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Issue 2, 2014
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Aerobic oxidative C–B bond cleavage of arylboronic acids mediated by methylhydrazines

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Abstract

The aerobic oxidative C–B bond cleavage and ipso-hydroxylation of arylboronic acids mediated by methylhydrazine have been developed under metal-free conditions. This transformation affords structurally diverse phenols in good to excellent yields (26 examples, 71–99%).

Graphical abstract: Aerobic oxidative C–B bond cleavage of arylboronic acids mediated by methylhydrazines

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Publication details

The article was received on 05 Nov 2013, accepted on 24 Dec 2013 and first published on 27 Jan 2014


Article type: Research Article
DOI: 10.1039/C3QO00026E
Citation: Org. Chem. Front., 2014,1, 151-154
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    Aerobic oxidative C–B bond cleavage of arylboronic acids mediated by methylhydrazines

    W. Ding, J. Chen, Y. Zou, S. Duan, L. Lu and W. Xiao, Org. Chem. Front., 2014, 1, 151
    DOI: 10.1039/C3QO00026E

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