New stereoselective routes from alcohols to secondary alkyl bromides with retention of configuration

M. Sevrin, A. Krief

    Research output: Contribution to journalArticlepeer-review

    Abstract

    Secondary alcohols can be converted into the corresponding bromides with high stereoselective retention of configuration; this two-step process proceeds by a double inversion involving the intermediate selenides.
    Original languageEnglish
    Pages (from-to)656-657
    Number of pages2
    JournalJournal of the Chemical Society, Chemical Communications
    Issue number14
    Publication statusPublished - 1 Jan 1980

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