| Literature DB >> 30372615 |
Trevor V Nykaza1, Julian C Cooper1, Gen Li1, Nolwenn Mahieu1, Antonio Ramirez2, Michael R Luzung2, Alexander T Radosevich1.
Abstract
A 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 Csp2-N (from arylboronic acids) and Csp3-N bonds (from alkylboronic acids) are demonstrated; the reaction is stereospecific with respect to Csp3-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.Entities:
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Year: 2018 PMID: 30372615 PMCID: PMC6235741 DOI: 10.1021/jacs.8b10769
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419