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  • 1
    Electronic Resource
    Electronic Resource
    Notiz über die Synthese von Benzo[α]fluoranthen (1979)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1979 (1979), S. 1443-1443 
    Details
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Note on the Synthesis of Benzo[α]fluorantheneCyclodehydrogenation of 9-phenylanthracene (1) by platinum gives benzo[α]fluoranthene (2).
    Notes: Benzo[α]fluoranthen (2) wird aus 9-Phenylanthracen (1) durch Cyclodehydrierung mit Platin erhalten.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.197919790917
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  • 2
    Electronic Resource
    Electronic Resource
    Notiz Über die Synthese von Benzo[ghi]fluoranthen (1983)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1983 (1983), S. 519-519 
    Details
    ISSN: 0170-2041
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Synthesis of Benzo[ghi]fluorantheneCyclodehydrogenation of benzo[c]phenanthrene (1) by platinum gives benzo[ghi]fluoranthene (2)
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.198319830316
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  • 3
    Electronic Resource
    Electronic Resource
    C26-Kohlenwasserstoffe als Schmieröl-Modellsubstanzen, II (1966)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 693 (1966), S. 90-98 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Zusammenhänge zwischen Konstitution und physikalischen Eigenschaften von Alkylderivaten des Benzols (1-5), Cyclohexans (6-8) und Tetralins (9-13) werden untersucht (Tab. 1).
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.19666930107
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  • 4
    Electronic Resource
    Electronic Resource
    Lupinen-Alkaloide, XVIII. Synthese und Konfigurationsbestimmung eines Alkaloids aus Nuphar japonicum DC (1961)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 94 (1961), S. 3151-3174 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Synthese des DL-Desoxy-nupharidins wird beschrieben. Von den acht möglichen Racematen wurden 6 isoliert und chromatographisch getrennt. Durch die Bestimmung der Konfiguration der vier isomeren 1.7-Dimethyl-chinolizidine und der vier 1.7-Dimethyl-chinolizidone-(4) sowie durch die Untersuchung der Stereochemie der Hydrierung und Reduktion von Dehydrochinolizidinen gelingt eine eindeutige konfigurative Zuordnung der isomeren Desoxynupharidine.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19610941202
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  • 5
    Electronic Resource
    Electronic Resource
    Notiz über die Synthese von Dibenz[a,j]anthracen (1978)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1978 (1978), S. 2105-2106 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Note on the Synthesis of Dibenz[a,j]anthraceneFriedel-Crafts reaction of 9,10-dihydrophenanthrene (1) with phenylacetyl chloride affords 2. Reduction of 2 by lithium tetrahydridoaluminate and dehydration gives 3, which is transformed by cyclodehydrogenation into dibenz[a,j]anthracene (4).
    Notes: Dibenz[a,j]anthracen (4) wurde aus 9,10-Dihydrophenanthren (1) durch Umsetzung mit Phenylessigsäurechlorid nach Friedel-Crafts zum Keton 2, Reduktion von 2 mit Lithiumtetrahydridoaluminat, Wasserabspaltung zu 3 und Cyclodehydrierung von 3 dargestellt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.197819781224
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  • 6
    Electronic Resource
    Electronic Resource
    C26-Kohlenwasserstoffe als Schmieröl-Modellsubstanzen, I (1965)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 685 (1965), S. 49-55 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Darstellung von 1.4-Dialkyl-benzolen (I-V) sowie von Alkylderivaten des Naphthalins (IX-XI) und Tetralins (VI-VIII) wird beschrieben. Die physikalischen Eigenschaften dieser Kohlenwasserstoffe werden auf Grund der intermolekularen Wechselwirkungen gedeutet. Die IR-Spektren werden diskutiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.19656850106
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  • 7
    Electronic Resource
    Electronic Resource
    Notiz über die Synthese von Indeno[1,2,3-cd]pyren (1978)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1978 (1978), S. 528-529 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Note on the Synthesis of Indeno[1,2,3-cd]pyreneIndeno[1,2,3-cd]pyrene (3) has been prepared from 1-pyrenylmagnesium bromide and cyclohexanone via 1-(1-cyclohexen-1-yl)pyrene (1) and 1-phenylpyrene (2).
    Notes: Indeno[1,2,3-cd]pyren (3) wird aus 1-Pyrenylmagnesiumbromid und Cyclohexanon über 1-(1-Cyclohexen-1-yl)pyren (1) und 1-Phenylpyren (2) dargestellt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.197819780313
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  • 8
    Electronic Resource
    Electronic Resource
    Notiz über die Synthese von Benzo[e]pyren (1978)
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1978 (1978), S. 530-531 
    Details
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Note on the Synthesis of Benzo[e]pyreneReaction of tetrahydrophenanthrenone 1 with phenyllithium affords 2. Dehydration of 2 gives 3. This is transformed by dehydrogenation (via 4) into benzo[e]pyrene (5).
    Notes: Benzo[e]pyren (5) wird aus dem Tetrahydrophenanthrenon 1 durch Umsetzung mit Phenyl-lithium zu 2, Wasserabspaltung zu 3 und Dehydrierung (über 4) dargestellt.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jlac.197819780314
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