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41Author    G. Waidmann, M. JansenRequires cookie*
 Title    Synthese und Charakterisierung des Fulleren-Kokristallisats C60*SiH(C6H5)3 Synthesis and Characterisation of the Fullerene Co-Crystal C60*SiH(C6H5)3  
 Abstract    A new fullerene co-crystal C60*SiH(C6H5)3 has been synthesized by crystallisation from a melt of SiH(C6H5)3 and C60 in sealed duran tubes at 80°C. X-ray investigations led to triclinic symmetry, space group P i, a = 10.086(1),/? = 14.431(2), c = 14.911(2) Ä, a = 79.13(1), ß = 74.943(9), 7 = 88.33(1)°, V = 2058.0(4) A 3, Z = 2. The crystal structure consists of isolated fullerene and silane molecules. At -80°C, C60 is still rotationally disordered. Temperature dependent Guinier powder diagrams do not show any phase transformation between 25 and -165°C. The compound is stable in air. 
  Reference    Z. Naturforsch. 53b, 161—164 (1998); eingegangen am 14. November 1997 
  Published    1998 
  Keywords    Fullerene C60, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0161.pdf 
 Identifier    ZNB-1998-53b-0161 
 Volume    53 
42Author    Thorsten Grob, FrankW. Eller, K. Urt, D. EhnickeRequires cookie*
 Title    Die Kristallstruktur von [Me3PN(H)PMe3]4l 28? einem Polyiodid mit I3~-, lg2--und I144"-Ionen Crystal Structure o f [M e3P N (H )P M e3]4I28, a Polyiodide w ith I3~, I82 -, and I 144~ Ions  
 Abstract    Black-red single crystals of [Me3PN(H)PMe3]4I28 have been prepared by the reaction of [Me3PNPMe3]I with iodine in dichloromethane solution in the presence of Me3SiI and traces of water. The polyiodide crystallizes triclinically in the space group Pi with two formula units per unit cell with the lattice dimensions a = 831.2(1), b = 1661.2(3), c = 1739.0(3) pm, q = 87.26(1)°, ß = 79.48(1)°, 7 = 78.17(1)°. The structure consists of [Me3PN(H)PMe3]2+ ions, linear I3~ ions, z-shaped I8: ~ ions, and zig-zag chains of I I44-ions, the terminal iodine atoms of which form I-H -N hydrogen bridges to the cations. 
  Reference    Z. Naturforsch. 53b, 552—556 (1998); eingegangen am 23. Februar 1998 
  Published    1998 
  Keywords    Polyiodide, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-0552.pdf 
 Identifier    ZNB-1998-53b-0552 
 Volume    53 
43Author    Wieslawa KudelskaRequires cookie*
 Title    Synthesis of Glycosyl Cyanides by the Reaction of 1-5-Phosphorothioates of Carbohydrates with Trimethylsilyl Cyanide  
 Abstract    A new procedure is described for the synthesis of a,/?-glycosyl cyanides by the reaction of per-O-benzylated S-a-D-glycopyranosyl phosphorothioates with trimethylsilyl cyanide in the presence of Lewis acid. Starting S-glycosyl phosphorothioates are prepared, directly, from O-benzyl protected reducing D-hexopyranoses (gluco-, galacto-, manno-) and alkylammonium salt of phosphorothioic acid under Lewis acid catalysis. 
  Reference    Z. Naturforsch. 53b, 1277—1280 (1998); received July 23 1998 
  Published    1998 
  Keywords    S-Glycosylphosphorothioates, Glycosyl Cyanides, Synthesis 
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 TEI-XML for    default:Reihe_B/53/ZNB-1998-53b-1277.pdf 
 Identifier    ZNB-1998-53b-1277 
 Volume    53 
44Author    Joachim Pethe, Joachim SträhleRequires cookie*
 Title    Synthese und Kristallstruktur von [Au(AuNCO)(AuPPh3)8]Cl Synthesis and Crystal Structure of [Au(AuNCO)(AuPPh3)8]Cl  
 Abstract    The photolysis of Cr(CO)6 and Ph3PAuN3 (1:2) in thf yields the unstable cluster cation [(Ph3PAu)5Cr(CO)4]+ that slowly decomposes to form the new homometallic gold cluster [Au(AuNCO)(AuPPh3)8]Cl. The cluster compound crystallizes in form of red needles in the tetragonal space group 14 with a = 2214.1(3), c = 1408.9(2) pm, and Z = 2. The inner skeleton of the cluster with the symmetry C4 consists of a centered square antiprism of nine Au atoms with the square faces of the antiprism being bridged by the AuNCO group, and a C P anion, respectively. The shortest Au-Au distances exist between the central and the 8+1 peripheral Au atoms ranging between 263.5(1) and 270.6(3) pm, the four Au-Cl distances are 280(1) pm. 
  Reference    Z. Naturforsch. 54b, 381—384 (1999); eingegangen am 3.Dezember 1998 
  Published    1999 
  Keywords    Gold Cluster, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-0381.pdf 
 Identifier    ZNB-1999-54b-0381 
 Volume    54 
45Author    A. N. Ägele3, E. A. Nokhinab, J. Sitarb, H.-JM. Eyer3, A. LachgarbRequires cookie*
 Title    Synthesis and Crystal Structures of ATi[Nb6Cli8] Compounds (A = K, Rb, Cs, In, Tl)  
 Abstract    New quaternary niobium cluster chlorides corresponding to the general formula ATi[Nb6Clis] (A = K, Rb, Cs, In, Tl) have been synthesized in sealed quartz tubes at 720 °C, starting from stoichiometric amounts of NbCls, niobium metal, TiCb, and AC1 (A = K, Rb, Cs), or In or Tl metals. The structures of RbTi[Nb6Clis] and CsTifNböClis] were determined using single­ crystal X-ray diffraction. RbTifNböClis] crystallizes in the rhombohedral crystal system, space group R3 (no. 148), Z = 3, with lattice parameters: a = 9.163(4), c = 25.014(14) A (hexagonal setting). The structure refinement converged to R] = 0.044 and wRi = 0.058 for all data. In this structure, discrete [NböClig]4-cluster units are linked by Rb+ and Ti3+ cations, located in a 12-coordinated anticubeoctahedral and octahedral chloride coordination environment, respectively. In contrast, CsTifNböClis] crystallizes in the trigonal crystal system, space group P31c (no. 163), Z = 2. The lattice parameters were determined to be a -9.1075(6), c = 17.0017(8) A. The structure refinement gives the reliability factors Ri = 0.029 and wRa = 0.063 for all data. The structure is built up of discrete octahedral [N bödis]4-cluster units, linked by Cs+ and Ti3+ cations which are located in a distorted hexagonal antiprismatic and octahedral chloride coordination environment, respectively. The structures of the compounds ATifNböClis] (A = K, In, Tl) were found to be isotypic with RbTi[NböCli8], and their unit cell parameters were refined using X-ray powder diffraction analysis. In tro d u ctio n 
  Reference    Z. Naturforsch. 55b, 139—144 (2000); received September 13 1999 
  Published    2000 
  Keywords    Niobium, Titanium, Cluster, Chlorides, Synthesis 
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 TEI-XML for    default:Reihe_B/55/ZNB-2000-55b-0139.pdf 
 Identifier    ZNB-2000-55b-0139 
 Volume    55 
46Author    K. EiseleRequires cookie*
 Title    Syntheses of Phenylserin Analogues and Their t-BOC-Derivatives  
 Abstract    The syntheses of phenylserinanalogues and their t-BOC-derivatives are described. 3,4-Methylendioxy-phenylserine is a new amino acid. 
  Reference    (Z. Naturforsch. 30c, 538 [1975]; received February 11 1975) 
  Published    1975 
  Keywords    Phenylserinanalogues, t-BOC-Derivatives, Syntheses 
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 TEI-XML for    default:Reihe_C/30/ZNC-1975-30c-0538_n.pdf 
 Identifier    ZNC-1975-30c-0538_n 
 Volume    30 
47Author    Requires cookie*
 Title    Übergangsmetall-Antimon(HI)bromide  
 Abstract    T ransition M etal-A n tim on y(III) Brom ides W o l f g a n g M a l i s c h und P e t e r P a n s t e r In stitu t Antim The reaction of SbBr3 with the complex metal carbonyl anions [jz-C5H 5(CO)3M]Na (M = Mo, W) leads to the formation of transition metal antimony bromides 7r-C5H 5(CO)3M -SbBr2, which can be further metallated, yielding the stable species jr-C5H 5(CO)3M -Sb-M / (CO)n7t-C5H 5 (M = M' = Mo, W) 
  Reference    (Z. Naturforsch. 30b, 229—234 [1975]; eingegangen am 16. Dezember 1974) 
  Published    1975 
  Keywords    ony-transition Metal Compounds, Synthesis, Coordination, Oxidation 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0229.pdf 
 Identifier    ZNB-1975-30b-0229 
 Volume    30 
48Author    Requires cookie*
 Title    Darstellung und Charakterisierung eines Di-w-amido-und von Di-^-hydroxokomplexen der  
 Abstract    Zusammensetzung [n>C5H5 Cr(NO)(NH2) ] 2 bzw. [7t-C5H 5Cr(NO)(OH)]2 (H 20) n (n = 0 -2) S ynthesis and C haracterization o f a D i-^-am ido-and D i-^-hydroxo Com plexes o f C om position [7r-C5H 5C r(N O)(N H 2)]2 and |>r-C5H 5Cr(NO)(OH)]2 • (H 20)" {n = 0 -2), R esp ectively G e r h a r d H o c h , H a n s -E c k a r d S a s s e und M a n f r e d L. Z i e g l e r The title compounds have been synthesized and characterized by elementary analysis, IR and NMR methods and their mass spectra. The compound [7i-C5H 5 Cr(NO)(NH2) ]2 is a di-^-amido complex, [jr-C5H 5Cr(NO)(OH) ] 2 -2 H 20 is its hydroxo analogon, elevation of the temperature causes the stepwise loss of the two water molecules yielding [7r-C5H 5 Cr(N0)(0 H)]2 -H 2 0 and [7i-C5H 5Cr(NO)(OH)]2. 
  Reference    (Z. Naturforsch. 30b, 704—709 [1975]; eingegangen am 24. Juni 1975) 
  Published    1975 
  Keywords    Synthesis, Characterization, Di-^-amido Complexes, Di-^-hydroxo Complexes 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0704.pdf 
 Identifier    ZNB-1975-30b-0704 
 Volume    30 
49Author    Dieter Mohr, Henning Wienand, ManfredL. Ziegler, M-O-S-RM. M—s—r, M. M. S—r, VsRequires cookie*
 Title    Darstellung und Charakterisierung von Sulfinatokomplexen 7r-C7H7Mo(C0)2S02R (R=-C6H5, -C6H4CH3) sowie von ein-und zweikernigen Thioarylverbindungen der Zusammensetzung 7r-C7H7Mo(CO)2SR' bzw. [^-C7H7Mo(CO)SR ]2 (R =-S-C6H5, -S-C6H4CH3, -S-C6F5, -S-C6H4N02)  
 Abstract    Synthesis and Characterization of Sulfinato Complexes 7r-C7H7Mo(C0)2S02R (R = -C6H5, -C6H4CH3) and of Mono and Dinuclear Thioaryl Compounds of Composition TT-C7H7MO(CO)2SR' resp. 0t-C7H7Mo(CO)SR']2 (R' = The aryl-sulfinato complexes ?r-C7H7Mo(CO)2S02R have been synthesized by re-action of JI-C7H7MO(CO)2J with the Ag-SC>2-R compounds. The sulfinate group is S-bonded. Mononuclear and dinuclear thioaryl complexes were isolated by reaction of 7r-C7H7Mo(CO)2Br with aryl mercaptanes R'-S-H in the presence of (CaHs^N which functioned as a proton acceptor. IR data indicate the dependence of the 7t-acceptor abilities of the sulfur atom from R'. Der Sulfinatrest -SO2-R kann sowohl als ein-zähniger als auch als zweizähniger Ligand fungieren. Als einzähniger Ligand kann er sowohl über das Schwefelatom (Sulfinato-S-Komplex) als auch über ein Sauerstoffatom (Sulfinato-O-Komplexe) gebun-den sein 1 . 0 0 0 0—s—0 II II /\ / \-o 7 Als zweizähniger Ligand ist die R-SCVGruppe intra-bzw. intermolekular an das Zentralatom koordiniert 1 . Die Darstellung der Sulfinatokomplexe gelingt im allgemeinen durch direkte Einschiebung von SO2 in eine Metall-Kohlenstoffbindung z.B. gemäß 2 -3 : 
  Reference    (Z. Naturforsch. 31b, 66—72 [1976]; eingegangen am 29. Juli 1975) 
  Published    1976 
  Keywords    Synthesis, Characterization, Sulfinato Complexes, Thiaryl Complexes 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0066.pdf 
 Identifier    ZNB-1976-31b-0066 
 Volume    31 
50Author    Nazmi Abd, Elatife Kassab, Sanaa Osman Abdallah, Hamed Abdel, Reheem Ead, Doreya ZakiRequires cookie*
 Title    Some New Tetrahydrothiopyrano[2,3-d]thiazole-2-thione Derivatives and their Biological Activities 3-Phenyl-2,4  
  Reference    (Z. Naturforsch. 31b, 376—379 [1976]; received August 14 1975) 
  Published    1976 
  Keywords    thiazolidinedithiones, 1, 4-Cycloaddition, Heterodienes, Synthesis, Biological Activities 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0376.pdf 
 Identifier    ZNB-1976-31b-0376 
 Volume    31 
51Author    Heinz-Joachim HübnerRequires cookie*
 Abstract    Manganese MnGa2Se4 and MnGa2Te4 were prepared by direct synthesis from the elements at 900-1000 °C. MnGa2Se4 (Space group l!, a = 5.676(2) A, c = 10.760(3) A, z = 2) is iso-typic with CdGa2S4. 
  Reference    (Z. Naturforsch. 31b, 886—887 [1976]; eingegangen am 12. März 1976) 
  Published    1976 
  Keywords    Gallium Selenide, Manganese Gallium Telluride, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0886_n.pdf 
 Identifier    ZNB-1976-31b-0886_n 
 Volume    31 
52Author    Kurt WalentaRequires cookie*
 Title    ZrSi04 mit monokliner Baddeleyitstruktur ? ZrSi04 with Monoclinic Baddeleyite Structure ?  
 Abstract    A new compound having the same composition as zircon, ZrSiC>4, but differing from it in its structure has been obtained by heating zircon particles to a temperature of 5000 to 10000 °K. According to X-ray powder diffraction data the structure and within limits of error also the unit-cell dimensions are identical with that of monoclinic baddeleyite, Zr02. This suggests that the baddeleyite lattice can not only accommodate 10 molecular % Si02 as is already known for some time, but substantially more, unless it is assumed that some kind of submicroscopic exsolution of amorphous Si02 has taken place. 
  Reference    (Z. Naturforsch. 31b, 1175—1178 [1976]; eingegangen am 31. Januar/24. März 1976) 
  Published    1976 
  Keywords    Zircon, Synthesis, Properties, Structure, Baddeleyite Lattice 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-1175.pdf 
 Identifier    ZNB-1976-31b-1175 
 Volume    31 
53Author    M. M., P. Či, S. InRequires cookie*
 Title    The Preparation of Some Unsymmetrically 2,2' -Disubstituted Stilbenes  
 Abstract    The new unsym m etrically 2,2'-disubstituted stilbenes with NO2 , F, Cl, Br, OCH3 , CH3 and NH2 groups as substituents have been prepared by W it t ig or P e r k i n reactions. The compounds 1 -8 were prepared due to the studies o f fragm entation on electron impact, photochem istry and photoelectron spectroscopy. Their geometrical configuration has been established by X H NMR and IR spectra. 
  Reference    (Z. Naturforsch. 32b, 181—183 [1977]; received October 18 1976) 
  Published    1977 
  Keywords    2, 2'-Disubstituted Stilbenes, Synthesis, Configuration 
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 TEI-XML for    default:Reihe_B/32/ZNB-1977-32b-0181.pdf 
 Identifier    ZNB-1977-32b-0181 
 Volume    32 
54Author    Friedhelm Lötz, Udo Kraatz, Friedhelm KörteRequires cookie*
 Title    Zur Synthese seitenkettenhydroxylierter Tetrahydrocannabinol Synthesis of Side Chain Hydroxylated Tetrahydrocannabinols  
 Abstract    The potential Zl 8 -tetrahydrocannabinol meta-bolites (6 a, b) were synthesized starting from (+)-fmris-p-menthadien-(2,8)ol(l) (2) and the resorcyl-alkyl esters (3 a, b). 
  Reference    Z. Naturforsch. 33b, 349—350 (1978); eingegangen am 30. Dezember 1977 
  Published    1978 
  Keywords    Zl 8 -Cannabinoids, Side Chain Hydroxylation, Synthesis 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0349_n.pdf 
 Identifier    ZNB-1978-33b-0349_n 
 Volume    33 
55Author    Max Schmidt, GerhardG. HoffmannRequires cookie*
 Title    Darstellung und Eigenschaften von Dihydrogensulfido-, Dihydrogenselenido-und Dinatriumsulfido-Komplexen von Palladium(II) und Platin(II) Synthesis and Properties of Di-hydrogensulfido, Di-hydrogenselenido and Di-sodiumsulfido Complexes of Palladium(II) and Platinum(II)  
 Abstract    Dichloro-bis(triphenylphosphine)platinum(II) (2) and Dichloro-l,2-bis(diphenylphos-phine)ethane-palladium(II) (3) do react with hydrogensulfide and sodiumsulfide under formation of the corresponding compounds Di-hydrogensulfido-l,2-bis(diphenylphos-phine)ethane-palladium(II) (4), Disodiumsulfido-l,2-bis(diphenylphosphine)ethane-palla-dium(II) (7), Di-hydrogensulfido-bis(triphenylphosphine)platinum(II) (1) and Di-sodium-sulfido-bis(triphenylphosphine)platinum(II) (8). 2 and 3 react with sodiumhydrogen-selenide under formation of Di-hydrogenselenido-l,2-bis(diphenylphosphine)ethane-palladium(II) (5) and Di-hydrogenselenido-bis(triphenylphosphine)platinum(II) (6). IR and *H NMR spectra are reported. 
  Reference    Z. Naturforsch. 33b, 1334—1337 (1978); eingegangen am 23. Mai 1978 
  Published    1978 
  Keywords    Platinum, Palladium, Dihydrogensulfido Complexes, Dihydrogenoselenido Complexes, Synthesis 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1334.pdf 
 Identifier    ZNB-1978-33b-1334 
 Volume    33 
56Author    Antonios Antoniadis, Udo KunzeRequires cookie*
 Title    Darstellung von Triphenylsilyl-diphenylphosphin * Synthesis of Triphenylsilyl Diphenylphosphine  
  Reference    (Z. Naturforsch. 34b, 116—117 [1979]; eingegangen am 29. August/25. September 1978) 
  Published    1979 
  Keywords    Syntheses, Triorganylelement(IVb)diorganylphosphines, Triphenyltindiphenylphosphine, Triphenylsilyldiphenylphosphine 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0116_n.pdf 
 Identifier    ZNB-1979-34b-0116_n 
 Volume    34 
57Author    Manfred Zabel, Sigrid Wandinger, Klaus-Jürgen RangeRequires cookie*
 Title    Ternäre Chalkogenide M3M2'X2 mit Shandit-Struktur Ternary Chalcogenides M3M2'X2 with Shandite-Type Structure  
 Abstract    Metal-rich ternary chalcogenides M3M2'X2 (M = Ni, Co, Pd, Rh; M' = In, Tl, Pb, Sn; X = S, Se) with Shandite-type structure were synthesized from mixtures of the elements and/or binary components. A single-crystal investigation on Co3ln2S2 verifies the rhombo-hedral unit cell of Shandite-type compounds, originally postulated by Peacock and McAndrew (Crystal data for Co3ln2S2: Rhombohedral, space group R3m; a = 549,31 (6) pm, a = 57.89°, Z= 1; 3 Co in 3d, 1 In(l) in la, 1 In(2) in lb, 2 S in 2c with x = 0.2790). 
  Reference    Z. Naturforsch. 34b, 238—241 (1979); eingegangen am 20. Oktober 1978 
  Published    1979 
  Keywords    Metal-rich Ternary Chalcogenides, Shandite-type, Synthesis, Crystal Structure 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0238.pdf 
 Identifier    ZNB-1979-34b-0238 
 Volume    34 
58Author    Friedhelm Lötz, Udo Kraatz, Friedhelm KörteRequires cookie*
 Title    Synthese Pyridin-analoger Tetrahydrocannabinol Synthesis of Pyridine-analogous Tetrahydrocannabinols  
 Abstract    Starting from 4-methylpyridine Si 3-B/ZR-zl 8 -tetrahydrocannabinol-analogous (2d) was prepared. The reaction sequence also includes the first synthesis of a 6H-benzo(4,5)-pyrano(2,3-c)-pyridin-6-on, a novel ring-system. The proposed structures were supported by spectroscopic data (X H NMR, IR, MS). 
  Reference    Z. Naturforsch. 34b, 306—312 (1979); eingegangen am 7. September 1978 
  Published    1979 
  Keywords    Aza-Cannabinoids, Benzopyrano Pyridines, Structural Identification, Synthesis 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0306.pdf 
 Identifier    ZNB-1979-34b-0306 
 Volume    34 
59Author    Gert Bauer, Gerhard HageleRequires cookie*
 Title    Reaktionen polyhalogenierter Cyclobutene mit Trimethylphosphit Reactions of Polyhalogenated Cyclobutenes with Trimethylphosphite  
 Abstract    Structure and reactive behaviour of polyhalogenated cyclobutenes towards trimethyl-phosphite are studied in detail. Stable phosphoranes RP(F)(OCH3)3 as intermediates of Arbuzov-type reactions are obtained. Controlled decomposition of phosphoranes leads to highly reactive c-yclobutenyl substituted phosphonic acid esters RP(0)(0CH3)2. Substitu-tion reactions at aliphatic and vinylic positions of RP(0)(0CH3)2 are observed. Biphos-phonic acid esters R[P(0)(0CH3)2]2 are synthesized. Some routes to perhalogenated cyclo-butenes are described. NMR and MS data for the hitherto unknown cyclobutenyl-sub-stituted organophosphorus compounds are given. 
  Reference    Z. Naturforsch. 34b, 1252—1259 (1979); eingegangen am 3. April/10. Mai 1979 
  Published    1979 
  Keywords    Phosphoranes, Phosphonic Acid Esters, Synthesis, NMR 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1252.pdf 
 Identifier    ZNB-1979-34b-1252 
 Volume    34 
60Author    Lothar Steiling, Ulrich WannagatRequires cookie*
 Title    Sila-Pharmaka, 15. Mitt. [1] Synthese und Eigenschaften des Sila-Pridinols Sila-Drugs, 15th Communication [1] Synthesis and Properties of Sila-Pridinol  
 Abstract    Synthesis of the silicon analogue VI b of the drug pridinol and of its homologue VI a was achieved via eq. (l-5b) (Scheme 1). The novel compounds IVa-VIb are described in their properties and confirmed in their structures (Tables I-IV). Some preliminary pharma-cological investigations suggest spasmolytical effects of sila-pridinol seeming to be somewhat better than those of pridinol itself. 
  Reference    Z. Naturforsch. 34b, 1413—1417 (1979); eingegangen am 25. Mai 1979 
  Published    1979 
  Keywords    Organosilicon Compounds, Syntheses, Chemical and Pharmacological Properties 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-1413.pdf 
 Identifier    ZNB-1979-34b-1413 
 Volume    34