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One-pot, three component tandem reaction of 2-aminopyridines, acetophenones and aldehydes: synthesis of 3-aroylimidazo[1,2-a]pyridines

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dc.contributor.author Kumar, Anil
dc.date.accessioned 2021-10-17T13:57:18Z
dc.date.available 2021-10-17T13:57:18Z
dc.date.issued 2015
dc.identifier.uri https://pubs.rsc.org/en/content/articlelanding/2015/ra/c4ra13056a
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2870
dc.description.abstract A 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.iso en en_US
dc.publisher RSC en_US
dc.subject Chemistry en_US
dc.subject 3-aroylimidazo en_US
dc.subject 2-aminopyridines en_US
dc.title One-pot, three component tandem reaction of 2-aminopyridines, acetophenones and aldehydes: synthesis of 3-aroylimidazo[1,2-a]pyridines en_US
dc.type Article en_US


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