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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/123456789/2814
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-14T13:10:04Z-
dc.date.available2021-10-14T13:10:04Z-
dc.date.issued2020-
dc.identifier.urihttps://pubag.nal.usda.gov/catalog/7074024-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2814-
dc.description.abstractA simple and facile method for the synthesis of 3-(arylthio)imidazo[1,2-a]pyridin-2-ols has been developed by a KOH-mediated reaction of 2-aminopyridinium bromides with aryl thiols. The method afforded a wide range of 3-(arylthio)imidazo[1,2-a]pyridin-2-ols in moderate to excellent (56–95%) yields with excellent functional group tolerance. Synthetic utility of the protocol was demonstrated by gram-scale reaction and preparation of 2-aryl-3-(p-tolylthio)imidazo[1,2-a]pyridines from 3-(p-tolylthio)imidazo[1,2-a]pyridin-2-ol.en_US
dc.language.isoenen_US
dc.publisherUSDAen_US
dc.subjectChemistryen_US
dc.subjectBromidesen_US
dc.subjectMethodologyen_US
dc.subjectPyridinesen_US
dc.subjectThiolsen_US
dc.subjectUtilitiesen_US
dc.titleKOH-mediated intramolecular amidation and sulfenylation: A direct approach to access 3-(arylthio)imidazo[1,2-a]pyridin-2-olsen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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