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Chemoselective Primary Amination of Aryl Boronic Acids by PIII/PV═O-Catalysis: Synthetic Capture of the Transient Nef Intermediate HNO : Chemoselective Primary Amination of Aryl Boronic Acids by P-III/P-V=O-Catalysis: Synthetic Capture of the Transient Nef Intermediate HNO

DC Field Value Language
dc.contributor.authorHong, Seung Youn-
dc.contributor.authorRadosevich, Alexander T.-
dc.date.accessioned2023-05-03T07:46:26Z-
dc.date.available2023-05-03T07:46:26Z-
dc.date.created2023-05-02-
dc.date.created2023-05-02-
dc.date.issued2022-05-
dc.identifier.citationJournal of the American Chemical Society, Vol.144 No.20, pp.8902-8907-
dc.identifier.issn0002-7863-
dc.identifier.urihttps://hdl.handle.net/10371/191831-
dc.description.abstractA catalytic approach to intercept the transient HNO for a chemoselective primary amination of arylboronic acids isreported. A phosphetane-based catalyst operating within PIII/PV???O redox cycling is shown to capture HNO, generated in situ byNef decomposition of 2-nitropropane, to selectively install the primary amino group at aryl Csp2centers. The method furnishesversatile primary arylamines from arylboronic acid substrates with the preservation of otherwise reactive functional groups-
dc.language영어-
dc.publisherAmerican Chemical Society-
dc.titleChemoselective Primary Amination of Aryl Boronic Acids by PIII/PV═O-Catalysis: Synthetic Capture of the Transient Nef Intermediate HNO-
dc.title.alternativeChemoselective Primary Amination of Aryl Boronic Acids by P-III/P-V=O-Catalysis: Synthetic Capture of the Transient Nef Intermediate HNO-
dc.typeArticle-
dc.identifier.doi10.1021/jacs.2c02922-
dc.citation.journaltitleJournal of the American Chemical Society-
dc.identifier.wosid000805981500005-
dc.identifier.scopusid2-s2.0-85131018318-
dc.citation.endpage8907-
dc.citation.number20-
dc.citation.startpage8902-
dc.citation.volume144-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorHong, Seung Youn-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.subject.keywordPlusAMMONIA EQUIVALENT-
dc.subject.keywordPlusPRIMARY ANILINES-
dc.subject.keywordPlusNITROXYL HNO-
dc.subject.keywordPlusHALIDES-
dc.subject.keywordPlusCHEMISTRY-
dc.subject.keywordPlusCHLORIDES-
dc.subject.keywordPlusAMINES-
dc.subject.keywordPlusALKYL-
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Inorganic Chemistry, Computational Modeling, Molecular Catalysis, Organic Synthesis, 무기화학, 전산모델링, 분자촉매, 유기합성

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