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  • 1985-1989  (2)
  • Organic Chemistry  (2)
  • Pesticides
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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 111-118 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Acidity and Complex Formation of CurcuminoidsThe stoichiometric acid dissociation constants of curcumin 1a and derivatives as well as the stoichiometric stability constants of the Cu(II)- and Ni(II)-complexes of these substances have been determined by pH-potentiometric titrations in dioxane-water mixture.The influence of different substituents on the pKa-values and the stability constants is discussed. The complexing properties of the —CO—CH2—CO— structural element of the ligands are not significantly changed when the phenyl group is substituted by the styryl group. Solid CuL2-complexes have been characterized. The coordination of the ester group in the tricarbonyl ligand systems 4 was excluded by i.r. spectroscopy.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 330 (1988), S. 241-247 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of N-(N′,N′-Dialkyl(aryl)amino-thiocarbonyl)benzimidoylchlorides with Potassium ThiocyanateThe treatment of the title compound N-(amino-thiocarbonyl)-benzimidoylchloride 1 with potassium thiocyanate leads in dependence on the solvents (methanol, acetic acid, acetone) either to the 1,3,5-thiadiazine-2-thione 2a-d or to the ring opened isothiocyanate 4a, b. In the case of methanol the N-(amino-thiocarbonyl)benzimidates were formed as by-products.The structure of the products is confirmed by analytical data and by chemical transformations. 2a reacts with methyl iodide to form the 2-methylthio-6-morpholino-4-phenyl-1,3,5-thiadiaziniumiodide 3a. From 4a and water the N-(morpholino-thiocarbonyl)benzamide 5a arises. The reaction of morpholine with 4a yields the benzamidine 6a.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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