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Crystal Structure and Biological Activities of (R)-N′-[2-(4-Methoxy-6-chloro)-pyrimidinyl]-N-[3-methyl-2-(4-chlorophenyl)butyryl]-urea
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作者 LI Jing-Zhi XUE Si-Jia LIU Guo-Hua 《Chinese Journal of Structural Chemistry》 SCIE CAS CSCD 北大核心 2006年第8期903-908,共6页
The title compound (R)-N′-[2-(4-methoxy-6-chloro)-pyrimidyl]-N-[3-methyl-2-(4- chlorophenyl)butyryl]-urea has been synthesized, and its crystal structure and biological behaviors were studied. Crystallographic ... The title compound (R)-N′-[2-(4-methoxy-6-chloro)-pyrimidyl]-N-[3-methyl-2-(4- chlorophenyl)butyryl]-urea has been synthesized, and its crystal structure and biological behaviors were studied. Crystallographic data: C17H18C12N4O3, Mr = 397.25, monoclinic, space group P21/c, a = 12.331(2), b = 14.025(3), c = 23.085(5) A, β = 99.607(4)°, Z = 8, V = 3936.2(13) A3, Dc = 1.341 g/cm^3, F(000) = 1648, R = 0.0718, wR = 0.1585 and/t(MoKα) = 0.353 mm^-1. The preliminary biological tests showed that the title compound has definite insecticidal and fungicidal activities. 展开更多
关键词 crystal structure biological activity (R)-3-methyl-2-(4-chlorophenyl)butyric acid 2-amino-6-chloro-4-methoxy-pyrimidine
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一种新型环己烯羧酸的合成及其对萤石的浮选性能 被引量:8
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作者 许海峰 钟宏 +2 位作者 王帅 黄志强 赵刚 《中国有色金属学报》 EI CAS CSCD 北大核心 2014年第11期2935-2942,共8页
在氢氧化钠和相转移催化剂四丁基氯化铵的催化下,正丁醛缩合生成1,3,5-三乙基-6-正丙基-2-羟基-3-环己烯甲醛中间体;该中间体经亚氯酸钠氧化生成1,3,5-三乙基-6-正丙基-2-羟基-3-环己烯甲酸(HPTECHFA)。用HPTECHFA浮选萤石纯矿物,在矿... 在氢氧化钠和相转移催化剂四丁基氯化铵的催化下,正丁醛缩合生成1,3,5-三乙基-6-正丙基-2-羟基-3-环己烯甲醛中间体;该中间体经亚氯酸钠氧化生成1,3,5-三乙基-6-正丙基-2-羟基-3-环己烯甲酸(HPTECHFA)。用HPTECHFA浮选萤石纯矿物,在矿浆pH为10、HPTECHFA用量为100 mg/L的条件下,萤石的回收率达90.60%。用HPTECHFA对坑口萤石实际矿石进行一次粗选浮选实验。结果表明:在30℃时,萤石粗精矿的品位和回收率分别达到82.71%和97.98%,与使用捕收剂油酸相比,CaF2的品位提高2.23%,回收率提高1.86%;在10℃时,萤石粗精矿回收率达到89.88%,与使用捕收剂油酸相比,CaF2的回收率提高16.09%。实际矿物浮选实验结果表明,HPTECHFA特别适合低温下萤石矿的浮选。红外光谱和Zeta电位测试表明,HPTECHCA能以化学作用方式吸附在萤石表面上。 展开更多
关键词 捕收剂 1 3 5-三乙基-6-正丙基-2-羟基-3-环己烯甲酸 羧酸 萤石 浮选
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7-羟甲基咪唑并[1,2-a]吡啶的合成 被引量:1
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作者 刘娥 《化学与生物工程》 CAS 2013年第12期43-44,共2页
以6-氨基-3-吡啶甲酸为起始原料,经过酯化反应、环合反应、还原反应得到7-羟甲基咪唑并[1,2-a]吡啶,总收率为42%。
关键词 7-羟甲基味唑并[1 2-a]吡啶 6-氨基-3-吡啶甲酸 合成
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N'-{1-[(6-氯吡啶-3-基)甲基]-5-甲基-1H-1,2,3-三唑-4-甲酰基}-N'-叔丁基-N-取代苯甲酰肼的合成与杀虫活性 被引量:2
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作者 Khalema Thandiwe D.L. 石德清 《有机化学》 SCIE CAS CSCD 北大核心 2010年第12期1925-1930,共6页
双酰肼化合物作为一类重要的昆虫生长调节剂,已广泛应用于农作物的保护中.为了发现新颖结构的高效、低毒双酰肼杀虫剂先导化合物,采用点击化学常用的1,2,3-三唑杂环将新烟碱杀虫剂的药效团2-氯-5-(氯甲基)吡啶引入到双酰肼分子骨架中,... 双酰肼化合物作为一类重要的昆虫生长调节剂,已广泛应用于农作物的保护中.为了发现新颖结构的高效、低毒双酰肼杀虫剂先导化合物,采用点击化学常用的1,2,3-三唑杂环将新烟碱杀虫剂的药效团2-氯-5-(氯甲基)吡啶引入到双酰肼分子骨架中,设计并合成了9种未见文献报道的含双杂环结构的双酰肼目标化合物,其结构经IR,1HNMR,ESI-MS和元素分析测试技术确证.初步的生物活性测定结果表明,部分目标化合物在200mg/L质量浓度下对小菜蛾(Spodoptera exigua)和甜菜夜蛾(Plutella xylostella)表现出中等程度的杀虫活性;但所有目标化合物在200mg/L浓度下对蚕豆蚜虫(Aphis fabae)的杀虫活性均较弱.. 展开更多
关键词 1-[(6-氯吡啶-3-基)甲基]-5-甲基-1H-1 2 3-三唑-4-甲酸 双酰肼化合物 杀虫活性
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An efficient regioselective sonochemical synthesis of novel 4-aryl-3-methyl-4,5-dihydro-1H-pyrazolo[3,4-b]pyridin-6(7H)-ones 被引量:1
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作者 Abbas Azimi Roshan Manouchehr Mamaghani +1 位作者 Nosrat Ollah Mahmoodi Farhad Shirini 《Chinese Chemical Letters》 SCIE CAS CSCD 2012年第4期399-402,共4页
An efficient ultrasound-assisted preparation of a series of novel 4-aryl-3-methyl-4,5-dihydro-l//-pyrazolo[34-b]pyridin-6(7H)ones via the reaction of 5-amino-3-methyl-1H-pyrazole,Meldrum's acid and various arylalde... An efficient ultrasound-assisted preparation of a series of novel 4-aryl-3-methyl-4,5-dihydro-l//-pyrazolo[34-b]pyridin-6(7H)ones via the reaction of 5-amino-3-methyl-1H-pyrazole,Meldrum's acid and various arylaldehydes using one-pot three-component approach is described.This rapid method produced the products in short reaction times(3-4 min) and excellent yields(87-95%). 展开更多
关键词 Pyrazolo[3 4-b]pyridin-6(7H)-one Meldrum's acid 5-amino-3-methylpyrazole One-pot Ultrasonic irradiation Three-component REGIOSELECTIVE
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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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Improved microwave-assisted catalyst-free synthesis of9-aryl-5,9-dihydropyrimido[4,5-d][1,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-dione derivatives
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作者 Mahnaz Farahi Bahador Karami Zohreh Banaki 《Chinese Chemical Letters》 SCIE CAS CSCD 2015年第9期1065-1067,共3页
Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-... Agreen regioselective synthesis of some new and known 9-aryl-5,9-dihydropyrimido[4,5-d][l,2,4]triazolo[1,5-a]pyrimidine-6,8(4H,7H)-diones has been described via the microwave-assisted one-pot reaction of 3-amino-1H-1,2,4-triazoles,aromatic aldehydes and barbituric acids under solvent- and catalyst-free conditions.This operationally simple procedure is less laborious and provides a better scope than previously reported procedures. 展开更多
关键词 9-Aryl-5 9-dihydropyrimido[4 5-d] [ 1 2 4]triazolo[1 5-a]pyrimidine- 6 8(4H 7H)-diones Barbituric acids 3-amino- 1 H- 1 2 4-triazoles Aryl aldehydes Microwave-assisted synthesis
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