Asymmetric synthesis of (-)-dihydroxanthatin by the stereoselective Oshima-Utimoto reaction

Org Lett. 2005 Jul 21;7(15):3371-3. doi: 10.1021/ol051276k.

Abstract

[reaction: see text]. The catalytic stereoselective Oshima-Utimoto reaction is useful for the construction of five-membered oxacycles from simple starting materials and was employed for the preparation of the lactone group in the asymmetric synthesis of (-)-11alpha,13-dihydroxanthatin. Completion of the synthesis is facilitated by ring-closing enyne metathesis and alkene cross metathesis reactions.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Catalysis
  • Crystallography, X-Ray
  • Cyclization
  • Furans / chemical synthesis*
  • Furans / chemistry
  • Molecular Conformation
  • Molecular Structure
  • Stereoisomerism

Substances

  • 11,13-dihydroxanthatin
  • Furans