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  • Thioacetals, semicyclic  (2)
  • Expression  (1)
  • NO3 radical  (1)
  • 1
    ISSN: 0014-5793
    Keywords: Affinity chromatography ; Baculovirus ; Expression ; Glycosylation ; β-adrenergic receptor
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of atmospheric chemistry 21 (1995), S. 275-291 
    ISSN: 1573-0662
    Keywords: Oxiranes ; NO3 radical ; monoalkenes ; mechanistic study ; product analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Geosciences
    Notes: Abstract The gas-phase reactions of NO3 with 2-methyl-2-butene, isobutene,trans-butene, 1-butene and propene, were investigated in a flow-tube at room temperature. Experiments were performed in the pressure range 1–1000 mbar in synthetic air as well as at a total pressure of 800 mbar with varying concentrations of oxygen in nitrogen. The main products found were oxiranes, nitroxy-carbonyl compounds (ketonitrates) and ketones or aldehydes. The product distribution was a function of pressure. In each case, in synthetic air, the oxirane yield increased with decreasing total pressure up to a value of about 100% at pressures less than 1 mbar. It was concluded that oxirane is a product of the excited adduct radical formed in the electrophilic addition of NO3 to the double bond. Experiments with very low partial pressures of oxygen showed that the quenched adduct radicals also produce the corresponding oxirane. Under tropospheric conditions (1000 mbar synthetic air) the following yields of the corresponding oxiranes were found: 2-methyl-2-butene 9%, isobutene 7%,trans-butene 12%, 1-butene 18%, propene 28%. In the case oftrans-butene the total oxirane yield consists of 72%trans- and 28%cis-isomer.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 1733-1737 
    ISSN: 0009-2940
    Keywords: Dithiolactones ; Electroreduction ; Haloalkanedithioates ; Thioacetals, semicyclic ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Intramolecular cyclization occurs on electroreduction of the methyl -haloalkanedithioates 1 in methanol. The expected semicyclic thioacetals 2 are formed according to an ECEH mechanism. The biheterocycles 12 result from dimerization of intermediate radicals whereas the semicyclic ketene dithio-acetals 13 are formed by non-electrochemical processes. The 2-(methylthio)thiolanes 2 a and 16 are obtained with much higher yields and better selectivity by co-electroreduction of the -dithio-lactones 15 in the presence of dimethyl sulfate.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1641-1646 
    ISSN: 0009-2940
    Keywords: Thioacetals, semicyclic ; Carbanions ; Alkylation ; Hydroxyalkylation ; Diastereoselectivity ; Thiolanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: C,C Coupling with Sulfur-Stabilized Carbanions, 2[1]. - Reactions of the 2-(Methylthio)thiolane Carbanion with Electrophiles[2]The „semicyclic” thioacetal 2-(methylthio)thiolane (4) is easily prepared from thiolane (tetrahydrothiophene). It is readily deprotonated by butyllithium to give the lithium derivative 5, which reacts with alkyl halides, saturated and α,β-unsaturated carbonyl compounds, and benzonitrile to form the alkyl derivatives 6, carbinols 7, allyl alcohols 8, and - after hydrolysis - the ketone 9. The diastereoselectivity of the C,C coupling reaction is discussed.
    Type of Medium: Electronic Resource
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