An Articulate Oxidative Transition-Metal-Free Homocoupling of Imidazo Heterocycles through C(sp2)–C(sp2) Bond Formation

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DC Field	Value	Language
dc.contributor.author	Sakhuja, Rajeev	-
dc.date.accessioned	2021-11-11T10:59:36Z	-
dc.date.available	2021-11-11T10:59:36Z	-
dc.date.issued	2017-03-13	-
dc.identifier.uri	https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201700238	-
dc.identifier.uri	http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3360	-
dc.description.abstract	Direct oxidative homocoupling of 2-arylimidazo heterocycles was achieved by using a phenyliodine diacetate-mediated BF3·OEt2-accelerated protocol at room temperature. A series of biimidazo heterocycles were synthesized under ambient conditions without prior activation of the C(sp2)–H bond. The desired biimidazo heterocycles were also obtained by using catalytic amounts of iodobenzene and m-CPBA/AcOH in an organocatalytic fashion.	en_US
dc.language.iso	en	en_US
dc.publisher	Wiley	en_US
dc.subject	Chemistry	en_US
dc.subject	Homocoupling	en_US
dc.subject	Imidazo Heterocycles through C(sp2)–C(sp2)	en_US
dc.subject	Bond Formation	en_US
dc.title	An Articulate Oxidative Transition-Metal-Free Homocoupling of Imidazo Heterocycles through C(sp2)–C(sp2) Bond Formation	en_US
dc.type	Article	en_US
Appears in Collections:	Department of Chemistry

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