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DC Field | Value | Language |
---|---|---|
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 |
Appears in Collections: | Department of Chemistry |
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