Total Synthesis of (+)-18-epi-Latrunculol A: Development of a Synthetic Route

نویسندگان

  • Brett D. Williams
  • Amos B. Smith
چکیده

The evolution of an enantioselective total synthesis of (+)-18-epi-latrunculol A, a congener of the marine-sponge-derived latrunculins A and B, is reported. Key steps include a late-stage Mitsunobu macrolactonization to construct the 16-membered macrolactone, a mild Carreira alkynylation to unite the northern and southern hemispheres, a diastereoselective, acid-mediated δ-hydroxy enone cyclization/equilibration sequence, and a functional-group-tolerant cross-metathesis to access the enone cyclization precursor.

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Total synthesis of (+)-18-epi-latrunculol A.

An enantioselective total synthesis of the cytotoxic latrunculin congener (+)-18-epi-latrunculol A has been achieved. Key steps in the synthetic route include an acid-mediated enone cyclization/equilibration sequence, a Carreira alkynylation, and a late-stage Mitsunobu macrolactonization to construct the macrolide skeleton.

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عنوان ژورنال:

دوره 79  شماره 

صفحات  -

تاریخ انتشار 2014