Ring expansion of cyclenones: An unusual regioselectivity

A. Krief, J.L. Laboureur

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Various cyclenones have been homologated by a two-step sequence involving a reaction with α-selenoalkyl-lithium compounds and further reaction of the resulting β-hydroxyselenides with thallium(I) ethoxide in chloroform; an unusually high propensity of the alkyl groups to migrate in place of the vinyl moiety has been observed.
    Original languageEnglish
    Pages (from-to)702-704
    Number of pages3
    JournalJournal of the Chemical Society, Chemical Communications
    Issue number9
    DOIs
    Publication statusPublished - 1 Jan 1986

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