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湖北省自然科学基金(2012FFB01103)

作品数:6 被引量:4H指数:1
相关作者:冯驸杨坤渹胡颖郭瑾匡仁云更多>>
相关机构:湖北民族大学华中师范大学井冈山大学更多>>
发文基金:湖北省自然科学基金国家自然科学基金更多>>
相关领域:理学医药卫生更多>>

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微波辐射硝基芴与丙烯酸酯Michael加成产物的合成与结构
2013年
以硝基芴和丙烯酸脂为原料,在碱性条件下,微波辐射(500 W)反应4~5 min,非常方便地合成了系列未见文献报道的Michael加成产物,该方法操作简单、产率较高(79%~87%)。其结构经IR、1H NMR、MS和元素分析进行表征,并利用X射线单晶衍射分析法测定了化合物3b的单晶结构。
胡卫兵黄猛冯驸崔治财刘信平
关键词:MICHAEL加成微波合成
新型N-芳基(芳基偶氮-1,3,4-噻二唑)磺酰胺类化合物的合成及抗癌活性被引量:3
2013年
目的研究N-芳基(芳基偶氮-1,3,4-噻二唑)磺酰胺类化合物的合成方法及抗癌活性。方法 以芳胺、水杨醛、氨基硫脲和苯磺酰氯为原料合成相应的目标化合物,采用MTT法研究了目标化合物体外抑制L1210和B16癌细胞的活性。结果合成了一系列新型的N-芳基(芳基偶氮-1,3,4-噻二唑)磺酰胺类化合物,其结构经元素分析、IR、MS及1H-NMR确证。化合物5a,5g表现出明显的体外抗癌活性。结论 N-芳基(芳基偶氮-1,3,4-噻二唑)磺酰胺类化合物有可能成为新型结构的抗癌药物。
胡颖杨坤渹冯驸
关键词:1,3,4-噻二唑抗癌活性
Synthesis and Crystal Structure of 1,2-Dis(1,3-diphenylpropan-2-yl)disulfane
2013年
A novel compound of 1,2-dis(1,3-diphenylpropan-2-yl)disulfane(C30H30S2,Mr=454.27)was synthesized in ethanol with 1,3-diphenyl-2-propanone as raw materials,giving high yield of product(90%).Its structure was determined by IR,1H NMR,MS,elemental analysis and X-ray diffraction.The crystal belongs to monoclinic,space group C2 with a=18.727(3),b=6.5179(9),c=13.7576(18),β=131.0610(10)o,V=1266.2(3)3,Z=2,Dc=2.136 g/cm3,μ=1.078 mm-1,F(000)=843,R=0.0490 and wR=0.1247 for 3211 observed reflections with I2(I).X-ray analysis reveals that the molecule is not symmetrical.There exist no classical hydrogen bonds andπ-πstacking interactions.Moreover,the thermal stability of compound 3 was investigated.
冯附黄猛王乾有段正超涂海洋张爱东胡卫兵
Synthesis of 3,3,5,5-tetrabenzyl-1,2,4-trithiol and 1,2-dis(1,3-arylpropan-2-yl)disulfane
2013年
Novel sulfur-containing compounds (3a-3c, 4a-4c) were obtained in ethanol with 1,3-diphenyl-2- propanone as the starting material. The advantages of this procedure were mild reaction conditions, simple protocol, and high yields. The structures of the products were characterized by IR, 1H NMR, MS and elementary analysis. The crystal of the new compound 4a belongs to monoclinic, space group C2 with a=18.727(3), b=6.5179(9), c=13.7576(18) A, fl=131.0610(10)°, V=I266.2(3)A3, Z=2, Dc=2.136g/cm3, μ=1.078mm 1, F(000)=843, R=0.0490 and wR=0.1247 for 3211 observed reflection with I 〉 2σ(I). X-ray analysis reveals that the molecule is not symmetrical, the molecular structure is stabilized by weak π-π stacking interactions, and no classical hydrogen bonds can be observed.
Fu FengMeng HuangZheng-Chao DuanWei-Bing Hu
3-羟基-苯并异噻唑-3(2氢)-酮-1,1-二氧化物的合成被引量:1
2013年
3-氯-2-甲基苯胺和盐酸以及亚硝酸钠反应生成重氮盐,重氮盐在催化剂存在下与二氧化硫进行反应,再和氨水反应,然后通过氧化、关环缩合反应,最后铜催化芳基卤的羟基化反应得到标题化合物。
匡仁云郭瑾罗秋燕
关键词:重氮化反应关环反应
Synthesis and Crystal Structure of a New Complex [Cu(C_(14)H_9O_3)_2(C_5H_5N)_2(C_2H_5OH)_2]
2014年
The title compound of Cu(C14H9O3)2(C5H5N)2(C2H5OH)2(1) was synthesized via the hy- drothermal reaction of CuCl2·2H2O and 9-hydroxy-fluorene-9-carboxylic acid(HHF) with pyridine, and characterized by elemental analysis and infrared spectra. The crystal belongs to triclinic, space group P1 with a = 8.8302(12), b = 10.1625(14), c = 12.2708(17), α = 86.207(2), β = 69.562(2), γ = 64.932(2)o, V = 930.3(2) 3, Z = 1, Mr = 764.30, Dc = 1.364 g/cm3, F(000) = 399, S = 1.059 and μ(MoKα) = 0.644 mm-1. The final R = 0.0459 and wR = 0.1274 for 3414 observed reflections with I 〉 2σ(I). The copper atom is six-coordinated by two oxygen atoms from two different 9-hydroxy-fluorene-9-carboxylate ligands, two pyridine nitrogen atoms and two ethanol oxygen atoms, forming a distorted octahedral coordination geometry. The extensive O–H···O hydrogen bonding connects the molecules to form a one-dimensional chain structure. Between adjacent one-dimensional chains, a two-dimensional layered structure was formed by fluorene ring π-π packing interaction. Between the layers, a three-dimensional structure was formed through the π-π packing interaction of the pyridine ring. Moreover, the thermal stability and photoluminescent property of the complex has been investigated.
胡卫兵宋楠楠黄猛冯驸田大听周红艳宋新建
关键词:SYNTHESIS
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