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Formation of the Tertiary Sulfonamide C(sp(3))-N Bond Using Alkyl Boronic Ester via Intramolecular and Intermolecular Copper-Catalyzed Oxidative Cross-Coupling

DC Field Value Language
dc.contributor.authorKim, Dong Sun-
dc.contributor.authorLee, Hong Geun-
dc.date.accessioned2022-05-04T01:45:43Z-
dc.date.available2022-05-04T01:45:43Z-
dc.date.created2022-03-08-
dc.date.issued2021-12-
dc.identifier.citationJournal of Organic Chemistry, Vol.86 No.23, pp.17380-17394-
dc.identifier.issn0022-3263-
dc.identifier.urihttps://hdl.handle.net/10371/179381-
dc.description.abstractA synthetic strategy for the formation of C(sp(3))-N bonds, particularly through a copper-catalyzed oxidative cross-coupling, is rare. Herein, we report a novel synthetic approach for the preparation of tertiary sulfonamides via copper-catalyzed intra-and intermolecular oxidative C(sp(3))-N cross-coupling reactions. This method allows the utilization of the readily available C(sp(3))-based pinacol boronate as a substrate and the tolerance of a wide range of functional groups under mild reaction conditions. The success of this strategy relies on the unprecedented additive effects of silanol and NaIO4 .-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleFormation of the Tertiary Sulfonamide C(sp(3))-N Bond Using Alkyl Boronic Ester via Intramolecular and Intermolecular Copper-Catalyzed Oxidative Cross-Coupling-
dc.typeArticle-
dc.identifier.doi10.1021/acs.joc.1c01759-
dc.citation.journaltitleJournal of Organic Chemistry-
dc.identifier.wosid000752848600099-
dc.identifier.scopusid2-s2.0-85119409484-
dc.citation.endpage17394-
dc.citation.number23-
dc.citation.startpage17380-
dc.citation.volume86-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorLee, Hong Geun-
dc.type.docTypeArticle-
dc.description.journalClass1-
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