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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 335 (1993), S. 345-350 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of α-Ketoenamines to 2-Acetyl-p-benzoquinoneAddition of 2-morpholino-2-cyclohex-1-en-one 2 to 2-acetyl-quinone 1 yields benzo[c][4 H]chromen-4,7,10-trion 4 which is unstable and rearranges to 5. 4 is converted to 3-(2,5-dihydroxy-phenyl)-2-morpholino-2-cyclohex-1-en-on 3 thermically and to dibenzo[b,d]furan-4-on 7 acid catalyzed. The structure of 7 is secured by independent synthesis. Dibenzo[b,d]furan-4-on 14 is the product of reaction from 2-(p-toluidino)-2-cyclohex-1-en-on 9 and 1 with benzo[c][4 H]chromen-4,7,10-trion 10 as intermediate. By proton catalysis 5-acetyl-6-hydroxy-carbazol-1-on 13 and 4-oxo-cyclohexa[c]isochinolinium hydrochlorid 15 is obtained from 10. 1 H-cyclopenta[d]furan-3-on 17 is formed by addition of 2-(p-toluidino)-2-cyclopent-1-en-on 16 to 1. It is rearranged by proton catalysis to 3-oxo-1 H-cyclopenta[c]isochinolinium salt 18. Reaction of cyclopentan-1,2-dione and 1 yields 3 aH-cyclopenta[c]isochromen-3,6,9-trion 20, rearranging to 1 H-cyclopenta[b]benzo[d]furan-3-on 21. The stereochemistry of adducts is discussed in connection with the course of the reaction, spectroscopical evidence, molecular modelling and calculation of HOMO/LUMO and AO-coefficients.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 607 (1992), S. 26-28 
    ISSN: 0044-2313
    Keywords: Tetrakis(di-tert.-butylphosphino)diphosphane ; [(tBu)2P]2P—P[P(tBu)2]2 ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal Structure of Tetrakis(di-tert.-butylphosphino)diphosphane [(tBu)2P]2P—P[P(tBu)2]2[(tBu)2P]2P—P[P(tBu)2]2 1 obtained at -20°C from a solution of (tBu)2P—P=P(Br)tBu2 forms yellow crystals (regular hexagons). 1 crystallizes monoclinic in the space group C2/c with a = 2145.6pm, b = 1137pm, c = 1696.1pm, β = 110.075° and Z = 4 formula units in the elementary cell. Due to high steric load the bond angles at the tertiary P atoms with δ = 115.7° are significantly larger than those at the primary P atoms with δ = 108.6°.
    Notes: [(tBu)2P]2P—P[P(tBu)2]2 1 sich aus (tBu)2P—P(Br)tBu2 (toluolische Lösung, -20°C) und fällt als gelbe Kristalle (regelmäßige Sechsecke) aus. 1 kristallisiert monoklin in der Raumgruppe C2/c mit den Gitterkonstanten a = 2145,6pm, b = 1137pm, c = 1696pm, β = 110,75°. Die Elementarzelle enthält 4 Formeleinheiten. Die Bindungswinkel an den tertiären P-Atomen mit δ = 115,7° sind infolge der hohen sterischen Belastung der tert. P-Atome gegenüber denen an den primären P-Atomen mit δ = 108,6° deutlich aufgeweitet.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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