Isoindolinones via Copper-Catalyzed Intramolecular Benzylic C-H Sulfamidation
Robin B. Bedford* , John G. Bowen and Carolina Méndez-Gálvez
*School of Chemistry, University of Bristol, Bristol BS8 1TS,
U.K.,
Email: r.bedford
bristol.ac.uk
R. B. Bedford, J. G. Bowen, C. Méndez-Gálvez, J. Org. Chem., 2017, 82, 1719-1725.
DOI: 10.1021/acs.joc.6b02970
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Abstract
2-Benzyl-N-tosylbenzamides and related substrates undergo copper-catalyzed intramolecular benzylic sulfamidation to provide N-arylsuflonyl-1-arylisoindolinones.
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Key Words
ID: J42-Y2017
