Solvent-Driven Iodine-Mediated Oxidative Strategies for the Synthesis of Bis(imidazo[1,2-a]pyridin-3-yl)sulfanes and Disulfanes

dc.contributor.authorMandal, S.K.
dc.date.accessioned2020-11-17T09:31:47Z
dc.date.available2020-11-17T09:31:47Z
dc.date.issued2017
dc.descriptionOnly IISERM authors are available in the record.
dc.description.abstractTwoefficient iodine-mediated strategies, which are economical and one-pot,are described to access bis(imi- dazo[1,2-a]pyridin-3-yl)sulfanes and bis(imidazo[1,2-a]pyri- din-3-yl)disulfanes in chloroform and acetic acid, respectively, by adirect oxidative homocoupli ng of imidazo-heterocycles using inexpensive sodiumsulfide as asulfur source.These strategies are scalable, andanarray of substrates delivered their corresponding stable sulfur-bridged imidazo-heterocy- cles in excellent yields.en_US
dc.identifier.citationChemistry - An Asian Journal, 12 (23)en_US
dc.identifier.other10.1002/asia.201701274
dc.identifier.urihttps://onlinelibrary.wiley.com/doi/full/10.1002/asia.201701274
dc.identifier.urihttp://hdl.handle.net/123456789/1688
dc.language.isoen_USen_US
dc.publisherWileyen_US
dc.subjectTwoefficienten_US
dc.subjectSolvent‐Drivenen_US
dc.subjectSulfur heterocyclesen_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

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