Combining Two-Directional Synthesis and Tandem Reactions, Part 8: A Novel Condensation/Michael Addition/Cycloaddition/Fragmentation/Lactamisation Cascade

Alex Sinclair, Louise Arini, Martin Rejzek, Peter Szeto, Robert Stockman

    Research output: Contribution to journalArticlepeer-review

    Abstract

    A tandem oxime formation/Michael addition/1,4-prototopic shift/[3+2]-cycloaddition of an acyclic symmetrical precursor results in a tricyclic isooxazolidine which then undergoes a further fragmentation/lactamisation cascade to generate a non-symmetrical tricyclic a-ketolactam as a single diastereomer
    Original languageEnglish
    Pages (from-to)2321-2324
    JournalSynlett
    Volume2006
    Issue number14
    DOIs
    Publication statusPublished - Sept 2006

    Keywords

    • Chemistry

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