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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 335 (1993), S. 95-97 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Negative Solvatochromism of Cyclohexa-2,5-diene-1-thion Derivatives
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1618-2650
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,3-Acylrearrangements by Cyclisation of Thioureas with Imidochlorides of Oxalic Acid - An Approach to interesting Thiocarbonylic SystemsBy cycloacylation of various substituted thioureas with bis-imidochlorides of oxalic acid the new thiazolidines 3, 4 and isomeric imidazolidines 5, 6 are obtained. Especially when triethylamine is used as a base the main products are the deeply coloured 4-arylimino-5-thioxo-imidazolidines which can be regarded as s-cis-configurated 1,4-dihetero-1,3-dienes. Some thiazolidines can be rearranged by means of anhydrous organic acids to parabanic acid derivatives; whereas the 5-thioxo-imidazolidines result from an intramolecular 1,3-acyl rearrangement during the reaction.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 333 (1991), S. 555-559 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Deep Coloured Systems with Oxalic Acid Substructure-a Structural CorrectionBasing on a recent spectroscopic investigation the structure of earlier described deeply coloured systems derived from oxalic acid imidochlorides and thioacetamide has to be revised. Due to the poor solubility of these systems their spectroscopic characterization led to the misinterpretation as tetramethin-bridged thiazolines 1. By means of 1H-NOE-Difference-Spectroscopy of newly synthesized derivatives with lipophilic substituents a imidazolin-thion substructure 4 has been found. Such an arrangement of the heteroatoms clearly reflects a 1,3-rearrangement with participation of the oxalic acid system.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 333 (1991), S. 855-862 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel Steroidal Orthoesters by Intramolecular Cyclisation of Ethynylcarbinol Derivatives with Organic HypoioditesThe iodination of the 17β-acetoxy-17-ethynylsteroid 2 using iodine/copper(II)-acetate in combination with the nucleophiles acetic acid, water and methanol is reported. Examples for chemical modification of the products are described. A cyclisation occurs in the case of iodomethoxylation as a formal through-space 1.4-addition of the reagent forming a mixture of 4 isomer iodomethylen-1,3-dioxolanes. The configuration and ratio of the isomers as well as analytical data of this hitherto unknown dioxolane-system are given.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 65-82 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: On the Reaction of Oxalic Amidines with Carbonic Acid Derived Heterocumulenes to Imidazolidine-DerivativesA useful synthetic route to nonsymmetric derivatives of imidazolidine (derivatives of parabanic acid) is demonstrated by the reaction of tetraarylated oxalic amidines 1 with different alkyl- and aryl substituted isothiocyanates 4, isoselenocyanates 31, and carbodiimides 30.Acylisothiocyanates 9 react differently leading to a mixture of three cycloacylation products 12, 13 and 14. Silylated heterocumulenes such as 25 and 26 react with 1 to give 28 and 29 transsilylation. Based on the 13C-n.m.r. spectroscopic investigation of the reaction between 1a and methyl isothiocyanate and phenyl isothiocyanate respectively a mechanism is proposed.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 332 (1990), S. 367-374 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Investigations on Regioselectivity of Wittig-Horner and Reformatsky-Reactions on Selected 3,17-Dioxo SteroidsThe Reformatsky synthesis and the Wittig-Horner olefination of 3,17-dioxo steroids like androsta-1,4-diene-3,17-dione (ADD) 1 and androst-4-ene-3,17-dione (AD) 2 is described. There are differences in the regioselective introduction of identical substructures with these two methods resulting from different nucleophilicity and stereoelectronical relations of these two reagents. In Reformatsky synthesis the oxo group in 3-position predominantly reacts, whereas in the Wittig-Horner olefination (in the case of 1) the reaction occurs mainly in the 17-position.The structures of all new compounds has been confirmed by spectroscopical data.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 551-560 
    ISSN: 0044-2313
    Keywords: Metal complexes ; Amidines ; Oxalic derivates ; Imidazolidines ; Diazadiene ligands ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nitrogen Derivates of Oxalic Acid as New Complexing AgentsHeterocycles with a exocylic 1,4-diaza-1, 3-diene structure 5a-d have σ-bonding and π-backbonding properties similar to the diazadienes (DAD) 1. The investigations of the molybdenum complexes 11 and 12 of the ligands 5 show a dominant σ-interaction and only a small π-backbonding, comparable with the compound (CO)4Mo(iPYC) 14, a complex of pyridinecarbaldehyde isopropylimine (iPYC).The oxalamidine (TPOA) 4 (precursor of the heterocycles 5a-d) are present in a s-trans (E/E)-form with two stable intra-molecular hydrogen bridges. 4 reacts with ferrous and cobaltous chloride to the polymer coordination compounds 8 and 9. According to the diazadiene 1 oxalamadine 4 substitutes two carbonyls in Mo(CO)6 by formation of (CO)4Mo(TPOA) 10. The coordinated ligand 4 shows in the complex 10 a s-cis(E/E)-form with respect to the free ligand and no H-bridges were observed. The crystal structures of TPOA 4 and (CO)4Mo(TPOA) 10 were determined. Cyclisation reactions on the coordinated oxalamidine are possible.
    Notes: Heterocyclen mit einer exocyclischen 1,4-Diaza-1,3-dien-Struktur 5a-d besitzen in Analogie zu den Diazadienen (DAD) 1 α-Donor und π-Akzeptoreigenschaften. Durch vergleichende Untersuchungen an deren Molybdäncarbonylkomplexen 11 und 12 konnte festgestellt werden, daß der σ-Bindungscharakter dominant ist und nur geringe π-Rückbindungsanteile vorliegen, vergleichbar mit Verbindung (CO)4Mo(iPYC) 14, einem Komplex des Pyridin-2-carbaldehyd-isopropylimins (iPYC).Der Vorläufer dieser Heterocyclen, das Oxalamidin 4 (TPOA), liegt als Molekül in einer s-trans-(E/E)-Form mit zwei stabilen intramolekularen Wasserstoffbrücken vor. 4 bildet mit Eisen(II)- bzw. Cobalt(II)-chloriden polymere Koordinationsverbindungen 8 und 9. Mit Molybdänhexacarbonyl reagiert 4 analog den Diazadienen 1 unter Substitution zweier Carbonyl-gruppen zu (CO)4Mo(TPOA) 10. In 10 liegt der Ligand 4 in der s-cis-(E/E)-Form vor, wobei keine Wasserstoffbrücken-bindungen mehr beobachtet werden. Von 4 und 10 wurden Röntgenstrukturanalysen angefertigt. Am koordinativ fixierten Oxalamidin in 10 können Cyclisierungsreaktionen durchgeführt werden.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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