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dc.contributor.authorKumar, Indresh-
dc.date.accessioned2021-10-27T04:27:21Z-
dc.date.available2021-10-27T04:27:21Z-
dc.date.issued2019-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2019/nj/c8nj04861d-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3162-
dc.description.abstractA direct method for the synthesis of new tetracyclic oxazepine-fused pyrroles has been developed through [3+2] annulation between aqueous succinaldehyde and dibenzo[b,f][1,4]-oxazepines under metal-free conditions. This one-pot synthetic protocol involves proline-catalyzed direct Mannich/cyclization between aqueous succinaldehyde and seven-membered oxazepine-imines, followed by an IBX-mediated oxidation sequence with high yields (up to 90%).en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectTetracyclic oxazepine-fuseden_US
dc.subjectOxazepinesen_US
dc.subjectAqueous succinaldehydeen_US
dc.titleA simple route to tetracyclic oxazepine-fused pyrroles via metal-free [3+2] annulation between dibenzo[b,f][1,4]oxazepines and aqueous succinaldehydeen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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