Synthesis of the optical antipodes of 4‐alkyl‐γ‐lactones

This publication has 20 references indexed in Scilit:

• Asymmetric synthesis of five- and six-membered lactones from chiral sulfoxides: application to the asymmetric synthesis of insect pheromones, (R)-(+)-.delta.-n-hexadecanolactone and (R)-(+)-.gamma.-n-dodecanolactone
  The Journal of Organic Chemistry, 1982
• A greatly improved procedure for ruthenium tetroxide catalyzed oxidations of organic compounds
  The Journal of Organic Chemistry, 1981
• Preparation d'alkyl-4 γ-lactones optiquement actives
  Tetrahedron Letters, 1980
• The first practical method for asymmetric epoxidation
  Journal of the American Chemical Society, 1980
• Broad-spectrum synthesis of enantiomerically pure lactones. 1. Synthesis of sex pheromones of the carpenter bee, rove beetle, Japanese beetle, black-tailed deer, and Oriental hornet
  The Journal of Organic Chemistry, 1979
• Photo-induced rearrangements of α,β-epoxy diazomethyl ketones
  Tetrahedron Letters, 1975
• Rearrangement and cyclization reactions of α,β-epoxy diazomethyl ketones catalyzed by boron trifluorioe
  Tetrahedron Letters, 1975
• Catalytic reduction. III. Hydrogenation of unsaturated compounds over borohydride reduced palladium
  The Journal of Organic Chemistry, 1974
• Reduction of unsaturated compounds containing oxygen
  The Journal of Organic Chemistry, 1971
• Synthesis of Optically Active γ- and δ-Lactones by Microbiological Reduction
  Nature, 1962