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Published on: April 1, 2013
Syntheses of C2'-Fluorinated Analogs of Solamin
Naoto Kojima1, Hiromi Hayashi2, Hiroki Iwasaki1
1Kyoto Pharmaceutical University.
Abstract:
The details of the total syntheses of C2'-fluorinated analogs of solamin, an antitumor annonaceous acetogenin, are described. Fluorine was enantioselectively introduced at the C2'-position by organocatalytic α-fluorination of the aldehyde according to a previously reported method. C2'-fluorinated solamin and its C2'-diastereomer were synthesized by the Sonogashira coupling of a tetrahydrofuran fragment and fluorine-containing γ-lactone fragments.
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