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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 1 (1975), S. 125-131 
    ISSN: 1573-1561
    Keywords: deer ; mammals ; odor preference ; odor specificity ; olfactory discrimination ; pheromone ; sexual isolation ; social odor ; tarsal scent
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Two subspecies of deer, black-tailed deer (Odocoileus hemionus columbianus) and Rocky Mountain mule deer (O. h. hemionus) were exposed to the tarsal scents of both subspecies in a social setting. The scent was sprayed on one individual in a group. The responses, consisting of sniffing, licking, and following, were stronger to each subspecies' own tarsal scent. This discrimination may be important for sexual isolation in areas where the ranges of the two species overlap.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 15 (1989), S. 887-893 
    ISSN: 1573-1561
    Keywords: Adirondacks ; beaver ; Castor canadensis ; castoreum ; nuisance beaver ; odors ; pheromone ; repellent ; scent marking ; territory ; wildlife damage
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Unoccupied beaver (Castor canadensis) sites in New York State were for two years experimentally scented with a mixture of beaver castoreum and anal gland secretion. These sites were colonized less often than unscented control sites. The beaver is the first mammal to have been shown experimentally to use intraspecific odor cues when settling in vacant habitat. Territorial pheromones may be useful as repellents for beaver or other rodents.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0009-2940
    Keywords: Aldehydes ; Ketones ; Titanium complexes ; Niobium complexes ; Tantalum complexes ; Phosphonium chlorides ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal-Activated Organic Compounds, XXXVII[1].  -  A Novel Reaction of Aldehydes and Ketones: Synthesis and Spectroscopic Investigation of α1-Phosphonioalkoxy Transition Metal ComplexesHerrn Professor Ulrich Schöllkopf zum 65. Geburtstag gewidmet.By treatment of aldehydes and ketones with one mole equivalent of a Lewis acid (TiCl4, NbCl5, TaCl5) and one mole equivalent of PPh3, or in one case of Ph2PCH2CH2PPh2, the aldehyde derivates [R1CH(P+Ph2R2)-OMCln]Cl- (4-8; M=Ti, Nb, Ta; R2=Ph or CH2CH2PPh2) and the ketone derivatives [R1R2C(P+Ph3)-ONbCl4]Cl- (9-10) were prepared. Complexes 4-10 were isolated as air-and water-sensitive solids. According to the NMR spectra some of the obtained aldehyde derivatives 4-8 exist in solution as a mixture of isomers or oligomers, whereas the ketone derivatives 9 and 10 form in solution an equilibrium with the free ketone and the complex NbCl5 · PPh3. The chloride ion of 4-10 is perhaps coordinated to the metal.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 701-704 
    ISSN: 0009-2940
    Keywords: N-Silyl amides ; Precursor ; 14N-NMR ; Titanium ; Tungsten ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of hexachlorodisilazanyllithium (Cl3Si)2NLi (1), with TiCl4 leads selectively to the novel fully chlorinated amides (Cl3Si)2NTiCl3 (2) or [(Cl3Si)2N]2 TiCl2 (3), respectively, depending on the molar ratio of the starting materials. The analogous reaction of 1 with WCl6 yielded the amide imide Cl3SiN=W(Cl3)N(SiCl3)2 (5) by elimination of SiCl4. The relative amounts of the starting materials had no effect on the formation of 5. 14/15N- and 29Si-NMR data on the starting materials and products show significantly different effects, when compared with those of analogous N-trimethylsilyl derivatives, due to the lower energy of the electrons in the N—Si and N—M ß bonds. The crystal structure of 5 (triclinic, space group P1) was determined by X-ray structure analysis.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0009-2940
    Keywords: Chemoselectivity ; Titanium complexes ; Niobium complexes ; Tantalum complexes ; Methylation of aldehydes and ketones ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Transition Metal-Activated Organic Compounds, XXXVIII[1].  -  Chemoselective Nucleophilic Methylation Reactions by In-Situ-Blocking of Aldehyde Groups by α1-Phosphonioalkoxide FormationHerrn Professor Ulrich Schöllkopf zum 65. Geburtstag gewidmet.For the selective methylation of a keto group in the presence of an aldehyde group the complex MeTiCl3·PPh3 and especially the reagent system [TiC]4·PPh3 + 0.5 Me2Zn] proved to be favourable. For instance, 6-oxoheptanal (8) was methylated by [TiCl4·PPh3 + 0.5 Me2Zn] at the keto group with 89% yield and 99:1 selectivity, whereas it was methylated by [TiCl4 + 0.5 Me2Zn] at the aldehyde group with 81% yield and 96:4 selectivity. A selective methylation of benzaldehyde in the presence of heptanal was achieved with MeNbCl4·PPh3 or [NbCl5·PPh3 + 0.75 Me2Zn] to give (1-chloroethyl)benzene (14; yield 92 or 53%; selectivity in each case 93:7) or with [TaCl5·PPh3 + 1.5 Me2Zn] to give mainly 1-phenylethanol (15) besides 16. A 96:4-selective benzylation (yield 74%) of a ketone in the presence of an aliphatic aldehyde was possible with [TiCl4·PPh3 + 1 PhCH2MgBr].  -  The high chemoselectivity is caused by irreversible blocking of aliphatic aldehyde groups by α1-phosphonioalkoxide formation[1], whilst the corresponding reaction of keto groups[1] and of benzaldehyde is reversible.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Journal of chemical ecology 17 (1991), S. 715-734 
    ISSN: 1573-1561
    Keywords: Adirondacks ; beaver ; bioassay ; Castor canadensis ; castoreum ; field study ; New York ; phenols ; pheromone ; scent marks ; territorial marking
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: Abstract Behavioral activity of single components of beaver castoreum was demonstrated for the first time. In four experiments samples were presented to free-ranging beaver in their family territories. First, responses to whole castoreum and anal gland secretion (AGS) from males and females were tested. Second, 24 compounds, known to be constituents of beaver castoreum, were individually screened for activity. Four of these consistently released immediate responses during the observation periods. These are the phenols 4-ethylphenol and 1,2-dihydroxybenzene and the ketones acetophenone and 3-hydroxyacetophenone. In the most complete responses, the beaver sniffed from the water, were attracted to the odor, swam toward its source, went on land, and then approached, sniffed, pawed, and scent-marked the artificial scent mound. 4-Ethoxyphenol, a compound not yet found in castoreum, also released these responses. Five additional compounds resulted in a few delayed visits to the samples during the night following the observations, as evidenced by destroyed scent mounds. These are 4-methyl-1,2-dihydroxybenzene, 4-methoxyacetophenone, 5-methoxysalicylic acid, salicylaldehyde, and 3-hydroxybenzoic acid. Third, mixtures of 24 and six compounds were tested. Responses to these mixtures could be as strong as those to whole castoreum. Fourth, the four regularly active compounds were tested in two additional beaver populations and proved to be active there, too. The response was strongest in the densest beaver population.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 13 (1971), S. 151-155 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 11 (1969), S. 1027-1032 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 10 (1874), S. 222-235 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 42 (1890), S. 1-18 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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