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  • General Chemistry  (80)
  • Industrial Chemistry  (68)
  • Carbohydrates  (12)
  • Structure  (6)
  • 1995-1999  (150)
  • 1920-1924  (9)
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  • 11
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 1014-1023 
    ISSN: 0947-6539
    Schlagwort(e): alkoxy radicals ; cyclizations ; pyridinethiones ; radicals ; tetrahydrofurans ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: A series of hitherto unknown N-(pent-4-enyl-1-oxy)pyridine-2(1 H)-thiones (6) were prepared from substituted pent-4-enyl tosylates or benzylic chlorides. On irradiation with incandescent light heterocycles 6 liberated alkoxy radicals 2, which were studied for rearrangement reactions. Surprisingly, all transformations involving the 1-phenylpent-4-enyl-1-oxy radical (2a), for example, to give the substituted thioether 8, 2-bro-momethyl-5-phenyltetrahydrofuran (11), or the tetrahydrofuran 14a, were not stereoselective. On the other hand 2-, 3- mono-, and 1,5-disubstituted pent-4-enyl-1-oxy radicals 2d-e and 2g cyclized in good yields and with good to excellent stereoselectivities to give the corresponding 2,4-cis- and 2,3-trans-phenyltetra-hydrofurfuryl radicals 3d-e, and the trans-2-benzyl-5-methyl substituted intermediate 3g. The major reaction mode of the 4-phenylpent-4-enyl-1-oxy radical (2f) was the 6-endo cyclization, which afforded 3-phenyltetrahydropyran (13f) as the major product (endo:exo = 93:7) after trapping with hydrogen donors. According to the experimental data of the present study, the unusual reactivity of the 1-phenylpent-4-enyl-1-oxy radical (2a) in 5-exo-trig ring closures could be caused by a coplanar arrangement of the benzyloxy moiety in the transition state of the cyclization. This interaction would lock the radical center in 2a in a preferred conformation, which would result in similar steric effects for both cis- and trans- cyclizations.
    Zusätzliches Material: 1 Ill.
    Materialart: Digitale Medien
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  • 12
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Chemistry - A European Journal 2 (1996), S. 1566-1571 
    ISSN: 0947-6539
    Schlagwort(e): amino acids ; asymmetric syntheses ; carbolines ; chiral auxiliaries ; Pictet-Spengler reaction ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Aromatic and aliphatic Schiff bases of tryptamine react with Fmoc- or phthaloyl-protected amino acid chlorides to form N-acyliminium intermediates, which, in the presence of titanium alkoxides at room temperature, undergo Pictet-Spengler reactions to give tetrahydro-β-carbolines with diastereomeric ratios of up to 99:1. The chiral auxiliary can be removed from the Pictet-Spengler adducts by means of a simple reduction. To rationalize the observed stereoselectivity a transition-state model is proposed in which the titanium atom coordinates both the carbonyl group of the N-acyliminium ion and the amino acid protecting group.
    Zusätzliches Material: 2 Tab.
    Materialart: Digitale Medien
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  • 13
    ISSN: 1434-1948
    Schlagwort(e): Aminoalanes ; Alanes ; Ab initio calculations ; 27Al-NMR spectroscopy ; Structure elucidation ; Substituent effects ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Reactions of metallated nucleophiles MIY [Y = OR, SR, NR2, PR2, AsR2, CR3, Si(SiMe3)3, R = organyl, H] with bis(2,2,6,6-tetramethylpiperidino)aluminum halides [tmp2AlX, (X = Cl, Br, I)] offer facile access to a variety of bis(amino)alanes of the type tmp2AlY. As indicated by 27Al-NMR spectroscopy, mass spectrometry and X-ray crystal structure determina-tions, all of these compounds are monomeric in the solid state, in solution, and in the gas phase. Even Al-E single bonds (E = Si, P, As etc.) that are not commonly encountered are stabilized by the supporting tmp fragments. The results of a systematic analysis of the bonding parameters determined for the tmp2AlY compounds, combined with a quantum mechanical study on model compounds (H2N)2AlY, not only reveal the presence of a highly polar Al-N bond, but at the same time rule out AlN-pp(π) bonding, in contrast to the situation in the analogous tmp2BY compounds. It is shown that the Al-N bond length depends on the acidic character of the protic species HY: the shorter d(Al-N), the less basic is Y.
    Materialart: Digitale Medien
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  • 14
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1998 (1998), S. 1609-1613 
    ISSN: 1434-193X
    Schlagwort(e): Glycals, nitro ; Michael additions ; Glycosylations ; Glycosides, galactosamine ; Reduction, nitro group ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: Formation of 3,4,6-tri-O-benzyl-2-nitro-D-galactal (3) was readily accomplished starting from tri-O-benzyl-D-galactal (1) by acetyl nitrate addition to 2 and base-promoted acetic acid elimination. Addition of alcohols to 3 under conditions of base catalysis afforded 2-deoxy-2-nitrogalactopyranosides 4a-e in high yields; high α-selectivity was obtained with strong bases, whereas weaker bases furnished mainly the corresponding β-galactopyranosides. Chemoselective nitro group reduction in these glycosides was successfully carried out in the case of disaccharide 4cα using Raney nickel as catalyst, thereby affording after N-acetylation the corresponding 2-acetylamino-2-deoxy derivative 5cα.
    Materialart: Digitale Medien
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  • 15
    ISSN: 1434-1948
    Schlagwort(e): Iridium ; Rhodium ; Amino acids ; Sandwich complexes ; Bioorganometallic chemistry ; Relativistic effects ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: η5-Pentamethylcyclopentadienyliridium(III) and -rhodium(III) sandwich complexes of the type [(η5-Cp*)M(η6-aa)](CF3SO3)2 (M = Ir, Rh; 3-14) containing L-tyrosine, L-tryptophan and L-phenylalanine derivatives (aa) can be prepared by treatment of [(η5-Cp*)ML3] (CF3SO3)2 [L = thf, (CH3)2CO, CH3CN] with the appropriate bioligand in thf for N-protected compounds and in CF3COOH for α-amino acids with unprotected amino groups. Coordination to the Cp*MIII fragments stabilizes the ketonic form of the tyrosine aromatic side chains, leading to a marked enhancement in the acidity of the p-hydroxy function. The crystal structure of [Cp*Ir(ActyrOMe)] (CF3SO3)2 (3b, ActyrOMe = N-acetyltyrosine methyl ester) confirms a marked distortion towards an η5-oxohexadienyl coordination mode as may be gauged from the tilting of the p-OH plane C13/C14/C15 by no less than θ = 12.9° from that of the remaining ring atoms. Facial isomers are present in an effective 1:1 ratio for all tryptophan derivatives. Whereas the Cp*IrIII sandwich complexes of aromatic α-amino acids are stable in polar solvents, rapid decay is observed for analogous Cp*RhIII complexes of N-unprotected derivatives in polar solvents. Comparative nonrelativistic and relativistic all-electron density functional calculations on the cationic sandwich complexes [Cp*M(η6-C6H5Me)]n+ (n = 2, M = Ir, Rh; n = 1, M = Ru) confirm that all three metals bind more tightly to Cp* than to toluene as gauged by the respective force constants (k1 〉 k2). A much larger relativistic enhancement of k2 for M = Ir (279 vs 207 Nm-1) could be responsible for the greater stability of Cp*IrIII complexes in solution.
    Zusätzliches Material: 7 Ill.
    Materialart: Digitale Medien
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  • 16
    ISSN: 1434-193X
    Schlagwort(e): Supramolecular chemistry ; Rotaxanes ; Mechanical bond ; Molecular recognition ; Chirality ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: In this paper we report on amide rotaxanes with tetrabenzoylglucose stoppers. When acetyl groups are used instead of benzoyl groups, merely a pseudo-rotaxane 5 is obtained. The circular dichroism measurements of the rotaxanes 6a and 6b differ significantly from that one of the free axle 7. Similarly, the Cotton effects of the mixtures of achiral wheels 2a and 2b and chiral axle indicate intermolecular host-guest interactions, likewise. After an addition of a solution of NaOMe the wheel is slipping off immediately and quantitatively by hydrolysis, as the benzoylglucose stoppers decrease in size by hydrolysis.
    Materialart: Digitale Medien
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  • 17
    ISSN: 1434-1948
    Schlagwort(e): Aluminum ; Chalcogens ; Cubanes ; Gallium ; Main group elements ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction of the trialkylalane (Me3Si)3CAlMe2 × THF (1) with H2S in toluene at room temperature results in the formation of the dimeric sulfido compound [(Me3Si)3CAl(μ-S)]2 × 2 THF (3), while the reaction of the homologous gallane (Me3Si)3CGaMe2 (2) with H2S under similar conditions affords the heterocubane [(Me3Si)3CGa(μ3-S)]4 (4). Heating of compound 3 in vacuo gives a mixture of the symmetrically substituted [(Me3Si)3CAl(μ3-S)]4 (5) and the unsymmetrically substituted heterocubane [{(Me3Si)3CAl(μ3-S)}3MeAl(μ3-S)] (6). Reaction of the trialkylmetalanes 1 and 2 with elemental selenium in refluxing toluene results in the formation of the corresponding selenolates [(Me3Si)3CMMe(μ-SeMe)]2 (7, M = Al; 8, M = Ga). The compounds exhibit a high thermal stability and can not be converted to the corresponding selenides [(Me3Si)3CM(μ3-Se)]n (M = Al, Ga) upon heating. In contrast, the trialkylalane 1 does not react with tellurium metal in refluxing toluene at all, while the trialkylgallane 2 affords the tellurolate [(Me3Si)3CGaMe(μ-TeMe)]2 (9) under similar conditions. Compounds 3-9 have been characterized by 1H- and 29Si-NMR, mass, and IR spectroscopy. Furthermore, the molecular structures of compounds 3· C6H6, 4· 1.5 C6H6, 6, 7· C6H6 and 9 have been determined by X-ray crystallography.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 18
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 785-787 
    ISSN: 1434-1948
    Schlagwort(e): Atom distribution ; Mixed crystals ; Scanning tunneling microscopy ; Layered compounds ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The layered compound Nb3(Se1-xIx)I7 is obtained when the I atoms at the face-capping sites of the layered compound Nb3I8 are replaced by Se atoms. The amount and distribution of the Se atoms in Nb3(Se1-xIx)I7 were examined by scanning tunneling microscopy. The analysis shows that the distribution of the Se atoms is completely random.
    Zusätzliches Material: 5 Ill.
    Materialart: Digitale Medien
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  • 19
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 863-867 
    ISSN: 1434-1948
    Schlagwort(e): Germanium ; Nitrogen ; Silicon ; Titanium ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reaction of dippNSiMe3Si(NH2)3 (1) (dipp = 2,6-iPr2C6H3) with Cp*TiMe3 (Cp* = C5Me5) and Me3SnCl yields the new heterocyclic adamantane (dippNSiMe3Si)2(Cp*Ti)2(NH)6 (2) containing the Si2Ti2(NH)6 core and the silicon-nitrogen six-membered ring compound [dippNSiMe3Si(NH2)NH]3 (4). [dippNSiMe3Ge(NH2)2]2NH (5) reacts with AlMe3 to give the germanium-nitrogen six-membered ring compound [dippNSiMe3Ge(NH2)NH]3 (6). The compounds 2, 4 and 6 have been structurally characterized by single-crystal X-ray structural analysis.
    Zusätzliches Material: 3 Ill.
    Materialart: Digitale Medien
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  • 20
    Digitale Medien
    Digitale Medien
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 1999 (1999), S. 869-872 
    ISSN: 1434-1948
    Schlagwort(e): Adamantane ; Liquid ammonia ; Oxygen ; Sulfur and selenium ; Tin ; Chemistry ; General Chemistry
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The reactions of trisSnBr3 (1) [tris = (Me3Si)3C] and nBuSnCl3 with Na2X (X = O, S, Se) yield the heterocyclic adamantanes 2-6. The reaction of 1 with Na2O is carried out in liquid ammonia under normal pressure at -78 °C to give (trisSn)4O6 (2). However, the reaction of 1 with Na2S and Na2Se under pressure at room temperature results in the formation of (trisSn)4S6 (3) and (trisSn)4Se6 (4). nBuSnCl3 reacts with Na2S and Na2Se in liquid ammonia at -33 °C under normal pressure to give (nBuSn)4S6 (5) and (nBuSn)4Se6 (6), respectively.
    Zusätzliches Material: 2 Ill.
    Materialart: Digitale Medien
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