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THE SYNTHESES OF 1,1,1-TRIFLUORO-2-SUBSTITUTED-PHENYL-2-PROPYL-3-^(14)C P- TOLUENESULFONATES
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作者 郭子丽 Arthur Fry 《Nuclear Science and Techniques》 SCIE CAS CSCD 1990年第4期239-242,共4页
1,1,1,-Trifluoro-2- substituted- phenyl- 2- propanols- 3- 14C were prepared from addition of methyl- 14C magnesium iodide to appropriate trifluoroacetophenone. These alcohols were converted into tosylatcs by reaction ... 1,1,1,-Trifluoro-2- substituted- phenyl- 2- propanols- 3- 14C were prepared from addition of methyl- 14C magnesium iodide to appropriate trifluoroacetophenone. These alcohols were converted into tosylatcs by reaction with n-butyllithium and then with p-toluenesulfonyl chloride. The yield, boiling point or melting point and pertinent spectral data of these compounds are reported. 展开更多
关键词 1 1- Trifluoro- 2- substituted- phenyl- 2- propanols- 3- 14C 1 1- Trifluoro- 2- substituted- phenyl- 2- propyl - 3- 14C P- toluenesulfonates Trifluoroacetophenones C- LABELLED compound
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Synthesis and Antibacterial Activities of 1,4-Disubstituted Phenyl-5-(halo-2-hydroxyphenyl)imino-1,2,3-triazole
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作者 ZHAO Xu LU Jun-rui +6 位作者 XIN Chun-wei LU Bo-wei BAO Xiu-rong LI Jian-fa LIU Ya YANG Xu-yun YUAN Yi 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第3期424-429,共6页
According to the superposition principle of reinforcement of biological activities, 24 novel 1,4- disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l,2,3-triazoles was synthesized and characterized by 1H NMR, ^13C ... According to the superposition principle of reinforcement of biological activities, 24 novel 1,4- disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l,2,3-triazoles was synthesized and characterized by 1H NMR, ^13C NMR, elemental analysis and IR. All the target compounds were screened for their antibacterial potential in vitro against Monilia albican, Escherichia coli and Staphylococcus aureus. It was shown that all the compounds possessed efficient antibacterial activities at a concentration of 0.1 mg/mL, even at a concentration of 0.01 mg/mL, some of the compounds still exhibited antibacterial activities against Escherichia coli and Monilia albican. At last, the struc- ture-activity relationship was discussed based on the antibacterial results. 展开更多
关键词 1 4-Disubstituted phenyl-5-(halo-2-hydroxyphenyl)imino-l 2 3-triazole Antibacterial activity Structure-activity relationship
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2-(2,4-二氟苯基)-5-烷氧甲基吡啶的合成 被引量:1
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作者 朱卫国 朱克明 +4 位作者 梁爱辉 罗剑 刘煜 马小云 朱美香 《湘潭大学自然科学学报》 CAS CSCD 北大核心 2009年第1期53-58,共6页
以2,5-二溴吡啶和溴代烷为原料,通过甲酰化、还原、成醚和Suzuki-Miyaura交叉偶联等反应,合成得到了2-(2,4-二氟苯基)-5-烷氧甲基吡啶衍生物,探讨了分子结构对成醚和Suzuki-Miyaura交叉偶联反应的影响,甲酰化、还原、成醚和Suzuki-Miya... 以2,5-二溴吡啶和溴代烷为原料,通过甲酰化、还原、成醚和Suzuki-Miyaura交叉偶联等反应,合成得到了2-(2,4-二氟苯基)-5-烷氧甲基吡啶衍生物,探讨了分子结构对成醚和Suzuki-Miyaura交叉偶联反应的影响,甲酰化、还原、成醚和Suzuki-Miyaura交叉偶联等反应的产率分别达到了49.8%、96.0%、90.3%和96.9%. 展开更多
关键词 2-(2 4-二氟苯基)-5-烷氧甲基吡啶 6-溴-3-吡啶甲醇 合成
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“一锅三步法”合成苯基-2-吡啶基甲醇 被引量:3
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作者 荆华青 李红亮 《精细化工》 EI CAS CSCD 北大核心 2020年第10期2150-2153,共4页
以2-苄基吡啶氮氧化物和三氟乙酸酐为原料,通过"一锅三步法"(串联"酰化、[3,3]σ重排和水解"反应)合成了关键药理活性中间体苯基-2-吡啶基甲醇,并对反应条件进行了优化。结果表明,当n(2-苄基吡啶氮氧化物)∶n(三氟... 以2-苄基吡啶氮氧化物和三氟乙酸酐为原料,通过"一锅三步法"(串联"酰化、[3,3]σ重排和水解"反应)合成了关键药理活性中间体苯基-2-吡啶基甲醇,并对反应条件进行了优化。结果表明,当n(2-苄基吡啶氮氧化物)∶n(三氟乙酸酐)=1.0∶1.2、N,N-二异丙基乙胺(DIPEA)为碱、甲苯为溶剂,室温反应6 h,经硅胶柱层析分离即可得到苯基-2-吡啶基甲醇,收率为81.0%。产物经1HNMR、13CNMR和HRMS进行结构确证。该反应以原子经济学的理念实现了由2-苄基吡啶氮氧化物到苯基-2-吡啶基甲醇的高效直接转化。 展开更多
关键词 酰化 [3 3]σ重排 水解 2-苄基吡啶氮氧化物 苯基-2-吡啶基甲醇 精细化工中间体
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Synthesis, Crystal Structure and Anti-parasitic Activity of 2-(2-Methoxy-4-nitrophenylcarbamoyl)phenyl 4-Fluorobenzoate
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作者 段李平 吴宁波 +3 位作者 刘丛珊 陶奕 张雪强 张浩冰 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 2013年第6期847-852,共6页
The title compound 2-(2-methoxy-4-nitrophenylcarbamoyl)phenyl-4'-fluorobenzoate (C21H15FN206, Mr = 410.35), a fluorine-containing derivative of salicylamide, was conve- niently synthesized through two steps and c... The title compound 2-(2-methoxy-4-nitrophenylcarbamoyl)phenyl-4'-fluorobenzoate (C21H15FN206, Mr = 410.35), a fluorine-containing derivative of salicylamide, was conve- niently synthesized through two steps and crystallized in the orthorhombic space group P21/c with a = 7.6453(15), b = 14.323(3), c = 17.035(3) A, V= 1865.4(6) A3, Z = 4, Dc = 1.461 Mg/m^3, 2 = 0.71073 A, μ(MoKa) = 0.115 mm-1, F(000) = 848, R = 0.0705 and wR = 0.1834 for 3267 independent refections with 1 〉 2σ(I). X-ray analysis reveals that the dihedral angles formed between the 2-methoxy-4-nitrobenzene and benzene ring, the benzene and 4-fluorobenzene, and the 2-methoxy-4-nitrobenzene and 4-fluorobenzene ring are 3.2(4), 69.8(3) and 72.9(2)~, respectively. Bioassay shows that the title compound has anti-parasitic activity against hydatid protoscoleces. 展开更多
关键词 2-(2-methoxy-4-nitrophenyicarbamoyl)phenyl-4'-fluorobenzoate synthesis ANTI-PARASITIC crystal structure
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Synthesis and Nonlinear Optical Properties of New Quadrupolar Chromophores 被引量:1
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作者 XiaoZhiGUO XiaoMeiWANG +4 位作者 YuKouDU NanPingHUA MingSHEN WanLiJIANG PingYANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第5期597-600,共4页
Two new symmetric chromophores: 2, 8-bis-[(2-4′-ethoxy phenyl-5-4′-styryl)-1, 3, 4- oxadiazole] didibenzothiophene (abbreviated as SO-G1) and 2, 8-bis-[(2-4′-ethoxy phenyl-5-4′- styryl)-1, 3, 4-oxadiazole]-N-ethyl... Two new symmetric chromophores: 2, 8-bis-[(2-4′-ethoxy phenyl-5-4′-styryl)-1, 3, 4- oxadiazole] didibenzothiophene (abbreviated as SO-G1) and 2, 8-bis-[(2-4′-ethoxy phenyl-5-4′- styryl)-1, 3, 4-oxadiazole]-N-ethyl carbazole (abbreviated as NO-G1) have been synthesized and characterized. Both chromophores exhibit strong two-photon absorption (TPA) with the cross-sections of 2.99×10-48 and 3.48×10-48 cm4?s?photon-1 in THF and large up-conversion emission, when pumped by Ti:sapphire femto-second laser at 720 nm. 展开更多
关键词 2 8-Bis-[(2-4′-ethoxy phenyl-5-4′-styryl)-1 3 4-oxadiazole] didibenzothiophene 2 8-Bis-[(2-4′-ethoxy phenyl-5-4′-styryl)-1 3 4-oxadiazole]-N-ethyl carbazole two-photon excited f luorescence two-photon absorption .
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A new phenolic compound from Crinum asiaticum L.
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作者 Qian Sun Wei Dong Zhang +2 位作者 Yun Heng Shen Chuan Zhang Hui Liang Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2008年第4期447-449,共3页
A new phenolic compound was isolated from the ethanol extract of the bulbs of Crinum asiaticum L.var.sinicum Baker.Its structure was defined as 1-(2-hydroxy-4-hydroxymethyl)phenyl-6-O-caffeoyl-β-D-gluco-pyranoside ... A new phenolic compound was isolated from the ethanol extract of the bulbs of Crinum asiaticum L.var.sinicum Baker.Its structure was defined as 1-(2-hydroxy-4-hydroxymethyl)phenyl-6-O-caffeoyl-β-D-gluco-pyranoside on the basis of spectroscopic evidences. 展开更多
关键词 Crinum asiaticum L.var.sinicum baker Amaryllideae Phenolic compound 1-(2-Hydroxy-4-hydroxymethyl)phenyl-6-O-caffeoyl-β-D-glucopyranoside
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An environmentally friendly synthesis of 1,4-dihydropyrano[2,3-c]pyrazole derivatives catalyzed by tungstate sulfuric acid 被引量:2
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作者 Mahnaz Farahi Bahador Karami +1 位作者 Iman Sedighimehr Hamideh Mohamadi Tanuraghaj 《Chinese Chemical Letters》 SCIE CAS CSCD 2014年第12期1580-1582,共3页
An efficient three-component synthesis of 6-amino-4-aryl-5-cyano-3-metriyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles via a reaction between 3-methyl-1-phenyl-2-pyrazolin-5-one,aromatic aldehydes and malononitrile usi... An efficient three-component synthesis of 6-amino-4-aryl-5-cyano-3-metriyl-1-phenyl-1,4-dihydropyrano[2,3-c]pyrazoles via a reaction between 3-methyl-1-phenyl-2-pyrazolin-5-one,aromatic aldehydes and malononitrile using tungstate sulfuric acid as a catalyst was described.Mild conditions,good to excellent yields,easily available catalyst and easy work-up are the key features of this method. 展开更多
关键词 6-Amino-4-aryl-5-cyano-3-methyl-1phenyl-1 4-dihydropyrano[2.3-c]pyrazoles 3-Methyl-1-phenyl-2-pyrazolin-5-one Aromatic aldehyde Malononitrile Tungstate sulfuric acid
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