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61Author    Hans-Peter Schrödel, Alfred SchmidpeterRequires cookie*
 Title    Phosphorandiyl-l,3,5-triphosphinane/ Phosphonio-l,3,5-triphosphinin Kationen Phosphoranediyl-l,3,5-triphosphinanes / Phosphonio-l,3,5-triphosphinine Cations  
 Abstract    Depending on the reaction conditions, the condensation of triphenylphosphonium bis(trimethylsilyl)methylide 1 with phosphorus trichloride and phosphorus tribromide gives the cyclic trimers (Ph3P=CP-X)3, X = Cl, Br, trihalo-tris(triphenylphosphoranediyl)-1,3,5-triphosphinanes 3 and 5. In solution the compounds dissociate to give the ionic forms 4 and 6 which rapidly exchange the halide between the halophosphine and the phosphenium moieties. The exchange is slowed down when the halide ion is replaced by a tosylate ion. Substitution of the covalent chloride of 4 for diphenylphosphino groups gives again an ionic product 10, while the introduction of a morpholino group as well as the replacement of all chloride by triflate give dicationic compounds 12 and 13. Reaction of 3 with gallium trichloride finally leads to the tris(triphenylphosphonio)-l,3,5-triphosphinine trication as a major equilibrium participant. 
  Reference    Z. Naturforsch. 52b, 162—168 (1997); eingegangen am 24. Oktober 1996 
  Published    1997 
  Keywords    Phosphonium Ylides, Halophosphines, Phosphenium Ions, 1, 3, 5-Triphosphinines, Halide Exchange 
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 TEI-XML for    default:Reihe_B/52/ZNB-1997-52b-0162.pdf 
 Identifier    ZNB-1997-52b-0162 
 Volume    52 
62Author    M. Ax Herberhold, U. Do Steffl, BerndW. RackmeyerRequires cookie*
 Title    l,3-Distanna-2-phospha-[3]ferrocenophanes -Synthesis, Reactivity and NMR Spectroscopic Properties  
 Abstract    -organo(R)-l,3-distanna-2-phospha-[3]ferrocenophanes [R = Me (2a), rBu (2b), CöH i i (2c), Ph (2d)] and one arsa-analogue 2d(As) were obtained from the reaction of l,l'-bis(chlorodim ethylstannyl)ferrocene 1 with either bis(trimethylsilyl)methylphosphane or the dilithio derivatives, Li2PR and Li^AsPh, respectively. All compounds 2 react with chalco-gens (oxygen, sulfur, selenium) by cleavage of the Sn-P bonds and formation of the known l,3-distanna-2-chalcogena-[3]ferrocenophanes. In contrast, 2d traps pentacarbonylmetal frag­ ments [M(CO)5] to give the stable phosphane complexes [M = Cr (4d), Mo (5d), W (6d)]. The l,l'-bis(diorganophosphanostannyl)ferrocenes [R = fBu (3b), Ph (3d)] were prepared for comparison of NMR data. The ferrocenophanes 2 are fluxional with respect to fast movement of the cyclopentadienyl rings which induces inversion at the pyramidal phosphorus atom. This dynamic process is slow in the cases of 2d(As) and of the pentacarbonyl complexes 4d -6d. All new compounds were characterised by 'H , i3C, 31P and 1 l9Sn NMR spectroscopy. Various 2D heteronuclear shift correlations {e.g. 11P /1H and ll9Sn/'H) were carried out for the com ­ pounds 2 and also for non-cyclic derivatives such as bis(trimethylstannyl)phenvlphosphane and -arsane in order to determine absolute signs of coupling constants [e.g. 7(n S n,''P) > 0 and 2J(] l9Sn,' l7Sn) < 0]. The NM R data suggest that the molecular frameworks of the ferroceno­ phanes 2 are not particularly strained. 
  Reference    (Z. Naturforsch. 54b, 57—62 [1999]; received July 28 1998) 
  Published    1999 
  Keywords    Ferrocene, Tin, Phosphorus, NMR Data, Coupling Signs l, l, 3, 3-Tetramethyl-2 
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 TEI-XML for    default:Reihe_B/54/ZNB-1999-54b-0057.pdf 
 Identifier    ZNB-1999-54b-0057 
 Volume    54 
63Author    Ralf Hautzel, Heidrun AnkeRequires cookie*
 Title    Screening of Basidiomycetes and Ascomycetes for Plant Growth Regulating Substances. Introduction of the Gibberellic Acid Induced de-novo Synthesis of Hydrolytic Enzymes in Embryoless Seeds of Triticum aestivum as Test System  
 Abstract    A new test system for the detection of plant growth regulating activities was successfully employed. In a screening for inhibitors of the gibberellic acid controlled synthesis of hydrolytic enzymes in embryoless wheat seeds (T riticum aestivum) 160 cultures of ascomycetes and basi­ diomycetes were tested. In the extracts of two cultures inhibitory activities were detected. From fermentations of a Hypholoma-species (basidiomycetes) 3,5-dichloro-4-methoxybenzyl alcohol \ yas isolated as the active principle. Galiellalactone and two other new phytotoxins were isolated from cultures of the ascomy-cete G aliella rufa. At concentrations of 50 |ig/ml all four compounds inhibited the de-novo synthesis of a-amylases, proteases, and phosphatases. Further investigations on the mode of action revealed, that all four metabolites interfere with early steps of the biosynthetic path­ ways induced by gibberellic acids. In vivo, the germination of the seeds of several plants was inhibited by these compounds. 
  Reference    Z. Naturforsch. 45c, 1093—1098 (1990); received July 19 1990 
  Published    1990 
  Keywords    Galiella rufa, Hypholoma species, a-Amylase, Plant Growth Regulator, Galiellalactone, 3, 5-Dichloro-4-methoxybenzyl Alcohol 
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 TEI-XML for    default:Reihe_C/45/ZNC-1990-45c-1093.pdf 
 Identifier    ZNC-1990-45c-1093 
 Volume    45 
64Author    Stefan Kremer, Olov Sterner, Heidrun AnkeRequires cookie*
 Title    Degradation of Pentachlorophenol by Mycena avenacea TA 8480 - Identification of Initial Dechlorinated Metabolites  
 Abstract    Cultures o f the basidiomycete M ycena avenacea TA 8480 were shown to m etabolize penta­ chlorophenol (PCP), 2,3,5,6-tetrachloro-/7-hydroquinone (TeCHQ), and 2,3,5,6-tetrachloro-/?-benzoquinone (TeCBQ). The first metabolite o f the PCP degradation pathway was identified as TeCBQ which in a second reaction is reduced to the hydroquinone TeCHQ. Subsequently dechlorination o f TeCHQ yielded 3,5,6-trichloro-2-hydroxy-/?-benzoquinone (TCOHBQ). The specific degradation rate for PCP was 1.4 mg x g dry m ycelia-1 x day-1. The initial de­ chlorination rate o f TeCHQ was 5.9 mg x g dry m ycelia"1 x h o u r '1. N one o f the com pounds supported growth o f the fungus. 
  Reference    Z. Naturforsch. 47c, 561 (1992); received April 1 1992 
  Published    1992 
  Keywords    Basidiomycete, M ycena avenacea, Pentachlorophenol, Dechlorination, 3, 5, 6-Trichloro-2-hydroxybenzoquinone 
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 TEI-XML for    default:Reihe_C/47/ZNC-1992-47c-0561.pdf 
 Identifier    ZNC-1992-47c-0561 
 Volume    47 
65Author    T. Sc HRequires cookie*
 Title    Departm ent o f Chemistry, The U niversity, Leicester LEI 7RH, England and  
  Reference    (Z. Naturforsch. 30b, 969 [1975]; received June 19 1975) 
  Published    1975 
  Keywords    Acetylisocyanate, Chlorosulfonylisocyanate, NMR, Mass Spectra, 3-Chlorosulfonyl-6-methyl-2 H-l, 3, 5-oxadiazine-2, 4-(3 H)-dione 
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 TEI-XML for    default:Reihe_B/30/ZNB-1975-30b-0969_n.pdf 
 Identifier    ZNB-1975-30b-0969_n 
 Volume    30 
66Author    Friedrich Boberg, Rainer VossRequires cookie*
 Title    Markierte Verbindungen, XXV 1 Chloraustausch zwischen und Antimon(III)-chlorid -das 1.2.3-Trichlorpropenylium-Ion On Labelled Compounds, XXV 1 Chlorine Exchange between 1,2,3,3-Tetrachloro-l-propene and Antimony(Ill)-chloride — the 1,2,3-Trichloropropenylium Ion  
  Reference    (Z. Naturforsch. 31b, 480—486 [1976]; eingegangen am 13. November 1975) 
  Published    1976 
  Keywords    Chlorine Exchange, 1, 2, 3, 3-Tetrachloro-l-propene, 1, 2, 3-Trichloropropenylium Ion, Ally lie Rearrangement, eis j trans-Isomerization 
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 TEI-XML for    default:Reihe_B/31/ZNB-1976-31b-0480.pdf 
 Identifier    ZNB-1976-31b-0480 
 Volume    31 
67Author    M. VeithRequires cookie*
 Title    Cyclische Diazastannylene, II 1 Intermolekulare Lewis-Säure-Base-Addukte bei 2 -Diazasilastannetidinen Cyclic Diazastannylenes, II 1 Intermolecular Lewis-Acid-Base Adducts of 1, 3,2,4A 2 -Diazasilastannetidines  
 Abstract    -diazasilastannetidines can be prepared as mono-mers (organyl = <erf-butyl) or dimers (organyl = isopropyl) in nonpolar solvents, depending on the organic nitrogen substituent. The formation of the dimer, which is due to an intermolecular Lewis-acid-base interaction of Sn(II) with nitrogen, can be initiated by solidification. When the tertf-butyl compound is cooled below 0 °C two crystalline modi-fications are found: a monoclinic phase (C 2/c; a= 10.655(5); b = 24.75(1); c = 17.334(9) Ä; ß = 106.9(1)°) and a triclinic phase (P I; a = 10.68(1); b = 13.51(1); c = 12.36(1) A; a = 96.2(1); ß = 102.6(1); y = 118.4(1)°). The crystal structures turn out to be built of dimeric and monomeric units in the first case and presumably only dimeric species in the second case. The isopropyl derivative crystallizes in the space group P 2i/b (a = 10.77(1); b= 12.14(2); c = 11.15(2) A; ß = 120.2(2)°) with only dimeric units being present, as in the liquid. Interrelationships between the three structures are discussed. 
  Reference    (Z. Naturforsch. 33b, 1—6 [1978]; eingegangen am 5. September/6. Oktober 1977) 
  Published    1978 
  Keywords    Diazastannylenes, Solid State, X-ray, Crystal Structure, NMR l, 3-Diorganyl-2, 2-dimethyl-I, 3, 2, 4A 2 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-0001.pdf 
 Identifier    ZNB-1978-33b-0001 
 Volume    33 
68Author    Ringverengungsreaktionen Von Chinolintrionen, Helga Wittmann, Friedrich GünzlRequires cookie*
 Title    Synthesen von Heterocyclen, CCVIII [1] Zur Chemie der vicinalen Triketone, XI [2]  
 Abstract    -lH,5H-benzo [ij] quinolizine (I) does not react with 2-aminopyridine to give a Schiff base [2], but reacts by ringcontraction to the spiro-indolone 1/1, which can be hydrolysed to l-(2-pyridyl-amino)l,2,5,6-tetrahydro-4H-pyrrolo[3,2,l-ij]quinoline-2-one (2/1). In the same way the reaction of I resp. 1-phenyl-quinolinetrione (LI) with tfert-butylamine in aliphatic alcohols yields by ringcontraction the indolone acid esters 5 a-c. Reaction of I with £er£-butylamine without solvent forms the ringcontracted amide 5c/I. 
  Reference    Z. Naturforsch. 33b, 1540—1546 (1978); eingegangen am 12. Juli 1978 
  Published    1978 
  Keywords    Quinolinetriones, Ringcontractions, 2-Aminopyridine, 2, 3-Diaminopyridine, Zerf-Butylamine l, 2, 3-Trioxo-2, 3, 6, 7-tetrahydro 
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 TEI-XML for    default:Reihe_B/33/ZNB-1978-33b-1540.pdf 
 Identifier    ZNB-1978-33b-1540 
 Volume    33 
69Author    MohamedHilmy Elnagdi, Mohamed Ezzat, KamalUsef Kandeel, SadekRequires cookie*
 Title    Reactions with Cyclic Amidenes III: Synthesis of Some New Fused Pyrazole Derivatives  
  Reference    Z. Naturforsch. 34b, 275—279 (1979); received August 28 1978 
  Published    1979 
  Keywords    Diazobetaienes, Dipolarcycloaddition, Pryazolo[4, 3-c]-l, 2, 3, 4-tetrazines, Ethoxycarbonyl Isothiocyanate, X H NMR 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0275.pdf 
 Identifier    ZNB-1979-34b-0275 
 Volume    34 
70Author    W. Neuenhaus, H. Budzikiewicz, H. Korth, G. PulvererRequires cookie*
 Title    Bakterieninhaltsstoffe, III [1] 3-Alkyl-tetrahydrochinolinderivate aus Pseudomonas Bacterial Constituents, III [1] 3-Alkyl-tetrahydroquinoline Derivatives from Pseudomonas  
  Reference    Z. Naturforsch. 34b, 313—315 (1979); eingegangen am 18. September 1978 
  Published    1979 
  Keywords    Bacterial Constituents, Pseudomonas, Iron Defficiency Growth, Fluorescent Compounds, 3-Alkyl-3-hydroxy-2, 4-dioxo-l, 2, 3, 4-tetrahydroquinolines 
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 TEI-XML for    default:Reihe_B/34/ZNB-1979-34b-0313.pdf 
 Identifier    ZNB-1979-34b-0313 
 Volume    34 
71Author    Manfred Weide, Helge Pesel, ++, Dang Van, Hieu ++Requires cookie*
 Title    mit starken intramolekularen sterischen Wechselwirkungen, IX [1] terf-Butylsubstituierte Di-und Trisiloxane Silicon Compounds with Strong Intramolecular Steric Interactions, IX [1] tert-Butyl Substituted Di-and Trisiloxane s  
  Reference    (Z. Naturforsch. 35b, 31—34 [1980]; eingegangen am 23. August 1979) 
  Published    1980 
  Keywords    l, l, 3, 3-Tetra-£er£-butyldisiloxane-l, 3-diol, Penta-fer£-butyldisiloxanol, Steric Hindrance, Mass Spectra 
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 TEI-XML for    default:Reihe_B/35/ZNB-1980-35b-0031.pdf 
 Identifier    ZNB-1980-35b-0031 
 Volume    35 
72Author    Rudolf Hansel, Faeis Khaliefi, Andrew PelterRequires cookie*
 Title    3.5-Dihydroxy  
 Abstract    6.7.8-trimethoxyflavon aus Heiichrysum graveolens: Bestätigung der Konstitution Confirmation of the Structure of an Extractive from Helichrysum graveolens as 3,5-Dihydroxy-6,7,8-trimethoxyflavone 
  Reference    Z. Naturforsch. 36b, 1171—1172 (1981); eingegangen am 12. Mai 1981 
  Published    1981 
  Keywords    3, 5-Dihydroxy-6, 7, 8-trimethoxyflavone, Isomeric a-Hydroxybenzalcumaranone, X ray, NMR Spectra 
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 TEI-XML for    default:Reihe_B/36/ZNB-1981-36b-1171.pdf 
 Identifier    ZNB-1981-36b-1171 
 Volume    36 
73Author    New Monocyclic Acyloxyfluoroboranes, Herbert Binder, Walter Matheis, Hans-Jörg Deiseroth, Han Fu-Son, ProfH. Dr, W. Binder, MatheisRequires cookie*
 Title    Über neue monocyclische Acyloxyfluoroborane Darstellung, Molekül-und Kristallstruktur  
 Abstract    Acyloxyfluoroboranes Trimeric alkoxydifluoroboranes (F2BOR)3 (2) react with organic acid anhydrides by substitution of a ring group OR forming monocyclic acyloxyfluoroboranes of the type 2,2,6,6-tetrafluoro-l,4-dialkyl-l,3,5-trioxa-2,6-diboracyclohexene (3). The X-ray crystal structure determination of 3a shows two conformational isomers: two planar and two non-planar six-membered rings are present in the unit cell. The ring conformation is influenced by weak intermolecular H — F interactions. 
  Reference    Z. Naturforsch. 38b, 554—558 (1983); eingegangen am 15. November 1982/26. Januar 1983 
  Published    1983 
  Keywords    6, 6-Tetrafluoro-l, 4-dialkyl-l, 3, 5-trioxa-2, 6-diboracyclohexenes: Synthesis, Molecular and Crystal Structure 
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 TEI-XML for    default:Reihe_B/38/ZNB-1983-38b-0554.pdf 
 Identifier    ZNB-1983-38b-0554 
 Volume    38 
74Author    Jacek Bielawski, Kurt Niedenzu, JeanS. StewartRequires cookie*
 Title    Preparation and Characterization of Some Isoelectronic Boron-Nitrogen Analogs of Substituted Uracil [1]  
 Abstract    Several l,3,5-triaza-2-boracyclohexa-4,6-diones, which are isoelectronic analogs of substituted uracil, have been prepared by condensation reactions of boranes with biurets. They include species containing a NH or BH unit as potentially reactive sites. The latter are extremely sensitive to hydrolysis but are readily handled as the 2-methylaminoethanol derivative containing four-coordinate boron. 
  Reference    Z. Naturforsch. 40b, 389—392 (1985); received November 18 1984 
  Published    1985 
  Keywords    Boron-Nitrogen Compounds, Azaborauracils, l, 3, 5-Triaza-2-boracyclohexa-4, 6-diones, Spiroboron Compound, NMR Spectra 
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 TEI-XML for    default:Reihe_B/40/ZNB-1985-40b-0389.pdf 
 Identifier    ZNB-1985-40b-0389 
 Volume    40 
75Author    IvanS. Alferiev, Sergey Yu, BobkovRequires cookie*
 Title    Cyclic Oligophosphonic Anhydrides Stable in Aqueous Media  
  Reference    Z. Naturforsch. 47b, 1213—1224 (1992) 
  Published    1992 
  Keywords    Amides, Phosphonylation, l-Alkylaminoalkane-l, l, 3, 3-tetrayl-tetrakis-phosphonic Anhydrides, Cyclic Dimeric Anhydrides, l-Aminoalkylidene-l, l-bis-phosphonic Acids 
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 TEI-XML for    default:Reihe_B/47/ZNB-1992-47b-1213.pdf 
 Identifier    ZNB-1992-47b-1213 
 Volume    47 
76Author    Rainer Gast, ThomasK. Aukorat, Ion Neda, Reinhard SchmutzlerRequires cookie*
 Title    Das 2-Halogen-5,6-benzo-1,3>2-dioxaphosphorinan-4-on-Ringsystem The 2-Halogeno-5,6-benzo-l,3,2-dioxaphosphorinan-4-one Ring System  
 Abstract    The reaction of salicylic acid with phosphorus trichloride furnished the previously known 2-chloro-5,6-benzo-l,3,2-dioxaphosphorinan-4-one heterocycle 1 which was unambiguously characterized, for the first time, by N M R spectroscopy and mass spectrometry. The fluorine and bromine analogues of 1, 2 and 3 were synthesized from 1, using exchange reactions. The iodo derivative, 4, owing to its instability, could be identified only in the reaction mixture by 'H and 31P N M R spectroscopy. The amine derivatives 5 -8 were obtained from 1 using stand­ ard exchange reactions, either with silylated amines or with secondary amines in the presence of base. There was no evidence by 'H N M R spectroscopy for intram olecular M e ,N -»P coordi­ nation in 6. The 31P N M R investigation of 7 revealed the presence o f two rotational isomers, presumably as a result of steric hindrance at the P -N bond by the methyl substituent of the piperidine group. The reaction of 6 with methyl iodide led to m ethylation at the nitrogen atom of the Me2N group, producing the ammonium iodide, 9. The reactions o f 5, 6 and 8 with nor-bornadiene tetracarbonyl molybdenum failed to furnish isolable products. 
  Reference    Z. Naturforsch. 48b, 867—874 (1993); eingegangen am 2. September 1992 
  Published    1993 
  Keywords    5, 6-Benzo-l, 3, 2-dioxaphosphorinan-4-one Derivatives, Halogen Substitution, Dialkylamino Substituents, R otational Isomers 
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 TEI-XML for    default:Reihe_B/48/ZNB-1993-48b-0867.pdf 
 Identifier    ZNB-1993-48b-0867 
 Volume    48 
77Author    M. Sekar, S. Vanitha, K. J. Rajendra, PrasadRequires cookie*
 Title    Synthesis of Novel 3-Acetyl-2-hydroxy-l-N,N-diacetylaminocarbazole Derivatives  
 Abstract    The synthesis of hitherto unknown 3-acetyl-2-hydroxy-l-N,N-diacetylaminocarbazole (3a-f), is reported. The hydroxyiminocarbazoles (2a-f), prepared from 1-oxo-1,2,3,4-tetra-hydrocarbazoles (la -f) on treatment with acetyl chloride in acetic anhydride yielded the title compounds (3a-f). 
  Reference    Z. Naturforsch. 49b, 687—690 (1994); received June 7/August 31 1993 
  Published    1994 
  Keywords    l-Hydroxyimino-l, 2, 3, 4-tetrahydrocarbazoles, 3-Acetyl-2-hydroxy-l-N, N-diacetylaminocar-bazoles, Aromatization, Thermal Fries Rearrangement, Antimicrobial Activities 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0687.pdf 
 Identifier    ZNB-1994-49b-0687 
 Volume    49 
78Author    Ralf Sonnenburg, Ion Neda, Axel Fischer, PeterG. Jones, Reinhard SchmutzlerRequires cookie*
 Title    Verbindungen mit dem 5,6-Benzo-l,3,2-diazaphosphorinan-4-on-Ringsystem: Synthese von 2-Chlor-, 2-N,N-dimethylamino-und 2-Bis-(2-chlorethyl)amino- substituierten Derivaten mit drei-und vierfach koordiniertem Phosphor Compounds Involving the 5,6-Benzo-l,3,2-diazaphosphorinane-4-one Ring System: Synthesis of 2-Chloro-, 2-N,N-dimethylamino-and 2-Bis-(2-chloroethyl)amino- Substituted Derivatives with Three-and Four-Coordinated Phosphorus  
  Reference    Z. Naturforsch. 49b, 788—8 (1994); eingegangen am 16. D ezem ber 1993 
  Published    1994 
  Keywords    5, 6-Benzo-l, 3, 2-diazaphosphorinan-4-one Derivatives, Dialkylamino Substituents, Bis-(2-chloroethyl)amino Substituents, Platinum Complex, NM R Spectra 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0788.pdf 
 Identifier    ZNB-1994-49b-0788 
 Volume    49 
79Author    Axel Fischer, Ion Neda, Thomas Kaukorat, Ralf Sonnenburg, PeterG. Jones, R.Einhard SchmutzlerRequires cookie*
 Title    Chemistry of the 4,5-Benzo-3-methyl-l,3,2-oxazaphosphorinan-6-one Ring System: X-Ray Crystal Structure Analysis of a Bis(2-chloroethyl)amino-and of an Acetam ido-Substituted Derivative  
  Reference    Z. Naturforsch. 49b, 939—949 (1994); eingegangen am 14. Februar 1994 
  Published    1994 
  Keywords    4, 5-Benzo-3-m ethyl-l, 3, 2-oxazaphosphorinan-6-one Derivatives, H alogen Substitution, Oxidation, X-Ray 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-0939.pdf 
 Identifier    ZNB-1994-49b-0939 
 Volume    49 
80Author    Axel Fischer, Ion Neda, PeterG. Jones, Reinhard SchmutzlerRequires cookie*
 Title    Darstellung und Kristallstrukturen einiger Ubergangsmetall-Komplexverbindungen mit Liganden mit dem 4,5-Benzo-3-methyl-l,3?2-oxazaphosphorinan-6-on-Gerüst Synthesis and X-Ray Crystal Structures of Some Transition-Metal Complexes Involving Ligands with the 4,5-Benzo-3-methyl-l,3,2-oxazaphosphorinan-6-one Framework  
  Reference    Z. Naturforsch. 49b, 1481—1493 (1994); eingegangen am 21. Februar 1994 
  Published    1994 
  Keywords    2-Substituted 4, 5-Benzo-3-m ethyl-l, 3, 2-oxazaphosphorinan-6-ones Ligands, Platinum Complexes, M olybdenum Complexes, Single Crystal X-Ray Structure Analysis 
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 TEI-XML for    default:Reihe_B/49/ZNB-1994-49b-1481.pdf 
 Identifier    ZNB-1994-49b-1481 
 Volume    49