Lipase-catalyzed kinetic resolution of methyl 4-hydroxy-5-tetradecynoate and its application to a facile synthesis of japanese beetle pheromone

This publication has 14 references indexed in Scilit:

• Preparation of Enantiomerically Enriched Compounds Using Enzymes; VII.¹A Synthesis of Japanese Beetle Pheromone Utilizing Lipase-Catalyzed Enantioselective Lactonization
  Synthesis, 1990
• Anhydrides as acylating agents in lipase-catalyzed stereoselective esterification of racemic alcohols
  The Journal of Organic Chemistry, 1988
• Lipase-catalyzed irreversible transesterifications using enol esters as acylating reagents: preparative enantio- and regioselective syntheses of alcohols, glycerol derivatives, sugars and organometallics
  Journal of the American Chemical Society, 1988
• Lipase catalyzed synthesis of macrocyclic lactones in organic solvents
  Tetrahedron Letters, 1987
• Quantitative analyses of biochemical kinetic resolutions of enantiomers
  Journal of the American Chemical Society, 1982
• Highly enantioselective reduction of alkynyl ketones by a binaphthol-modified aluminum hydride reagent. Asymmetric synthesis of some insect pheromones
  Tetrahedron Letters, 1981
• Asymmetric synthesis of .gamma.-lactones. A facile synthesis of the sex pheromone of the Japanese beetle
  The Journal of Organic Chemistry, 1981
• The synthesis of naturally occurring 4-alkyl- and 4-alkenyl-γ-lactones using the asymmetric reducing agent B-3-pinanyl-9-borabicyclo[3.3.1]nonane
  Tetrahedron Letters, 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
• Identification of the Female Japanese Beetle Sex Pheromone: Inhibition of Male Response by an Enantiomer
  Science, 1977