Lewis Acid Catalyzed Regioselective Hydroheteroarylation of Pentafulvenes

Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/2812

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 acetonitrile cyclopentadienyl 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
URI:	http://hdl.handle.net/123456789/2812
Appears in Collections:	2016

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