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dc.contributor.authorNykaza, Trevor Vincent
dc.contributor.authorCooper, Julian Colton
dc.contributor.authorLi, Gen
dc.contributor.authorMahieu, Nolwenn
dc.contributor.authorRamirez, Antonio
dc.contributor.authorLuzung, Michael R.
dc.contributor.authorRadosevich, Alexander T.
dc.date.accessioned2020-01-24T15:44:55Z
dc.date.available2020-01-24T15:44:55Z
dc.date.issued2018-10-29
dc.date.submitted2018-10-06
dc.identifier.issn0002-7863
dc.identifier.issn1520-5126
dc.identifier.urihttps://hdl.handle.net/1721.1/123674
dc.description.abstractA main group-catalyzed method for the synthesis of aryl- and heteroarylamines by intermolecular C-N coupling is reported. The method employs a small-ring organophosphorus-based catalyst (1,2,2,3,4,4-hexamethylphosphetane) and a terminal hydrosilane reductant (phenylsilane) to drive reductive intermolecular coupling of nitro(hetero)arenes with boronic acids. Applications to the construction of both C[subscript sp2]-N (from arylboronic acids) and C[subscript sp3]–N bonds (from alkylboronic acids) are demonstrated; the reaction is stereospecific with respect to C[subscript sp3]-N bond formation. The method constitutes a new route from readily available building blocks to valuable nitrogen-containing products with complementarity in both scope and chemoselectivity to existing catalytic C-N coupling methods. Keywords: functionalization; catalysts; coupling reactions; chemical reactions; cyclizationen_US
dc.language.isoen
dc.publisherAmerican Chemical Society (ACS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1021/jacs.8b10769en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePMCen_US
dc.titleIntermolecular Reductive C–N Cross Coupling of Nitroarenes and Boronic Acids by P[superscript III]/P[superscript V]═O Catalysisen_US
dc.typeArticleen_US
dc.identifier.citationNykaza, Trevor V. et al. "Intermolecular Reductive C–N Cross Coupling of Nitroarenes and Boronic Acids by P[superscript III]/P[superscript V]═O Catalysis." Journal of the American Chemical Society 140, 45 (2018): 15200-15205 © 2018 American Chemical Societyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Chemistryen_US
dc.relation.journalJournal of the American Chemical Societyen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2020-01-06T17:31:57Z
dspace.date.submission2020-01-06T17:32:00Z
mit.journal.volume140en_US
mit.journal.issue45en_US
mit.metadata.statusComplete


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