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Issue 7, 2018
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Cp2TiCl2-catalyzed highly regioselective hydroamination of styrenes with hydroxylamines

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Abstract

A Cp2TiCl2-catalyzed highly regioselective hydroamination of styrene derivatives with O-benzoylhydroxylamines in the presence of isopropylmagnesium chloride to afford α-branched tertiary alkylamines in high yields has been described.

Graphical abstract: Cp2TiCl2-catalyzed highly regioselective hydroamination of styrenes with hydroxylamines

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Publication details

The article was received on 29 Nov 2017, accepted on 29 Jan 2018 and first published on 30 Jan 2018


Article type: Research Article
DOI: 10.1039/C7QO01068K
Citation: Org. Chem. Front., 2018,5, 1184-1187
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    Cp2TiCl2-catalyzed highly regioselective hydroamination of styrenes with hydroxylamines

    X. Luo, S. Wang and C. Xi, Org. Chem. Front., 2018, 5, 1184
    DOI: 10.1039/C7QO01068K

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