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  • 2010-2014
  • 1975-1979  (7)
  • 1965-1969  (4)
  • 1920-1924
  • 2013
  • 1978  (7)
  • 1966  (4)
  • Synthetic methods
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 476-486 
    ISSN: 0570-0833
    Keywords: Intramolecular reactions ; Ene reaction ; Synthetic methods ; Cyclization ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Thermal cyclizations of appropriate dienes, enynes and related unsaturated systems, some of them carried out on an industrial scale, demonstrate increasingly the preparative power of the intramolecular ene reaction. A variety of substituted, fused and bridged ring systems, including natural products, are thus easily accessible in a regio- and stereo-selective manner. Numerous examples are discussed systematically illustrating the possibilities, limitations, and common features of this cyclization reaction and its reverse ring-opening process.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 27-37 
    ISSN: 0570-0833
    Keywords: Organomercury compounds ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Organomercurials have been known since 1850 and many synthetic routes to these compounds presently exist. The ability of these compounds to accommodate a wide variety of functional groups and to tolerate quite diverse reaction conditions makes them attractive as synthetic intermediates. While the solvomercuration-demercuration and divalent carbon transfer reactions remain the most widely used of the organomercurial reactions, a number of new synthetic procedures employing organomercurials have been developed in recent years. Many of these involve transmetallation reactions with palladium salts.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0570-0833
    Keywords: Oxygenation ; Alkanes ; Synthetic methods ; Superacidic systems ; Catalysis ; Magic acid ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Owing to the ready availability of the starting materials, the functionalization of saturated hydrocarbons for preparing chemical intermediates and products represents an attractive goal. The possibility of converting alkane in a controlled way into alcohols, ketones etc., i.e. to oxyfunctionalize them, is particularly challenging. After a short account of previous methods used for the oxidation of alkanes, particular emphasis will be given to recently developed reactions of alkanes with oxygenating agents in superacidic media.
    Additional Material: 16 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 169-175 
    ISSN: 0570-0833
    Keywords: Organoaluminum compounds ; Selectivity ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: With the aid of selected examples an overview is given of the development trends in highly discriminative reactions using organoaluminum compounds. (1) Isomerization of substituted oxiranes into allyl alcohols has been effected both stereo- and regioselectively by means of a new organoaluminum reagent, diethylaluminum 2,2,6,6-tetramethylpiperidide (DATMP); this reaction which provides a new route for the regiospecific transformation of allyl alcohols into 1,3-dienes. (2) A novel nonenzymic heterolysis of allylic phosphates of terpenoids has been effected by organoaluminum compounds and has enabled development of a new method for the selective synthesis of cyclic terpenes. (3) The reductive condensation of α-haloketones with carbonyl compounds in the presence of diethylaluminum chloride and zinc affords β-hydroxy-carbonyl derivatives in good yields with exclusion of undesired self-condensations products.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 487-496 
    ISSN: 0570-0833
    Keywords: Alumina surfaces ; Synthetic methods ; Surface chemistry ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Recent examples are given to emphasize that alumina can cause many different and often unexpected chemical reactions of adsorbed organic molecules. Recent developments are summarized to publicize that reagent-doped alumina can be used deliberately to achieve some very mild and highly selective organic transformations. The scope and limitations of organic reactions at alumina surfaces are discussed, and the advantages of these heterogeneous reactions over the corresponding homogeneous ones are pointed out. The role of the alumina and future problems are discussed briefly.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 17 (1978), S. 505-515 
    ISSN: 0570-0833
    Keywords: Pyridines ; Alkynes ; Nitriles ; Synthetic methods ; Cobalt catalysts ; Catalysis ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Soluble organocobalt catalysts permit selective formation of substituted pyridines under mild conditions in a single step: mono-, di-, and trisubstituted pyridines can be obtained at will in high conversions and high yields from nitriles and alkynes. Polynuclear derivatives such as bipyridines can also be prepared by this method.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0570-0833
    Keywords: 4-Dialkylaminopyridines ; Amino pyridines ; Acylation ; Catalysis ; Synthetic methods ; Pyridines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The synthesis of 4-dialkylaminopyridines can be accomplished in two steps starting from pyridine. Compared to pyridine, these derivatives are approximately 104 times more active when used as acylation catalysts. Dialkylaminopyridines are being used with ever-increasing frequency for acylation reactions which proceed either incompletely or not at all in pyridine. This article reviews the various possible applications of 4-dialkylaminopyridines in terpene, steroid, carbohydrate and nucleoside chemistry as well as in the transformation of amino acids into α-acyl aminoketones and polymerization of isocyanates. In addition, N-substituted 4-dialkylaminopyridinium salts can be used for the transfer of sensitive groups to nucleophiles in aqueous medium. The exceptional catalytic effect of these derivatives, even in non-polar solvents, is due, in part, to the formation of high concentrations of N-acylpyridinium salts which are present in solution as loosely-bound, highly reactive ion pairs.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 435-446 
    ISSN: 0570-0833
    Keywords: C-C coupling ; Ring closure ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Carbon monoxide undergoes catalytic reactions with unsaturated compounds to give heterocyclic carbonyl compounds. This cyclization has led to new syntheses of imides, lactams, lactones, phthalimidines, indazolones, and tetrahydroquinazolines.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 5 (1966), S. 447-461 
    ISSN: 0570-0833
    Keywords: Thiocarboxamides ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methods for the preparation of thiocarboxamides are described with special reference to progress achieved in the last few years. The discussion is arranged according to the eight most important reaction types.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    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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  • 11
    ISSN: 0570-0833
    Keywords: Carboxylic acids ; 1,1-Dichloroethylene ; Synthetic methods ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Many β-alkyl- and β-arylpropionic acids are readily obtainable by the reaction of secondary or tertiary alcohols, esters of these, or olefins with the inexpensive 1, 1-dichloroethylene in sulfuric acid. The success of the synthesis depends on the bulk and energy of the carbonium ion intermediate formed from the alcohols or olefins. With carbonium ions having one H atom attached to the carbonium C atom, electrophilic substitution of the 1,1-dichloroethylene takes place to a small extent. Dicarboxylic acids and carboxylic acids with higher molecular weights are sometimes formed as a result of side reactions.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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