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  • 1970-1974
  • 1965-1969  (5)
  • 1890-1899
  • 1965  (5)
  • Heterocycles  (3)
  • Phosphorus  (3)
  • 1
    Electronic Resource
    Electronic Resource
    New Methods in the Chemistry PyridazonesPublished on the occasion of the 100th anniversary of the establishment of Badische Anilin- & Soda-Fabrik AG., on April 6th, 1965. (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 292-300 
    Details
    ISSN: 0570-0833
    Keywords: Pyridazones ; Heterocycles ; Mucochloric acid ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A new synthesis of mucochloric acid by chlorination of butynediol has facilitated the preparation of a series of 4,5-dichoropyridazones. The high reactivity of these compounds has been investigated and applied in several ways. New classes of compounds, some with biological activity, were obtained by displacement of the chlorine atoms. New heterocyclic systems were prepared by condensation and rearrangement reactions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196502921
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Color and Constitution of Azo Compounds (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 457-471 
    Details
    ISSN: 0570-0833
    Keywords: Color ; Azo compounds ; Azobisphosphoric acid ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Attempts to explain the surprising violet color of the new azobisphosphonic acid derivatives Y2OP—N=N—POY2 have led to the preparation and spectroscopic characterization of more than 60 azo compounds. The long-wavelength n → π* transitions on which the color depends exhibit regularities which justify the assumption of substitutent-specific absorption increments. The complex relation between color and constitution of azo compounds can be qualitatively explained with the aid of orbital models. Infrared and ultraviolet spectral data show that conjugation is inhibited by tetra-coordinated phosphorus (V). the π-system of these compounds therfore comprises only for atoms, P·N·N·P. The unexpected violet color of the phosphorus azo compounds can be ascribed to a π*/d orbital interaction. The substituent effects described have general significance, and n→π*transitions of other chromophores are similarly affected.
    Additional Material: 14 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196504571
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  • 3
    Electronic Resource
    Electronic Resource
    The Hetarynes (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 543-557 
    Details
    ISSN: 0570-0833
    Keywords: Hetarynes ; Heterocycles ; Alkynes ; Arynes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations carried out during the last six years have shown that, as in the case of benzene, an extra bond can be introduced into heteroaromatic rings. Since this possibility does not appear to be confined to exceptional cases, the heterocyclic arynes (hetarynes) promise a much wider variety than the carbocyclic arynes. Hetarynes occur mainly as intermediates in nucleophilic substitutions on halogenated heterocyclic compounds. Since the replacement of a CH group in dehydrobenzene by a nitrogen atom and the condensation of benzene rings have stabilizing effects, the stability of hetarynes is expected to increase with the number of N atoms and with the number of condensed aromatic rings.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196505431
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  • 4
    Electronic Resource
    Electronic Resource
    Heterocycles Containing Phosphorus (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1023-1038 
    Details
    ISSN: 0570-0833
    Keywords: Heterocycles ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The preparation of heterocycles containing phosphorus is described. The chemical behavior of ring systems containing trivalent phosphorus is mainly determined by their phosphine character; heterocyclic behavior in the ordinary sense is shown by rings containing functional groups. Syntheses and reactions of cyclic compounds of pentavalent and hexavalent phosphorus are particularly interesting.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196510231
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  • 5
    Electronic Resource
    Electronic Resource
    New Products of Reaction of Organometallic Compounds with Sulfur, Selenium, Tellurium, and Phosphorus (1965)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 4 (1965), S. 1007-1013 
    Details
    ISSN: 0570-0833
    Keywords: Sulfur ; Selenium ; Tellurium ; Phosphorus ; Organometallic compounds ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bond fission of molecular sulfur, selenium, and tellurium by lithiotriphenylmetal compounds (of Ge, Sn, Pb) is summarized. The products are suitable as starting materials for synthesis of new “ether analogues”. Transphenylation with tetraphenylstannane is interpreted as a high-temperature variant of the usual fission of chalcogen molecules by nucleophilic reagents. In principle, transphenylation can be applied also to other elements, as is illustrated for phosphorus. In the syntheses achieved, many of the tin-phosphorus compounds arising as intermediates can be isolated.
    Additional Material: 6 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196510071
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