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Two calix[4]arene derivatives containing 1,2,3-triazole moiety were synthesized via K2CO3-catalyzed1,3-dipolar cycloaddition reaction between calix[4]arene-based azide and active methylene compounds in good yields.The structures of the two compounds synthesized herein were fully confirmed by 1HNMR,,(13)C NMR,and MS(ESI).The thermal analysis showed that the mass losses of the synthesized compounds 4 and 5 containing 1,2,3-triazole groups are similar to each other. 相似文献
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Zai-Gang Luo Yu Zhao Chao Ma Xue-Mei Xu Xiao-Mei Zhang Nian-Yu Huang Hong-Qiu He 《中国化学快报》2014,25(5):737-740
A series of novel calix[4]arene derivatives incorporating two triazolyl 1 3-diketo subunits in alternate positions at the lower rim were synthesized and screened for HⅣ integrase inhibition activity.The chemical structures of these compounds were confirmed by means of1H NMR 13C NMR,and ESI-MS.Preliminary bioassays indicated that calix[4]arene derivatives proved to be more active than p-tertbutylcalix[4]arene derivatives.In particular,compound 4g presented the most potent integrase strand transfer inhibitory activity with an IC50value of 6.1 mmol/L. 相似文献
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LUO Zai-Gang MA Chao WU Li-Mei YUAN Meng-Hong XU Chuan-Hao HU Jing-Song XU Xue-Mei 《结构化学》2014,33(6):865-870
The title complex(C66H76O8·CH3CN) was synthesized and structurally determined by single-crystal X-ray diffraction method. It crystallizes in monoclinic, space group P21/c with a = 22.384(13), b = 13.413(7), c = 21.867(12), β = 112.257(7)°, C68H78NO8, Mr = 1037.31, Dc = 1.133 g/cm3, V = 6076(6) 3, Z = 4, F(000) = 2224, μ(MoKa) = 0.073 mm-1, T = 296(2) K, 10276 independent reflections with 5469 observed ones(I 2σ(I)), R = 0.0797 and wR = 0.2316 with GOF = 1.027(R = 0.1442 and wR = 0.2689 for all data). The calixarene moiety maintains the symmetric cone conformation through intramolecular O–H···O hydrogen bonds. The inhibition of the strand transfer process of HIV-1 integrase of the title compound was also evaluated. Preliminary bioassays indicated that it has a low inhibition ratio(24.85%) at the concentration of 50 μM. 相似文献
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The title compound(C50H44O10) was synthesized and structurally determined by single-crystal X-ray diffraction method. It crystallizes in monoclinic, space group P21/c with a = 16.713(4), b = 13.189(3), c = 19.434(5) , β = 104.411(4)°, Mr = 804.85, Dc = 1.288 g/cm3, V = 4149.2(17) 3, Z = 4, F(000) = 1696, μ(MoKa) = 0.089 mm-1, T = 296(2) K, 7279 independent reflections with 3172 observed ones(I 2σ(I)), R = 0.0520 and wR = 0.1203 with GOF = 0.928(R = 0.1464 and wR = 0.1657 for all data). The calixarene moiety maintains the symmetric cone conformation through intramolecular O–H···O hydrogen bonds. Preliminary bioassays indicated that the title compound has a potent inhibitory activity against the strand transfer process of HIV-1 integrase. 相似文献
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Li Zheng-Fa Zhu Ling-Yun Chen Shi-Qian Chen Zai-Gang Gou Xiang-Feng 《Nonlinear dynamics》2022,109(3):1297-1324
Nonlinear Dynamics - Multi-state meshing characteristics induced by backlash and contact ratio in the gear pair are an unsolved puzzle about its relationship to safety characteristics of the gear... 相似文献
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Cs2CO3-mediated decomposition of N-tosylhydrazones for the synthesis of azines under mild conditions
Luo Zai-Gang Liu Peng Fang Yu-Yu Xu Xue-Mei Feng Cheng-Tao Li Zhong Zhang Xiao-Mei He Jie 《Research on Chemical Intermediates》2017,43(2):1139-1148
Research on Chemical Intermediates - A facile, environmentally and efficient Cs2CO3-mediated decomposition of N-tosylhydrazones reaction has been developed for the synthesis of functionalized... 相似文献
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