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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 118 (1985), S. 1058-1070 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Regioselective Addition of Grignard Reagents to 3-Methoxy- and 3-Nitrophthalic AnhydrideThe regioselectivity in the addition of the grignard reagents 5a and 6a to the anhydrides 1 and 2 is determined by the solvent system: in a highly selective manner (3: 97), the meta carbonyl group is attacked in tetrahydrofuran/tetramethylethylenediamine, while predominant, but relatively unselective (maximum 78:22) addition to the ortho carbonyl group is observed in diethyl ether. The influence of the solvent system on the regioselectivity is discussed. The LUMO-coefficients of the carbonyl carbon atoms in 1 and 2 were calculated.
    Notes: Die Addition der Grignard-Reagenzien 5a und 6a an die Anhydride 1 und 2 wird entscheidend vom Reaktionsmedium beeinflußt: in Tetrathydrofuran/Tetramethylethylendiamin wird hochselektiv (3: 97) die meta-ständige, in Diethylether dagegen überwiegend, aber mit nur geringer Selektivität (maximal 78: 22), die ortho-Carbonylgruppe angegriffen. Die Strukturen der dabei erhaltenen Addukte werden durch Umwandlung in die Ester 7-10, in die Lactone 11 sowie in die Ketone 12 und 13 bewiesen. Im Zusammenhang mit dem Versuch, die lösungsmittelabhängige Regioselektivität zu interpretieren, wurden die LUMO-Koeffizienten der Carbonylkohlenstoff-atome in 1 und 2 berechnet.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 265-268 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The reaction of the aldehyde 1 with aluminium trichloride in benzene affords the dihydrobenzanthrone 2. The structure is confirmed by an X-ray analysis. Dehydrogenation of 2 yields the benzanthrone 3, which shows a greenish yellow fluorescence. According to the 1H-NMR and mass spectra, the deuterated products 5 and 6 are formed, when the key reaction is carried out in [D6]benzene.
    Notes: Die Umsetzung des Aldehyds 1 mit Aluminiumtrichlorid in Benzol führt zum Dihydrobenzanthron 2, dessen Konstitution durch eine Röntgenstrukturanalyse bewiesen wird. Die Dehydrierung von 2 liefert das grüngelb fluoreszierende Benzanthron 3. Wird die Schlüsselreaktion in [D6]Benzol durchgeführt, so bilden sich laut 1H-NMR- und Massenspektren die [D8]Produkte 5 bzw. 6.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1989 (1989), S. 99-101 
    ISSN: 0170-2041
    Keywords: 1,3-Indandiones, 2-aryl ; Keto-enol tautomerism ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: As evaluated by 1H- and 13C-NMR spectroscopy, the keto-enol equilibrium of 2-phenyl-, 2-(2-methoxyphenyl)-, and 2-(3-methoxyphenyl)-1,3-indandione in chloroform lies far on the side of the diketo forms 1a-c. Whereas the enol tautomers 2a and 2c are favoured in dimethyl sulfoxide, 2-(2-methoxyphenyl)-1,3-indandione prefers the diketo form 1b even in this solvent.
    Additional Material: 2 Tab.
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  • 4
    Publication Date: 1986-01-01
    Print ISSN: 0040-4039
    Electronic ISSN: 1873-3581
    Topics: Chemistry and Pharmacology
    Published by Elsevier
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