期刊文献+

含二茂铁基的取代缩氨基脲、取代缩氨基硫脲的合成和性质 被引量:2

The Syntheses and Properties of Substituted Semicarbazones and Thiosemicarbazones Containing Ferrocenyl Group
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摘要 缩氨基脲、缩氨基硫脲既是很好的金属离子配体,又有很好的生物活性,如抗细菌、病毒、抗结核、抗麻疯病、抗风湿、抗嗜眠等,文献曾有一些报道。其中有些在结构上调整,引入二茂铁基,显示了一些特殊性质。本文在此基础上进一步合成了12个新型结构的含二茂铁基的缩氨基脲(或硫脲),对它们的性质作了初步研究。 This paper reports twelve new substituted semicavbazones and thiosemicarbazones which contain ferrocenyl group. All of these compounds are characterized on the basis of elemental analysis, IR and 1H NMR. A number of transition element (Cu, Co, Ni, Zn) complexes with thiosemicar-bazone prepared from formylferrcene and thiocarbohydrazide have been prepared and characterized. Using some of these compounds and Cu(Ⅱ) complexes, we have observed the bacteriostatic activity of them. It is shown that those compounds have significant bacteriostasis on Staphylococcus autreus, Bacillus Subtilis and Escherichia Coli
机构地区 兰州大学化学系
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 1990年第3期307-309,共3页 Chemical Journal of Chinese Universities
关键词 二茂铁 羰基化合物 缩氨基脲 合成 Ferrocene, Ferrocenyl carbonyl compound, Ferrocenyl semicarbazone, Transition metal complex
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参考文献1

  • 1Wei H H,J Chin Chem Soc(Taipei),1976年,25卷,17页

同被引文献12

  • 1张有明,任海仙,魏太保.间苯二甲醛缩双芳氨基硫脲的合成及阴离子识别研究[J].高等学校化学学报,2006,27(11):2079-2083. 被引量:22
  • 2HAIFENG DU,BAOGUO ZHAO,YIAN SHI,et al.Pd (0)-catalyzed diamination of trans-1-phenyl-1,3-butadiene with ditert-butyldiaziridinone as nitrogen source[J].Org.Synth,2009,86:315-324.
  • 3MAJER P,RANDAD RS.A safe and efficient method for preparation of N,N'-unsymmetrically disubstituted ureas utilizing triphosgene[J].J.Org.Chem,1994,59:1937-1938.
  • 4MATSUMURA,Y,SATOH Y,ONOMURA O,et aLA new method for synthesis of unsymmetrical ureas using electrochemistry prepared trifluoroethyl carbmates[J] J.OrgChem,2000,65:1549-1551.
  • 5KITTERINGHAM J,SHIPTON MR,VOYLE M.A simple method for the synthesis of unsymmetrical ureas[J].Synth.Commun,2000,30:1937-1943.
  • 6SHI M,SHEN YM.Transition-metal-catalyzed reactions of propa rgylamine with carbon dioxide and carbon disulfide[J] J.Org.Chem.,2002:67,16.
  • 7ISABELLE GALLOU,MAGNUS ERIKSSON,XINGZHONG ZENG,et al.Practical synthesis of unsymmetrical ureas from isopropenyl carbamates[J].J.Org.Chem.,2005,70:6960-6963.
  • 8SANG HYUEP LEE,HANA MATSUSHITA,BRUCE CLAPHA-M,et al.The direct conversion of carbamates to ureas using aluminum amides[J].Tetrahedron,2004,60:3439-3443.
  • 9DEVIN M,SWANSON,ADRIENNE E,et al.Identification and biological evaluation of 4-(3-trifluoromethylpyridin-2-yl)piperazine-1-carboxylic acid (5-trifluromethylpyridin-2-yl)amide,a high affinity TRPV1 (VR1) vanilloid receptor antagonist[J].J.Med.Chem.,2005,48:1857-1872.
  • 10JOHN AW,KRUIJTZER,DIRK J,LEFEBER,ROB M J LISKAMP.Approaches to the synthesis of ureapeptoid peptidomimetics[J].Tetrahedron Letters,2005,38:5335-5338.

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