磺酰基
- 名sulfonyl;suIfonyl
-
聚苯乙烯负载磺酰基化合物的制备及其在固相有机合成中的应用
Preparation of Polystyrene-Supported Sulfonyl Compounds and Their Applications in Solid-Phase Organic Synthesis
-
疟疾防治药物的研究&Ⅵ.2,4-二氨基-6-取代氨基-磺酰基喹唑啉衍生物的合成及其抗疟作用
Studies on antimalarials ⅵ . synthesis and antimalarial activities of some 2,4-di amino - 6-substituted amino sulfonyl quinazoline derivatives
-
N-苯磺酰基甲基苯胺与芳醛的缩合反应
Condensation of N - [ ( Phenylsulfonyl ) methyl ] - aniline with Aromatic Aldehydes
-
从反应混合物中分离得副产物N,O-二(对甲苯磺酰基)双(2-羟乙基)胺。
An intermediate , N , O-di ( p-toluenesulfonyl ) his ( 2-hydroxyethyl ) amine , was isolated from tEe reaction mixture .
-
抗坏血酸(维生素C)作为众所周知的天然抗氧化剂,在光诱导电子转移反应中被成功地运用到α-苯磺酰基苯乙酮衍生物磺酰基基团的移除反应中。
Ascorbic acid ( vitamin C ), a well-known natural antioxidant , was successfully used to remove the sulfonyl group of α - phenylsulfonyl acetophenone derivatives by photochemical method .
-
氟苯尼考-β-环糊精包合物的研制Gabriel法合成2-(4-氟苯磺酰基)-乙胺
Preparation of Inclusion Complex of Florfenicol - β - Cyclodextrin Gabriel-wise synthesis of 2 - ( 4-fluorophenylsulfony ) ethylamine
-
目的设计合成2-(E)-(4-甲磺酰基)亚苄基环戊酮Mannich碱类化合物,并对其抗炎活性进行初步评价。
Aim The Mannich bases of 2 - ( E ) - ( 4-methanesulfonyl ) benzylidene cyclopentanone were designed and synthesized for studying their anti-inflammatory activities .
-
结论对甲磺酰基苯乙烯环酬类衍生物的抗炎作用较强,GI不良反应小,值得进一步研究。
Conclusion p - ( Methanesulfonyl ) styrene-linked cyclic ketone derivatives showed strong anti-inflammatory activity but few GI side effects and deserve to be further investigated .
-
由N-苯磺酰基甲基苯胺与芳醛反应得到了7种缩合产物,其结构经元素分析、1HMR、MS和IR所确证。
N - [ ( Phenylsulfonyl ) methyl ] - aniline was treated with aromatic aldehydes in the presence of sodium ethoxide and the structure of the seven condensation products was confirmed by elemental analyses , IR , 1H NMR and MS spectra .
-
苯磺酰基取代的α,β-不饱和酮的合成及其在不对称催化Diels-Alder反应中的研究
The Research about the Synthesis of Phenylsulfonyl α, β - unsaturated Ketones and Their Applications in Asymmetric Diels-Alder Reaction Catalyzed by Lewis Acid and Chiral Titanium Reagents . The Mechanism Was Approached
-
本文提出一类含有羧甲磺酰基(&SO2CH2COOH)的新的水溶性分散染料。
This paper studies water soluble disperse dyes containing carboxy-methyl-sulfonyl group ( - SO2CH2COOH ) .
-
其中在最后两步脱砜(脱苯磺酰基)脱苄基反应和氧化后所生成的几何异构体比例方面我们作了大量的研究和分析工作,对辅酶Q10的合成具有一定的参考价值。
During the course , we did a lot of work in two aspects : how to remove benzenesulfonyl and benzyl groups , then analyzed the ratio of geometrical isomers after oxidation . It has great consult value on synthesis of Coenzyme Q10 .
-
对甲苯磺酰基酰胺和2-苯基-N,N'-二甲基苯并咪唑啉(PDMBI)之间的光诱导电子转移反应,为酰胺的保护基&对甲苯磺酰基的脱除反应,提供了一条有效途径。
The photoinduced electron transfer reaction between N-tosyl amides and2-phenyl-N , N ' - dimethyl benzimidazoline ( PDMBI ) provides an efficient approach for the deprotection of N-tosyl amides .
-
N-(6-羟基-2,3,5-三氯苯磺酰基)对氯苯胺的结构与活性
Structure and activity of n - ( 6-hydroxy-2,3,5-trichloro-benzenesulfonyl ) - 4-chloroaniline
-
溴化氢的冰乙酸溶液脱除苯磺酰基的研究
Investigation of Cleavage of Benzenesulfonyl by Hydrogen Bromide in Acetic Acid
-
α-亚磺酰基-N,N-二取代酰胺的简便合成
A Convenient Synthesis of α - Sulfinyl-N , N-disubstituted Amides
-
N-2-(1-羟基-对甲磺酰基苯乙基)-1,2,3,4-四氢异喹啉类化合物的合成及Ⅲ类抗心律失常活性
Synthesis and antiarrhythmic activity of N-2-hydroxyl-2 - ( 4-methansulfonamidophenyl ) - ethyl-1,2,3,4-tetrahydroisoquinolines derivatives
-
苯磺酰基α,β&不饱和酮的合成
The Synthesis of Phenylsulfonyl α,β - Unsaturated Kelones
-
方法以对甲磺酰基苯乙酮为原料,经溴代、缩合和环合三步反应合成了产物。
METHOD The title compound was synthesized from p-methylsulfonyl-acetophenone via bromination , condensation and cyclization .
-
测定了一批具有大小不同碳环的苯磺酰基环烷烃甲酸酯对发光菌的毒性数据。
Batch data for the toxicity of phenylsulfonyl-cycloalkane carboxylates containing different sizes of carboatomic rings to photoluminescence bacteria have been measured .
-
从邻甲基苯甲酸合成间甲酚的动力学模型泰必利中间体-2-甲氧基-5-甲磺酰基苯甲酸的新合成法
A Kinetic Model of the Synthesis of m-cresol from o-toluic Acid A novel synthesis of 2-methoxy-5-methylsulfonyl benzoic acid & An intermediate for Tiapride
-
替硝唑是甲硝唑的乙磺酰基衍生物,属于新一代硝基咪唑类药物,具有良好的抗厌氧菌和抗原虫活性。
Tinidazole is a new drug of nitromidazole . It is a derivative of metronidazole , with better activity of ani-anaerobic bacteria and anti-protozoan .
-
2-(4-氟苯磺酰基)-乙胺及烟酸衍生物的合成研究黄原酸乙酰苯胺衍生物的合成及其摩擦学性能
Study on the Synthesis of 2 - ( 4-fluorophenylsulfonyl ) - ethylamine and Nicotinic Acid Derivatives SYNTHESIS AND TRIBOLOGICAL PROPERTIES OF XANTHOGENATE ACETANILIDE DERIVATIVES
-
目的研究对甲磺酰基苯丙烯酸的异羟肟酸和酰脲衍生物的合成及其抗炎活性。
Aim To study on synthesis and anti-inflammatory activity of hydroxamic acid and acyl urea derivatives ofp - ( me thanesulfonyl ) phenylpropenoic acids .
-
下沿含苯磺酰基杯芳烃衍生物与Eu~(3+)配合物的光谱性质研究带有核苷酸识别基团的杯芳烃衍生物对核苷酸的分子识别作用初探
Spectroscopic Properties of Calixarene Derivative with Eu ~ ( 3 + ) Complex Primary Study on the Molecular Recognition of Uracil-containing Calixarene Derivative to Nucleotide
-
四氢叶酸模型化合物碘化1,2二甲基3对甲氧苯磺酰基咪唑啉的还原及产物结构分析
The Tetrahydrofolate Model Compounds The Reduction and The Structures Analysis on the Reaction Product of 1,2 - dimethyl - 3 - ( P-Methoxybenzenesulfonyl ) imidazolinium iodide
-
本文研究了四氢叶酸模型化合物碘化1,2二甲基3对甲氧苯磺酰基咪唑啉的还原反应,生成了一种新化合物;
This paper has Studied the reduction of 1 , 2 - dimethyl - 3 - ( p - methoxy-benzenesulfony ) imidazolinium iodide , as tetrahydrofolate model compounds .
-
本文以季铵碱树脂作为聚合物固载的相转移催化剂,在50%氢氧化钠水溶液中催化α-苯磺酰基苯乙酮(1)的α-亚甲基的烷基化反应。
The alkylation of α - methylene of β - phenylsulfonyl acetophenone ( 1 ) with alkyl halides catalyzed by quaternary ammonium base resin in 50 % aqueous sodium hydroxide solution was investigated .
-
报道了甲酸氧化态四氢叶酸辅酶模型&碘化-2,3-二甲基-1-对氯苯磺酰基咪唑啉的合成以及该模型化合物与双中心亲核试剂(乙二胺、邻苯二胺、邻氨基苯酚)的反应。
The synthesis of a tetrahydrofolate coenzyme model & 1 p chlorobenzene sulfonyl 2,3 dimethyl imidazolinium iodide , and the reactions of the model compound with some bifunctional nucleophiles ( ethylenediamine , 1,2 diaminobenzene , 2 aminophenol ) are reported .
-
用热塑性聚(氧-1,4-亚苯基磺酰基-1,4-亚苯基)(聚醚砜)树脂作粘接剂,制备耐高温摩阻材料,探索了材料的压制工艺。
Employing thermoplastic poly ( oxy - 1 , 4-phenylene sulfonyl - 1 , 4-phenylene )( polyethersulfone or PES in brief ) resin as binder , friction materials for high temperature services were fabricated . The technology of compression moulding was explored .