国家自然科学基金(20172039)

作品数:16被引量:30H指数:3
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相关作者:纪顺俊顾大公李建国崔洪华史丽颖更多>>
相关机构:苏州大学更多>>
相关期刊:《分析化学》《有机化学》《Chinese Journal of Structural Chemistry》《合成化学》更多>>
相关主题:FACILEACETYLFERROCENESOLVENTCRYSTAL_STRUCTURESYNTHESES更多>>
相关领域:理学化学工程更多>>
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酸性离子液体催化合成1,5-苯并二氮衍生物被引量:2
《合成化学》2005年第5期496-497,共2页徐秋艳 纪顺俊 顾大公 
国家自然科学基金资助项目(20172039);江苏省精细石油化工重点实验室开放基金赞助项目(KF0402)
以邻苯二胺和酮为原料,酸性离子液体[hm im]HSO4和乙醇为催化体系,合成了一系列1,5-苯并二氮衍生物,其结构经1HNMR,IR和元素分析表征。催化体系可循环使用3次。
关键词:苯并二氮衍生物 酸性离子液体 催化 合成 
Syntheses and Crystal Structures of Pyrazoline Derivants被引量:1
《Chinese Journal of Structural Chemistry》2005年第5期586-590,493,共6页史海斌 纪顺俊 张勇 
The project was supported by the National Natural Science Foundation of China (20172039, 20472062) and Natural Science Foundation of Jiangsu Province (No. BK2004038)
Two pyrazoline derivants 1-(2-benzothiazole)-3-phenyl-5-(3-thiophene)-2- pyrazoline (BPTP) and 1-(2-benzothiazole)-3-(2-thiophene)-5-phenyl-2-pyrazoline (BTPP) have been synthe- sized and their crystal structures were...
关键词:PYRAZOLINE 2-hydrazinobenzothiazole crystal structure 
微波辐射下1-氨基烷基膦酸酯的一锅合成被引量:4
《合成化学》2005年第2期185-186,195,共3页顾大公 纪顺俊 史海斌 周民锋 
国家自然科学基金资助项目(20172039); ;江苏省精细石油化工重点实验室开放基金资助项目(KF0402)
以醛、胺及膦酸二乙酯为原料,微波辐射3min^5min,高产率地一锅合成了一系列的1-氨基烷基膦酸酯。其结构经1HNMR,IR和元素分析表征。
关键词:氨基烷基膦酸酯 微波辐射 合成 
水相中6-甲基-6-苯基-7-烯-1,5-辛二醇的合成被引量:3
《苏州大学学报(自然科学版)》2004年第3期61-64,共4页胡丽华 纪顺俊 
国家自然科学基金资助项目(20172039)
以DHP为原料,通过在锌介入下水相中的烯丙基化反应,合成目标产物6 甲基 6 苯基 7 烯 1,5 辛二醇.产物结构经核磁共振光谱、红外光谱和质谱得到了证实.
关键词:二醇 甲基 苯基 合成 水相 烯丙基 原料 产物结构 红外光谱 质谱 
Synthesis and Crystal Structure of (2S,5S)-1-Aza-2- (2-pyridyl)-3-oxa-4,4-diphenylbicyclo [3.3.0] Octane
《Chinese Journal of Structural Chemistry》2004年第6期527-530,共4页LU Jun JI Shun-Jun QIAN Rong JIANG Zhao-Qin ZHANG Yong LANG Jian-Ping 
the National Natural Science Foundation of China (No. 20172039)
The title compound (C23H22N2O) 3 has been synthesized by the reaction of (S)- (-)-1,1-diphenyl-2-pyrrolidinemethanol 1 with 2-pyridinecarboxaldehyde 2 in refluxing benzene catalyzed by TsOH, and its structure was dete...
关键词:SYNTHESIS crystal structure (2S 5S)-1-aza-2-(2-pyridyl)-3-oxa-4 4- diphenylbicyclo [3.3.0] octane 
Facile Ionic Liquids-Promoted One-Pot Synthesis of Polyhydroquinoline Derivatives under Solvent Free Conditions被引量:1
《有机化学》2004年第z1期257-258,共2页JIANG,Zhao-Qin LU,Jun ZHOU,Min-Feng JI,Shun-Jun 
Project supported by the National Natural Science Foundation of China (No. 20172039).
In recent years, much attention has been directed towards the syntheses of 1,4-dihydropyridyl compounds due to the fact that 1,4-dihydropyridyl compounds possess a variety of biological activities.[1] In view of the i...
Novel Base-Promoted Syntheses ofβ-Indolylketones via a Three- Component Condensation under Ultrasound Irradiation
《有机化学》2004年第z1期259-,共1页SHEN,Zhi-Liang WANG,Shun-Yi JI,Shun-Jun 
Project supported by the National Natural Science Foundation of China (No. 20172039).
  In recent years, a wide variety of organic compounds bearing indole fragment have been attracted much attention due to the fact that many of them are pharmacologically and biologically active compounds.[1] Among t...
An Expeditious Synthesis of β-Indolylketones Catalyzed by p-Toluenesulfonic Acid (PTSA) Using Ultrasonic Irradiation
《有机化学》2004年第z1期260-261,共2页WANG,Shun-Yi SHI,Hai-Bin JI,Shun-Jun 
Project supported by the National Natural Science Foundation of China (No. 20172039).
  The investigation of the chemistry of indoles has been, and continues to be, one of the most active areas of heterocyclic chemistry.[1] In particular, β-indolylketones have received much attention as important bu...
Facile Synthesis of 3,3-Di(1H-indol-3-yl)indolin-2-ones Catalyzed by Ceric Ammonium Nitrate (CAN) under Ultrasound Irradiation
《有机化学》2004年第z1期262-263,共2页WANG,Shun-Yi ZENG,Xiao-Fei ZHOU,Wei-Juan JI,Shun-Jun 
Project supported by the National Natural Science Foundation of China (No. 20172039).
Indole fragment is featured widely in a wide variety of pharmacologically and biologically active compounds.[1] The 3,3-bis(3-indolyl)oxindole has been shown to possess antibiotic activities against Escherichia coli, ...
An Environmentally-Friendly and Catalytic Procedure for Mukaiyama Aldol Reaction Using Organic Catalyst DBU under Solvent Free Conditions
《有机化学》2004年第z1期264-,共1页SHEN,Zhi-Liang JI,Shun-Jun LOH,Teck Peng 
Project supported by the National Natural Science Foundation of China (No. 20172039) and the Foundation of National University of Singapore.
  Recently, methods based exclusively on organic catalysts have become of major significance in synthetic chemistry.Mukaiyama-aldol reaction, as one of the most important and frequently utilized methods for C-C bond...
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