4.8 Article

Total Synthesis of the Cyanolide A Aglycon

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JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 133, 期 25, 页码 9727-9729

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AMER CHEMICAL SOC
DOI: 10.1021/ja204228q

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  1. National Institute of General Medical Sciences [GM-43854]
  2. Lilly Graduate Research Fellowship

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The synthesis of the potent molluscicide cyanolide A has been achieved in 10 steps without the use of protecting groups. The synthesis features a key Sakurai macrocyclization/dimerization reaction that simultaneously forms both tetrahydropyran rings and the macrocycle of the natural product.

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