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Issue 11, 1993
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Organoselenium-induced cyclization of γ,δ-alkenimine to nitrogen heterocycles

Abstract

γ,δ-Alkenimines undergo electrophile-induced cyclization by means of phenylselenenyl bromide to produce cyclic iminium salts which are reduced to functionalized pyrrolidines or piperidines.

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Article type: Paper
DOI: 10.1039/C39930000916
Citation: J. Chem. Soc., Chem. Commun., 1993, 916-918
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    Organoselenium-induced cyclization of γ,δ-alkenimine to nitrogen heterocycles

    N. De Kimpe and M. Boelens, J. Chem. Soc., Chem. Commun., 1993, 916
    DOI: 10.1039/C39930000916

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