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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/xmlui/handle/123456789/3177
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dc.contributor.authorKumar, Indresh-
dc.date.accessioned2021-10-27T04:28:04Z-
dc.date.available2021-10-27T04:28:04Z-
dc.date.issued2012-
dc.identifier.urihttps://pubs.rsc.org/en/content/articlelanding/2012/RA/c2ra21258g-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/3177-
dc.description.abstractA robust method for the synthesis of substituted pyrrole-3-carboxaldehydes from N-PMP aldimines and succinaldehyde is reported. This reaction involves an organocatalytic direct Mannich reaction, and an acid catalyzed cyclization and oxidative aromatization sequence with high yields (up to 82%).en_US
dc.language.isoenen_US
dc.publisherRSCen_US
dc.subjectChemistryen_US
dc.subjectOrganocatalyticen_US
dc.subjectMannich/cyclization/aromatizationen_US
dc.subjectPyrrole-3-carboxaldehydesen_US
dc.titleOrganocatalytic Mannich/cyclization/aromatization sequence: direct synthesis of substituted pyrrole-3-carboxaldehydesen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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