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  • Title: Total synthesis of buergerinin F via effective construction of the asymmetric quaternary carbons using an enantioselective aldol reaction.
    Author: Shiina I, Kawakita Y, Ibuka R, Yokoyama K, Yamai YS.
    Journal: Chem Commun (Camb); 2005 Aug 28; (32):4062-4. PubMed ID: 16091800.
    Abstract:
    An efficient method for the synthesis of (+)-buergerinin F is established via the enantioselective aldol reaction of a tetra-substituted ketene silyl acetal with crotonaldehyde, followed by intramolecular Wacker-type ketalization.
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