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  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Alkoxy-β-ketosulfones, 2.1. Mitteil.: K. Schank, Liebigs Ann. Chem. 716, 87 (1968). Particulars and Optimal Reaction Conditions with regard to S-Alkylation of Sulfinate Anions by α-Halogen α-Acyl EthersDuring SN reactions with α-halogen ethers sulfinate anions are alkylated both at O and S. The dependence of reaction course on external (solvent, concentration) and internal (substituent and cation effects at the nucleophile; alkylating reagent) factors is investigated with α-halogen α-acyl ethers and is exploited for specific S-alkylation.
    Notes: Sulfinatanionen werden bei SN-Reaktionen mit α-Halogenäthern sowohl O- als auch S-alkyliert. Am Beispiel von α-Halogen-α-acyl-äthern wird die Abhängigkeit der Reaktionsrichtung von externen (Lösungsmittel; Konzentration) und internen (Substituenten- und Kationeneffekte beim Nucleophil; Alkylierungsmittel) Faktoren untersucht und zur gezielten S-Alkylierung ausgewertet.
    Additional Material: 5 Tab.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3769-3771 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 3036-3040 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polyacetylenic Compounds, 211. Synthesis of Enolether-polyynes from Anaphalis- and Gnaphalium SpeciesThe structures of four enolethers (3-5 and 14) isolated from Anaphalis species have been confirmed by synthesis of the racemates. For the compounds isolated from Gnaphalium species a further synthesis is described.
    Notes: Die Strukturen von vier aus Anaphalis-Arten isolierten Enoläthern (3-5 und 14) werden durch Synthese der Racemate gesichert. Für die aus Gnaphalium-Arten isolierten Verbindungen wird eine weitere Synthese beschrieben.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 2745-2748 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 368-376 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Steric and Stereoelectronic Factors Concerning the Intramolecular Addition of Hydroxy-to Imonium CompoundsDehydrogenation of both 1-methyl--3[2-hydroxyethyl]- (13a) and 1-methyl--3[3-hydroxy-propyl]-piperidine (13b) with mercuric EDTA yields two isomeric -2 and 6-piperidones. The structures are assigned to the isomers and their proportion is determined by comparison with unequivocal synthesized compounds. The validity of the postulated reaction mechanism) is confirmed and extended to piperidine derivatives bearing C-hydroxyalkyl substituents.
    Notes: Entgegen früheren Angaben entstehen bei der Quecksilber(II)-ÄDTA-Dehydrierung von 1-Methyl--3[2-hydroxy-äthyl]-piperdin (13a) und 1-Methyl--3[3-hydroxy-propyl]-piperidin (13b) jeweils zwei isomere Lactame mit -2 bzw. 6-Piperidon-Struktur. Mit Hilfe unabhängig synthetisierter Vergleichssubstanzen wird die Zuordnung und das Mengenverhältnis der Isomeren bestimmt. Die Gültigkeit des postulierten Reaktionsmechanismus wird bestätigt und auf Piperidinderivate mit einer C-[Hydroxy-alkyl]-Seitenkette ausgedehnt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3020-3025 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Polyacetylenic Compounds, 219. On the Biogenesis of C17-ene-diyne-dienesBy feeding labelled compounds the biogenesis of the aldehyde 17 has been investigated. Only the esters 8, 9, and 11 are incorporated, while several others are not useful as precursors showing that at least in this case the single steps are not exchangeable.
    Notes: Durch Verfütterung markierter Verbindungen wird die Biogenese des Aldehyds 17 untersucht. Nur die Ester 8, 9 und 11 werden eingebaut, während mehrere andere nicht als Vorstufen brauchbar sind, was anzeigt, daß zumindest in diesem Fall die einzelnen Schritte nicht austauschbar sind.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 2305-2309 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Condensed Ring System, V. Synthesis and Spectroscopic Properties of cis- and trans- 1,5-Dimethyl-1,3,7-diheterobicycol-[3.3.0]octanesThe synthesis of 1,5-dimethyl-3,7-dithiabicyclo [3.3.0]octane yields the cis (4a) and the trans-isomer (5a) in a ratio of 1:1 Small amounts of the cis-(4b) and the trans-isomer (5b) of 1,5-dimethyl-3-oxa-7-thiabicyclo[3.3.0]octane are formed as side products. The configuration of the isomers can be deduced from their n.m.r. spectra by comparing the spectra with those of dihetero[3.3.n.]propellanes1) having cis-configuration.
    Notes: Bei der Synthese des 1,5-Dimethyl-3,7-dithiabicyclo[3.3.0]octans entstehen das cis (4a) und trans-Isomere (5a) im Verhältnis 1:1. Als Nebenprodukte erhält man in geringen Mengen das cis- (4b) und trans-Isomere (5b) des, 1,5-Dimethyl-3-oxa-7-thiabicyclo [3.3.0]octans. Der Vergleich ihrer 1H-NMR-Spektren mit denen der cis-konfigurierten Dihetero[3.3.n]propellane1) ermöglicht die Konfigurationszuordnung.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 869-875 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Glycosides of Amino Sugars, IV. Synthesis of Disaccharides of 2-Amino-2-deoxy- and 3-Amino-3-deoxy-D-glucoseThe solvent dependency of the Koenigs-Knorr reaction between two derivatives of 2-amino-2-deoxy-D-glucose (3 and 4) was investigated. The highest yield of the α-disaccharide 5 was obtained in the system toluene/1,2-dimethoxyethane. The condensation of two derivatives of 3-amino-3-deoxy-D-glucose (11 and 13) under similar conditions yielded the 1,6-linked α-and β-disaccharides (15, 14) of this sugar which were unknown until now.
    Notes: Die Koenigs-Knorr-Reaktion zwischen zwei Derivaten der 2-Amino-2-desoxy-D-glucose (3 und 4) wurde in Abhängigkeit vom Lösungsmittel untersucht. Die höchste Ausbeute an α-Disaccharid 5 konnte in einem Gemisch von Toluol und 1,2-Dimethoxyäthan erhalten werden. Die Kondensation zweier Derivate der 3-Amino-3-desoxy-D-glucose (11 und 13) unter ähnlichen Bedingungen führte zu den bisher unbekannten 1,6-verknüpften α- und β-Disacchariden (15 bzw. 14) dieses Zuckers.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1478-1489 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Pyridones, III. Influence of Substituents on the Oxidation of Quaternary Pyridinium CompoundsBy hexacyanoferrate(III) oxidation of 3-substituted 1-methylpyridinium compounds two isomeric pyridones are normally formed. Only from the 3-carboxylic acid or the 3-nitro derivative results exclusively the corresponding 6-pyridone.
    Notes: Bei der Hexacyanoferrat(III)-Oxydation 3-substituierter 1-Methyl-pyridiniumverbindungen entstehen normalerweise zwei isomere Pyridone. Lediglich bei dem 3-Carboxy- bzw. dem 3-Nitro-Derivat resultiert ausschließlich das entsprechende Pyridon-(6).
    Additional Material: 2 Ill.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1518-1523 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 2′.4′.5′-Trihydroxylated Isoflavones2′.4′.5′-Trihydroxylated isoflavones are synthesized by condensation of chromanones (1a, b and 5) with 4.5-dimethoxy-o-benzoquinone (2). The total synthesis of dehydroneotenone (6) is described.
    Notes: Durch Kondensation von Chromanonen (1a, b und 5) mit 4.5-Dimethoxy-o-benzochinon (2) werden 2′.4′.5′-trihydroxylierte Isoflavone dargestellt. Die Totalsynthese des Dehydroneotenons (6) wird beschrieben.
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