Decarboxylative 1-aza-1′-oxa [3,3]sigmatropic rearrangements of enolizable or enolized N-aryl-N,O-diacylhydroxylamines to o-(N-acylamino)aryl ketones, esters, and amides: A new synthetic method for ortho alkylation [13]

Robert M. Coates, Ikram Md Said

    Research output: Contribution to journalArticle

    37 Citations (Scopus)
    Original languageEnglish
    Pages (from-to)2355-2357
    Number of pages3
    JournalJournal of the American Chemical Society
    Volume99
    Issue number7
    Publication statusPublished - 1977

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    Carboxy-Lyases
    Alkylation
    Ketones
    Amides
    Esters

    ASJC Scopus subject areas

    • Chemistry(all)

    Cite this

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    title = "Decarboxylative 1-aza-1′-oxa [3,3]sigmatropic rearrangements of enolizable or enolized N-aryl-N,O-diacylhydroxylamines to o-(N-acylamino)aryl ketones, esters, and amides: A new synthetic method for ortho alkylation [13]",
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    year = "1977",
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    journal = "Journal of the American Chemical Society",
    issn = "0002-7863",
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    T2 - A new synthetic method for ortho alkylation [13]

    AU - Coates, Robert M.

    AU - Said, Ikram Md

    PY - 1977

    Y1 - 1977

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