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41.
Three divalent transiton‐metal complexes of 2,3‐pyridinedicarboxylate (2,3‐pda2), [Mn(2,3‐pda)‐(H2O)3]∞ ( 7 ), [Ni(2,3‐pda)(H2O)3]∞ ( 8 ), and [Cd2(2,3‐pda)2(H2O)]∞ ( 9 ) have been hydrothermally synthesized and structurally characterized. X‐ray diffraction analyses reveal that compounds 7 and 8 are zigzag‐ and linear‐type one‐dimension (1D) coordination polymers, respectively, whereas compound 9 is a three‐dimension (3D) coordination polymer. A simple comparison of the coordination geometries with the available neutral analogues {Mx(2,3‐pda)x(H2O)y}∞ containing one or two divalent transition‐metal atoms and equal ligands in the presence or absence of coordinated water molecules is also presented. 相似文献
42.
Lee JC Chang SW Liao CC Chi FC Chen CS Wen YS Wang CC Kulkarni SS Puranik R Liu YH Hung SC 《Chemistry (Weinheim an der Bergstrasse, Germany)》2004,10(2):399-415
A novel and convenient route for the synthesis of biologically potent and rare L-hexose derivatives from D-glucose is described. Conversion of diacetone-alpha-D-glucose (14) into 1,2:3,5-di-O-isopropylidene-beta-L-idofuranose (19) was efficiently carried out in two steps. Orthogonal isopropylidene rearrangement of compound 19 led to 1,2:5,6-di-O-isopropylidene-beta-L-idofuranose (27), which underwent regioselective epimerization at the C3 position to give the L-talo- and 3-functionalized L-idofuranosyl derivatives. Hydrolysis of compound 19 under acidic conditions furnished 1,6-anhydro-beta-L-idopyranose (35) in excellent yield, which was successfully transformed into the corresponding L-allo, L-altro, L-gulo, and L-ido derivatives via regioselective benzylation, benzoylation, triflation and nucleophilic substitution as the key steps. Applications of these 1,6-anhydro-beta-L-hexopyranoses as valuable building blocks to the syntheses of 4-methylcoumarin-7-yl-alpha-L-iduronic acid and the disaccharide moieties of bleomycin A(2) as well as heparan sulfate are highlighted. 相似文献
43.
A new chiral aminophosphine ligand 6,6′-dimethoxy-2,2′-bis(diphenylphosphinoamino)biphenyl(DMBDPPABP) was prepared and its rhodium complex was found to be an effective catalyst for the asymmetric hydrogenation of amidoacrylic acid and its dervatives.The effects of solvent and reaction temperature on enantioselectivity were also studied. 相似文献
44.
Synthesis of camphor derived chiral allenes and their hydroboration-oxidation reactions are described. Reaction of (1R)-(+)-camphor with alkynyllithium followed by the reduction of the resulted propargyl alcohol derivatives using AlH3 furnished chiral allenes 2a-g in excellent yields with high diastereoselectivity. Reduction of the propargyl alcohols with aluminum hydride proceeded through selective intermolecular anti-addition of hydride ion. The stereochemistry of the chiral allenes 2 was assigned based on lanthanide shift studies and chemical correlations. Diastereoselectivity was observed in the hydroboration-oxidation of 2 which produced a mixture of (E,R) and (E,S) stereoisomers in a ratio of 6:1 to 18:1. 相似文献
45.
Fluorescence lifetimes of vibrational levels of the first electronically excited state (ā 2 A′) of HSO, determined by the technique of discharge flow and laser-induced fluorescence, are 81 ± 10, 74 ± 8, and 76 ± 14 μs for υ3′ = 0, 1 and 2, respectively. The rate coefficients of quenching of each level by He, N2, O2 and O3 were measured; the coefficients for HSO (ā, υ3′ = 0 – 2) quenched by O3 arc 35–50 times as great as those of HSO by He. 相似文献
46.
Two new esters, methyl 4‐(prenyloxy)dihydrocinnamate and methyl 4‐(geranyloxy)dihydrocinnamate, together with fourteen known compounds have been isolated from the stem bark of Zanthoxylum pistaciiflorum. The structures of two new compounds were determined through spectral analyses. Among the isolates, four compounds exhibited effective cytotoxicities against P‐388 and HT‐29 cell lines in vitro. 相似文献
47.
The self association of cumyl hydroperoxide and its complexing with polar monomers have been studied by proton magnetic resonance. These complexations are exothermic and strongly temperature dependent. It has been suggested that the complexation of cumyl hydroperoxide by polar monomers could be one of the causes of its efficiency in initiating the radical polymerization of vinyl monomers on an ethyl-zinc terminated polyethylene chain to form radical block copolymers. However, if this phenomenon has an effect on the initiation, it should not affect the propagation mechanisms, because the hydroperoxide is destroyed by ZnEt2 during initiation. Moreover, the tacticity of radical polymethylmethacrylate, obtained at 60° with (ZnEt2—cumyl hydroperoxide) in heptane does not differ from the conventional radical polymer. 相似文献
48.
血清必需元素测定中样品预处理方法的探讨 总被引:2,自引:0,他引:2
对血清必需元素测定的样品预处理方法进行了研究,用火焰原子吸收法测定了经不同处理的血清样品中的锌,铜,铁,钙,镁含量,结果显示,预处理方法不同,其测定结果有较大差异,变异系数,镁为7.94%,锌,铜,铁,钙在15.19%~53.53%之间,并对各样品作了精密度和准确度实验。 相似文献
49.
Under various basic solutions and reaction durations, 3-substituted 4-formyIsydnones and nitroalkanes containing α-active hydrogen (e.g. nitromethane and nitroethane) are converted to β-nitroalcohols, nitroalkenes and dinitroalkanes. β-Nitroalcohols are obtained only by electrochemical reaction on an electrogenerated base (EGB). The mechanism of overall reaction steps in particular is discussed. 相似文献
50.
The pigments Luteoskyrin (Ls) and Rugulosin (Rg) might adopt a priori two extreme conformations, a planar and an angular one. To determine the predominant conformation in solution, the nature of the lowest energy transition of the chromophores and the presence of intramolecular H-bonding have been investigated. The solvent effects on electronic absorption and CD spectra indicated the π-π* nature of the lowest energy transition. Treatments of the electronic absorption results according to McRae and Kosower relations, IR absorption and PMR spectra suggested the presence of strong intra-molecular H-bonds. From these results it was concluded that Ls and Rg adopted in a variety of solvents the most planar conformation. 相似文献