Synthesis of the C1-C9 fragment of the potent antitumor agent dictyostatin
We describe herein a short and efficient synthesis of the C1-C9 fragment of the potent antitumor agent dictyostatin. Notable features of this approach include a Sharpless asymmetric epoxidation followed by epoxide opening under Myashita's conditions to introduce the stereogenic centers at C6 an...
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Veröffentlicht in: | Journal of the Brazilian Chemical Society 2012-02, Vol.23 (2), p.344-348 |
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container_title | Journal of the Brazilian Chemical Society |
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creator | Dias, Luiz C. Sant'Ana, Danilo P. Vieira, Ygor W. Gonçalves, Caroline C. S. Lima, Dimas J. P. |
description | We describe herein a short and efficient synthesis of the C1-C9 fragment of the potent antitumor agent dictyostatin. Notable features of this approach include a Sharpless asymmetric epoxidation followed by epoxide opening under Myashita's conditions to introduce the stereogenic centers at C6 and C7, and a Horner-Wadsworth-Emmons type reaction under Ando's conditions to construct the Z-double bond of the 1,3-(Z,E)-diene system. |
doi_str_mv | 10.1590/S0103-50532012000200022 |
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title | Synthesis of the C1-C9 fragment of the potent antitumor agent dictyostatin |
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