Lewis Acid Catalyzed Regioselective Hydroheteroarylation of Pentafulvenes

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DC Field	Value	Language
dc.contributor.author	Sarath Chand, S	-
dc.contributor.author	Greeshma, Gopalan	-
dc.contributor.author	Santhini, P V	-
dc.contributor.author	Preethanuj, P	-
dc.contributor.author	Jubi, John	-
dc.contributor.author	Dominique, Harakat	-
dc.contributor.author	Florian, Jaroschik	-
dc.contributor.author	Radhakrishnan, K V	-
dc.date.accessioned	2017-05-25T06:38:03Z	-
dc.date.available	2017-05-25T06:38:03Z	-
dc.date.issued	2016-02-10	-
dc.identifier.citation	Organic letters 18:964−967	en_US
dc.identifier.uri	http://hdl.handle.net/123456789/2812	-
dc.description.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	en_US
dc.language.iso	en	en_US
dc.publisher	ACS publication	en_US
dc.subject	exocyclic carbon	en_US
dc.subject	acetonitrile	en_US
dc.subject	cyclopentadienyl	en_US
dc.subject	endocyclic ring	en_US
dc.title	Lewis Acid Catalyzed Regioselective Hydroheteroarylation of Pentafulvenes	en_US
dc.type	Article	en_US
Appears in Collections:	2016

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