Facile β-Alkyl and β-Hydride Elimination in the Nickel-Catalyzed Annulation of o-Iodophenyl Ketones and Aldehydes with Bicyclic Alkenes

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DC Field	Value	Language
dc.contributor.author	Shukla, Paritosh	-
dc.date.accessioned	2021-11-11T10:54:03Z	-
dc.date.available	2021-11-11T10:54:03Z	-
dc.date.issued	2006-05-26	-
dc.identifier.uri	https://pubs.acs.org/doi/10.1021/ol061051p	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3291	-
dc.description.abstract	o-Iodoaryl aldehydes react with bicyclic alkenes in the presence of NiBr2(dppe) and Zn powder in acetonitrile at 80 °C undergoing annulation to give polycyclic ketone derivatives. Surprisingly, o-iodoaryl alkyl ketones also react with bicyclic alkenes to form polycyclic ketones with structures the same as those from the corresponding o-iodoaryl aldehydes.	en_US
dc.language.iso	en	en_US
dc.publisher	ACS	en_US
dc.subject	Chemistry	en_US
dc.subject	Hydrocarbons	en_US
dc.subject	Annulations	en_US
dc.subject	Reaction products	en_US
dc.title	Facile β-Alkyl and β-Hydride Elimination in the Nickel-Catalyzed Annulation of o-Iodophenyl Ketones and Aldehydes with Bicyclic Alkenes	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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