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61.
Masao Tokuda Yasufumi Yamada Toshiya Takagi Hiroshi Suginome Akio Furusaki 《Tetrahedron letters》1985,26(49):6085-6088
Neutral aminyl radicals generated by anodic oxidation of lithium alkenylamides 2 undergo a stereoselective cyclization to give -1-methyl-2,5-disubstituted pyrrolidines 4. Their stereochemistry was confirmed by a comparison with -1,2-dimethyl-5-phenylpyrrolidine, the structure of which was established by X-ray crystallographic analysis of its quarternary ammonium bromide 6. 相似文献
62.
Tanaka H Yamada T Sugiyama S Shiratori H Hino R 《Journal of colloid and interface science》2005,286(2):812-815
Using a hydroxyl group appended free base porphyrin derivative (HP), porphyrin-introduced silica gels were synthesized by a sol-gel process. The HP content in the materials linearly increased with increasing the HP concentration. Meanwhile, free base tetraphenylporphyrin (TPP) with no hydroxyl groups were almost not incorporated into the silica gels. These facts suggested that the interaction between hydroxyl groups of the HP molecules and silica network is considerably strong. The UV-vis characters of HP-introduced materials were almost the same as pure HP molecules. The Beer's plot indicated that the HP molecules in the materials are dispersed. 相似文献
63.
S. Kulprecha T. Nihira C. Shimomura K. Yamada N. Nilubol T. Yoshida H. Taguchi 《Tetrahedron》1984,40(15):2843-2846
The microbiological transformation of lithocholic acid (3α-hydroxy-5β-cholanic acid) into 3α, 15β-dihydroxy-5β-cholanic acid by Cunninghamella sp. is Investigated. The structure has been determined on the basis of two-dimensional 1H-NMR. 相似文献
64.
A. E. Stuchbery H. H. Bolotin C. E. Doran I. Morrison L. D. Wood H. Yamada 《Zeitschrift für Physik A Hadrons and Nuclei》1985,320(4):669-674
The gyromagnetic ratios of the 4 1 + , 6 1 + , and 2 2 + states in186W were measured relative to that of the 2 1 + level by means of the transient field implantation perturbedγ-ray angular distribution technique. The nuclei in the states of interest were Coulomb excited using a beam of 220-MeV63Cu projectiles and recoiled swiftly through a thin, polarized Fe foil. The present measurements yielded ratiosg(4 1 + )/g(2 1 + )=1.04±0.07,g(6 1 + )/g(2 1 + )=1.03 ±0.20 andg(2 2 + )/g(2 1 + )=0.63±0.13. The sizable disparity between the measuredg-factors of the ground- and excited-band is examined within the context of the interacting boson approximation model. 相似文献
65.
Antianoxic action and active constituents of evodiae fructus 总被引:1,自引:0,他引:1
J Yamahara T Yamada T Kitani Y Naitoh H Fujimura 《Chemical & pharmaceutical bulletin》1989,37(7):1820-1822
In order to develop new drugs from natural products, constituents of natural medicines were examined for their effectiveness in the KCN-induced anoxia model in mice. Methanol extract from a Chinese medicine, evodia (fruits of Evodia rutaecarpa Benth. or E. officinalis Dode), had a significant effect in the KCN-induced anoxia model in mice and therefore the active constituents were further examined. The results indicated that the antianoxic action of evodia was found in the fraction containing evodiamine. Further analysis of the active constituent indicated that evodiamine and rutaecarpine, indole-alkaloids found in large amounts in the Chinese medicine evodia, were mainly responsible for the antianoxic action. 相似文献
66.
67.
Phenotyping of erythrocyte acid phosphatase (EAP) and esterase D (ESD) by cellulose acetate membrane isoelectric focusing (CAM-IEF) under a nonequilibrium condition is described. In an attempt to improve the method of CAM-IEF, we shortened the electrode distance to provide a higher field strength at a given (low) voltage. Various carrier ampholytes for EAP typing and various chemical separators for ESD typing were also tested. Good separations were obtained after 30 min IEF for EAP typing and 25 min for ESD typing. When applied to blood stains and stored for various periods at room temperature, the stains up to 8 months old could still be phenotyped for EAP and those up to 4 weeks old for ESD. CAM-IEF is suitable for routine forensic work of EAP and ESD phenotyping. 相似文献
68.
69.
Funyu S Isobe T Takagi S Tryk DA Inoue H 《Journal of the American Chemical Society》2003,125(19):5734-5740
Visible light irradiation of a reaction mixture of carbonyl-coordinated tetra(2,4,6-trimethyl)phenylporphyrinatoruthenium(II) (Ru(II)TMP(CO)) as a photosensitizer, hexachloroplatinate(IV) as an electron acceptor, and an alkene in alkaline aqueous acetonitrile induces selective epoxidation of the alkene with high quantum yield (Phi = 0.6, selectivity = 94.4% for cyclohexene and Phi = 0.4, selectivity = 99.7% for norbornene) under degassed conditions. The oxygen atom of the epoxide was confirmed to come from a water molecule by an experiment with H(2)(18)O. cis-Stilbene was converted into its epoxide, cis-stilbeneoxide, without forming trans-stilbeneoxide. trans-Stilbene, however, did not exhibit any reactivity. Under neutral conditions, an efficient buildup of the cation radical of Ru(II)TMP(CO) was observed at the early stage of the photoreaction, while an addition of hydroxide ion caused a rapid reaction with the cation radical to promote the reaction with reversion to the starting Ru(II)TMP(CO). A possible involvement of a higher oxidized state of Ru such as Ru(IV), Ru(V), Ru(VI) through a dismutation of the Ru(III) species was excluded by an experiment with Ru(VI)TMP(O)(2). Decarbonylation of the Ru complex was also proven to be invalid. A reaction mechanism involving an electron transfer from the excited triplet state of Ru(II)TMP(CO) to hexachloroplatinate(IV) and subsequent formation of OH(-)-coordinated Ru(III) species, leading to an oxo-ruthenium complex as the key intermediate of the photochemical epoxidation, was postulated. 相似文献
70.
Y. Yamada M. Itoh K. Egawa N. Kiriyama K. Komura K. Ueno 《Journal of Radioanalytical and Nuclear Chemistry》1992,164(1):47-57
Various f-elements are separated as anionic complexes from both acidic and alkaline solutions by precipitation with alkylpyridinium salts. The precipitates are also cationic surfactants where the simple counter-ion (e.g. nitrate or chloride) is replaced by the negatively charged complex anion of an actinide or lanthanide. The low solubility of these precipitates is explained by a strong affinity of divalent complex counter-ions of f-elements to the quaternary nitrogen. Precipitations in solutions of nitric acid allow to separate tetravalent f-elements from other metals, in alkaline carbonate solutions tetravalent and hexavalent actinides are precipitated simultaneously. The last procedure yields precipitates, which are very intimate mixtures of hexavalent and tetravalent actinides. This allows to prepare mixed oxides in a simple way. 相似文献