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- W2949628168 abstract "The tedanolide and myriaporone classes of natural products represent interesting targets for synthesis because of their structural similarity and biological activity. The asymmetric preparation of a potential common intermediate in the total synthesis of each of these targets is presented. The key step, a Zr-mediated allylation, allows for the efficient preparation of the hydroxypropionate structural unit." @default.
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- W2949628168 date "1998-12-01" @default.
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- W2949628168 title "A divergent approach to the myriaporones and tedanolide: Enantioselective preparation of the common intermediate" @default.
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- W2949628168 doi "https://doi.org/10.1016/s0040-4039(98)02110-8" @default.
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