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On the Stereochemistry of Vincetene

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Summary.

 The absolute configuration of the centre of asymmetry in the side chain of the alkaloid vincetene (1) was determined by ozonolysis and subsequent unequivocal transformations affording the (S)-enantiomer of 1,2-propanediyl dibenzoate (4).

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Authors and Affiliations

  1.  Institute of Pharmacy, University of Regensburg, D-93040 Regensburg, Germany, , , , , , DE

    David Jirovsky, Andreas Sellmer, Pierre Guiswe & Wolfgang Wiegrebe

  2.  Department of Analytical Chemistry, Palacky University, CZ-77146 Olomouc, Czech Republic, , , , , , CZ

    Karel Lemr

Authors
  1. David Jirovsky
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  2. Andreas Sellmer
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  3. Pierre Guiswe
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  4. Karel Lemr
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  5. Wolfgang Wiegrebe
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Additional information

Received February 22, 2001. Accepted March 1, 2001

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Jirovsky, D., Sellmer, A., Guiswe, P. et al. On the Stereochemistry of Vincetene. Monatshefte fuer Chemie 132, 765–768 (2001). https://doi.org/10.1007/s007060170092

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  • DOI: https://doi.org/10.1007/s007060170092

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