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  • Cycloadditions  (1)
  • Stegobinone  (1)
  • 1
    ISSN: 1434-193X
    Keywords: Cycloadditions ; Leishmaniasis ; Lutzomyia longipalpis ; Pheromones ; Sandfly ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Four stereoisomers (1a-d) of (±)-3-methyl-α-himachalene were synthesized by employing the intramolecular Diels-Alder reaction of (±)-14 to (±)-18 as the key-step. The male-produced sex pheromone of the sandfly Lutzomyia longipalpis was shown to possess the structure and relative configuration as depicted in 1c.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-193X
    Keywords: Heterocycles ; Lipases ; Oxidations ; Pheromones ; Stegobinone ; Stegobium paniceum ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Crystalline (-)-stegobinone [(2S,3R,1′R)]-2,3-dihydro-2,3,5-trimethyl-6-(1′-methyl-2′-oxobutyl)-4H-pyran-4-one (1)], the major component of the female-produced sex pheromone of the drugstore beetle (Stegobium paniceum L.), was synthesized by oxidation of crystalline and the minor component (-)-stegobiol [(2S,3R,1′S,2′S)-2,3-dihydro-2,3,5-trimethyl-6-(2′-hydroxy-1′-methylbutyl)-4H-pyran-4-one (2)] under the appropriate conditions using Jones's chromic acid, Dess-Martin's periodinane or Ley's ruthenium reagent. The latter (2) was synthesized by employing lipase and the Sharpless epoxidation for the introduction of the proper chiral centers. The streostructure of 1 was comfirmed by X-ray analysis.
    Type of Medium: Electronic Resource
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