Stereochemistry of Hydroboration of Methylenecyclohexanes

J. Klein, D. Lichtenberg

    Research output: Contribution to journalArticlepeer-review

    43 Scopus citations

    Abstract

    Hydroboration of 3- and 4-methyl- and 3- and 4-t-butylmethylenecyelohexanes yielded, after oxidation, predominantly the axial-equatorial disubstituted cyclohexanes. Similar results were obtained when dichloroborane was used as the hydroborating agent. Dicyclohexylborane gave equal amounts of axial and equatorial products.

    Original languageEnglish
    Pages (from-to)2654-2656
    Number of pages3
    JournalJournal of Organic Chemistry
    Volume35
    Issue number8
    DOIs
    StatePublished - 1 Aug 1970

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