Please use this identifier to cite or link to this item:
Title: Lewis Acid Catalyzed Regioselective Hydroheteroarylation of Pentafulvenes
Authors: Sarath Chand, S
Greeshma, Gopalan
Santhini, P V
Preethanuj, P
Jubi, John
Dominique, Harakat
Florian, Jaroschik
Radhakrishnan, K V
Keywords: exocyclic carbon
endocyclic ring
Issue Date: 10-Feb-2016
Publisher: ACS publication
Citation: Organic letters 18:964−967
Abstract: A diverse approach toward the catalytic regioselective nucleophilic addition of nitrogen heterocycles to Lewis acid activated pentafulvenes has been established. The developed protocol introduces pentafulvenes as nonsymmetrical alkenes for the hydroheteroarylation reaction, providing alkylidenecyclopentenylation at the C-3 position of indoles and the C-2 position of pyrrole
Appears in Collections:2016

Files in This Item:
File Description SizeFormat 
lewics acid-organic letters-sarath chand.pdf629.32 kBAdobe PDFView/Open

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.