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Publications by Kozo MACHIYA
Activity of Four Stereoisomers of 6-Acetoxy-5-Hexadecanolide, the Oviposition Pheromone of Culicine Mosquitos
Medical Entomology and Zoology
A Convenient Synthesis of Four Stereoisomers of 6-Acetoxy-5-Hexadecanolide, the Major Component of the Mosquito Oviposition Attractant Pheromone.
Agricultural and Biological Chemistry
Related publications
Bidirectional Synthesis of 6Acetoxy-5-Hexadecanolide the Mosquito Oviposition Pheromone of Culex Quinquefasciatus, From a C2Symmetric Building Block Using Olefin Metathesis Reactions
Oviposition Pheromone in the Simulium Damnosum Complex: Biological Activity of Chemical Fractions From Gravid Ovaries
Physiological Entomology
Evolution
Ecology
Insect Science
Systematics
Behavior
Physiology
Preparation and Characterization of Four Stereoisomers of Monatin
Chemical and Pharmaceutical Bulletin
Medicine
Drug Discovery
Chemistry
Four Stereoisomers of the Novel Μ-Opioid Receptor Agonist Tapentadol Hydrochloride
Acta Crystallographica Section C Crystal Structure Communications
Mosquitos and Malaria: The Infection of Birds by Mosquitos
BMJ
2-Isopropyl-5-Methylcyclohexyl 5-Acetoxy-1,3-Oxathiolane-2-Carboxylate
Acta Crystallographica Section E Structure Reports Online
3β-Acetoxy-5α-Cholestan-6-One 2-Cyanoacetylhydrazone
Acta Crystallographica Section E Structure Reports Online
Structure Assignment of Lagunapyrone B by Fluorous Mixture Synthesis of Four Candidate Stereoisomers
