Pd(ii)-catalyzed annulation of terminal alkynes with 2-pyridinyl-substituted p-quinone methides: direct access to indolizines

dc.contributor.authorAhmad, Feroz
dc.contributor.authorRanga, Pavit K.
dc.contributor.authorPankhade, Yogesh A.
dc.contributor.authorFatma, Shaheen
dc.contributor.authorGouda, Ashrumochan
dc.contributor.authorAnand, Ramasamy Vijaya
dc.date.accessioned2023-08-21T14:27:14Z
dc.date.available2023-08-21T14:27:14Z
dc.date.issued2022
dc.descriptionOnly IISER Mohali authors are available in the record.en_US
dc.description.abstractA Pd-catalyzed direct method has been developed to access 1,3-disubstituted indolizines. This reaction proceeds through a regiospecific annulation of terminal alkynes with 2-pyridinyl-substituted p-quinone methides and, in most of the cases, the desired 1,3-disubstituted indolizines were obtained in moderate to good isolated yields. The control experiments suggested that the reaction does proceed through a substrate-controlled regiospecific formal [3 + 2]-annulation pathway.en_US
dc.identifier.citationChemical Communications, 58(95), 13238-13241.en_US
dc.identifier.urihttps://doi.org/10.1039/d2cc04395e
dc.identifier.urihttp://hdl.handle.net/123456789/4986
dc.language.isoen_USen_US
dc.publisherRoyal Society of Chemistryen_US
dc.subjectPd(ii)-catalyzed annulationen_US
dc.subjectterminal alkynesen_US
dc.subject2-pyridinyl-substituted p-quinone methidesen_US
dc.titlePd(ii)-catalyzed annulation of terminal alkynes with 2-pyridinyl-substituted p-quinone methides: direct access to indolizinesen_US
dc.typeArticleen_US

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