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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Helvetica Chimica Acta 67 (1984), S. 1957-1962 
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Irradiation (λ 〉 280 nm) of 3-hydroxy-1H-pyrrole-2-carboxylates 1 in CH3CN gives the [2.2′-bi(3-oxo-2,3-dihydro-1H-pyrrole)]-2-,2′-dicarboxylates 2 in reasonable to good yields. The corresponding N-methylpyrroles 3 only undergo slow photodecomposition under similar conditions. Several 2-methyl-3-oxo-2,3-dihydro-1H-pyrrole-2-carboxylates 4 and 5 were synthesized to compare their spectral data with those of the dehydrodimers 2. A X-ray structure analysis was performed for diethyl [2,2′-bi(4,5-dimethyl-3-oxo-2,3-dihydro-1 H-pyrrole)]-2,2′-dicarboxylate (2b). The originally proposed [3,3′-bi(3H-pyroole)] structure for compounds 2a-e proves incorrect.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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