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  • Wiley-Blackwell  (2)
  • Cambridge University Press  (1)
  • EMBO Press
  • 1995-1999
  • 1970-1974  (3)
  • 1974  (3)
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Years
  • 1995-1999
  • 1970-1974  (3)
Year
  • 1
    Electronic Resource
    Electronic Resource
    Cambridge : Cambridge University Press
    The @journal of modern African studies 12 (1974), S. 409-421 
    ISSN: 0022-278X
    Source: Cambridge Journals Digital Archives
    Topics: Ethnic Sciences , History , Political Science , Economics
    Notes: It is known that the forms of physical education practised among ancient Greek communities reflected the differential importance attached to military and artistic activities.1 Similarly, today, variations in the relative pre-eminence of collective over individual sports are likely to reflect contrasts in the socio-economic and cultural profiles of contemporary societies.2 Moreover, modes of social participation in a particular game should be affected by the patterns of interaction prevailing in the society at large.
    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. 2537-2543 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 6-(Pyrido[2,3-d]pyrimidin-8-yl)hexanoic AcidsBy way of nucleophilic substitution, 4-chlorouracil (8) reacts with 6-aminohexanoic acids (9,10) to yield 6-(4-pyrimidinylamino)hexanoic acids (4,5). These undergo cyclocondensation with 3-amonoacroleins and 2-(hydroxymethylene)cycloalkanones (2), respectively, to yield 6-(pyrido[2,3-d]pyrimidin-8-yl)hexanoic acids (6,7). The 1H and 13C n. m. r. spectra of these carboxylic acids substituted with heterocycles are discussed.
    Notes: Aus 4-Chloruracil (8) und 6-Aminohexansäuren (9,10) entstehen durch nucleophile Substitution 6-(4-Pyrimidinylamino)hexansäuren (4,5). Diese cyclokondensieren mit 3-Aminoacroleinen bzw. 2-(Hydroxymethylen)cycloalkanonen (2) zu 6-(Pyrido[2,3-d]pyrimidin-8-yl)-hexansäuren (6,7). Die 1H- und 13C-NMR-Spektren dieser heterocyclisch substituierten Carbonsäuren werden diskutiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Chemie in unserer Zeit 8 (1974), S. 33-43 
    ISSN: 0009-2851
    Keywords: Chemistry ; Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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