Synthesis of the Four Stereoisomers of 6‐Acetoxy‐19‐methylnonacosane, the Most Potent Component of the Female Sex Pheromone of the New World Screwworm Fly, with Special Emphasis on Partial Racemization in the Course of Catalytic Hydrogenation

This publication has 10 references indexed in Scilit:

• Highly Potent Chiral Labeling Reagents for the Discrimination of Chiral Alcohols
  Analytical Sciences, 2003
• Synthesis of the Enantiomers of 21-Methyl-7-hentriacontanone and a Stereoisomeric Mixture of 5-Acetoxy-19-methylnonacosane, Candidates for the Female Sex Pheromone of the Screwworm Fly…
  Bioscience, Biotechnology, and Biochemistry, 2003
• Determination of the Absolute Configuration at the Two Cyclopropane Moieties of Plakoside A, an Immunosuppressive Marine Galactosphingolipid
  European Journal of Organic Chemistry, 2002
• Syntheses of Four Methyl-branched Secondary Acetates and a Methyl-branched Ketone as Possible Candidates for the Female Pheromone of the Screwworm Fly,Cochliomyia hominivorax
  Bioscience, Biotechnology, and Biochemistry, 2002
• A solution of the“intrinsic problem”of diastereomer method in chiral discrimination
  Proceedings of the Japan Academy, Series B, 2002
• Synthesis of All the Stereoisomers of 7-Methylheptadecane and 7,11-Dimethylheptadecane, the Female Sex Pheromone Components of the Spring Hemlock Looper and the Pitch Pine Looper
  European Journal of Organic Chemistry, 1999
• Semiochemicals – Synthesis, Stereochemistry, and Bioactivity
  European Journal of Organic Chemistry, 1998
• Identification of compounds in an HPLC fraction from female extracts that elicit mating responses in male screwworm flies,Cochliomyia hominivorax
  Journal of Chemical Ecology, 1993
• Hydrogenation and hydrogenolysis in synthetic organic chemistry
  Published by Springer Nature ,1977
• Improved Carbon‐Carbon Linking by Controlled Copper Catalysis
  Angewandte Chemie International Edition in English, 1974