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Issue 12, 1996
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Reductive cyclization of γ,δ-unsaturated selenothioic acid S-esters leading to tetrahydroselenophenes

Abstract

Reductive cyclization of γ,δ-unsaturated selenothioic acid S-esters with NaBH4 or LiAlH4 proceeds viaδ,ε-unsaturated selenols to afford tetrahydroselenophenes in good to high yields.

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Article type: Paper
DOI: 10.1039/CC9960001461
Chem. Commun., 1996, 1461-1462

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    Reductive cyclization of γ,δ-unsaturated selenothioic acid S-esters leading to tetrahydroselenophenes

    T. Murai, M. Maeda, F. Matsuoka, T. Kanda and S. Kato, Chem. Commun., 1996, 1461
    DOI: 10.1039/CC9960001461

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