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  • Chemistry  (25)
  • N-(2-hydroxy-4-methoxybenzyl)  (2)
  • Osteoarthritis  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Skeletal radiology 18 (1989), S. 199-205 
    ISSN: 1432-2161
    Keywords: Osteoarthritis ; Joint utilisation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Two subjects were studied for 1 to 3 weeks during the course of their normal domestic activities. Utilisation profiles were derived for ten joints, using a systematic time-series sampling technique adapted from behavioural biology. At each joint the proportion of the available range utilised was noted. The results were compared with the known regional prevalence of primary osteoarthritis. There was a correlation between the degree to which a joint was incompletely utilised, and its susceptibility to osteoarthritis. The hypothesis is advanced that primary osteoarthritis may be due to incomplete joint utilisation.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Skeletal radiology 19 (1990), S. 327-333 
    ISSN: 1432-2161
    Keywords: Osteoarthritis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Radiology is dependent on an accurate understanding of the pathological process. This review of primary osteoarthritis identifies eight areas in which widely held concepts are either demonstrably false or fall short of proof. In some, the concepts have been disproved by the gradual accumulation of evidence. In others, the error is due to radiological misinterpretation while in a third group, the evidence is not in dispute, but the logical framework used in its assessment is flawed. Awareness of these deficiencies simplifies radiological interpretation and clarifies research objectives.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1573-3904
    Keywords: amyloid ; circular dichroism ; ‘difficult sequence’ ; in situ neutralisation ; N-(2-hydroxy-4-methoxybenzyl) ; tetramethylfluoroformamidinium hexafluorophosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Summary A peptide corresponding to residues 106–126 of the human prion protein (PrP) possesses the neurotoxic and amyloidogenic properties of the infectious form of the parental protein. This peptide is now identified as a ‘difficult sequence’ and synthesis using conventional manual Fmoc chemistry was unsuccessful with acylation terminating at a central core of hydrophobic amino acids. The use of tetramethylfluoroformamidinium hexafluorophosphate and 1-methyl-2-pyrrolidone as anti-aggregatory agents in the coupling steps improved the synthesis but still resulted in an incomplete peptide. The incorporation ofN-(2-hydroxy-4-methoxybenzyl)protection at glycine residues 119 and 124 enabled synthesis of the full length peptide in low yield. Synthesis using Boc chemistry within situ neutralisation gave the full length peptide in high yield.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-3904
    Keywords: amyloid ; circular dichroism ; 'difficult sequence' ; in situ neutralisation ; N-(2-hydroxy-4-methoxybenzyl) ; tetramethylfluoroformamidinium hexafluorophosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A peptide corresponding to residues 106-126 of the human prion protein (PrP) possesses the neurotoxic and amyloidogenic properties of the infectious form of the parental protein. This peptide is now identified as a 'difficult sequence' and synthesis using conventional manual Fmoc chemistry was unsuccessful with acylation terminating at a central core of hydrophobic amino acids. The use of tetramethylfluoroformamidinium hexafluorophosphate and 1-methyl-2- pyrrolidone as anti-aggregatory agents in the coupling steps improved the synthesis but still resulted in an incomplete peptide. The incorporation of N-(2-hydroxy-4-methoxybenzyl) protection at glycine residues 119 and 124 enabled synthesis of the full length peptide in low yield. Synthesis using Boc chemistry with in situ neutralisation gave the full length peptide in high yield.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0935-6304
    Keywords: Gas chromatography ; Capillary columns ; Simulated distillation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The characterization of heavy petroleum fractions is essential for the design and improvement of cracking plants converting heavy feedstock into valuable “white” products. Conventional simulated distillation methods using packed columns are unsuitable for this purposes, being limited to boiling points up to about 600°C. The method presented is able to cover a boiling points interval ranging from about 150°C up to around 800°C. It employs a short, nonpolar, highly thermostable capillary column routinely operated at temperatures around 430°C. The analytical system is based on a high temperature versions of a fully automatic, capillary dedicated gas chromatograph. The experimental data demonstrate that cold on-column injection is the sole sampling system suitable for such heavy compounds. The conversion of the retention times into boiling points, based on the use of low molecular weight polyethylenes, is extremely reliable, as demonstrated by the excellent retention time reproducibilities. The lower part (up to 550-600°C TBP) of the boiling point distribution curves of heavy petroleum fractions obtained on capillary columns fits well with the corresponding distribution curves based on packed column data. For the petroleum fractions fully eluted from the column the quantitative results obtained either using internal standards or by direct processing of the elution curves are in excellent agreement (less than 0.3 weight% differences). The method has been applied to the determination of the true boiling points corresponding to short path vacuum distillation (DISTACT) cut points over 300°C.
    Additional Material: 18 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 8 (1985), S. 39-41 
    ISSN: 0935-6304
    Keywords: Liquid chromatography, HPLC ; Mass detector ; Carbohydrates ; Heavy petroleum distillates ; Hormonal steroids ; Nonionic surfactants ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0935-6304
    Keywords: Coupled HPLC-GC ; Retention gap ; Partially concurrent solvent evaporation ; Gasoline ; Group-type separation ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two-dimensional chromatography of gasoline by on-line coupled HPLC-HRGC, as described in this paper, allows separate GC analysis of paraffins and aromatics. The GC system contains a retention gap of only 10 m length for introducing HPLC fractions of 100 μl volume. This becomes possible through evaporation of part of the solvent during introduction of the HPLC eluent. This “partially concurrent solvent evaporation” technique allows transfer of large volumes of HPLC eluent into relatively short retention gaps, maintaining the full efficiency of the solvent effects in reconcentrating the bands of the early eluted solutes.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 0269-3879
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Medicine
    Notes: A method for extracting spiramycin by an octadecylsilica cartridge is described for plasma or vitreous samples. The macrolide antibiotic is then measured by reversed-phase HPLC with UV detection. The limit of detection is estimated to be 50 ng/mL. The coefficient of variation for the procedure is 6.1% and 5.2% for the range of concentrations 0.2 μg/mL and 10 μg/mL respectively. By this method, pharmokinetic profiles were performed for five adult patients. Spiramycin could be accurately measured in the vitreous humour, allowing the determination of antibiotic at its site of action.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 38 (1991), S. 1137-1143 
    ISSN: 0006-3592
    Keywords: organic-phase biocatalysis ; equillibrium ; reaction rates ; log P ; solvent choice ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Porcine pancreatic lipase immobilized on celite particles has been employed as a catalyst for the esterification of dodecanol and decanoic acid in a predominantly organic system. Solvent influence on the equilibrium position and on the catalyst activity has been studied using 20 solvents, including aliphatic and aromatic hydrocarbons, ethers, ketones, nitro- and halogenated hydrocarbons, and esters. The equilibrium constant for esterification correlates well with the solubility of water in the organic solvent, which in turn shows a good relationship with a function of Guttman's donor number and the electron pair acceptance index number of the solvent. This may be rationalized in terms of the requirements for solvation of water and of the reactants. The catalyst activity, measured as the initial rate of the esterification reaction, is best correlated as a function of both n-octanol-water partition coefficient (log P) and either the electron pair acceptance index or the polarizability.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 1479-1488 
    ISSN: 1434-1948
    Keywords: Phosphorus heterocycles ; Cations ; Tungsten complexes ; Coordination modes ; Phosphaalkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1,1,3-tris(diisopropylamino)diphosphirenium salt 1 reacts with lithium aluminium hydride leading to the P-hydrogeno-C-phosphinophosphaalkenes 2, which on treatment with a catalytic amount of BF3·OEt2 afford the 1,3-bis(diisopropylamino)-1H-diphosphirene 3. The corresponding η1-coordinated 1H-diphosphirene 6 can be prepared by treatment of 2 or 3 with one equivalent of [W(CO)5(thf)]. Alternatively, the diphosphirenium salt 1 reacts with an excess of [W(CO)5(thf)], affording the corresponding η1-coordinated diphosphirenium salt complex 4, which is converted into the P-hydrogenophosphaalkene complex 5 with lithium aluminium hydride. The dinuclear tungsten complexes 7 and 8 are obtained by treatment of the free 1H-diphosphirene 3 with two equivalents of [W(CO)5(thf)] or one equivalent of [W(CO)4(thf)2], respectively. Compound 6 reacts with two equivalents of hydrogen chloride, giving the 1-chloro-3-diisopropylamino-1H-diphosphirene 9, which can be subsequently converted into the 1-diisopropylamino-, 1-azido, or 1-phenyl-3-diisopropylamino-1H-diphosphirenes 6, 10 and 11 by nucleophilic substitution with diisopropylamine, azidotrimethylsilane or sodium tetraphenylborate, respectively. The [η2-(3-diisopropylaminodiphosphirenylium salt)·W(CO)5] complexes 12a-c can be prepared by reaction of 9 with silver trifluoromethanesulfonate, aluminium or gallium trichloride or, alternatively, by treatment of 6 with two equivalents of trifluoromethanesulfonic acid. Reaction of 12a with diisopropylamine, water, bis(triphenylphosphoranylidene)ammonium chloride or tetrabutylammonium fluoride gives the corresponding 1H-diphosphirene complexes 6, 13, 9, or 14, respectively. Compound 12a also reacts with one or two equivalents of [W(CO)5(thf)], leading to the di- and tri-nuclear complexes 15and 16, respectively.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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