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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 63 (1980), S. 1932-1946 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Twelve tricyclic ethers of the labdane and ent-labdane series, 5-16, have been synthesized; compounds 6-15 are new. The intramolecular C18-acetals 1-4 and the tricyclic ethers 5-16 were submitted to an olfactory test which was characterized by an exceptionally high percentage of ‘wrong’ answers (cf. Table 1, footnote b). For most compounds specific anosmia, rapidly ensuing fatigue and a high percentage of odor deviation were the most salient features.Pronounced ambergris-like odors were only noted in compounds of the labdane series, and were strongest in ethers 1, 5 and 15, followed by the ethers 9 and 11. In contrast, both labdane derivatives 3 and 7 were practically odorless. Their enantiomers 4 and 8, on the other hand, have relatively strong odors which can only to a limited extent be associated with ambergris-type odors. The pairs of ethers 3/4 and 7/8 are the first recorded examples of optical antipodes in which only one isomer possesses olfactory properties.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Photo-oxygenation of (E)-7-methyl-β-ionone ((E)-1) and (E)-8-methyl-β-ionone ((E)-2) gave rise to the formation of the hydroperoxy-enones (E)-10 and (E)-15, respectively, which, in part, underwent intramolecular epoxidation to the hydroxy-epoxy-ketones 11 and 16, respectively, The product distribution of the photo-oxidation of (Z)-1 shows a marked influence of the skewed ground-state conformation of the dienone chromophore. Thus, singlet oxygen (1O2) was added to C(γ) of the dienone chromophore leading to the spirocyclic peroxy-hemiacetal 12 and to the endoperoxide 13. In addition, the tricyclic peroxide 14 was formed as a new type of product via primary addition of 1O2 to C(γ) of the dienone chromophore. The structure of 14 was established by X-ray crystal-structure analysis of the hemiacetal 22.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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