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  • 11
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 1810-1814 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses of Bicyclic Heterocyclic Ring Systems, I. Imidazo[1.2-b]-s-triazolesWhereas in basic media treatment of 3.5-diamino-s-triazole (1) with acyloins (2) merely results in acylation with formation of 4, under acidic reaction conditions condensation takes place to yield imidazo[1.2-b]-s-triazoles (3). The latter can be characterized via the 2-aminogroup as Schiff′s bases (3c and f). An independent synthesis of 3 is the reaction of 1 with the corresponding α-chlorocarbonyl compounds 5.
    Notes: Während bei der Umsetzung von 3.5-Diamino-s-triazol (1) mit Acyloinen (2) in basischem Medium nur Acylierung unter Bildung von 4 eintritt, erfolgt unter sauren Reaktionsbedingungen Kondensation zu Imidazo[1.2-b]-s-triazolen (3). Diese können über die 2-Aminogruppe als Schiffsche Basen (3c und f) charakterisiert werden. Eine Gegensynthese von 3 ist die Reaktion von 1 mit den entsprechenden α-Chlor-carbonylverbindungen 5.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 2998-3013 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XVIII. Syntheses of 2.4-Diamino-2.4-didesoxy-D-galactose and -D-glucoseSyntheses of the title compounds were accomplished by single resp. double inversion at C-4 of suitable derivatives of D-glucose. Both sugars were obtained as free hydrochlorides.
    Notes: Die Synthese der Titelverbindungen erfolgte durch ein- bzw. zweimalige nucleophile Substitution am 4-C geeignet substituierter Derivate der D-Glucose. Beide Zucker wurden als freie Hydrochloride erhalten.
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 995-996 
    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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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 2418-2423 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Elimination Reactions of a Pyranose Enolacetate. A Pyranose Amino ReductoneThe α-azidoketone 1 is easily transformed either directly or via the enolacetate 2 into the vinylogous amide 4 which on acid treatment yields 8. 4 and 8 show the typical reactions of reductones. On reduction 8 yields derivatives of 2-amino-2-deoxy-D-allose only.
    Notes: Das α-Azido-keton 1 geht leicht direkt oder über das Enolacetat 2 in das vinyloge Säureamid 4 über, Aus dem mit Säure 8 entsteht. 4 und 8 zeigen die typischen Reaktionen von Reduktonen. Bei der Reduktion gibt 8 ausschließlich Derivate der 2-Amino-2-desoxy-D-allose.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1-3 
    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, III. Synthesis of Strophanthidin-3-(3′-amino-3′-deoxy-β-D-glucopyranoside)3-Amino-3-deoxy-1.2;5.6-di-O-isopropylidene-α-D-glucofuranose was transformed into the bromide 5 which in a Koenigs-Knorr reaction with strophanthidin yielded the β-glycoside.
    Notes: 3-Amino-3-desoxy-1.2:5.6-di-O-isopropyliden-α-D-glucofuranose wurde in das Bromid 5 übergeführt und dieses in einer Königs-Knorr-Reaktion mit Strophanthidim zum β-Glykosid umgesetzt.
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  • 16
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1976-1980 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Di- and Polyamino Sugars, XVI. Synthesis of 2.3.4.6-Tetraamino-2.3.4.6-tetradeoxy-D-galactoseBenzyl 2-acetamido-2-deoxy-α-D-glucopyranoside was converted into the corresponding allo derivative which was trimesylated and reacted with sodium azide in phosphoric tris-(dimethylamide). After deblocking the free sugar was isolated as its crystalline tetrahydrochloride.
    Notes: Die Synthese der Titelverbindung erfolgte aus Benzyl-2-acetamino-2-desoxy-α-D-glucopyranosid über die entsprechende allo-Verbindung, in die nach Trimesylierung die Stickstoff-Funktionen mit Natriumazid in Hexamethylphosphorsäuretriamid eingeführt wurden. Nach Entfernung der Schutzgruppen wurde der Zucker als Tetrahydrochlorid kristallin isoliert.
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 105 (1972), S. 2546-2557 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Structure Elucidation of the Gentamycins - Structure and Synthesis of Gentosamine and GarosamineBy methylation and degradation 3-deoxy-3-methylamino-D-xylose - identical with Gentosamine - was prepared from 3-amino-3-deoxy-D-glucose. Dehydrogenation to the 4-ketone and Grignard reaction yielded 3-deoxy-3-methylamino-4-C-methyl-L-arabinose and -D-xylose. The configuration of the L-arabino derivative - identical with Garosamine - was proved by i.r. spectroscopy and by cyclization to a 3.4-oxazolidone.
    Notes: Durch Methylierung und Kettenverkürzung wurde aus der 3-Amino-3-desoxy-D-glucose die 3-Desoxy-3-methylamino-D-xylose - identisch mit dem Gentosamin - dargestellt. Dehydrierung zum 4-Keton und Grignardierung ergaben die 3-Desoxy-3-methylamino-4-C-methyl-L-arabinose und -D-xylose. Die Konfiguration des L-arabino-Derivates - identisch mit dem Garosamin - wurde IR-spektroskopisch und durch Cyclisierung zum 3.4-Oxazolidon bewiesen.
    Type of Medium: Electronic Resource
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  • 18
    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.
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  • 19
    ISSN: 0018-019X
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A procedure was developed for the biosynthetic preparation of 15N-labelled guanosine and inosine through the action of a mutant Bacillus subtilis strain. Crude [N2,1,3,7,9-15N]guanosine and [1,3,7,9-15N]inosine were isolated from the culture filtrate by precipitation and anion-exchange chromatography (Scheme 1). No cell lysis and no enzymatic degradation was necessary. The per-isobutyrylated derivatives 1 and 2 were isolated from a complex mixture, purified by virtue of their different lipophilicity, and separated in three steps involving normal-and reversed-phase silica-gel chromatography. One litre of complex nutrient medium yielded 8.44 mmol of guanosine derivative and 2.84 mmol of inosine derivative with high average 15N enrichment (83.5 and 91.9 atom-%, resp.). [N6,1,3,7,9-15N]Adenosine (4) was obtained from 2′,3′,5′-tri-O-isobutyryl[1,3,7,9-15N]inosine (1) through the ammonolysis of its 1,2,4-triazolyl derivative with aqueous 15NH3 (Scheme 2).
    Additional Material: 4 Ill.
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  • 20
    ISSN: 0009-2940
    Keywords: Isothiazole complexes ; Dinuclear silver(I) complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of isothiazole-based potential ligands bearing substituents with additional donor sites in the 5-position of the heterocycle was synthesized [3-Me-5-R-C3HNS; R = CH=N(CH2)2py (1), CH=NCH2py (2), CH2N(CH2CH2NEt2)2 (4), (CH2)2SMe (5)]. Upon reaction with AgO3SCF3 they formed complexes [(1)AgOSO2CF3]2 (6), [(2)AgOSO2CF3]2 (7), [(4)Ag]2+2(O3SCF-3)2 (8) and [(5)AgOSO2CF3]2 (9), respectively. 6, 8 and 9 were shown by X-ray structural analyses to consist of dimeric units L2Ag2+2, either discrete (8), coordinated by terminal CF3SO-3 units (6). In 8 and 9 the isothiazole moiety is bonded to the metal center via the ring-N. The coordination potential of the isothiazole heterocycle is discussed.
    Additional Material: 5 Ill.
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