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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/3360
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T10:59:36Z-
dc.date.available2021-11-11T10:59:36Z-
dc.date.issued2017-03-13-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.201700238-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3360-
dc.description.abstractDirect 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.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectHomocouplingen_US
dc.subjectImidazo Heterocycles through C(sp2)–C(sp2)en_US
dc.subjectBond Formationen_US
dc.titleAn Articulate Oxidative Transition-Metal-Free Homocoupling of Imidazo Heterocycles through C(sp2)–C(sp2) Bond Formationen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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