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  • Articles: DFG German National Licenses  (7)
  • Organic Chemistry  (6)
  • Yttrium complexes  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 589 (1954), S. 82-90 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 724 (1969), S. 102-121 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Syntheses in the Bicyclo[3,2,Z/nonane and Bicyclo[4,2, I] nonane SeriesThe epimeric 6-ethoxycarbonyl-8-bicyclo[3,2,2]nonenes (1a and 2a) are prepared; their configurations are established from Curtius degradation giving exo-and endo-6-amino-8-bicyclo-[3,2,2]nonene (1c and 2c). Synthesis of 6-bicyclo[3,2,2]nonene (4) and 6-bicyclo[3,2,2]-nonanone (6) from the mixture of the epimers 1a and 2a is described. Reduction of 6 and equilibration of the obtained mixture of alcohols afford the exo/endo isomers of 6-bicyclo[3,2,2]nonanol (7 and 8). The configurations and conformations of these alcohols are discussed. - 2-Bicyclo[4,2,1]nonanone (11) is produced by Ziegler ring closure of the dinitrile 14d obtained from ethyl 4-(3-ethoxycarbonyl-2-oxocyclopentyl)butyrate (13). In the same way cyclization of cis-3-(3-cyanomethylcyclopentyl)propionitrile (17d) yields 3-bicyclo[4,2,1] nonanone (16). The latter is also obtained by deamination of 3-aminomethyl-3-bicyclo[3,2,1]octanol (19). The Tiffeneau-Demjanov reaction of 2-aminomethyl-2-bicyclo[3,2,1]octanol (20) gives 80% 11 and 17% 16, which on reduction by the Wolff-Kishner method yield bicyclo[4,2,1]nonane (12).
    Notes: Die epimeren 6-Äthoxycarbonyl-bicyclo[3.2.2]nonene-(8) (1a und 2a) werden dargestellt; ihre Konfiguration wird zugeordnet durch Curtius-Abbau zu exo- bzw. endo-6-Aminobicyclo[3.2.2]nonen-(8) (1c und 2c) und durch die Synthesen von Bicyclo[3.2.2]nonen-(6) (4) bzw. Bicyclo[3.2.2]nonanon-(6) (6). Durch Reduktion von 6 und Äquilibrierung des Alkoholgemisches entstehen die exo/endo-isomeren Bicyclo[3.2.2]nonanole-(6) (7 und 8), deren Konfigurationen und Konformationen diskutiert werden. - Aus 4-[3-Äthoxycarbonyl-2-oxocyclopentyl]-buttersäureäthylester (13) wird über das Dinitril 14d durch Zieglerschen Ringschluß Bicyclo[4.2.1]nonanon-(2) (11) erhalten. Die analoge Cyclisierung des cis-3-[3-Cyanmethyl-cyclopentyl]-propionitrils (17d) ergibt Bicyclo[4.2.1]nonanon-(3) (16), das auch bei der Desaminierung von 3-Aminomethyl-bicyclo[3.2.1]octanol-(3) (19) entsteht. Die Tiffeneau-Demjanow-Reaktion von 2-Aminomethyl-bicyclo[3.2.1]octanol-(2) (20) verläft unter Bildung von 80% 11 und 17% 16, deren Wolff-Kishner-Reduktion zum Bicyclo[4.2.1]nonan (12) führt.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 729 (1969), S. 8-20 
    ISSN: 0075-4617
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Wagner- Meerwein Rearrangements in the Bicyclo[3.2.2rsqb;nonane Series I )Deamination of the epimeric 6-aminobicyclo[3.2.2]non-8-enes (6 and 7) and 6-aminobicyclo-[3.2.2]nonanes (8, X = NH2 and 9) mainly proceeds via a stereospecific rearrangement to yield exo-alcohols of hte bicyclo[3.3.1]nonane or bicyclo[4.2.1]nonane series with high stereospecifity. In addition, tricyclo[4.2.1.02.8]nonan-7-ol (10) was produced from the endo-amin 7. - In the presence of silver bromide 2-bromobicyclo[3.2.2]nonane (8, X = Br) rearranges to 2-bromobicyclo[3.3.1]nonane (2, Y = Br). - Both the dehydration of bicyclo[3.2.2]nonan-6-ol (1, X = OH) with phosphoric acid and the acid-catalyzed rearrangement of bicyclo-[3.2.2]non-6-ene (12) give rise to bicyclo[3.3.1]non-2-2ne (11, X = H). The reaction of 12 with an excess of monoperphthalic acid yields syn- and anti-bicyclo[3.3.1.13.9]decane (17). -The deamination of 2e-aminomethylbicyclo[3.2.1]octane (18 gives a mixture of alcohols consisting of bicyclo-[4.2.,1]nonan-3-ol (36), bicyclo[4.2.1]nonan-2-ol (3, Y = OH), bicyclo[3.3.1]nonan-2-ol (2, Y = OH), and 2a-and 2e-methylbicyclo[3.2.1]octan-2e- and 2a-ols (20 and 19).
    Notes: Die Desaminierungen der epimeren 6-Amino-bicyclo[3.2.2]nonene-(8) (6 und 7) und 6-Aminobicyclo[3.2.2]nonane (8, X = NH2, und 9) führen stereospezifisch zu exo-Alkoholen der Bicyclo[3.3.1]nonan- oder Bicyclo[4.2.1]nonan-Reihe. Das endo-Amin 7 liefert daneben Tricyclo[4.2.1.02.8]nonanol-(7) (10). - 6-Brom-bicyclo[3.2.2]nonan (8, X = Br) lagert sich in Gegenwart von AgBr in 2-Brom-bicyclo[3.3.1]nonan (2, Y = Br) um. -Die Dehydratisierung von Bicyclo[3.2.2]nonanol-(6) (1, X = OH) mit Phosphorsäure und die säurekatalysierte Umlagerung von Bicyclo[3.2.2]nonanol-(6) (1, X = OH) mit Phosphorsäure und die säurekatalysierte Umlagerung von Bicyclo[3.2.2]nonen-(6) (12) führen zu Bicyclo[3.3.1]nonen-(2) (11, X = H). - Aus 12 bilden sich mit überschüss. Monoperphthalsäure syn- und anti- Bicyclo[3.3.1]nonen-(2)-ol-(9) (14 und 15) sowie vermutlich 10-Oxatricyclo[3.3.1.13.9]decan (17). - Bei der Desaminierung des 2e-Aminomethyl-bicyclo[3.2.1]octans (18) entstehen Bicyclo[4.2.1]nonanol-(3) (36), Bicyclo[4.2.1]nonanol-(2) (3), Y = OH), Bicyclo[3.3.1]nonanol-(2) (2, Y = OH) sowie 2a und 2e-Methyl-bicycol[3.2.1]octanol-2c und 2a) (20 und 19).
    Additional Material: 1 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 21 (1963), S. 59-64 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird die Synthese des geschützten Tetrapeptides S-Benzyl-N-carbobenzoxy-L-cysteinyl-L-threonyl-L-seryl-L-isoleucin-methylester nach verschiedenen Methoden beschrieben. Dieses Tetrapeptid entspricht der Aminosäuresequenz 7-10 der A-Kette des Schweine- bzw. Wal-Insulins.
    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 6 (1958), S. 1-3 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    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 14 (1961), S. 1-3 
    ISSN: 0021-8383
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die Umsetzung α,α-disubstituierter Malonsäureester mit Formamid in alkoholischer Lösung und in Gegenwart von Natriumalkoholat führt zur Bildung der entsprechend substituierten Malonsäurediamide.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 0044-2313
    Keywords: Yttrium complexes ; yttrium tris[bis(trimethylsilyl)amide] ; yttrium tris[bis(trimethylsilyl)methanide] ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Bis(trimethylsilyl)amides and -methanides of Yttrium  -  Molecular Structures of Tris(diethylether-O)lithium-(μ-chloro)-tris[bis(trimethylsilyl)methyl]yttriate, solvent-free Yttrium Tris[bis(trimethylsilyl)amide] as well as the Bis(benzonitrile) ComplexThe reaction of yttrium(III) chloride with the three-fold molar amount of LiE(SiMe3)2 (E = N, CH) yields the corresponding yttrium derivatives. Yttrium tris-[bis(trimethylsilyl)amide] crystallizes in the space group P31c with a = 1 636,3(2), c = 849,3(2) pm, Z = 2. The yttrium atom is surrounded trigonal pyramidal by three nitrogen atoms with Y—N-bond lengths of 222 pm. Benzene molecules are incorporated parallel to the c-axes. The compound with E = CH crystallizes as a (Et2O)3LiCl-adduct in the monoclinic space group P21/n with a = 1 111,8(2), b = 1 865,2(6), c = 2 598,3(9) pm, β = 97,41(3)° and Z = 4. The reaction of yttrium tris[bis(trimethylsilyl)amide] with benzonitrile yields the bis(benzonitrile) complex, which crystallizes in the triclinic space group P1 with a = 1 173,7(2), b = 1 210,3(2), c = 1 912,4(3) pm, α = 94,37(1), β = 103,39(1), γ = 117,24(1)° and Z = 2. The amido ligands are in equatorial, the benzonitrile molecules in axial positions.
    Notes: Die Reaktion von Yttrium(III)-chlorid mit der dreifachen molaren Menge LiE(SiMe3)2 (E = N, CH) ergibt die entsprechenden Yttrium-Derivate. Yttrium-tris[bis(trimethylsilyl)amid] kristallisiert in der Raumgruppe P31c mit a = 1 636,3(2), c = 849,3(2) pm, Z = 2. Das Yttriumatom ist trigonal pyramidal koordiniert mit Y—N-Bindungslängen von 222 pm. Entlang der c-Achse sind Benzolmoleküle eingeschlossen. Die Verbindung mit E = CH kristallisiert als (Et2O)3LiCl-Addukt in der monoklinen Raumgruppe P21/n mit a = 1 111,8(2), b = 1 865,2(6), c = 2598,3(9) pm, β = 97,41(3)° und Z = 4. Die Umsetzung von Yttrium-tris[bis(trimethylsilyl)amid] mit Benzonitril ergibt einen Bis(benzonitril)-Komplex, der in der triklinen Raumgruppe P1 mit a = 1173,7(2), b = 1210,3(2), c = 1912,4(3) pm, α = 94,37(1), β = 103,39(1), γ = 117,24(1)° und Z = 2 kristallisiert. Die Amido-Liganden sind äquatorial, die Benzonitril-Moleküle axial koordiniert.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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