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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1809-1817 
    ISSN: 0009-2940
    Keywords: Lithiation ; Mannich reaction ; Alkylation ; Grignard reaction ; Condensation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Phenols and naphthols are benzotriazolylmethylated by 1-(hydroxymethyl)-1H-benzotriazole (13) (a formaldehyde derivative) in the o- or (if both o-positions are occupied) in the p-position. The reaction can be extended to other aldehydes in the case of the naphthols. The methylene group in the o-(benzotriazolylmethyl)phenols can be lithiated (but only after trimethylsilyl protection of the hydroxy group) and then substituted by various electrophiles. The benzotriazole residues in both the primary products and in their substituted derivatives can be displaced by the alkyl anions of Grignard reagents or by hydride ions allowing the elaboration of many new types of substituted phenols.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 1819-1826 
    ISSN: 0009-2940
    Keywords: Lithiation ; Grignard reaction ; Condensation ; Aryl ethers ; Diarylmethanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Methoxybenzenes and -naphthalenes are benzotriazolylmethylated in the para-position or if this is blocked in an ortho- position. The methylene groups in the products are readily substituted by electrophiles via the lithiated derivatives. Displacement of the benzotriazole group can be effected by organometallic reagents or by electron-rich benzoid compounds to afford a versatile method for the synthesis of substituted aryl ethers.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 27 (1989), S. 1090-1093 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 1-Substituted pyridinium salts ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR chemical shifts of a series of 1-substituted pyridinium salts were measured in dimethyl sulfoxide. The effect of the quaternary pyridinium ring on the resonance of the methylene group of the substituent is reported. Increments of δ1H = 3.89 ± 0.16 ppm and δ13C = 47.5 ± 3.7 ppm and are estimated for replacing YCH2H with YCH2Py+. The effects of 1-substituents on the pyridinium ring chemical shifts are discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 29 (1991), S. 2-8 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; Ethenyl-substituted benzenoid aromatics ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1H and 13C NMR studies were carried out on 1-ethenylnaphthalene, 2-ethenylnaphthalene, 9-ethenylanthracene, 9-ethenylphenanthrene, 1-ethenylpyrene and 1-ethenylperylene. Assignments of proton and carbon resonances were made with the aid of 2D COSY, 2D HETCOR, 2D COLOC, 2D COLOCS, 3J(H,C) INAPT, and NOE difference spectral techniques.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Chichester : Wiley-Blackwell
    Organic Magnetic Resonance 28 (1990), S. 914-917 
    ISSN: 0749-1581
    Keywords: 1H NMR ; 13C NMR ; 4-substituted and 4,6-disubstituted dibenzothiophenes ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The proton and carbon NMR spectra of several 4-substituted- and 4,6-disubstituted-dibenzothiophenes have been measured, and their chemical shifts assigned employing spin decoupling and COSY and HETCOR two-dimensional techniques. This work rectifies several literature misassignments of 13C chemical shifts of 4-substituted dibenzothiophenes and also examines the effects of substituents on the chemical shifts. Hence this study will be useful in the future structure determinations of mono- and multisubstituted dibenzothiophenes.
    Additional Material: 5 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Angewandte Chemie International Edition in English 15 (1976), S. 1-9 
    ISSN: 0570-0833
    Keywords: Betaines ; Synthetic methods ; Cycloaddition ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The cycloadditions of 3-hydroxy-1-methylpyridinium betaines with electron-deficient olefins have been extended to a variety of 1-substituents in place of methyl. Application of resonance theory and later of quantum chemical methods led to rationalization of preceding results and prediction of new reactions. Thermal additions of 2π- and 6π-electron addends at the 2,6-positions and of 4π-electron addends at the 2,4-positions are described. The cycloadducts are highly interesting potential synthetic building blocks.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0570-0833
    Keywords: Pyrylium salts ; Pyridinium salts ; Synthetic methods ; Amines ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The first pyrylium salt was isolated some 80 years ago, yet up to the 1950s only moderate interest was taken in the preparation, properties and uses of such salts. However, the past thirty years has seen a phenomenal growth in the literature pertinent to this area of chemistry: the importance of pyrylium salts as intermediates has been realized. They are readily prepared by a variety of generally applicable routes, and they are highly reactive towards nucleophiles. Together, this enables the convenient synthesis of a great variety of acyclic and heterocyclic compounds. We have used highly substituted pyrylium salts for the two-step conversion of the amino group in alkylamines RNH2 into numerous other functionalities. In the first step, the pyrylium salts are converted with the amines into N-substituted pyridinium salts, which, in the second step, react with Nu⊖ to give the desired products RNu. In some cases the R moiety is also changed, e.g. by elimination. Studies of the reactions of these pyridinium salts have allowed interesting insights into the mechanisms of nucleophilic substitution, in addition to rendering aliphatic amines important synthetic intermediates. Thus, the method complements the diazotization procedure for the transformation of arylamines.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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