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Please use this identifier to cite or link to this item: http://10.10.120.238:8080/xmlui/handle/123456789/777
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dc.contributor.authorSharma A.en_US
dc.contributor.authorKour H.en_US
dc.contributor.authorKour J.en_US
dc.contributor.authorKamal N.en_US
dc.contributor.authorSawant S.D.en_US
dc.date.accessioned2023-11-30T08:49:28Z-
dc.date.available2023-11-30T08:49:28Z-
dc.date.issued2022-
dc.identifier.issn1359-7345-
dc.identifier.otherEID(2-s2.0-85139378809)-
dc.identifier.urihttps://dx.doi.org/10.1039/d2cc03319d-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/777-
dc.description.abstractA catalytic oxidative addition of sulfoximines to naphthoquinones via C-H functionalization has been achieved using an iron catalytic system, which exhibits good reactivity and high regioselectivity in the presence of visible light. This is the first report offering an efficient protocol for obtaining (naphtho)quinone-sulfoximine hybrid analogs in moderate to good yields with wide scope for both the substrates. This protocol has also been applied on natural products for their modification, including vitamin K3, Juglone and some other modified natural scaffolds as well. © 2022 The Royal Society of Chemistry.en_US
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.sourceChemical Communicationsen_US
dc.titleVisible-light-promoted iron-catalyzed C-H functionalization of 1,4-naphthoquinones via oxidative coupling with sulfoximinesen_US
dc.typeJournal Articleen_US
Appears in Collections:Journal Article

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