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1.
Qiu Hong WU He Xiang WANG Kun GAO State Key Laboratory of Applied Organic Chemistry College of Chemistry Chemical Engineering Lanzhou University Lanzhou 《中国化学快报》2006,17(2)
Many Ligularia species have long been used as traditional folk medicine for theirantibiotic, antiphlogistic and antitussive activities1, and were found to be an importantsource of eremophilane. In the course of our search for bioactive sesquiterpenoids, w… 相似文献
2.
Controlled growth of calcium carbonate by poly(ethylenimine) at the air/water interface 总被引:1,自引:0,他引:1
Two metastable calcium carbonate polymorphs, hemispherical vaterite and needle-like aragonite, are selectively formed at the air/water interface by the mediation of poly(ethyleneimine)(with molecular weights of 25000 and 2000, respectively) dissolved in supersaturated calcium bicarbonate solution. 相似文献
3.
表面涂覆CeO2对Co—40Cr合金氧化行为的影响 总被引:1,自引:0,他引:1
研究了表面涂覆CeO2对Co-40Cr合金在1000℃、空气中恒温氧化和循环氧化的影响。并用扫描电镜/能谱(SEM/EDXS)、电子探针(EPMA)、高分辩率显微镜(HREM)等测试手段对氧化膜的形貌和成分进行了观察了监测。结果表明,涂覆CeO2后极大地提高了合金的抗循环氧化性能。研究表明,涂覆的CeO2主要以细小颗粒 蒿度弥散存在于氧化膜的外表面,并且主要分布于氧化物晶界上,其中C 相似文献
4.
Qiang ZHAO Qian Kun ZHUANG 《中国化学快报》2005,16(9):1237-1240
With 1-Pymnebutyric acid (PBA) and multiwalled carbon nanotubes (MWNTs), glassy carbon electrode modified was successfully prepared. In phosphate buffer solution (pH 7,0), the direct electrochemistry of cytochrome C (Cyt C) was realized. In the cyclic voltammetry experiment two pairs of redox peaks ofCyt C were observed at 0.018 V and -0.314 V (vs. SCE), respectively. The redox reaction at 0.018 V was diffusion controlled, while the redox reaction at -0.314 V was adsorption controlled. 相似文献
5.
6.
Furostanol saponins with inhibitory action against COX-2 production from Tupistra chinensis rhizomes
Kun Zou Jun Zhi Wang Jun Wu Yuan Zhou Chuang Liu Fei Jun Dan Ya Xiong Zhang Jin Yang 《中国化学快报》2007,18(10):1239-1242
Two furostanol saponins were obtained from the n-butanol fraction of methanol extract from Tupistra chinensis rhizomes,a folk medicine of Shennongjia Forest District of Hubei Province.Their structures were determined as (25S)-26-O-(β-D-glucopyranosyl)- furost-1β,3β,22α,26-tetrol-3-O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→2)-β-D-glucopyranoside (1) and (25R)- 26-O-(β-D-glucopyranosyl)-furost-1β,3β22α,26-tetrol 3-O-β-D-glucopyranosyl-(1→4)-β-D-glucopyranosyl-(1→2)-β-D-glu- copyranoside (2),on basis of chemical and spectroscopic evidences.1 and 2 displayed marked inhibitory action towards COX-2 production in macrophages of the rat abdomen induced by LPS at 20μg/mL. 相似文献
7.
Kun Guo YANG Rui Mao HUA* Hai WANG Bo Qing XU* Department of Chemistry Tsinghua University Key Laboratory of Organic Optoelectronics & Molecular Engineering of Ministry of Education Beijing Department of Chemistry Chemical Engineering Guangxi Normal University Guilin 《中国化学快报》2005,16(4)
Diphenylmethane and substituted diphenylmethane are important compounds forsynthesis chemistry as well as industrial chemistry. These compounds are easilysynthesized by the benzylation of aromatic compounds with benzyl chloride or benzylalcohol catalyzed by homogeneous acid catalysts, such as AlCl3, FeCl3, H2SO4, HF andBF3. However, these catalytic systems are highly corrosive, and usually proceed withlow selectivity. In addition, they are less satisfactory from the environmen… 相似文献
8.
Li Jing FANG Jin Chun CHEN Guo Jun ZHENG Yu Kun GUAN Yu Lin LI* State Key Laboratory of Applied Organic Chemistry Institute of organic chemistry Lanzhou University Lanzhou 《中国化学快报》2004,(11)
The eudesmane derivative, (-)-10-epi-α-cyperone 1, is widely used as a chiral starting material for the synthesis of other fused-ring sesquiterpenes1. The first synthetic work was reported by Howe and co-workers via condensation of (+)-dihydrocarvone 2 with 1-diethylaminopentan-3-one methiodide in 32% yield2. Previously, our group reported the synthesis of compound 1 by treating ketone 2 with ethyl vinyl ketone (EVK) directly under different conditions1a, but the yields were not satisfacto… 相似文献
9.
In this paper a modified two-step procedure for synthesis of N-(1-naphthyl) suecinimide (NaS) was developed, and the molecular structure of NaS was properly characterized by XRD, FT-IR, 1H NMR, DSC, etc. The results show that the melting point of our product is 159 ℃-160.5 ℃, and the characteristic infrared absorption band of carbonyl group splits into two peaks (1705cm^-3/1779cm^-3), which are found to be quite different from the documented data (rap 147℃ -149℃; IR C=0-1700cm^-3). Besides, photophysical spectroscopy was found to be powerful to study the molecular structure and crystal morphology of NaS compound. 相似文献
10.