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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3356
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dc.contributor.authorSakhuja, Rajeev-
dc.date.accessioned2021-11-11T10:59:10Z-
dc.date.available2021-11-11T10:59:10Z-
dc.date.issued2017-09-26-
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/10.1002/asia.201701274-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3356-
dc.description.abstractTwo efficient iodine-mediated strategies, which are economical and one-pot, are described to access bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and bis(imidazo[1,2-a]pyridin-3-yl)disulfanes in chloroform and acetic acid, respectively, by a direct oxidative homocoupling of imidazo-heterocycles using inexpensive sodium sulfide as a sulfur source. These strategies are scalable, and an array of substrates delivered their corresponding stable sulfur-bridged imidazo-heterocycles in excellent yields.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectSolvent-Drivenen_US
dc.subjectSynthesis of Bis(imidazo[1,2-a]pyridin-3-yl)en_US
dc.subjectDisulfanesen_US
dc.titleSolvent-Driven Iodine-Mediated Oxidative Strategies for the Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and Disulfanesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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