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

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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


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