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triazole
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  三唑
     Crystal Structure of 1H 2,5 bi (2′ Bromopheny1) 1,3,4 triazole
     1H-2,5-双(2′-溴苯基)-1,3,4-三唑的晶体结构
短句来源
     2 Aryl 5 mercapto 1,3,4 triazole Derivatives
     2-芳基-5-巯基-1,3,4-三唑衍生物的合成
短句来源
     In the substitution of triazolenitride derivatives,1substitution of 1,2,3triazole and 2substitution of 1,2,3,4tetrazole are the best.
     同时Triazolenitride杂环的取代中1,2,3三唑1取代和1,2,3,4四唑2取代最好;
短句来源
     A Novel Magenta Coupler:Synthesis of 1 H-Pyrazolo[5,1-C][1,2,4] Triazole
     新型品成色剂1H-Die吡唑并[5,1-C][1,2,4]三唑的合成
短句来源
     Synthesis and Characterization of 4—Substitution Phenyl —3,5 —Bis(2—Picolinoyl) —1,2,4 —Triazole
     4—取代苯基—3,5—二(2—吡啶基)—1,2,4—三唑的合成及表征
短句来源
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  三唑类
     Syntheses and bioactivity of 3,5 disubstituted 4 amino 1,2,4 triazole derivatives
     3,5-二取代-4-氨基-1,2,4-三唑类衍生物的合成及生物活性研究
短句来源
     The biological activities of sixteen new triazole compounds as a formula (CH 3) 3C(X)CH(Tr)CH 2(Y)R,in which X means CO,CHOH;
     测定了16个通式为(CH3)3C(X)CH(Tr)CH2(Y)R的新三唑类化合物[式中,X=CO,CHOH;
短句来源
     Aim To improve the synthetic process of 4-[4-(5oxo-1,5-dihydro-triazoyl-4-yl)phenyl] piperazine-1-carboxylic t-butyl ester,which is used as the key intermediate of triazole antifungal agents.
     目的改进三唑类抗真菌药物关键中间体4-[4-(5-氧代-1,5-二氢-[1,2,4]三唑-4-基)苯基]哌嗪-1-羧酸叔丁酯的合成工艺。
短句来源
     Objective:[ST5”,6BZ]To study the antifungal activities of 23 1 [2 (N methyl N substituted benzyl) amino 2 (2,4 difluorophenyl)ethyl] 1 H 1,2,4 triazole compounds in vitro and to discuss their structure activity relationship.
     目的 :研究 2 3个 1- [2 - (N-甲基 - N-取代苄基 )氨基 - 2 - (2 ,4-二氟苯基 )乙基 ]- 1H - 1,2 ,4-三唑类化合物的体外抗真菌活性 ,并初步探讨其构效关系。
短句来源
     The results showed that they were relatively sensitive to the triazole fungicides which were hexaconazole,tebuconazole,myclobutanil,flusilazole and difenoconazole. Their EC50 values were less than 1μg/mL,and the EC90 values were less than 10μg/mL.
     结果表明:苹果斑点落叶病菌对三唑类杀菌剂己唑醇、戊唑醇、腈菌唑、氟硅唑和苯醚甲环唑的敏感性依次下降,EC50值均在1μg/mL以下,EC90值均低于10μg/mL;
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  “triazole”译为未确定词的双语例句
     Synthese and Crystal Structure of a Triazole Complex Cu_2(CH_3COO)_4(C_4H_8N_4)_2·2CH_3CN
     三氮唑配合物[Cu_2(CH_3COO)_4(C_4H_8N_4)_2]·2CH_3CN的合成及晶体结构(英文)
短句来源
     Single crystals of the new title compound [Cu2(CH3COO)4(C4H8N4)2]·2CH3CN are obtained from the reaction of Cu(CH3COO)2 and 4 amino 3,5 dimethyl 1,2,4 triazole.
     Cu(CH3COO)2 和4 氨基 3,5 二甲基 1,2,4 三氮唑反应制得标题化合物的单晶[Cu2(CH3COO)4(C4H8N4)2]·2CH3CN。
短句来源
     Synthesis of 7-phenylmethylamino-9, 10-dihydro [1,2,4] triazole[4,3-a]quinoline derivatives
     7-苄氨基-9,10-二氢-1,2,4-三氮唑并[4,3-a]喹啉衍生物的合成
短句来源
     Synthesis and cyclolization of 7-phenylmethylamino-9,10-dihydro[1,2,4] triazole[4,3-a]quinoline derivatives
     7-苄氨基-9,10-二氢-1,2,4-三氮唑并[4,3-a]喹啉衍生物的合成及环合反应的探讨
短句来源
     SYNTHESIS OF 1,2,4 TRIAZOLE 3 ONE DERIVATIVES
     1,2,4-三唑酮-3衍生物的制备
短句来源
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  triazole
The model with three common biophoric sites such as center of triazole ring for A, center of phenyl ring for B, and charge heteroatom for C.
      
Synthesis, structure and biological activity of 1-(1-methoxy-1-ferrocenyl-3-arylpropan-2-yl)-1H-1,2,4-triazole derivatives
      
A total of eleven new 1-(1-methoxy-1-ferrocenyl-3-arylpropan-2-yl)-1H-1,2,4-triazole derivatives have been synthesized from acetylferrocene.
      
1-(N-Silatranylmethyl)-1,2,4-Triazole: Synthesis and Molecular Structure
      
Determination of the Optical Purity of Fungicides of the Triazole Series
      
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The octadeoxynucleotide, d-GGAAACCA, which corresponds to the nucleotide sequence 10-17 in the 26-nucleotide-long lower chain of the gone for Lou-enkephalin, was synthesized by an improved phosphotriester mehod. The synthetic d-(DMT) ibGibGbzA, d-(DMT)bzAbzA and d-(DMT)anCanC were phosphorylated with p-chlorophenylphosphorodichloridate in the presence of triazole, producing d-(DMT) ibGibGbzAOH, d-(DMT) bzAbzAOH and d-(DMT) anCanCOH. Starting from d-bzAobz, by successive condensation with d-(DMT)anCanCOH,...

The octadeoxynucleotide, d-GGAAACCA, which corresponds to the nucleotide sequence 10-17 in the 26-nucleotide-long lower chain of the gone for Lou-enkephalin, was synthesized by an improved phosphotriester mehod. The synthetic d-(DMT) ibGibGbzA, d-(DMT)bzAbzA and d-(DMT)anCanC were phosphorylated with p-chlorophenylphosphorodichloridate in the presence of triazole, producing d-(DMT) ibGibGbzAOH, d-(DMT) bzAbzAOH and d-(DMT) anCanCOH. Starting from d-bzAobz, by successive condensation with d-(DMT)anCanCOH, d-(DMT)bzA bzAOH and d-(DMT) ibGibGbzAOH, d-(DMT) ibGibGbzAbzAbzAanCanC bzAobz was cbtained. Mositylenosulfonyl nitroimidazole (MSNI) was used as condensing reagent in all condensation reactions concerned. After removal of all protecting groups and purification by DEAE-Sephadex A-25 chromatography, d-GGAAAGGA was obtained and identified by sequence analysis.

本文报道了脑啡肽基因下链26核苷酸中八核苷酸片段d-GGAAACCA(10~17)的合成。合成系采用改良的三酯法,先合成和,再用对氯苯基磷酰二氯在1,2,4-三氮唑存在下磷酰化得到和,然后由bzAobz开始,依次同和缩合得到。在所有的缩合反应中,缩合剂均采用2,4,6-三甲基苯磺酰硝基咪唑。所得的全保护八核苷酸用浓氨水和80%醋酸脱去保护基后再经DEAE-葡聚糖凝胶A-25(7M尿素)柱层析分离纯化并去盐后,即得到d-GGAAACCA。产物经5'-~(32)P标记后,同系层析均一,蛇毒磷酸二酯酶部分酶解后的电泳-同系层析双向图谱能够得到预期的核苷酸排列顺序。

The octadeoxynucleotide, d-GGAAACCA, which corresponds to the nucleotidesequence 10-17 in the 26-nucleotide-long lower chain of the gene for Leu-enkephalin,was synthesized by an improved phosphotriester method. The synthetic d-(DMT)ibG*ibG*bzA, d-(DMT)bzA*bzA and d-(DMT)anC*anC were phosphorylated withp-chlorophenylphosphorodichloridate in the presence of triazole, producing d-(DMT)ibG*ibG*bzA*OH, d-(DMT)bzA*bzA*OH and d-(DMT)anC*anC*OH. Starting fromd-bzAobz, by successive condensation with d-(DMT)anC*anC*OH,...

The octadeoxynucleotide, d-GGAAACCA, which corresponds to the nucleotidesequence 10-17 in the 26-nucleotide-long lower chain of the gene for Leu-enkephalin,was synthesized by an improved phosphotriester method. The synthetic d-(DMT)ibG*ibG*bzA, d-(DMT)bzA*bzA and d-(DMT)anC*anC were phosphorylated withp-chlorophenylphosphorodichloridate in the presence of triazole, producing d-(DMT)ibG*ibG*bzA*OH, d-(DMT)bzA*bzA*OH and d-(DMT)anC*anC*OH. Starting fromd-bzAobz, by successive condensation with d-(DMT)anC*anC*OH, d-(DMT)bzA*bzA*OH and d-(DMT)ibG*ibG*bzA*OH, d-(DMT)ibG*ibG*bzA*bzA*bzA*anC*anC*bzAobz was obtained. Mesitylenesulfonyl nitroimidazole (MSNI) was used as condensingreagent in all condensation reactions concerned. After removal of all prefecting groupsand purification by DEAE-Sephadex A-25 chromatography, d-GGAAACCA wasobtained and identified by sequence analysis.

本文报道了脑啡肽基因下链26核苷酸中八核苷酸片段d-GGAAACCA(1~17)的合成。合成系采用改良的三酯法,先合成(DMT)ibG?ibG?bzA(DMT)bzA?bzA和(DMT)anC?anC(?2代表),再用对氯苯基磷酸二氯在1,2,4-三氮唑存在下磷酰化得到(DMT)ibG?ibG?bzA?OH、(DMT)bzA?bzA?OH和(DMT)anC?anC?OH,然后由bzAobz开始,依次同(DMT)anC?anC?OH、(DMT)bzA?bzA?OH和(DMT)ibG?ibG?bzA?OH缩合得到(DMT)ibG?ibG?bzA?bzA?bzA?anC?anC?bzAobz。在所有的缩合反应中,缩合剂均采用2,4,6-三甲基本磺酰硝基咪唑。所得的全保护八核苷酸用浓氨水和80%醋酸脱去保护基后再经DEAE-葡聚糖凝胶A-25(7M尿素)柱层析分离纯化并去盐后,即得到d-GGAAACCA。产物经5′-~(32)P标记后,同系层析均一,蛇毒磷酸二酯酶部分酶解后的电泳-同系层析双向图谱能够得到预期的核苷酸排列顺序。

Some derivatives of imidazole and 1, 2, 4-triazole have been introduced as very effective systemic fungicides. The synthesis of 10 species are described and the methods are improved to obtain higher yields.

本文介绍了1—(2—苯基—1,3—二氧戊环—2—甲基)—1,2,4—三唑类和1—(2—苯基—1,3—二氧戊环—2—甲基)—1,3—味唑类等十种内吸性杀菌剂的合成方法,着重报导了合成实验,测定了它们的物理常数,并做了某些化合物的红外光谱。

 
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