Abstract
A copper-catalyzed aminooxygenation reaction of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives has been developed. The aminooxygenation product could be converted into the corresponding alcohol or free amine through the cleavage of the N-O or C-N bond of the N-hydroxyphthalimide moiety.
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Li, Y., Zhou, X., Zheng, G., & Zhang, Q. (2015). Copper-catalyzed aminooxygenation of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives. Beilstein Journal of Organic Chemistry, 11, 2721–2726. https://doi.org/10.3762/bjoc.11.293
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