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  • Inorganic Chemistry  (1,444)
  • SPACE SCIENCES
  • 1980-1984  (706)
  • 1935-1939  (738)
  • 1982  (706)
  • 1936  (738)
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Publisher
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  • 1980-1984  (706)
  • 1935-1939  (738)
Year
  • 1
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of 3-Oxo-8-oxabicyclo[3.2.1]oct-6-ene-2-carbonitriles from γ-Bromo-β-oxonitriles and Furan via [4 + 3] Cycloaddition of 1-Cyanoallylium-2-olatesSome γ-bromo-β-oxonitriles 3 react with furan in the presence of silver oxide to form stereoselectively the title compounds 7. Satisfying yields are obtained only with those bromides 3, whose γ-carbon ist tertiary or which are monoalkylated both at the α- and γ-carbon atoms. The results are explained by a [4 + 3] cycloaddition of 1-cyanoallylium-2-olate intermediates (14) to the 1,3-diene system of the furan. With cyclic γ-bromo-β-oxonitriles (6) two types of cycloadducts were observed: 3-bromo-3-methyl-2-oxocyclohexanecarbonitrile (6b) and 3-bromo-2-oxocyclododecanecarbonitrile (6d) form the tricyclic [4 + 3] cycloadducts 10b and d, analogs of the bicyclic adducts 7. With 3-bromo-2-oxocyclohexanecarbonitrile (6a) and 3-bromo-5-tert-butyl-2-oxocyclohexanecarbonitrile (6e), however, the carbonyl oxygen is connected with an α-carbon of the furan to give the tricyclic [3 + 2] cycloadducts 12Aa and Ae. The structure of endo-2,endo-4-dimethyl-3-oxo-8-oxabicyclo[3.2.1]oct-6-ene-exo-2-carbonitrile (7eα) was determined by X-ray analysis.
    Notes: Verschiedene γ-Brom-β-oxonitrile 3 reagieren in Gegenwart von Silberoxid mit Furan stereoselektiv zu den Titelverbindungen 7. Befriedigende Ausbeuten werden nur mit solchen Bromiden 3 erhalten, deren γ-Kohlenstoff tertiär ist oder die sowohl am α- als auch γ-Kohlenstoff monoalkyliert sind (3c, e-h). Die Befunde werden durch eine [4 + 3]-Cycloaddition von intermediären 1-Cyanallylium-2-olaten (14) an das 1,3-Dien-System des Furans erklärt. Mit cyclischen γ-Brom-β-oxonitrilen (6) wurden zwei Typen von Cycloaddukten beobachtet: 3-Brom-3-methyl-2-oxocyclohexancarbonitril (6b) und 3-Brom-2-oxocyclododecancarbonitril (6d) reagieren zu den tricyclischen [4 + 3]-Cycloaddukten 10b und d, Analoga der Bicyclen 7. Bei 3-Brom-2-oxocyclohexancarbonitril (6a) und 3-Brom-5-tert-butyl-2-oxocyclohexancarbonitril (6e) wurde jedoch der Carbonyl-Sauerstoff mit einem α-Kohlenstoffatom des Furans verknüpft, wobei die tricyclischen [3 + 2]-Cycloaddukte 12Aa und Ae entstanden. Die Struktur von endo-2,endo-4-Dimetyl-3-oxo-8-oxabicyclo[3.2.1]oct-6-en-exo-2-carbonitril (7eα) wurde durch eine Röntgenstrukturanalyse bestimmt.
    Additional Material: 1 Ill.
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal-π-Complexes of Benzene Derivatives, XV. Bis(η6-naphthalene)chromium(0): X-Ray Structure Determination and Investigation by Nuclear Magnetic Resonance SpectroscopyBis(η6-naphthalene)chromium(0) (2) crystallizes in the space group P21/n with two molecules in the unit cell. The ligands in individual molecules of 2 are syn-oriented. The implied presence of a center of symmetry in 2 is caused by disorder that consists in the statistical occupation by chromium atoms of two equivalent sites between the six membered ring of pairs of parallel naphthalene ligands. The 1H and 13C NMR spectra of 2 are analysed and the spectroscopic parameters are discussed with reference to the respective data of free naphthalene as well as other (η-naphthalene)metal complexes.
    Notes: Bis(η6-naphthalin)chrom(0) (2) kristallisiert in der Raumgruppe P21/n mit zwei Molekülen in der Elementarzelle. Die Liganden in individuellen Molekülen von 2 nehmen dabei eine syn-Anordnung ein. Das Vorliegen eines Symmetriezentrums in 2 wird durch eine Fehlordnung vorgetäuscht, die darin besteht, daß in Paaren parallel angeordneter Naphthalin-Liganden linke und rechte Lücken zwischen den Sechsringen statistisch mit Chromatomen besetzt sind. Die 1H- und 13C-NMR-Spektren von 2 werden analysiert, und die spektroskopischen Parameter werden im Vergleich mit entsprechenden Daten des freien Naphthalins sowie anderer (η-Naphthalin)metall-Komplexe diskutiert.
    Additional Material: 7 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 393-395 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Refinement of the Crystal Structure of (Ethylenediamine)zinc(II) Benzohydroxamate Hydrate, ZnC23H29N5O7The already known structure1) of the title compound has been refined and slightly corrected from new data.
    Additional Material: 3 Tab.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 3904-3907 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of Allylidenephosphoranes with Heterocumulenes, II. New Syntheses of 1,2,4-Pentatrienes and 2-Pentene-1,5-dionesCinnamylidenetriphenylphosphorane (2a) undergoes Wittig reaction with ketenes to afford monomeric and dimeric 1,2,4-pentatrienes 4 and 5, resp. 4b reacts further with an excess of ketene via a [2 + 2]-cycloaddition, whereby the 3-styryl-1-naphthyl diphenylacetate 12 is formed. In contrast, with the α-phenylsubstituted phosphorane 2b, instead of the Wittig reaction addition of ketene takes place at both the α- and the γ-positions. The 1,3-diacyl-3-triphenylphosphonio-1-propen-3-enolate 6 readily hydrolyzes to the 2-pentene-1,5-dione 9.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2668-2673 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Contributions to the Chemistry of Boron, 127. Hexamethylborazine-Gallium Trichloride: Structure in Solution and in the Solid StateHexamethylborazine forms a 1:1 adduct 1 with gallium trichloride. It is isostructural with hexamethylborazine-aluminium tribromide. The BN heterocycle is no longer planer, and the molecule adapts almost Cs symmetry and contains a tetracoordinated nitrogen atom. 1 shows fluctional behavior in toluene solution at room temperature. The coordinated GaCl3 will no longer change its coordination site at T 〈 220 K (two signals each for the CH3N-and CH3B-protons). However, at T 〈 195 K an additional splitting of the signals is observed - three signals for each type of CH3 groups: this would be consistent with a pentacoordinated gallium atom and a bidentate borazine ligand.
    Additional Material: 1 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982) 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2679-2681 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Preparation of Cyclic Nitrones from Heterocyclic N-(Benzyloxy)aminesTreatment of heterocyclic N-(benzyloxy)amines 1 with concentrated hydrogen peroxide solution in acetic acid enables the preparation of 7-membered cyclic nitrones in respectable yields. This one-pot procedure offers some advantages compared with conventional routes.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2674-2678 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Vinyl Carbanions, 13. Convenient Synthesis of Oxaloacetic Acid DerivativesThe vinyllithium derivatives 2a, b and 9a, b, obtained by direct lithiation of the functionally substituted acrylic acid derivatives 1a, b and 8a, b, respectively, react with heterocumulenes A-E such as phenyl isocyanate, phenyl isothiocyanate, and carbon dioxide to give derivatives of oxaloacetic acid. In a single step reaction the oxaloacetic acid monoester 6a and monoamide 6b were synthesized.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 115 (1982), S. 2683-2696 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis of a [3]-PrecatenaneStarting from the previously synthesised compound 9a, the cyclophane 13 is prepared. Acetalisation with 1,25-dichloro-13-pentacosanone followed by nitration and reduction afforded the diamine 16. By cyclization of this compound in isoamyl alcohol with sodium carbonate and sodium iodide under high dilution conditions the monomeric products 17, 18, and 19 are obtained in yields of 5.0, 2.4, and 0.1%, respectively. On the basis of mass, 13C and 1H NMR spectra the structures of these compounds are discussed. The attempted transformation of the [3]-precatenane 17 into the [3]-catenane 24 gives a mixture of products among which 24 could not be identified with certainty.
    Notes: Ausgehend von der bereits früher hergestellten Verbindung 9a wird das Cyclophan 13 synthetisiert. Durch dessen Acetalisierung mit 1,25-Dichlor-13-pentacosanon, nachfolgende Nitrierung und Reduktion wird das Diamin 16 erhalten. Dessen Cyclisierung in Isoamylalkohol in Gegenwart von Natriumcarbonat und Natriumiodid unter Verdünnungsbedingungen ergibt die monomeren Cyclisierungsprodukte 17, 18 und 19 in Ausbeuten von 5.0, 2.4 und 0.1%. Die Struktur dieser Verbindungen wird anhand der Massen-, 13C-und 1H-NMR-Spektren diskutiert. Die versuchte Umwandlung des [3]-Praecatenans 17 in das [3]-Catenan 24 führt zu einem Produktgemisch, in dem 24 nicht mit Sicherheit identifiziert werden konnte.
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