1)pyrrolo[2,1-b]thiazole吡咯[2,1-b]噻唑
2)imidazo [2,1-b] thiazole咪唑[2,1-b]噻唑
英文短句/例句
1.Synthesis and Characterization of Imidazo [2,1-b] thiazoles Polyamine Conjugates咪唑[2,1-b]噻唑多胺缀合物的合成与表征
2.One-Pot Synthesis of Thiazolo[3,2-b](1,2,4)-triazoles一步法合成噻唑并[3,2-b](1,2,4)-三唑类衍生物的研究
3.Synthesis of 6-Chloroimidazo[1,2-b] pyridazine6-氯咪唑并[1,2-b]哒嗪的合成
4.Therefore, it can be concluded that both imidazole ring and thiazole ring have bioactivity.因而我们可以确信咪唑环和噻唑环是具有生物活性的。
5.The Synthesis and Molecular Structure Characterization of the Derivatives of Imidazole or Thiazole Possessing Potential Bioactivity;具有潜在生物活性的咪唑或噻唑类衍生物的合成与结构表征
6.Study on Syntheses, Characterizations and Properties of 2, 5-Thiophenediacylhydrazones and 4, 5-imidazolediacylhydrazones;2,5-噻吩、4,5-咪唑双酰腙的合成、表征及性能研究
7.Synthesis of Thiadiazine、Thiosemicarbazide、Thiadiazole Derivatives Containing Benzimidazole under Microwave Irradiation;微波辐射下含取代苯并咪唑基噻二嗪、酰氨基硫脲、噻二唑衍生物的合成
8.Studies on the Syntheses of Imidazo[1,2-b] Pyridazine and Derivatives;咪唑并[1,2-b]哒嗪及其衍生物的合成研究
9.Study on the Spectral Character and Analysis of Thiabendazole, Ortho-phenylphenol, and Biphenyl Residues in Fruits and Vegetables;果蔬保鲜剂噻苯咪唑、邻苯基苯酚、联苯的光谱特性及残留分析研究
10.Objective To optimize the reaction condition of2- mercaptobenzothiaozole ramification.目的:探索出在咪唑啉酮2号位引入2-巯基苯骈噻唑的适宜反应条件。
11.Study the Ramifications of Thiadiazole and Schiff-Base Imidaozline Corrosion Inhibition for Steel in 1MHCl Medium and for Copper in NaHCO_3 Medium;席夫碱基咪唑啉和噻二唑衍生物对钢在盐酸介质中和铜在碳酸氢钠介质中缓蚀性能的研究
12.Synthesis of 2-Bromo-1,3,4-Thiadiazole2-溴-1,3,4-噻二唑的合成
13.Synthesis of Spiro-Heterocycle Compounds of Oxazole, Thiazole and Quinoline Derivatives;含噁唑、噻唑基螺杂环化合物的合成
14.Studies on the Synthesis of Thia/Oxadiazole and Triazole Compounds噻(噁)二唑及三唑类化合物的合成研究
15.Synthesis of Aminothiazole and Thiazolidinone Derivatives in Ionic Liquid;在离子液中合成氨基噻唑、噻唑琳酮类化合物
16.polybenzimidazoleamide fibre聚苯并咪唑酰胺纤维
17.lysidine tartrate酒石酸甲基二氢咪唑
18.Study Insectifuge of Mebendazole and Albendazole by Thermal Analysis;驱虫药甲苯咪唑、丙硫咪唑的热分析研究
相关短句/例句
imidazo [2,1-b] thiazole咪唑[2,1-b]噻唑
3)imidazolo[2,1-b]-1,3,4-thiadiazole咪唑[2,1-b]-1,3,4-噻二唑
1.Synthesis and Biological Activities of Imidazolo[2,1-b]-1,3,4-thiadiazole,S-Triazole[3,4-b]-1,3,4-thiadiazole Derivatives Bearing 1H-1,2,4-triazole;含有1H-1,2,4-三唑咪唑[2,1-b]-1,3,4-噻二唑、S-三唑[3,4-b]-1,3,4-噻二唑衍生物的合成及生物活性
2.A series of imidazolo[2,1-b]-1,3,4-thiadiazoles were synthesized by the reaction of 2-(2-phenyl- 1,2,3-triazol-4-yl)-5-amino-1,3,4-thiadiazole with ω-bromoacetophenones or ω-bromo-ω-(1H-1,2,4-triazol- 1-yl)acetophenones in reflux EtOH.以2-(2-苯基-1,2,3-三唑-4-基)-5-氨基-1,3,4-噻二唑(1)为原料分别与ω-溴代芳基乙酮、ω-溴代-ω-(1H-1,2,4-三唑-1-基)芳基乙酮反应,合成了一系列新型咪唑[2,1-b]-1,3,4-噻二唑类化合物2a~2e和3a~3e。
4)spiro[imidazo〔2,1-b〕benzo〔d〕thiazole螺咪唑并〔2,1-b〕苯并噻唑
5)s-triazolo[2,1-b]-1,3,4-thiadiazole均三唑并[2,1-b]-1,3,4-噻二唑
6)imidazolothiadiazole咪唑并[2,1-b][1,3,4]噻二唑
延伸阅读
唑唑oxazole含有一个氧和一个氮杂原子的五元杂环化合物。分子式C3H3NO。环中的氧和氮原子分别占1,3两位,又称氮代呋喃。若氧和氮原子分别占1,2位,则称为异唑。唑和异唑在自然界都不存在。为具有吡啶气味的液体。沸点69~70℃。碱性很弱,盐类不稳定,但可与氯化汞形成络合物。唑对氢化非常稳定,氧化则可将环破裂,环的稳定性与环上取代基的性质有关。唑的芳香性很弱。唑可由4-唑羧酸失羧而制得。4-(3-苯基-5-甲基)异唑羧酸是苯唑青霉素的侧链部分,具有某些杀菌能力。异唑氮-氧之间的键在一定条件下易断裂,利用这一性质,可在有些有机合成中用作试剂。有些磺胺制剂是异唑的衍生物。