18 research outputs found

    THE TOTAL SYNTHESIS OF (+,-)-JATROPHONE (+,-)-EPI-JATROPHONE AND NORMETHYLJATROPHONE.

    No full text
    Abstract Not Available

    THE TOTAL SYNTHESIS OF (+,-)-JATROPHONE (+,-)-EPI-JATROPHONE AND NORMETHYLJATROPHONE.

    No full text
    Abstract Not Available

    Asymmetric Synthesis and Absolute Configuration of Streptophenazine G

    No full text
    The asymmetric synthesis of the antibacterial natural product, streptophenazine G, has been achieved by employing asymmetric alkylation and asymmetric aldol reactions using chiral oxazolidinones as the key steps. The originally proposed structure for streptophenazine G has been revised, and its absolute configuration has been determined to be 1′<i>S</i>,2′<i>R</i>,6′<i>S</i>. The asymmetric total synthesis of 6′-<i>epi</i>-streptophenazine G is also described
    corecore