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961.
Zhi-Kun Rao Jing Long Cong Li Sui-Shuan Zhang Mei He Ling-Cheng Ou Yong-Tang Zheng Yan-Ping He 《Monatshefte für Chemie / Chemical Monthly》2008,139(8):967-974
Several 2-heteroaryl-, 2-heteroarylcarbonylmethyl-, 2-arylcarbonylmethyl, and 2-arylethyl derivatives of S-dihydro(alkyloxy)benzyloxypyrimidines have been synthesized and the anti-HIV activities of these compounds were tested in
C8166 cell and against RT enzyme. It was found that some of these compounds showed good activity against HIV-1 (EC
50 = 0.014–0.8 μM) with low toxicity (CC
50 value of 222–564 μM) and high selectivity (SI value of 278–37743). The structure-activity relationships (SAR) of these compounds have also been discussed.
First two authors contributed equally to this work
Correspondence: Yan-Ping He, Key Laboratory of Medicinal Chemistry for Natural Resource Ministry of Education, School of Chemical
Science and Technology, Yunnan University, Kunming 650091, People’s Republic of China; Yong-Tang Zheng, Laboratory of Molecular
Immunopharmacology, Key Laboratory of Animal Models and Human Disease Mechanisms, Chinese Academy of Sciences, Kunming Institute
of Zoology, Kunming, Yunnan 650223, People’s Republic of China. 相似文献
962.
苯酚在Ti/PbO2电极上的电氧化反应 总被引:1,自引:0,他引:1
利用线性伏安法和恒电流电解法研究了苯酚在Ti/PbO2电极上的电催化氧化反应,通过电氧化过程中反应物和中间物的高效液相色谱测定,研究了苯酚在Ti/PbO2电极上电催化氧化的反应机理.实验发现,Ti/PbO2电极对水溶液中苯酚的电氧化具有显著的催化作用,25℃时,对初始浓度为2mmol/L的苯酚水溶液,恒定电流密度为50mA/cm2,电解3h,苯酚转化率为98.02%,有机碳去除率为54.36%.苯酚在Ti/PbO2电极上电催化氧化要经过对苯二酚或邻苯二酚、对苯醌、反丁烯二酸和草酸,最终变成二氧化碳和水的历程.第一步反应苯酚转化的主产物是对苯二酚.对苯二酚转化为苯醌和苯醌转化为反丁烯二酸的反应为慢反应,反丁烯二酸转化为草酸的反应为快反应. 相似文献
963.
环境中铬形态分析研究进展 总被引:4,自引:0,他引:4
对近10年来国内外在环境中铬形态方面的分析研究进展作了综述,内容包括样品预处理、分离富集方法和样品检测方法(引述文献61篇). 相似文献
964.
利用高效液相色谱法测定了苹果、山楂等制品中的展青霉素.样品经乙酸乙酯提取、碳酸钠净化后进行检测,通过对流动相、检测波长等试验条件的优化,消除了5-羟甲基糠醛对展青霉素测定的干扰,方法的回收率为95.2%~107.1%;检出限(3S/N)为0.04 mg·L-1,线性范围在0.14~2.8 mg·L-1. 相似文献
965.
Dr. Yanbo Mei Prof. Dr. Xiaodan Chen Dr. Rui Wei Dr. Xiao-Yong Chang Prof. Dr. Lizhi Tao Prof. Dr. Liu Leo Liu 《Angewandte Chemie (International ed. in English)》2023,62(52):e202315555
Featuring an extra electron in the π* antibonding orbital, species with a 2-center-3-electron (2c3e) π bond without an underlying σ bond are scarcely known. Herein, we report the synthesis, isolation and characterization of a radical anion salt [K(18-C-6)]+{[(HCNDipp)2Si]2P2}⋅− (i.e. [K(18-C-6)]+ 3 ⋅−) (18-C-6=18-crown-6, Dipp=2,6-diisopropylphenyl), in which 3 ⋅− features a perfectly planar Si2P2 four-membered ring. This species represents the first example of a Si- and P-containing analog of a bicyclo[1.1.0]butane radical anion. The unusual bonding motif of 3 ⋅− was thoroughly investigated via X-ray diffraction crystallography, electron paramagnetic resonance spectroscopy (EPR), and calculations by density functional theory (DFT), which collectively unveiled the existence of a 2c3e π bond between the bridgehead P atoms and no clearly defined supporting P−P σ bond. 相似文献
966.
Qin Wang Yong Jiang Nina Wei Jindong Li Mei Zhang Linwei Chen 《Journal of separation science》2023,46(24):2300518
967.
Shanshan Sun Litao Wang Jiasheng Wang Wenjing Lv Qinghua Yu Dong Pei Siqi Han Xingyu Li Miao Wang Sheng Liu Xiangao Quan Mei Lv 《Journal of separation science》2023,46(16):2200935
In this work, homochiral reduced imine cage was covalently bonded to the surface of the silica to prepare a novel high-performance liquid chromatography stationary phase, which was applied for the multiple separation modes such as normal phase, reversed-phase, ion exchange, and hydrophilic interaction chromatography. The successful preparation of the homochiral reduced imine cage bonded silica stationary phase was confirmed by performing a series of methods including X-ray photoelectron spectroscopy, thermogravimetric analysis, and infrared spectroscopy. From the extracted results of the chiral resolution in normal phase and reversed-phase modes, it was demonstrated that seven chiral compounds were successfully separated, among which the resolution of 1-phenylethanol reached the value of 3.97. Moreover, the multifunctional chromatographic performance of the new molecular cage stationary phase was systematically investigated in the modes of reversed-phase, ion exchange, and hydrophilic interaction chromatography for the separation and analysis of a total of 59 compounds in eight classes. This work demonstrated that the homochiral reduced imine cage not only achieved multiseparation modes and multiseparation functions performance with high stability, but also expanded the application of the organic molecular cage in the field of liquid chromatography. 相似文献
968.
Four symmetric and non-symmetric chiral liquid crystal dimers containing trifluoromethyl groups, termed as TFBA-PD-TFBA, UEBBA-PD-TFBA, UEBA-PD-TFBA and UEA-PD-TFBA, respectively, have been synthesised and characterised. UEA-PD-TFBA exhibited chiral nematic phase, whereas the other three dimers displayed chiral smectic A phase. X-ray diffraction (XRD) has revealed the structure of the smectic A phase for TFBA-PD-TFBA to be intercalated, whereas that for UEBBA-PD-TFBA and UEBA-PD-TFBA to be monolayer and interdigitated, respectively. In addition, the weaker peak corresponding to a shorter layer spacing was observed for UEBBA-PD-TFBA and UEBA-PD-TFBA. Considering the results of XRD measurements and computer simulations, the structural model corresponding to the shorter layer spacing is assigned as horseshoe-like shape. The absence of smectic behaviour for UEA-PD-TFBA reveals that the weaker aromatic–aromatic interactions cannot stabilise the smectic A phase. 相似文献
969.
Chiral Phosphoric Acid Catalyzed Asymmetric Ugi Reaction by Dynamic Kinetic Resolution of the Primary Multicomponent Adduct
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Yun Zhang Dr. Yu‐Fei Ao Prof. Dr. Zhi‐Tang Huang Prof. Dr. De‐Xian Wang Prof. Dr. Mei‐Xiang Wang Prof. Dr. Jieping Zhu 《Angewandte Chemie (International ed. in English)》2016,55(17):5282-5285
Reaction of isonitriles with 3‐(arylamino)isobenzofuran‐1(3H)‐ones in the presence of a catalytic amount of an octahydro (R)‐binol‐derived chiral phosphoric acid afforded 3‐oxo‐2‐arylisoindoline‐1‐carboxamides in high yields with good to high enantioselectivities. An enantioselective Ugi four‐center three‐component reaction of 2‐formylbenzoic acids, anilines, and isonitriles was subsequently developed for the synthesis of the same heterocycle. Mechanistic studies indicate that the enantioselectivity results from the dynamic kinetic resolution of the primary Ugi adduct, rather than from the C?C bond‐forming process. The resulting heterocycle products are of significant medicinal importance. 相似文献
970.