Frontispiece: Cyclopenta[b]annulation of Heteroarenes by Organocatalytic γ′[C(sp3)−H] Functionalization of Ynones

dc.contributor.authorRaghu, M.
dc.contributor.authorGrover, J.
dc.contributor.authorRamasastry, S.S.V.
dc.date.accessioned2020-12-01T04:12:58Z
dc.date.available2020-12-01T04:12:58Z
dc.date.issued2016
dc.description.abstractIntramolecular Hydroalkylation Organocatalytic γ’[C(sp3)−H] functionalization of ynones has been achieved for the first time. Nucleophilic addition of an organophosphine to the designed ynones leads to the formation of heteroaryl‐based ortho‐quinodimethane (oQDM) intermediates, which undergo an unusual carbocyclization to provide functionalized cyclopenta‐fused heteroarenes. The present study can have potential implications on the development of new organocatalytic C(sp3)−H‐functionalization pathways.en_US
dc.identifier.citationChemistry - A European Journal, 22(51).en_US
dc.identifier.otherhttps://doi.org/10.1002/chem.201685161
dc.identifier.urihttps://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/chem.201685161
dc.identifier.urihttp://hdl.handle.net/123456789/2390
dc.language.isoenen_US
dc.publisherWiley‐VCH Verlag GmbH & Co. KGaA, Weinheimen_US
dc.subjectCyclopentannulationen_US
dc.subjectHeterocyclesen_US
dc.subjectHydroalkylationen_US
dc.subjectOrganophosphinesen_US
dc.titleFrontispiece: Cyclopenta[b]annulation of Heteroarenes by Organocatalytic γ′[C(sp3)−H] Functionalization of Ynonesen_US
dc.typeArticleen_US

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