Beilstein Journal of Organic Chemistry (May 2014)

cis–trans Isomerization of silybins A and B

  • Michaela Novotná,
  • Radek Gažák,
  • David Biedermann,
  • Florent Di Meo,
  • Petr Marhol,
  • Marek Kuzma,
  • Lucie Bednárová,
  • Kateřina Fuksová,
  • Patrick Trouillas,
  • Vladimír Křen

DOI
https://doi.org/10.3762/bjoc.10.105
Journal volume & issue
Vol. 10, no. 1
pp. 1047 – 1063

Abstract

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Methods were developed and optimized for the preparation of the 2,3-cis- and the 10,11-cis-isomers of silybin by the Lewis acid catalyzed (BF3∙OEt2) isomerization of silybins A (1a) and B (1b) (trans-isomers). The absolute configuration of all optically pure compounds was determined by using NMR and comparing their electronic circular dichroism data with model compounds of known absolute configurations. Mechanisms for cis–trans-isomerization of silybin are proposed and supported by quantum mechanical calculations.

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