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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Journal of Chromatography A 479 (1989), S. 243-250 
    ISSN: 0021-9673
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 54 (1989), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: 1,3-Bis(carboxymethyl)imidazole was identified in a model reaction mixture derived from glycine, glyoxal, and formaldehyde. The same compound was also found in the reaction of glycine with glyoxal. The structure of this compound was elucidated from the measured molecular, mass and 1H-NMR and 13C-NMR spectral data and confirmed by X-ray crystallographic measurements. Similarly, a 2-methyl-, 4-methyl-, and 2,4-dimethyl-1,3-bis(carboxymethyl)-imidazole were formed in reactions of glycine with glyoxal or methylglyoxal and formaldehyde or acetaldehyde. These 1,3-symmetrically substituted imidazoles represent quite a new group of N-containing heterocyclic compounds originating in model systems containing amino acids and α-dicarbonyl compounds and probably also in natural systems.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 56 (1991), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: In model aqueous solutions containing 3-chIoro-l,2-propanediol (arising by the interaction of hydrochloric acid with lipids in protein hydrolysate and ammonia, 3-amino-1,2-propanediol was found as the main reaction product together with smaller amounts of glycerol. The reaction mechanism of formation of these two compounds was outlined and discussed as well as the possibilities of formation of some other amino analogues of glycerol chlorohydrins. 3-Amino-1,2-pro-panediol was also identified in commercially available seasonings (hydrolyzed vegetable protein) being present in concentrations of 30 mg kg-1.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of food science 56 (1991), S. 0 
    ISSN: 1750-3841
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, Nutrition , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Glycerol monochlorohydrin, (3-chloro-1,2-propanediol), which occurs in chemical hydrolysates of proteins, reacted with amino acids in model aqueous solutions to form the corresponding glycerylamino acids, i.e. N-(2,3-dihydroxypropyl)-amino acids. N-(2,3-dihydroxy-propyl)-derivatives of 15 amino acids were prepared and analyzed by gas chromatography and gas chromatography-mass spectrometry. No N-(2,3-dihydroxypropyl)-amino acid was detected in a freshly produced commercial soybean hydrolysate. Amounts up to ∼1 mg-kg-1 of N-(2,3-dihyproxypropyl)-serine and -threonine were found in a stored hydrolysate. Higher amounts of N-(2,3-dihydroxypropyl)-amino acids (up to about 10 mg-kg-1) were found in the alkaline treated and with 3-chloro-1,2-propanediol fortified hydrolysate. N-(2,3-dihydroxypropyl)-amino acids represent a new class of amino acids not previously reported in foodstuffs.
    Type of Medium: Electronic Resource
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