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  • 1985-1989
  • 1980-1984
  • 1960-1964  (6)
  • 1950-1954
  • 1870-1879
  • 1964  (6)
  • 1950
  • Catalysis  (3)
  • Cyclooctatetraenes  (2)
  • Organopotassium compounds  (2)
Datenquelle
Materialart
Erscheinungszeitraum
  • 1985-1989
  • 1980-1984
  • 1960-1964  (6)
  • 1950-1954
  • 1870-1879
Jahr
Schlagwörter
  • 1
    Digitale Medien
    Digitale Medien
    The Valence Tautomerism of Cyclooctatetraene (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 83-85 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Valence tautomerism ; Cyclooctatetraenes ; Bicyclooctatriene ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The Diels-Alder adducts of cyclooctatetraene and its derivatives are derived from the bicyclo[4,2,0]octane structure. A kinetic investigation shows that the Diels-Alder addition of dienophiles to cyclooctatetraene and phenylcyclooctatetraene is preceded by a valence tautomerism equilibrium with bicyclo[4,2,0]octa-2,4,7-triene or its 7-phenyl derivative.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196400831
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  • 2
    Digitale Medien
    Digitale Medien
    Proton Transfer, Acid-Base Catalysis, and Enzymatic Hydrolysis. Part I: ELEMENTARY PROCESSESPart II (Catalytic Mechanisms) will appear shortly in this journal.Dedicated to Dr. W. Foerst on the occasion of his 65th birthday (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 1-19 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Proton transfer ; Catalysis ; Enzyme catalysis ; Hydrolysis ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The proton occupies a special position as a promoter and mediator in chemical reactions occurring in solution. Many reactions in organic chemistry are catalysed by acids or bases; likewise, most enzymes contain active groups which promote acid-base catalysis. To understand the reaction mechanisms involved, it is necessary to identify the elementary steps as well as their course in time. Systematic investigation of these elementary steps as well as their course in time. Systematic investigation of these elementary steps has become possible only with the development of new methods for studying very fast reactions. The present paper reviews the information obtained in this type of investigation. The result is a relatively complete picture of the elementary proton transfer mechanisms and a comprehensive description of the modes and laws of acid-base and enzymatic catalysis.
    Zusätzliches Material: 12 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196400011
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  • 3
    Digitale Medien
    Digitale Medien
    The Mechanism of the Action of Organometallic CatalystsDedicated to Prof. Dr. Karl Winnacker on the occasion of his 60th birthday. (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 93-101 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Organometallic catalysts ; Catalysis ; Reaction mechanisms ; Lithium ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Kinetic investigations of the polyreaction of isoprene with organolithium compounds as initiators in n-heptane as solvent indicate the following sequence of reactions: 1. formation of an adduct between a monomeric form of the organolithium compound and the isoprene and 2. reaction of this adduct with an associated form of the organolithium compound with insertion of the isoprene. The adduct formation is considered to be due to chemisorption, and proof of such chemisorption of a monomer (ethylene) is also demonstrated for a homogeneous Ziegler-type catalyst. All the reactions can be formulated in the form of cyclic structures with electron-deficient character. Postulation of such ring structures explains the surprising values obtained for the frequency factors and equilibrium constants.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196400931
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  • 4
    Digitale Medien
    Digitale Medien
    Coordination Chemistry and Catalysis. Investigations on the Synthesis of Cyclooctatetraene by the Method of W. Reppe (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 185-191 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Coordination modes ; Catalysis ; Cyclooctatetraenes ; Reppe chemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The relationship between the structure and the catalytic activity of nickel(II) complexes in the synthesis of cyclooctatetraene by the method of W. Reppe is discussed. The cyclotetramerization of acetylene takes place within labile Ni(II)-acetylene π-complexes. Inhibition tests have made it probable that four molecules of acetylene are grouped around the nickel ion in the transition state, in a configuration which favors the formation of the eight-membered ring.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196401851
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  • 5
    Digitale Medien
    Digitale Medien
    Organosodium and Organopotassium Compounds Part I: Properties and ReactionsFor earlier reviews see [1a-1g]. (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 287-306 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Organopotassium compounds ; Organosodium compounds ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Zusätzliches Material: 7 Tab.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196402871
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  • 6
    Digitale Medien
    Digitale Medien
    Organosodium and Organopotassium Compounds. Part II: Preparation and Synthetic ApplicationsPart I: Properties and Reactions: M. Sclilosser, Angew. Chem. 76, 124 (1964); Angew. Chem. internat. Edit. 3, 287 (1964). (1964)
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 362-373 
    Details
    ISSN: 0570-0833
    Schlagwort(e): Organopotassium compounds ; Organosodium compounds ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A selection of well established procedures for the preparation of the most common organosodium and organopotassium compounds is given. The wide synthetic applicability of organoalkali-metal compounds is shown by means of examples. Unlike Part I, Part II deals not only with “true”organoalkali compounds, but also with salt-like compounds such as sodium acetylides and sodiocarboxylic esters, since these posses considerable preparative value.
    Zusätzliches Material: 8 Tab.
    Materialart: Digitale Medien
    URL: http://dx.doi.org/10.1002/anie.196403621
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