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  • 1960-1964  (8)
  • 1935-1939
  • 1920-1924
  • 1963  (5)
  • 1962  (3)
  • Phosphorus  (4)
  • Catalysis
  • Heterocycles
  • Key words
  • 1
    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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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Further Contributions to the Knowledge of SemimetalsDedicated to Dr. W. Foerst on the occasion of his 65th birthday (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 523-530 
    Details
    ISSN: 0570-0833
    Keywords: Semimetals ; Metallic structure ; Nonmetallic structure ; Antimony ; Arsenic ; Bismuth ; Phosphorus ; Tellurium ; Tin ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Measurements on semimetals have been continued. Studies of the dependence on temperature of various properties have provided details regarding the transition from the nonmetallic to the more metallic structure. A second-order transition has been found for tin at 170 °C, in which the c-axis remains unchanged, while the a-axis undergoes a small, discontinuous elongation.
    Additional Material: 13 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196305231
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  • 4
    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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  • 5
    Electronic Resource
    Electronic Resource
    New Developments in the Chemistry of PolyphosphanesDedicated to Prof. Dr. Karl Winnacker on the occasion of his 60th birthday (1963)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 2 (1963), S. 646-654 
    Details
    ISSN: 0570-0833
    Keywords: Polyphosphanes ; Phosphanes ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: While silicon and sulfur, which are situated to the left and to the right of phosphorus in the periodic table, from numerous chain and cyclic Si-Si and S-S-compounds with varying numbers of members, until recently the polyphosphance chemistry has been limited to the two-membered compounds diphosphane P2H4 and its derivatives. A number of results obtained in studies on polyphosphanes carried out in recent years will therefore be discussed, which, together with some more recent work by other authors, have led to an expansion of our knowledge of the prepration and properties of straight and branched-chain as well as of cyclic and polycylic -P-P-systems.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196306461
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  • 6
    Electronic Resource
    Electronic Resource
    The Oxidation of Olefins with Palladium Chloride Catalysts (1962)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 80-88 
    Details
    ISSN: 0570-0833
    Keywords: Oxidation ; Palladium ; Catalysis ; Alkenes ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The oxidation of olefins to carbonyl compounds with palladium compounds, especially the oxidation of ethylene to acetaldehyde, is at present carried out on a technical scale. The reaction takes place via a palladium-olefin complex, the formation of which is inhibited by halide ions. Hydrolysis to the carbonyl compound is inhibited by hydrogen ions. The knowledge gained by studying the reaction of olefins with pure solutions of palladium salts allows important conclusions to be drawn concerning the action of technical catalyst solutions containing copper and palladium chloride.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196200801
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  • 7
    Electronic Resource
    Electronic Resource
    Isocyanates of Esters of Some Acids of Phosphorus and SilicionDedicated to Prof. Dr. Otto Bayer on the occasion of his 60th birthday (1962)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 617-621 
    Details
    ISSN: 0570-0833
    Keywords: Isocyanates ; Phosphorus ; Silicon ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Several aminoaryl esters of phosphoric and thiophosphoric acids were prepared by the reaction of phosphorus pentahalides with nitrophenols, followed by catalytic hydrogenation, or by treating aminophenols with phosphorus trihalides and oxidation to pentavalent phosphorus. These amino esters were then converted into isocyanato esters by the action of phosgene. Isocyanates of phosphonates have been synthetized on the same principle, as well as via the Arbusov reaction of halogen-substituted isocyanates with trialkyl phosphites. The reaction of silicon halides or alkylhalogenosilanes with aminophenols yielded aminoaryl esters of silicic acid or its derivatives, which could also be treated with phosgene to convert them into isocyanato esters.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196206171
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  • 8
    Electronic Resource
    Electronic Resource
    β-Chloroethylphosphonic Dichloride: Its Synthesis and Use (1962)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 1 (1962), S. 652-656 
    Details
    ISSN: 0570-0833
    Keywords: β-Chloroethanephosphonic dichloride ; Phosphorus ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ethylene, phosphorus trichloride, and oxygen react together to give β-chloroethylphosphonic dichloride in good yields. Being a bifunctional acid chloride, this compound undergoes polycondensation reactions with other, at least bifunctional, compounds affording polyesters, polyamides, epoxy resins, etc. β-Chloroethylphosphonic dichloride also may be converted into vinylphosphonic dichloride, thus serving as a starting material for the preparation of vinylphosphonic acid and its derivatives. These undergo both homopolymerization and copolymerization with compounds containing olefinic double bonds. The products are used in the field of synthetic resins, for dressing textiles, and as protective surface coatings.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/anie.196206521
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