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 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.

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Bibliographic Details
Main Authors: Dias,Luiz C., Sant'Ana,Danilo P., Vieira,Ygor W., Gonçalves,Caroline C. S., Lima,Dimas J. P.
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2012
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000200022
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