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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 335 (1993), S. 351-358 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ring Transformations of Heterocyclic Compounds. I. 2-Amino-benzophenones and 7-Oxo-hepta-2,4-dienenitriles by Reaction of 2,4,6-Triarylpyrylium Salts with 4-Nitrobenzyl Cyanide2,4,6-Triarylpyrylium salts 1 react with 4-nitrobenzyl cyanide in the presence of sodium acetate, triethylamine or triethylamine/acetic acid to give 7-oxo-hepta-2,4-dienenitriles 2. With stronger bases such as sodium methanolate or ethanolate a ring transformation of the salts 1 occurs giving rise to 2-amino-benzophenones 3 which can also be obtained by cyclization of the nitriles 2. Under the same conditions the 3-methyl-2,4,6-triphenylpyrylium salt 4 forms the 4-methyl-7-oxo-hepta-2,4-dienenitrile 5 by regioselective addition of the 4-nitrobenzyl cyanide at C-2 or it is converted to the 2-amino-5-methyl-benzophenone 6. The ring transformation of the pyrylium salts 1/4 by 4-nitrobenzyl cyanide represents a new and simple method for the preparation of 2-amino-benzophenones. - Spectroscopic data of the novel compounds are discussed; the structure of 5 was confirmed by a single crystal X-ray analysis.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 337 (1995), S. 46-49 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The hitherto unknown stereochemistry of N,N,N′,N′-tetrasubstituted 2-arylthioacrylamides 1 has been determined by X-ray crystal analysis and systematic NMR-investigations. Provided that the 2-aryl group lacks ortho substituents, compounds 1 exist predominantly as Z-isomers. In contrast, the major isomer has an E-s-trans configuration if the 2-aryl group is ortho-substituted. Substitution of the 3-amino group of 1 by glycinates, giving 3-aminothioacrylamides 2, generally preserves the original stereochemistry.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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