Total synthesis of natural products having 1,3- -polyol, δ-lactone of (2 ,5 ,7 ,9 ,11 )-tetrahydroxyhexacos-2-enoic acid and 4,6,8,10,12,14,16,18,20-all- -nonamethoxy-1-pentacosene

This publication has 7 references indexed in Scilit:

• Stereoselective reduction of β-alkoxy ketones: a synthesis of syn-1,3-diols
  Tetrahedron Letters, 1988
• Determination of stereostructure of naturally occurring α, β-unsaturated δ-lactone derivatives through a stereoselective synthesis
  Tetrahedron Letters, 1987
• An introduction of chiral centers into acyclic systems based on stereoselective ketone reduction
  Accounts of Chemical Research, 1984
• Asymmetric carbon-carbon bond formation via .beta.-allyldiisopinocampheylborane. Simple synthesis of secondary homoallylic alcohols with excellent enantiomeric purities
  Journal of the American Chemical Society, 1983
• Direct synthesis of Z-unsaturated esters. A useful modification of the horner-emmons olefination.
  Tetrahedron Letters, 1983
• Isotactic polymethoxy-1-alkenes from the blue-green alga Tolypothrix conglutinata var. Chlorata
  Phytochemistry, 1979
• δ-Lactones of polyhydroxy-C26 acids in Eupatorium pilosum
  Phytochemistry, 1978