• Media type: E-Article
  • Title: Asymmetric total synthesis of smyrindiol employing an organocatalytic aldol key step
  • Contributor: Enders, Dieter; Fronert, Jeanne; Bisschops, Tom; Boeck, Florian
  • Published: Beilstein Institut, 2012
  • Published in: Beilstein Journal of Organic Chemistry, 8 (2012), Seite 1112-1117
  • Language: English
  • DOI: 10.3762/bjoc.8.123
  • ISSN: 1860-5397
  • Keywords: Organic Chemistry
  • Origination:
  • Footnote:
  • Description: The first organocatalytic asymmetric synthesis of smyrindiol, by using an (S)-proline catalyzed enantioselective intramolecular aldol reaction as the key step, is described. Smyrindiol was synthesized from commercially available 2,4-dihydroxybenzaldehyde in 15 steps, with excellent stereoselectivity (de = 99%, ee = 99%). In the course of this total synthesis a new and mild coumarin assembly was developed.
  • Access State: Open Access