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  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 114 (1981), S. 3170-3175 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The Chemistry of Amino Oximes, XIV Synthesis and Reaction of 2-[α-(E)-(Hydroxyimino)benzyl]-3-imidazoline 3-Oxides2-Benzoyl-4-phenyl-1-(p-tolyl)-3-imidazolin 3-oxide (3b) has been prepared by cyclocondensation of α-(p-toluidino)acetophenone oxime (1a) with phenylglyoxal and transferred into 2-[α-(E)-(hydroxyimino)benzyl]-4-phenyl-1-(p-tolyl)-3-imidazoliune 3-oxide (5a). 5a is identical with the product prepared by oxidation of 1a, with FeCl3.
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  • 3
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Ring Closures of syn-(E)- and (E)-(2-Quinolylmethyl)- and -(1-Isoquinolylmethyl)ketoximes to Pyrazolo[1,5-a]quinolines and Pyrazolo[5,1-a]isoquinolinesThe (2-quinolylmethyl)- and (1-isoquinolylmethyl)ketoximes 2a -e and 4a -d have been prepared and the oxime configurations determined. The Pyrazolo[1,5-a]quinolines 7a, b and the pyrazolo[5,1-a]isoquinoline 8a are formed by Beckmann reaction of the anti-isomers 2a, b and 4a, while O mesitylsulfonylhydroxylamine yields the pyrazolo compounds 7 and 8, independent of the oxime configuration.
    Notes: Die (2-Chinolylmethyl)- und (1-Isochinolylmethyl)ketoxime 2a-e und 4a-d wurden synthetisiert und die Oximkonfigurationen ermittelt. Durch Beckmann-Reaktion entstehen aus den anti-Isomeren 2a, b und 4a die Pyrazolo[1,5-a]chinoline 7a, b bzw. das Pyrazolo[5,1-a]isochinolin 8a, während mit O-Mesitylsulfonylhydroxylamin die Pyrazoloverbindungen 7 und 8 unabhängig von der Oximkonfiguration entstehen.
    Additional Material: 6 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Electrophoresis 4 (1983), S. 148-152 
    ISSN: 0173-0835
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Chemistry and Pharmacology
    Notes: It is demonstrated that photoacoustic spectroscopy is a superior tool in the evaluation of electropherograms. The locla distribution of proteins in ultrathin layers of polyacrylamide gels used for isoelectric focusing is mapped with a resolution equal to or better than a laster densitomer. Even unstained samples of colored proteins can be mapped with excellent sensitivity and resolution due to the fact that the photoacoustic effect is caused only by the absorbed fraction of the incident light; scapttered light therefore doesse not cause a signal. in situ photoacosutic spectra of previously localzed zones allow the identification of the prosthetic groups of these proteins.
    Additional Material: 7 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 755 (1972), S. 191-193 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of 2,3,4,6-Tetramethyl-D-glucono-1.5-lactoneBy one-step-methylation with dimethyl sulfate in presence of Ba(OH)2 and BaO α-methyl-D-glucopyranoside is converted to α-methyl-2,3,4,6-tetramethyl-D-glucopyranoside using dimethylformamide/dimethyl sulfoxide (5 : 2) as solvent.  -  The permethylated product is saponified specifically at the glycosidic group by a strongly acidic cation exchanger giving 2,3,4,6-tetramethyl-D-glucopyranose. This compound is oxidized with bromine and the corresponding tetramethylgluconic acid obtained is converted to the lactone in the conventional way.
    Notes: Durch einstufige Methylierung mit Dimethylsulfat in Gegenwart von Ba(OH)2 und BaO wird α-Methyl-D-glucopyranosid unter Verwendung von Dimethylformamid/Dimethylsulfoxid (5 : 2) als Lösungsmittel in das α-Methyl-2.3.4.6-tetramethyl-D-glucopyranosid übergeführt.  -  Das permethylierte Produkt wird mittels stark sauren Kationenaustauschers spezifisch an der glykosidischen Gruppe verseift. Die entstandene 2.3.4.6-Tetramethyl-D-glucopyranose wird durch Brom zur entsprechenden Tetramethylgluconsäure oxydiert und diese auf üblichem Wege zum Lacton umgesetzt.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1974 (1974), S. 169-175 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Isolation and Structure of Larreagenin AFour glycosides have been isolated from leaves of the central american plant Larreu divaricata Cav.; the structure of one of the aglycons, larreagenin A, has been elucidated by means of 1H-NMR- and 13C-NMR-investigation together with other spectroscopic data as 3β-hydro-xy-29-nor-urs-13(18)-en-20β,28β-olide (4). Larreic acid, isolated from the same plant as glycoside, can be isomerized to larreagenin A.
    Notes: Aus Blättern der mittelamerikanischen Pflanze Lurrea divaricata Cav. wurden 4 Glykoside isoliert; die Struktur eines der Aglyka, das Larreagenin A wurde mit Hilfe von 1H-NMR- und 13C-NMR-Untersuchungen sowie anderer spektroskopischer Daten als 3β-Hydroxy-29-nor-urs-l3(18)-en-20β,28β-olid (4) aufgeklärt. Die aus der gleichen Pflanze als Glykosid isolierte Larreasäure läßt sich zu Larreagenin A isomerisieren.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 323 (1981), S. 747-754 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Protected Aminooxazolines of Arabinose and RiboseThe reaction of D-arabinose or D-ribose with cyanamide afforded 2-amino-1,2-oxazolines 1 which were treated with dihydropyran or ethylvinylether. In the presence of PTS the 3′,5′-di-THP- or 3′,5′-di-O-ethoxyethyl-D-arabino-(ribo)-furo-[1′,2′:4,5]-2-oxazolines 2 and 3 could be isolated as useful intermediates for the preparation of nucleosides.When the 2-aminooxazolines are treated with benzyloxycarbonylchloride or its p-substituted derivatives the N-3 atom of the oxazoline ring is preferentially substituted. Under these conditions the exocyclic amino function is always replaced and 2-oxo-3-benzyloxycarbonylderivatives 4 are obtained; only traces of the corresponding 2-aminoderivatives 5 are formed. Treatment of 4 with acetic anhydride, benzoylchloride, and benzoylcyanide, respectively, results in the 3′-, 5′-di-O-acyl derivatives 6. Mild hydrolysis of the benzyloxycarbonyl group with trifluoroacetic acid yields the 3′,5′-di-O-acyl-D-arabino-(ribo)-furo-[1′,2′:4,5]-2-oxooxazolidines as further intermediates for the synthesis of nucleosides.
    Additional Material: 1 Ill.
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  • 8
    ISSN: 0025-116X
    Keywords: Chemistry ; Polymer and Materials Science
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology , Physics
    Additional Material: 24 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 410 (1974), S. 165-178 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Surface Composition, Solubility, and the Ion Activity Product of Calcite in Solutions with Auxiliary IonsUsing the method of simultaneous ion and isotope exchange the chemical composition of the surface layer of calcite powder in equilibrium with solutions of varying Me/Ca molar ratios is determined (Me = Mg2+, Co2+, Ni2+, and Fe2+ ions). The ion exchange isotherms show a marked bend in the surface reactivity when a surface molar ration of ∼1 and ∼3 is reached. The solubility of calcite initially decreases on the addition of Co2+ or Ni2+ ions to the solution whereas it increases in the presence of Mg2+ or Fe2+ ions. The activity product of the pseudo compound, CaxMe(1-x)CO3, decreases in the Ni2+, Co2+ or Fe2+ exchange experiments, however, it increases considerably in those with Mg2+ ions.
    Notes: Mit der Methode des gleichzeitigen Ionen- und Isotopenaustausches wird die chemische Zusammensetzung der Oberfläche eines Calcitpulvers im Gleichgewicht mit Lösungen verschiedener Me/Ca- Verhältnisse bestimmt (Me = Mg2+, Co2+, Ni2+, Fe2+). Alle Austauschisothermen zeigen eine deutliche Änderung der Oberflächenreaktivität, wenn eine Zusammensetzung auf der Oberfläche von (Me/Ca)Obfl.∼1 und ∼3 erreicht wird. Die Löslichkeit des Calcits nimmt anfänglich bei Zugabe von Co2+ oder Ni2+ ab, während sie bei Mg2+ oder Fe2+ im ganzen Bereich der Untersuchung zunimmt. Das Ionenaktivitätsprodukt für die „Pseudoverbindung“ in der Oberfläche nimmt in den Ni2+-, Co2+- und Fe2+-Austauschexperimenten ab, in Gegenwart von Mg2+-Ionen jedoch zu.
    Additional Material: 6 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 504 (1983), S. 155-162 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Investigation of CuGaSe2 and CuGaTe2 under High PressureThe X-ray powder diffraction analysis at 300 K in dependence on the pressure gives a transition from the chalcopyrite-type to the NaCl structure for CuGaSe2 at 12.5 GPa and for CuGaTe2 at 8 GPa. The phase transition is associated with a discontinuity of the volume of 8.6 and 3.8%. These results were discussed in relation to other tetrahedrally coordinated compounds.
    Notes: Röntgenuntersuchungen bei 300 K in Abhängigkeit vom Druck ergaben, daß CuGaSe2 bei 12,5 GPa und CuGaTe2 bei 8 GPa von der Chalcopyrit-Struktur in die NaCl-Struktur übergehen. Dabei tritt ein Volumensprung von 8,6 bzw. 3,8% auf. Diese Ergebnisse werden im Zusammenhang mit Hochdruckuntersuchungen an anderen tetraedrisch koordinierten Verbindungen diskutiert.
    Additional Material: 5 Ill.
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