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Issue 2, 1994
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N-hydroxy γ-lactams or cyclic N-hydroxy imidates from the organoselenium-induced cyclization of β,γ-unsaturated hydroxamic acids

Abstract

The organoselenium-induced ring-closure reactions of γ-substituted β, γ-unsaturated hydroxamic acids afforded cyclic phenylseleno N-hydroxy imidates or phenylseleno N-hydroxy γ-lactams as the kinetically or thermodynamically controlled products, respectively.

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Article type: Paper
DOI: 10.1039/C39940000221
Citation: J. Chem. Soc., Chem. Commun., 1994, 221-222
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    N-hydroxy γ-lactams or cyclic N-hydroxy imidates from the organoselenium-induced cyclization of β,γ-unsaturated hydroxamic acids

    M. Tiecco, L. Testaferri, M. Tingoli and F. Marini, J. Chem. Soc., Chem. Commun., 1994, 221
    DOI: 10.1039/C39940000221

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