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  • 1
    ISSN: 0947-3440
    Schlagwort(e): Ring transformation ; Nitrogen heterocycles ; Cyclizations ; Substituted 5-[2-(N-phenylsulfamoyl)vinyl]-pyrimidines ; Masked 1,3-dicarbonyl compounds ; Chemistry ; Organic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: As a masked 1,3-dicarbonyl compound, the 1,1-dioxo-2H-1,2-thiazine-4-carbaldehyde 1 undergoes ring transformation with amidines to produce 2-substituted 4-methyl-5-[1-methyl-2-methylthio-2-(N-phenylsulfamoyl)vinyl]pyrimidines 3a-f. For 3b, an X-ray structure analysis is reported. From the 4-methyl-2-methylthio-5-[1-methyl-2-methylthio-2-(N-phenylsulfamoyl)vinyl]pyrimidine (3e), the substituted pyrimidinone 4 is obtained by acidic hydrolysis.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1213-1218 
    ISSN: 1434-193X
    Schlagwort(e): Cycloadditions ; Diazatetraasteranes ; Crystal structure ; Solid-state chemistry ; Photochemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Upon irradiation, crystalline 4-methoxyphenyl-1,4-dihy-dropyridines 1 undergo nearly quantitative [2+2]cyclo-addition to form, via the ring-open intermediates 2, the centrosymmetric, polyfunctionalized 3,9-diazatetraasteranes 3. The centrosymmetric character of 3 was confirmed by 1H NMR spectral data as well as by X-ray crystal structure analysis. The dimerization reactions prove to be topochemically controlled by the nearest distance between potentially reacting double bonds, as well as by the conformationally determined packing restraints. This latter factor is shown by the X-ray crystal structure analysis of one dimerizing and one photostable derivative of the monomers 1.
    Materialart: Digitale Medien
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  • 3
    ISSN: 1434-193X
    Schlagwort(e): Lawesson's reagent ; Thiolation of cyclic ketones ; Anchimeric effect ; cis-Bicyclo[3.3.0]octane-3,7-diones ; 9-Thiatricyclo[3.3.1.03,7]nonane ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A simple and efficient approach to the 9-thiatricyclo[3.3.1.03,7]nonane ring system (5) has been found by treating cis-bicyclo[3.3.0]octane-3,7-diones (1) with Lawesson's reagent or phosphorus pentasulfide. When dione 1 is treated with Lawesson's reagent tetramethyl 3(4aH)oxo-1,4-dihydrophenanthro[9,10-a]pentalene-1,2,4,4a-tetracarboxylate (6) is obtained as a by-product as shown by X-ray structural analysis.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 2000 (2000), S. 245-249 
    ISSN: 1434-193X
    Schlagwort(e): Cycloadditions ; Cage compounds ; Dimerizations ; Steric hindrance ; Photochemistry ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: ---On irradiation at λ ≥ 270 nm solutions of 4-aryl-1,4-dihydropyridines 1 yield cage dimers 2 as the main products beside small amounts of anti dimers 3. 1H-NMR data and X-ray crystal structure prove centrosymmetrical properties for both dimers with axially orientated 4-aryl substituents. Irradiation with filtered light (λ 〉 313 nm) leads to syn and anti dimers 4 and 3 in nearly equal yields. The poor yields of anti dimers 3 on irradiation with unfiltered light are demonstrated to result from a partial cleavage back to their monomeric starting materials 1.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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  • 5
    ISSN: 0009-2940
    Schlagwort(e): Amides ; Pyrrolyl complexes ; Chelate complexes ; Transition-metal complexes ; Metallacycles ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Intramolecularly Stabilized Metal Amides: 2-(Dimethylaminomethyl)pyrrolyl Complexes of Titanium(III), Vanadium(III), Chromium(III), Cobalt(II) and Nickel(II)By the metallation of 2-(dimethylaminomethyl)pyrrol (HL) with butyllithium the lithium pyrrolide LiL (1) was obtained. The reactions of 1 with TiBr3 · 3 THF, VBr3 · 3 THF, CrBr3 · 3 THF, CoBr2 · 2 THF, and NiBr2 · 1.67 THF result in the formation of the 2-(dimethylaminomethyl)pyrrolyl complexes of type ML3 (2-4), and ML2 (5, 6), respectively. The structures of these new compounds are discussed on the basis of magnetic and visible absorption measurements. An X-ray crystal structure determination of 4 reveals a strongly distorted octahedral environment of the chromium atom with facial arrangement of the ligands.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 6
    ISSN: 0009-2940
    Schlagwort(e): Bis(phosphido)-bridged diiron hexa(penta)carbonyl complexes, molecular structures ; Steric strain ; Iron-iron double bond ; Calculations, EHT ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: An Unusual Pair of Bis(phosphido)-Bridged Diiron Carbonyl Complexes: [Fe2(CO)n{μ-P(tBu)2}(μ-PCy2)] (n = 5 and 6)Treatment of Na[Fe2(CO)6(μ-CO){μ-P(tBu)2}] with Cy2PCl gives [Fe2(CO)6{μ-P(tBu)2}(μ-PCy2)] (1) which loses CO on heating in toluene to afford [Fe2(CO)5{μ-P(tBu)2}(μ-PCy2)] (2). Complexes 1 and 2 have been characterized spectroscopically and by X-ray analyses. The central Fe2P2 unit in 1 is exactly planar whereas in 2 it is somewhat folded.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1941-1945 
    ISSN: 0044-2313
    Schlagwort(e): Zinc complexes ; oxygen, nitrogen chelate ligands ; crystal structure ; diethyl zinc ; Chemistry ; Inorganic Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Beschreibung / Inhaltsverzeichnis: Synthese und Molekülstruktur von 2-(1-Methyliminoethyl)phenolatozinkkomplexenDie Reaktion zwischen 2-(1-Methyliminoethyl)phenol (1 a) und Zinkdiethyl ergibt Bis[2-(1-methyliminoethyl)phenolato]zink (3) und [2-(1-Methyliminoethyl)phenolato]ethylzink (2) als Intermediat. Der Komplex 3 wird auch in der Reaktion von Zink-bis(trimethylsilyl)amid mit 1 a gebildet. Die Verbindungen wurden durch Elementaranalyse, NMR (1H, 13C) und IR-Spektroskopie charakterisiert. Die Röntgenkristallstrukturanalyse von 2 und 3 zeigt, daß beide Verbindungen in der festen Phase dimer sind, in denen die monomeren Einheiten durch zwei Sauerstoffatome und Ausbildung eines planaren Zn2O2-Ringes mit tetraedrischer [ZnO2NC]- bzw. trigonal-bipyramidaler [ZnO3N2]-Koordination des Zinkatoms verbrückt sind.
    Notizen: 2-(1-Methyliminoethyl)phenol (1 a) reacts with diethyl zinc to give bis[2-(1-methyliminoethyl)phenolato]zinc (3) via [2-(1-methyliminoethyl)phenolato]ethylzinc (2) as an intermediate. The complex 3 is also formed in the reaction of bis(trimethylsilyl)amide zinc with 1 a. The compounds were characterized by microanalysis, NMR (1H, 13C) and IR spectroscopy. X-ray structure analysis of the compounds 2 and 3 revealed that both compounds form in the solid state dimeric species where the monomeric units are bridged via two oxygen atoms forming a planar Zn2O2 ring with tetrahedral [ZnO2NC] and trigonal-bipyramidal [ZnO3N2] coordination of the zinc atom, respectively.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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