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131.
[reaction: see text] A series of chiral pyrrolidinylmethanol-based dendritic ligands were synthesized for application in enantioselective aryl transfer reactions to aldehydes with the (ArBO)3/ZnEt2 system in up to 98% ee. 相似文献
132.
Chun Hua Ge Xiang Dong Zhang Yong Chao Ma Lei Guan Chun Yue Shi Xiao Yan Zhang Ya Nan Guo Qi Tao Liu College of Chemistry Liaoning University Shenyang China 《中国化学快报》2007,(11)
The preparation and crystal structure of complex Co(Hsae)_2·2H_2O (1,H_2sae=N-salicylidene-2-iminoethanol) are reported.X- ray analysis revealed that every six Co(Hsae)_2 forms a cyclic chip and every 12 water forms a novel gear-like cluster.Acting as building blocks,the gear-like water cluster and complex chip are connected in A-B fashion and extend into one-dimensional supramolecular chain.Hydrogen bond is the primary bridging force in the formation of supramolecular framework. 相似文献
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136.
铟锡氧化物纳米网的微波法制备及其光催化特性研究 总被引:2,自引:0,他引:2
By using ultrasonic and chemical liquid coprecipitation, the precursor was prepared with high purity In, SnCl4·5H2O and urea. The In2O3·SnO2 nanonets were obtained from precursor by heating in microwave oven. The powders were characterized by XRD, TEM. The analyzed results show the sample is In2O3·SnO2, and In2O3is rhombohedral system while SnO2 is tetragonal system. The sample is in spherical grain shape, with average granularity of 35 nm, and the mesh diameter of 10~80 nm. The sample was with fluorescence and good photocatalytic performance for degradation of organic dyestuff. 相似文献
137.
研究了一系列二芳甲酰甲烷化合物在不同溶剂中的分子内氢键及酮-烯醇互变异构平衡。δ_(OH)和lgK与取代基常数(σ)之间均有良好的线性关系存在。+I和+R取代基使分子内氢键增强,而使烯醇式含量降低。 相似文献
138.
Densities have been measured for the electrolyte (NaCl, NaBr and NaI)‐monosaccharide (D ‐mannose and D‐ribose)‐water solutions at 298.15 K. These data have been used to calculate the apparent molar volumes of the saccharides (VΦ,S) and electrolytes (VΦ,E) in the studied solutions. Infinite dilution apparent molar volumes, VΦ,S0 and VΦ,E0, have been evaluated, together with the standard transfer volumes of the saccharides (ΔtVS0) from water to aqueous electrolyte solutions and those of the electrolytes (ΔtVE0) from water to aqueous saccharide solutions. It was shown that both the ΔtVS0 and ΔtVE0 values are positive and increase with increasing molalities of sodium halides and saccharides, respectively. Overall, the ΔtVS0 and ΔtVE0 values have the order of NaCl > NaBr > NaI except for NaI‐ribose and NaI‐ribose. Volumetric interaction parameters for the electrolyte‐monosaccharide pairs in water were obtained and interpreted by the stereochemistry of the monosaccharide molecules and the structural interaction model. 相似文献
139.
Huan Yang QI Chao Feng ZHANG Mian ZHANG Jian Qun LIU Zheng Tao WANG 《中国化学快报》2005,16(8):1050-1052
Three new anthraquinones, emodin-8-β-D-(2"-O-coumarate)glucoside 1, emodin-8-β-D-(6'-O-acetyl)glucoside 2 and physicon-8-β-D-(6'-O-acetyl)glucoside 3, were isolated from the roots of Polygonum cillinerve and their structures were established by spectroscopic methods. The biological activity indicated that compound 1 had the scavenging activity on 1,1-diphenyl-2-picrylhydrazyl (DPPH) radicals (the IC50 = 8.5 μmol/L), and compound 1-3 showed no activities against HL-60 and BCJC-823 cells by MTT method in vitro. 相似文献
140.
Chao Zhang 《Tetrahedron》2007,63(26):5832-5838
The ability to inhibit any protein kinase of interest with a small molecule is enabled by a combination of genetics and chemistry. Genetics is used to modify the active site of a single kinase to render it distinct from all naturally occurring kinases. Next, organic synthesis is used to develop a small molecule, which does not bind to wild-type kinases but is a potent inhibitor of the engineered kinase. This approach, termed chemical genetics, has been used to generate highly potent mutant kinase-specific inhibitors based on a pyrazolopyrimidine scaffold. Here, we asked if the selectivity of the resulting pyrazolopyrimidines could be improved, as they inhibit several wild-type kinases with low-micromolar IC50 values. Our approach to improve the selectivity of allele-specific inhibitors was to explore a second kinase inhibitor scaffold. A series of 6,9-disubstituted purines was designed, synthesized, and evaluated for inhibitory activity against several kinases in vitro and in vivo. Several purines proved to be potent inhibitors against the analog-sensitive kinases and exhibited greater selectivity than the existing pyrazolopyrimidines. 相似文献