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Issue 36, 2008
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Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons

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Abstract

Benzylic and allylic hydrocarbons are selectively converted to the corresponding sulfonamides by a ZnBr2–H2O-catalyzed reaction with PhI[double bond, length as m-dash]NTs; saturated adamantane is aminosulfonated at the tertiary C–H bond.

Graphical abstract: Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons

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Publication details

The article was received on 08 Apr 2008, accepted on 16 Jun 2008 and first published on 05 Aug 2008


Article type: Communication
DOI: 10.1039/B805783D
Citation: Chem. Commun., 2008,0, 4291-4293

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    Hydrous zinc halide-catalyzed aminosulfonation of hydrocarbons

    B. Kalita, A. A. Lamar and K. M. Nicholas, Chem. Commun., 2008, 0, 4291
    DOI: 10.1039/B805783D

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