Metal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids

dc.contributor.authorKumar, Anil
dc.date.accessioned2021-10-14T13:09:52Z
dc.date.available2021-10-14T13:09:52Z
dc.date.issued2020
dc.description.abstractA simple and straightforward approach has been realized for the direct benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acids in the presence of K2S2O8 as an oxidant. Various functional groups were tolerated on both imidazoheterocycles and arylglyoxylic acids and a wide range of C5-benzoyl-imidazoheterocycles were obtained in good to high yields (50–84%). Radical trapping experiments confirmed the involvement of the radical pathway. The developed protocol is amenable for a scale-up reaction.en_US
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2020/ob/d0ob01842b
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2811
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectBenzoylationen_US
dc.subjectImidazoheterocyclesen_US
dc.subjectArylglyoxylic acidsen_US
dc.titleMetal-free benzoylation of imidazoheterocycles by oxidative decarboxylation of arylglyoxylic acidsen_US
dc.typeArticleen_US

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