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  • 1
    ISSN: 0947-3440
    Keywords: Spiranes ; Liquid crystals ; Structure-property relations of LC substances ; TosMIC ; Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A number of terminally substituted spiranes were prepared from 9-pentyl-3-spiro[5.5]undecanone (7), which was obtained in a five-step synthesis starting from 4-pentylcyclohexanone (1), using an intramolecular cyclisation with 4-toluenesulfonylmethyl isocyanide (TosMIC) as a key step. By a comparison of the physical data of the new spiro[5.5]undecane derivatives I with those of several well-known, analogous substituted compounds - solely differing in their central building unit - conclusions regarding the effects of the spiro ring system on its mesogenic potential are drawn.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photochemistry of Small Rings, XXVIII1). - Dibenzo[2.4]spirenes and Their Derivatives via Photofragmentation and Thermolysis of SpiropyrazolesPhotofragmentation of the spiropyrazoles 3 leads to the dibenzo[2.4]spirenes 4 in good to average yields. Thermolysis of 3 at lower temperatures also gives 4. At higher temperature, however, the pentalene derivatives 9 are formed. This rearrangement involves spirenes 4. The vinylcarbene 11 or the diradical 13 are intermediates in the reaction 3 → 4. Rearrangement 4 → 9 can proceed synchronously or via the diradical 15.
    Notes: Die Photofragmentierung der Spiropyrazole 3 ergibt in guten bis mittleren Ausbeuten die Dibenzo[2.4]spirene 4. Die Thermolyse von 3 führt bei tieferen Temperaturen ebenfalls zu 4, bei höheren Temperaturen werden die Pentalen-Derivate 9 gebildet. Bei dieser Umlagerung treten die Spirene 4 als Zwischenprodukte auf. Die Reaktion 3 → 4 dürfte über das Vinylcarben 11 oder das Diradikal 13 als Zwischenstufen verlaufen. Die Umlagerung 4 → 9 kann entweder synchron oder über ein Diradikal 15 formuliert werden.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1974 (1974), S. 1140-1149 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N-Heterocycles via 1,3-DipolarAddition and 1,5-Sigmatropic Shifts1,3-Dipolar cycloaddition of diazofluorene (1a) to the alkynes 2 affords the diaza[4.4]spirenes 3. With the other diazocyclopentadienes 1b-e the primary adduct 3 undergoes a 1,5-sigma- tropic shift to give the azaindolizines 4 or the 3aH-indazoles 5. Acid-catalyzed rearrangement of 3 produces the 1H-indazoles 6. Substituent effects on cycloaddition and 1,5-rearrangement are discussed. An alternative mechanism is proposed for the van Alphen rearrangement 3 → 6.
    Notes: Die 1,3-dipolare Cycloaddition von Diazofluoren (1a) an die Alkine 2 ergibt die Diazat[4.4]spirene 3. Bei den anderen Diazocyclopentadienen 1b-e geht das primär gebildete 3 eine 1,5-sigmatrope Umlagerung zu den Azaindolizinen 4 oder den 3aH-Indazolen 5 ein. Die säurekatalysierte Umlagerung von 3 liefert die 1H-Indazole 6. Substituenteneffekte der Cycloaddition und der 1,5-Umlagerungen werden diskutiert. Für die van-Alphen-Umlagerung 3 → 6 wird ein alternativer Mechanismus vorgeschlagen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Sulfur Compounds in Crude Oil, IV. - Alkaline Cleavage of 4,5-Annulated Cyclopenta[b]-thiophen-6-ones2-Aryl-4-(carboxyaryl)-3-thiophenecarboxylic acids 6a - c or esters 5 are formed from 4,5-annulated methyl 2-aryl-6-oxo-6H-cyclopenta[b]thiophene-3-carboxylates 1 by cleavage of the cyclopentadienone ring with methanolic potassium hydroxide. The mechanism is discussed.
    Notes: 4,5-Anellierte 2-Aryl-6-oxo-6H-cyclopenta[b]thiophen-3-carbosäure-methylester 1 reagieren mit methanolischem Kaliumhydroxid unter Spaltung des Cylopentadienon-Ringes zu 2-Aryl-4-(carboxyaryl)-3-thiophencarbonsäuren 6a - c order Estern 5. Der Mechanismus wird diskutiert.
    Type of Medium: Electronic Resource
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