Isoindolinones |
Issue Date: | 9-Nov-2017 |
Publisher: | Wiley |
Abstract: | A modular synthesis of azepino-fused isoindolinones has been developed in form of a sequential copper- and palladium-catalyzed tandem reaction. The developed protocol involved the formation of one carbon–nitrogen and two carbon–carbon bonds in a one-pot fashion. The palladium-catalyzed intramolecular direct-arylation step involves the formation of an unusual eight-membered palladacycle. |
URI: | https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/ejoc.201701379 http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2829 |
Appears in Collections: | Department of Chemistry |
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.