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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/123456789/2812
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-14T13:09:56Z-
dc.date.available2021-10-14T13:09:56Z-
dc.date.issued2020-09-15-
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.202000996-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2812-
dc.description.abstractSynthesis of 3-(arylthio)imidazo[1,2-a]pyridin-2(3H)-ols has been achieved through a catalyst-free, one-pot reaction of 2-aminopyridinium bromides with sodium arenesulfinates. The tandem reaction involved intramolecular amidation followed by sulfenylation and afforded a wide range of 3-(arylthio)imidazo[1,2-a]pyridin-2(3H)-ols in moderate to excellent (33–85 %) yields. The method exhibited broad substrate scope with a wide range of functional group tolerance, and is amenable for gram-scale synthesis.en_US
dc.language.isoenen_US
dc.publisherEJOCen_US
dc.subjectChemistryen_US
dc.subjectFacile Synthesisen_US
dc.subjectSodium Arenesulfinatesen_US
dc.subject2-Aminopyridinium Bromidesen_US
dc.titleA Facile Synthesis of 3-(Arylthio)imidazo[1,2-a]pyridin-2(3H)-ones from 2-Aminopyridinium Bromides and Sodium Arenesulfinatesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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