• Media type: E-Article
  • Title: Total Synthesis of Blennolide Mycotoxins: Design, Synthetic Routes and Completion
  • Contributor: Meister, Anne C.; Encinas, Arantxa; Sahin, Hülya; Singer, Emilie M. C.; Nising, Carl F.; Nieger, Martin; Bräse, Stefan
  • imprint: Wiley, 2014
  • Published in: European Journal of Organic Chemistry
  • Language: English
  • DOI: 10.1002/ejoc.201402083
  • ISSN: 1434-193X; 1099-0690
  • Keywords: Organic Chemistry ; Physical and Theoretical Chemistry
  • Origination:
  • Footnote:
  • Description: <jats:title>Abstract</jats:title><jats:p>Mycotoxins of the tetrahydroxanthone class of natural products possess a large number of interesting biological properties. In this full paper, we present our synthetic strategy to some members of this class of compounds, namely the blennolides A and C. We disclose the scope and limitations of the functionalization of various xanthones derived from a domino oxa‐Michael‐aldol condensation and pursue dimerization of these xanthones. Furthermore, the first crystal structure of blennolide C has been obtained.</jats:p>