Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/5035
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dc.contributor.authorPandey, Rajat-
dc.contributor.authorSingh, Gurdeep-
dc.contributor.authorGour, Vinod-
dc.contributor.authorAnand, Ramasamy Vijaya-
dc.date.accessioned2023-08-22T12:03:14Z-
dc.date.available2023-08-22T12:03:14Z-
dc.date.issued2021-
dc.identifier.citationTetrahedron, 82, 131950.en_US
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0040402021000417?via%3Dihub-
dc.identifier.urihttp://hdl.handle.net/123456789/5035-
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractA one-pot approach has been developed for the synthesis of 2,3-disubstituted indoles through a base-mediated N-alkylation of 2-(tosylamino)aryl-substitued para-quinone methides with halomethylaryl ketones followed by intramolecular cyclization and tosyl group elimination sequence. This one-pot protocol provides direct access to a wide range of 2,3-disubstituted indoles in moderate to good yields under mild conditions.en_US
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.subjectIndolesen_US
dc.subjectHeterocyclesen_US
dc.titleBase-mediated sequential one-pot approach for the synthesis of 2,3-disubstituted indoles from 2-(tosylamino)aryl-substituted para-quinone methidesen_US
dc.typeArticleen_US
Appears in Collections:Research Articles

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