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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Monatshefte für Chemie 117 (1986), S. 617-619 
    ISSN: 1434-4475
    Keywords: Catalysis ; Photochemistry ; Supported platinum complex
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Ultraviolettbetrahlung des siliziumverknüpften Komplexes Pt(C2O4)L 2 [L=(H3CO)3Si(CH2)2PEt 2] ergab eine [SiO2]-L 2Pt-Spezies, die die Hydrosilierung von Olefinen katalysiert oder unter Bildung eines Oberflächen-Dicarbonylkomplexes 2 CO addiert.
    Notes: Abstract Ultraviolet irradiation of the silica attached complex Pt(C2O4)L 2, [L=(H3CO)3Si(CH2)2PEt 2], yields a [SiO2]-L 2Pt species that catalyzes olefin hydrosilation or adds 2 CO to yield a surface dicarbonyl complex.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1434-4475
    Keywords: Catalysis ; Dinitrogen complexes ; Ethyldiazoacetate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Komplexetrans-[Mo(N2)2(dppe)2] (dppe=Ph 2PCH2CH2PPh 2) reagieren mit NN=CHCOOEt in benzolischer Lösung zuPh-N=N-CH3 als organischem Hauptprodukt. Andererseits wird bei der Bestrahlung vontrans-[W(N2)2(dppe)2] inTHF-Lösung in der Gegenwart von Ethyldiazoacetat das PhosphazenPh 2P(N2CHCOOEt)(CH2CH2)P(N2CHCOOEt)Ph 2 gebildet; in feuchter Lösung erleidet die Phosphazen-Bindung eine teilweise Hydrolyse und die Phosphonium-Spezies [Ph 2P(NHNCHCOOEt)(CH2CH2)P(NHNCHCOOEt)Ph 2]2+ scheint gebildet zu werden.
    Notes: Abstract Complextrans-[Mo(N2)2(dppe)2] (dppe=Ph 2PCH2CH2PPh 2) reacts with NN=CHCOOEt in benzene solution to afford benzene-azomethane,Ph-N=N-CH3, as the main organic product. However, the phosphazene speciesPh 2P(N2CHCOOEt)(CH2CH2)P(N2CHCOOEt)Ph 2 is formed by irradiating aTHF solution oftrans-[W(N2)2(dppe)2] in the presence of ethyldiazoacetate; in moist solution, the phosphazene bonds undergo a partial hydrolysis, and the phosphonium species [Ph 2P(NHNCHCOOEt)(CH2CH2)P(NHNCHCOOEt)Ph 2]2+ appears to be formed.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0570-0833
    Keywords: Cholesterol homeostasis ; Receptors ; Catalysis ; Nobel lecture ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 16 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 508-524 
    ISSN: 0570-0833
    Keywords: Cross-coupling ; Organotin compounds ; Electrophilicity ; Palladium ; Catalysis ; C-C coupling ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cross-coupling of organotin reagents with a variety of organic electrophiles, catalyzed by palladium, provides a novel method for generating a carbon-carbon bond. Because this mild, versatile reaction is tolerant of a wide variety of functional groups on either coupling partner, is stereospecific and regioselective, and gives high yields of product, it is ideal for use in the synthesis of elaborate organic molecules. When the coupling reaction is carried out in the presence of carbon monoxide, instead of a direct coupling, carbon monoxide insertion takes place, stitching the two coupling partners together and generating a ketone.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 25 (1986), S. 960-970 
    ISSN: 0570-0833
    Keywords: Phase-transfer catalysis ; Catalysis ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The development of Phase Transfer Catalysis (PTC) represents a major step forward in the employment of many organic reactions and renders them very convenient and useful processes. These reactions involve the application of nucleophiles in general, anions and bases in particular, in reactions carried out in a water-organic solvent system. They can be performed both in the laboratory and on an industrial scale. The ease of application of PTC processes is the main reason for their increasing utilization in industry. An outstanding achievement of this technique is the employment of aqueous bases in reactions which traditionally would otherwise require a strong base in a nonaqueous medium. The classical procedures that require severe anhydrous conditions, expensive solvents and dangerous bases such as metal hydrides and organometallic reagents are now replaced by aqueous solutions of, e.g., sodium or potassium hydroxides (PTC/OH processes). In contrast to the extensive synthetic applications of PTC/OH systems, the detailed mechanisms of these processes have been the subject of a great deal of controversy and various mechanisms have been suggested. However, it would seem that our knowledge concerning the mechanistic aspects of such reactions has now reached the stage where it can be used to advantage in synthesis planning. A better understanding of the various factors which influence the reaction would undoubtedly help to optimize PTC/OH processes such as to enable higher yields in shorter reaction times at lower temperatures. The importance of, inter alia, the catalyst will be pointed out and it is highly recommended that such catalysts be always available in the laboratory, for the range of organic reactions that they can efficiently, conveniently and safely catalyze is vast indeed.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 0570-0833
    Keywords: Proton transfer ; Catalysis ; Enzyme catalysis ; Hydrolysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 12 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 93-101 
    ISSN: 0570-0833
    Keywords: Organometallic catalysts ; Catalysis ; Reaction mechanisms ; Lithium ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 3 (1964), S. 185-191 
    ISSN: 0570-0833
    Keywords: Coordination modes ; Catalysis ; Cyclooctatetraenes ; Reppe chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 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.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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