Copper-Catalyzed C(sp3)? Functionalization and Annulation of 2-Bromoaryl Oximes with Active Methylene Compounds towards Synthesis of Isoquinoline N-Oxides

dc.contributor.authorPatel, Chandresh K.
dc.contributor.authorGujjarappa, Raghuram
dc.contributor.authorKant, Kamal
dc.contributor.authorGhanta, Susanta
dc.contributor.authorSingh, Virender
dc.contributor.authorKabi, Arup K.
dc.contributor.authorAl-Zaqri, Nabil
dc.contributor.authorMalakar, Chandi C.
dc.date.accessioned2024-01-21T10:33:08Z
dc.date.accessioned2024-08-13T11:16:20Z
dc.date.available2024-01-21T10:33:08Z
dc.date.available2024-08-13T11:16:20Z
dc.date.issued2023-06-09T00:00:00
dc.description.abstractThe established process proceeds through copper (II)-catalyzed C(sp3)? functionalization of ?-diketones/?-ketoesters with 2-bromobenzaldehyde oximes followed by the intramolecular cyclization of in situ generated acylated intermediates to deliver isoquinoline N-oxides. The copper(II) acetate catalyzed C?H functionalization showed maximum efficacy at 60 �C in methanol/toluene as solvent. The described reaction conditions were applicable over a wide range of substrates with a variety of functional groups to yield isoquinoline N-oxides in yields up to 85%. The developed approach was further elucidated by means of control experiments and DFT calculations. � 2023 Wiley-VCH GmbH.en_US
dc.identifier.doi10.1002/adsc.202300217
dc.identifier.issn16154150
dc.identifier.urihttps://kr.cup.edu.in/handle/32116/3277
dc.identifier.urlhttps://onlinelibrary.wiley.com/doi/10.1002/adsc.202300217
dc.language.isoen_USen_US
dc.publisherJohn Wiley and Sons Incen_US
dc.subjectActive methylene compoundsen_US
dc.subjectC(sp<sup>3</sup>)? activationen_US
dc.subjectCopper catalysisen_US
dc.subjectIsoquinoline N-oxideen_US
dc.subjecttrans-esterificationen_US
dc.titleCopper-Catalyzed C(sp3)? Functionalization and Annulation of 2-Bromoaryl Oximes with Active Methylene Compounds towards Synthesis of Isoquinoline N-Oxidesen_US
dc.title.journalAdvanced Synthesis and Catalysisen_US
dc.typeArticleen_US
dc.type.accesstypeClosed Accessen_US

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