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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-17T13:55:55Z-
dc.date.available2021-10-17T13:55:55Z-
dc.date.issued2015-10-19-
dc.identifier.urihttps://pubs.acs.org/doi/abs/10.1021/acs.orglett.5b02539-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2852-
dc.description.abstractThe vanadium-catalyzed oxidative coupling of substituted 2-arylimidiazo[1,2-a]pyridines to N-methylmorpholine oxide, which acts as both a coupling partner and an oxidant, has been achieved. This reaction was applied to various substituted imidiazo[1,2-a]pyridine and indole substrates, resulting in yields as high as 90%. Mechanistic investigations indicate that the reaction may proceed via a Mannich-type process. This work demonstrates how oxidative aminomethylation can be used as a useful method to introduce tertiary amines into heterocycles, thus providing an alternative method for conventional Mannich-type reactions.en_US
dc.language.isoenen_US
dc.publisherACSen_US
dc.subjectChemistryen_US
dc.subjectCatalystsen_US
dc.subjectOxidative couplingen_US
dc.subjectAnionsen_US
dc.subjectByproductsen_US
dc.subjectIonsen_US
dc.titleNEXT Oxidative Cross-Coupling of sp3- and sp2-Hybridized C–H Bonds: Vanadium-Catalyzed Aminomethylation of Imidazo[1,2-a]pyridinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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