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  • Electronic Resource  (7)
  • 1975-1979
  • 1960-1964  (7)
  • 1945-1949
  • 1935-1939
  • 1915-1919
  • 1880-1889
  • 1850-1859
  • 1830-1839
  • 1820-1829
  • 1964  (2)
  • 1963  (5)
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  • 1948
  • 1858
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  • 1835
  • Heterocycles  (4)
  • Dyes/Pigments  (3)
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  • Electronic Resource  (7)
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  • 1975-1979
  • 1960-1964  (7)
  • 1945-1949
  • 1935-1939
  • 1915-1919
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  • 1
    Electronic Resource
    Electronic Resource
    New Reactive DyesDedicated to Professor H. Bredereck on the occasion of his 60th birthday (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 408-416 
    Details
    ISSN: 0570-0833
    Keywords: Reactive dyes ; Dyes/Pigments ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two new groups of reactive dyestuffs have been developed. One group (Levafix® dyes) comprises compounds which contain —SO2NH—CH2—CH2—OSO3H or —CH2—N(alkyl)-CH2—CH2—OSO3H as reactive groups. The dyes of this group react with cellulose fibers to form cellulose ethers, e.g. R—SO2NH—CH2—CH2—O—cellulose. The substances in the second group (Levafix-E® dyes) consist of the amides formed from 2,3-dichloroquinoxaline-6-carboxylic acid and dyestuffs containing primary or secondary amino groups.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196404081
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    Paper (German National Licenses)
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  • 2
    Electronic Resource
    Electronic Resource
    Three-Membered Rings Containing Two Hetero-Atoms (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 333-341 
    Details
    ISSN: 0570-0833
    Keywords: Strained molecules ; Heterocycles ; Diaziridines ; Diazirines ; Oxaziranes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Since their discovery five years ago, the diaziridines have become an extensive and easily accessible class of compounds. Hydrolysis of these compounds effects a simple synthesis of hydrazine, alkylhydrazines, and N,N′-dialkylhydrazines. They are also powerful oxidizing agents. The rigidity of the three-membered ring gives rise to a few stereoelectronic peculiarities. Investigations on the mechanism of formation of the three-membered rings led to a new synthesis of oxaziranes and to discovery of the isomeric oximes with a three-membered ring structure. The latter decompose readily to form diimide. Diazirines are cyclic isomers of the aliphatic diazo compounds and are surprisingly easy to obtain by dehydrogenation of suitable diaziridines; they are chemically much more stable than the linear isomers. Grignard reagents add onto the N=N double bond without destruction of the three-membered ring. Thermal decomposition yields carbenes.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196403331
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  • 3
    Electronic Resource
    Electronic Resource
    Kinetics and Mechanism of 1,3-Dipolr CycloadditionsExtended version of a lecture given at the Annual Meeting of the Dechema in Frankfurt/Main on June 14th, 1962, and of the Max Tishler Lecture at Harvard University on December 10th, 1962. (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 633-645 
    Details
    ISSN: 0570-0833
    Keywords: Kinetics ; Dipolar cycloaddition ; Cycloaddition ; Heterocycles ; Reaction mechanisms ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Criteria for the mechanism of 1,3-dipolar cycloadditions which lead to 5-membered rings are provided by the stereoselectivity observed with cis-trans isomeric dipolarophiles, by the effect of solvent and substituents on the rate constants, by the activation parameters, and by orientation phenomena. A concerted addition, which can also be described in terms of molecular orbitals and in which the two new σ-bonds are formed simultaneously, although not necessarily at equal rates, offers the best explanation of the experimental facts.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196306331
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  • 4
    Electronic Resource
    Electronic Resource
    Reactive Dyes Containing Vinylsulfonyl GroupsPublished on the occasion of the 100th anniversary of the founding of Farbwerke Hoechst AG. on January 11th, 1963 (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 20-23 
    Details
    ISSN: 0570-0833
    Keywords: Reactive dyes ; Dyes/Pigments ; Reactive dyes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Compounds and dyes containing vinylsulfonyl groups or groupings which readily yield vinylsulfonyl groups possess a marked ability to add onto many compounds containing active hydrogen under alkaline conditions. They also react with natural substances of high molecular weight, e.g. wool and cellulose, which contain amino- or hydroxyl groups. These reactions lead to the formation of strong covalent bonds between the reactants. As a result of this finding, reactive dyes for nitrogenous and cellulose fibers have been developed.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196300201
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  • 5
    Electronic Resource
    Electronic Resource
    Polycondensation Dyes. A New Principle for the Preparation of Wash-Fast Cotton DyeingsPublished on the occasion of the 100th anniversary of the foundation of Farbwerke Hoechst on January 11th, 1963 (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 30-31 
    Details
    ISSN: 0570-0833
    Keywords: Polycondensation ; Dyes/Pigments ; Bunte salts ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Dyes which contain only thiosulfate residues as water-solubilizing groups are readily polycondensed on cellulose under mild conditions in the presence of condensing agents such as sodium sulfide to give insoluble, high molecular-weight dyes. This type of fixation leads to wash-fast dyeings and, in contrast to reactive dyes, involves no reaction with the fiber. The preparation and application of the dyes are described.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196300301
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  • 6
    Electronic Resource
    Electronic Resource
    Syntheses of Heterocyclic Compounds from Aminoguanidine (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 459-476 
    Details
    ISSN: 0570-0833
    Keywords: Aminoguanidine ; Heterocycles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Due to its unique structure, aminoguanidine is capable of reacting as a derivative of hydrazine, guanidine or formamidine. Addition and condensation reactions yield products which can be cyclized to heterocyclic compounds. Frequently, heterocyclics are directly accessible from aminoguanidine in one stage.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196304591
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  • 7
    Electronic Resource
    Electronic Resource
    1,3-Dipolar Cycloadditions. Past and FutureExtended version of lectures given at the Chemists' Meeting in Vienna (Austria) October 1961, and at the Gordon Research Conference, New Hampton (U.S.A.), 1961. (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 565-598 
    Details
    ISSN: 0570-0833
    Keywords: Dipolar cycloaddition ; Cycloaddition ; Heterocycles ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: In contrast to the very large number of special methods applicable to syntheses in the heterocyclic series, relatively few general methods are available. The 1,3-dipolar addition offers a remarkably wide range of utility in the synthesis of five-membered heterocycles. Here the “1,3-dipole”, which can only be represented by zwitterionic octet resonance structures, combines in a cycloaddition with a multiple bond system - the “dipolarophile” - to form an uncharged five-membered ring. Although numerous individual examples of this reaction were known, some even back in the nineteenth century, fruitful development of this synthetic principle has been achieved only in recent years.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196305651
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