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  • Chemistry  (4)
  • Arfsciliaprotein traffickingreleasing factorssmall G proteins  (1)
  • Wiley-Blackwell  (4)
  • Nature Publishing Group (NPG)  (1)
  • American Chemical Society
  • International Union of Crystallography (IUC)
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  • 1974  (2)
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  • Wiley-Blackwell  (4)
  • Nature Publishing Group (NPG)  (1)
  • American Chemical Society
  • International Union of Crystallography (IUC)
  • Oxford University Press
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  • 2010-2014  (1)
  • 1975-1979  (2)
  • 1970-1974  (2)
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  • 1915-1919
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  • 1
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several long chain primary alcohols (saturated, monoolefinic and methyl branched) have been converted via their mesylates into various long chain alkylated aromatic compounds with basic character, and their mass spectra compared. The spectra of 2-alkylaminopyridines and to some extent those of 3-alkylaminopyridines exhibit most clearly the structure of the aliphatic chain, allowing the localization of branchings and double bonds.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 424-441 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Thermolysis of Acetoxy-alkylbenzene and Hydroxy-alkylbenzene DerivativesThe thermolysis of long chain acetoxy-alkylbenzene and hydroxy-alkylbenzene derivatives at 340-350°C affords, probably via a radical reaction, products in which acetoxy or hydroxy groups and/or alkyl residues are substituted by hydrogen (tables 1, 2). The yields vary with type, number, and position of substituents on the benzene ring. The thermolysis of hydroxydialkylbenzene derivatives 14 and 20 gives in addition hydroxy-triaklylbenzene derivatives formed by transfer of alkyl radicals.
    Notes: Die Thermolyse von langkettigen Acetoxy-alkylbenzolen und Hydroxy-alkylbenzolen bei 340-350°C liefert in einer vermutlich radikalisch ablaufenden Reaktion Produkte, in denen Acetoxy-bzw. Hydroxygruppen und/oder Alkylreste durch Wasserstoff ersetzt sind (Tab. 1, 2). Die Ausbeuten sind von der Art, der Anzahl und der Stellung der Substituenten am Benzolkern abhängig. Die Thermolyse der Dialkyl-hydroxybenzole 14 und 20 ergibt zusätzlich Trialkyl-hydroxybenzole, die durch Übertragung von Alkyl-Radikalen entstehen.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 111 (1978), S. 791-796 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Enehydrazines, 20: Pyrazolinium Betaines from 1,1-Dimethylhydrazine and 3-Phenylglycidic EstersEthyl trans-3-phenylglycidate and 1,1-dimethylhydrazine give the trans-4-hydroxy-5-phenyl-pyrazolinium betaine 1a, whereas the cis-phenylglycidic ester forms the cyclic cis-betaine 1b. Some degradation reactions are described.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 409 (1974), S. 285-298 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrosolates and Nitrosolatocompounds. III. Synthesis and Structures of Nitrosolate Derivatives of Organosubstituted Compounds of Antimony(V(, Tellurium(IV), and Iodine(III)In solution the derivatives of the nitrosolates of acetic and benzoic acids and of the ions (C6H5)4Sb+, (CH3),Sb+, (C6H5)3Te+, and the derivative of the nitrosolate of acetic acid and of the ion C12H8I+ show ionic or covalent structures, depending on the polarity of the solvent. In the solid state only the derivatives of (C12H5)4Sb+ unequivocally do not display salt character. The structure of (C6H5)4Sb · O2N2C-CH3 was determined by X-ray methods. The compound consists of separated molecules with slightly distorted trigonal-bipyramidonal environment of the antimony atom. The nitrosolato ligand is oxygen bonded to one of the apical positions. According to the electronic spectra of the solutions of the nitrosolate derivatives the nitrosolate ions react in the covalent forms either as uni-dentate ligands with O-coordination or as bidentate chelating or bridging ligands with O,O′-coordination.
    Notes: Die Acet- und Benznitrosolsäurederivate der Ionen (C6H5)4Sb+, (CH3)4Sb+, (C6H5)3Te+ und das Acetnitrosolsäurederivat des Ions C12H8J+ zeigen in Lösung je nach Polarität des Lösungsmittels ionische oder kovalente Strukturen. Im festen Zustand besitzen nur die Derivate von (C6H5),Sb+ eindeutig keinen Salzcharakter. Die Struktur von (C6H5)4Sb · O2N2C-CH3 wurde röntgenographisch bestimmt. Die Verbindung besteht aus diskreten Molekeln mit leicht verzerrter trigonal-bipyramidaler Umgebung des Antimon-atoms. Der Nitrosolatoligand besetzt eine der axialen Positionen und ist über Sauerstoff gebunden. Kach Aussage der Elektronenspektren der Lösungen der Nitrosolsäurederivate fungieren die Nitrosolationen in den kovalenten Formen entweder als einzähnige Liganden rnit O-Koordination oder als zweizähnige Chelat- bzw. Brückenliganden mit O, O′-Koordination.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Publication Date: 2012-10-18
    Description: The EMBO Journal 31, 4085 (2012). doi:10.1038/emboj.2012.257 Authors: Shehab A Ismail, Yong-Xiang Chen, Mandy Miertzschke, Ingrid R Vetter, Carolin Koerner & Alfred Wittinghofer Access to the ciliary membrane for trans-membrane or membrane-associated proteins is a regulated process. Previously, we have shown that the closely homologous small G proteins Arl2 and Arl3 allosterically regulate prenylated cargo release from PDEδ. UNC119/HRG4 is responsible for ciliary delivery of myristoylated cargo. Here,
    Keywords: Arfsciliaprotein traffickingreleasing factorssmall G proteins
    Print ISSN: 0261-4189
    Electronic ISSN: 1460-2075
    Topics: Biology , Medicine
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