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Please use this identifier to cite or link to this item: http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19068
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dc.contributor.authorKumar, Anil-
dc.date.accessioned2025-07-24T06:19:06Z-
dc.date.available2025-07-24T06:19:06Z-
dc.date.issued2024-11-
dc.identifier.urihttps://aces.onlinelibrary.wiley.com/doi/full/10.1002/asia.202401104-
dc.identifier.urihttp://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/19068-
dc.description.abstractA ruthenium(II)-catalyzed direct C−H/C−H (4+2) annulation of 2-aryl-N-heterocycles such as 2-aryl-4H-pyrido[1,2-a]pyrimidin-4-ones, 2-arylimidazo[1,2-a]pyridines, 2-aryl-2H-indazoles and 2-arylquinolin-4(1H)-ones with vinylene carbonate has been described. This one-pot cascade strategy provided the diversely substituted fused-polyheterocycles such as 7H-benzo[h]pyrido[2,1-b]quinazolin-7-ones, naphtho[1′,2′:4,5]imidazo[1,2-a]pyridines, indazolo[2,3-a]quinolines and benzo[c]acridin-7(12H)-ones in moderate to excellent yields. The developed protocol exhibited a broad substrate scope with good functional group tolerance and acid/base-free conditions. Based on a preliminary mechanistic investigation, a tentative mechanism of Ru(II)-catalyzed (4+2) annulation reaction has been proposed.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectChemistryen_US
dc.subjectRuthenium(II) catalysisen_US
dc.subjectC–H/C–H annulationen_US
dc.subjectVinylene carbonateen_US
dc.titleRuthenium(ii)-catalyzed C−H/C−H(4+2) annulation of 2-aryl-N-heterocycles with vinylene carbonateen_US
dc.typeArticleen_US
Appears in Collections:Department of Chemistry

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