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  • Carbodiimides  (2)
  • Wiley-Blackwell  (2)
  • American Institute of Physics
  • Blackwell Publishing Ltd
  • 1965-1969  (2)
  • 1966  (2)
Collection
Publisher
  • Wiley-Blackwell  (2)
  • American Institute of Physics
  • Blackwell Publishing Ltd
Years
  • 1965-1969  (2)
Year
  • 1966  (2)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 470-477 
    ISSN: 0570-0833
    Keywords: Isoureas ; Alkylation ; Carbodiimides ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The CuCl2-catalysed addition of alcohols to aliphatic caribodiimides (particularly diisopropylcarbodiimide) to form O,N,N′-trialkylisoureas may, in the case of bifunctional hydroxy compounds (esters of α-hydroxycarboxylic acids, diols, halogeno alcohols, amino alcohols, and cyclic hydroxy ethers), continue to give 5-, 6-, and 7-membered 1,3-O,N or 1,3-N,N heterocycles. O,N,N′-Trialkylisoureas are selective alkylating agents. Thus alcohols with allyl structures can be etherified with diisopropylcarbodiimide; a new method of esterification via O,N,N′-trialkylisoureas has been applied to mesitylenecarboxylic acid.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 704-712 
    ISSN: 0570-0833
    Keywords: Isocyanates ; Carbodiimides ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of 1,3-disubstituted ureas and 1-arylsulfonyl-3-alkylureas with phosgene permits the preparation of a number of isocyanates and sulfonyl isocyanates that had not previously been described, or that were difficult to prepare. 1,3-Disubstituted thioureas and 1-aryl-(or alkyl)sulfonyl-3-alkylthioureas give carbodiimides. Thionyl chloride and phosphorus pentachloride react with the urea derivatives in the same way as phosgene. Oxalyl chloride reacts with ureas to form parabanic acid derivatives, whereas with thiourea it gives 2-imino-1,3-thiazolidine-4,5-diones, which can isomerize to parabanic acid derivatives.
    Additional Material: 9 Tab.
    Type of Medium: Electronic Resource
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