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Issue 4, 2009
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Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions

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Abstract

The highly regioselective, stereospecific ring-opening of trisubstituted N-tosylaziridines possessing vinyl and hydroxymethyl groups by sulfone- and sulfide-stablised carbanions is reported.

Graphical abstract: Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions

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Publication details

The article was received on 12 Sep 2008, accepted on 28 Oct 2008 and first published on 26 Nov 2008


Article type: Communication
DOI: 10.1039/B815971H
Citation: Chem. Commun., 2009,0, 451-453

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    Highly regioselective ring-opening of trisubstituted aziridines by sulfur-stabilised carbanions

    S. Carballares, D. Craig, C. J. T. Hyland, P. Lu, T. Mathie and A. J. P. White, Chem. Commun., 2009, 0, 451
    DOI: 10.1039/B815971H

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