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Synthesis 1997; 1997(8): 953-956
DOI: 10.1055/s-1997-1279
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Allylic Hydroxylation of Vinyl Fluorides

Thomas Ernet, Günter Haufe*
  • *Organisch-Chemisches Institut, Universität Münster, Corrensstraße 40, D-48149 Münster, Germany, Fax +49(251)8339772; E-mail: haufe@uni-muenster.de
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Publication History

Publication Date:
31 December 2000 (online)

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Terminal and non-terminal vinyl fluorides have been hydroxylated regioselectively in the allylic position adjacent to the fluorine bearing carbon using selenium dioxide and tert-butyl hydroperoxide.

Terminal and non-terminal vinyl fluorides have been hydroxylated regioselectively in the allylic position adjacent to the fluorine bearing carbon using selenium dioxide and tert-butyl hydroperoxide