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Copper-catalyzed aminooxygenation of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives.

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.

SUBMITTER: Li Y

PROVIDER: S-EPMC4734344 | biostudies-literature | 2015

REPOSITORIES: biostudies-literature

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Copper-catalyzed aminooxygenation of styrenes with N-fluorobenzenesulfonimide and N-hydroxyphthalimide derivatives.

Li Yan Y Zhou Xue X Zheng Guangfan G Zhang Qian Q

Beilstein journal of organic chemistry 20151224

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. ...[more]

PMID: 26877794

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