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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

Cited 16 time in Web of Science Cited 16 time in Scopus
Authors

Hong, Seung Youn; Radosevich, Alexander T.

Issue Date
2022-05
Publisher
American Chemical Society
Citation
Journal of the American Chemical Society, Vol.144 No.20, pp.8902-8907
Abstract
A 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
ISSN
0002-7863
URI
https://hdl.handle.net/10371/191831
DOI
https://doi.org/10.1021/jacs.2c02922
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  • College of Natural Sciences
  • Department of Chemistry
Research Area Inorganic Chemistry, Computational Modeling, Molecular Catalysis, Organic Synthesis

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