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dc.contributor.authorKumar, Anil-
dc.date.accessioned2021-10-17T13:57:18Z-
dc.date.available2021-10-17T13:57:18Z-
dc.date.issued2015-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2015/ra/c4ra13056a-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2870-
dc.description.abstractA facile synthesis of 3-aroylimidazo[1,2-a]pyridine derivatives has been achieved through the one-pot, three-component tandem reaction of acetophenones, arylaldehydes and 2-aminopyridines in the presence of a catalytic amount of copper(II) chloride and air as the sole oxidant. The developed one-pot method is atom-economical and utilizes readily available precursors to offer highly functionalized N-fused imidazoles in moderate to good yields (26–82%). The presented tandem process is expected to proceed via crossed aldol condensation, Michael addition, copper catalyzed oxidative cyclization and subsequent aromatization.en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subject3-aroylimidazoen_US
dc.subject2-aminopyridinesen_US
dc.titleOne-pot, three component tandem reaction of 2-aminopyridines, acetophenones and aldehydes: synthesis of 3-aroylimidazo[1,2-a]pyridinesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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