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Iterative Polyketide Synthesis via a Consecutive Carbonyl-Protecting Strategy
1Institute of Industrial Science , The University of Tokyo , 4-6-1 Komaba, Meguro-ku , Tokyo 153-8505 , Japan.
Abstract:
To address the difficulty in protecting a β-polycarbonyl compound, a method for the sequential protection of elongating carbonyl groups was demonstrated. The iterative chain elongation of a carboxylic acid with malonic acid half thioester followed by the protection of the resulting β-ketothioester was performed via the stepwise formation of an isoxazole ring using an O-protected oxime functionality. Yangonin and isosakuranetin were synthesized according to this procedure.
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