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An Efficient Deselenenylation Reaction to the Synthesis of 3, 5-Disubstituted Isoxazoline and Isoxazole
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作者 Wei Ming XU Yu Guang WANG +1 位作者 Zhen Hua CHEN Xian HUANG 《Chinese Chemical Letters》 SCIE CAS CSCD 2005年第8期995-996,共2页
A mild deselenenylation reaction protocol for the preparation of 3, 5-disubstituted isoxazolines and their further application to 3-methyl-5-substituted isoxazoles both in solution phase and solid phase was reported.
关键词 Deselenenylation reaction ISOXAZOLINE isoxazole.
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Palladium-catalyzed Suzuki-Miyaura cross-coupling reaction of organoboronic acids with N-protected 4-iodophenyl alanine linked isoxazoles 被引量:4
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作者 E.Rajanarendar G.Mohan +1 位作者 E.Kalyan Rao M.Srinivas 《Chinese Chemical Letters》 SCIE CAS CSCD 2009年第1期1-4,共4页
Suzuki-Miyaura coupling reaction of N-protected 4-iodopheyl alanine isoxazoles with arylboronic acids,catalyzed by palladium,efficiently produce benzyl-N-(4-bipheyl)-2-(3-methyl-5(E)-2-aryl-1-ethenyl-4-isoxazolyl... Suzuki-Miyaura coupling reaction of N-protected 4-iodopheyl alanine isoxazoles with arylboronic acids,catalyzed by palladium,efficiently produce benzyl-N-(4-bipheyl)-2-(3-methyl-5(E)-2-aryl-1-ethenyl-4-isoxazolyl)-amino-2-oxoethyl)carba- mates in good yields.This process is first of its kind to construct carbon-carbon bond formation having biaryl motif on amino acid linked isoxazole moiety. 展开更多
关键词 Suzuki-Miyaura coupling C-C bond formation Amino acid linked isoxazoles
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Synthesis and Herbicidal Activities of 3-(Substituted phenyl)isoxazole Derivatives 被引量:3
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作者 Yu Han ZHOU, Wei Rong MIAO, Lu Bai CHEN State Key Laboratory of Fine Chemicals, Dalian University of Technology, Dalian 116012 《Chinese Chemical Letters》 SCIE CAS CSCD 2003年第9期897-900,共4页
Several novel 3-(substituted phenyl)isoxazole derivatives were prepared from phenyl butan-1,3-dione. Their structures were confirmed by 1H NMR, IR, and CIMS. Preliminary bioassay showed that some of them exhibited goo... Several novel 3-(substituted phenyl)isoxazole derivatives were prepared from phenyl butan-1,3-dione. Their structures were confirmed by 1H NMR, IR, and CIMS. Preliminary bioassay showed that some of them exhibited good activities toward various weeds. 展开更多
关键词 Protox-inhibitor isoxazole derivatives herbicidal activity.
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Design,Synthesis and Insecticidal Activities of Novel Phenyl Substituted Isoxazolecarboxamides 被引量:2
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作者 LIU Peng-fei ZHANG Ji-feng +2 位作者 YAN Tao XIONG Li-xia LI Zheng-ming 《Chemical Research in Chinese Universities》 SCIE CAS CSCD 2012年第3期430-433,共4页
Thirteen novel phenyl substituted isoxazolecarboxamides were synthesized, and their structures were characterized by IH NMR, elementary analysis and high-resolution mass spectrometry(HRMS) techniques. Their evaluate... Thirteen novel phenyl substituted isoxazolecarboxamides were synthesized, and their structures were characterized by IH NMR, elementary analysis and high-resolution mass spectrometry(HRMS) techniques. Their evaluated insecticidal activities against oriental armyworm(Mythimna separata) indicate that the phenyl substituted isoxazolecarboxamides exhibited moderate insecticidal activities, among which compounds 9c and 9k showed com- paratively higher activities. 展开更多
关键词 Insecticidal activity isoxazole Anthranilic diamide isoxazolecarboxamide
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Basic fibroblast growth factor increases the numbe of endogenous neural stem cells and inhibits the expression of amino methyl isoxazole propionic acid receptors in amyotrophic lateral sclerosis mice
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作者 Weihui Huang Dawei Zang Yi Lu Ping Jiang 《Neural Regeneration Research》 SCIE CAS CSCD 2012年第10期761-765,共5页
This study aimed to investigate the number of amino methyl isoxazole propionic acid (AMPA) receptors and production of endogenous neural stem cells in the SOD1 G93AG1H transgenic mouse model of amyotrophic lateral s... This study aimed to investigate the number of amino methyl isoxazole propionic acid (AMPA) receptors and production of endogenous neural stem cells in the SOD1 G93AG1H transgenic mouse model of amyotrophic lateral sclerosis, at postnatal day 60 following administration of basic fibroblast growth factor (FGF-2). A radioligand binding assay and immunohistochemistry were used to estimate the number of AMPA receptors and endogenous neural stem cells respectively. Results showed that the number of AMPA receptors and endogenous neural stem cells in the brain stem and sensorimotor cortex were significantly increased, while motor function was significantly decreased at postnatal days 90 and 120. After administration of FGF-2 into mice, numbers of endogenous neural stem cells increased, while expression of AMPA receptors decreased, whilst motor functions were recovered. At postnatal day 120, the number of AMPA receptors was negatively correlated with the number of endogenous neural stem cells in model mice and FGF-2-treated mice. Our experimental findings indicate that FGF-2 can inhibit AMPA receptors and increase the number of endogenous neural stem cells, thus repairing neural injury in amyotrophic lateral sclerosis mice. 展开更多
关键词 amino methyl isoxazole propionic acid receptor amyotrophic lateral sclerosis basic fibroblast growth factor endogenous neural stem cells
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Traceless solid-phase synthesis of 3-substituted isoxazoles from polystyrene-supported vinyl selenide
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作者 Qin Xin Shou Ri Sheng +2 位作者 Shu Ying Lin Xiao Ling Liu Xian Huang 《Chinese Chemical Letters》 SCIE CAS CSCD 2007年第1期1-3,共3页
A novel facile procedure for traceless solid-phase synthesis of 3-substituted isoxazoles in good yields and with excellent purities using polymer-supported vinyl selenide has been developed.
关键词 Solid phase organic synthesis Polystyrene-supported vinyl selenide isoxazole
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Ru(Ⅲ)-catalyzed construction of variously substituted quinolines from 2-aminoaromatic aldehydes(ketones)and isoxazoles:Isoxazoles as cyclization reagent and cyano sources
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作者 Di Hu Chao Pi +3 位作者 Wei Hu Xiliang Han Yangjie Wu Xiuling Cui 《Chinese Chemical Letters》 SCIE CAS CSCD 2022年第8期4064-4068,共5页
A Ru(Ⅲ)-catalyzed annulation reaction of 2-aminoaromatic aldehydes(ketones)and isoxazoles to afford diverse 3-cyanoquinolines has been developed.Notably,isoxazole acted as a cyclization reagent and nontoxic cyano sou... A Ru(Ⅲ)-catalyzed annulation reaction of 2-aminoaromatic aldehydes(ketones)and isoxazoles to afford diverse 3-cyanoquinolines has been developed.Notably,isoxazole acted as a cyclization reagent and nontoxic cyano source via N-O bond cleavage and fragmentation.Variously substituted(especially 6-or 7-substituted)quinolines could be easily afforded.This procedure features wide functional group compatibility,efficiency and avoiding toxic cyano source.Meanwhile,this protocol could be successfully applied to scale-up synthesis.Further chemical transformations of 3-cyanoquinoline could give some valuable skeletons,demonstrating its potential in synthetic application. 展开更多
关键词 isoxazoleS Cyclization reagent Cyano sources Variously substituted 3-cyanoquinolines
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Synthesis and Spectral Identification of Novel Stable Triazene: As Raw Material for the Synthesis Biocompatible Surfactants-Pyrazole-Isoxazole-Dihydropyrimidine-Tetrahydropyridine Derivatives
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作者 Mohamed Ahmed Mahmoud Abdel Reheim Ahmed Mahmoud El-Sayed Tolba 《International Journal of Organic Chemistry》 CAS 2016年第1期44-54,共11页
The chemical reactivity of novel stable triazene 3 toward some nucleophilic and electrophilic reagents was investigated. Traizene 3 was used as a key precursor for the synthesis of some novel important heterocyclic co... The chemical reactivity of novel stable triazene 3 toward some nucleophilic and electrophilic reagents was investigated. Traizene 3 was used as a key precursor for the synthesis of some novel important heterocyclic compounds such as Pyrazole, Isoxazole, Dihydropyrimidine, Tetrahydro-pyridine derivatives with expected antimicrobial activity. The synthesized compounds were obtained in good yields. The structures of the newly synthesized compounds were confirmed by elemental analysis, IR, 1H-NMR and Ms spectral data. 展开更多
关键词 Biocompatible Surfactants Pyrazole isoxazole Dihydropyrimidine Tetrahydropyridine Derivatives Spectral Characteristics
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Synthesis and Antitumor Activity of 3-[2-(4-Hydroxy-Phenyl)-Ethyl]-Benzo[d] Isoxazole-4,6-Diol
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作者 Li Wang 《International Journal of Organic Chemistry》 CAS 2023年第1期1-6,共6页
A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characteriz... A new phloretin derivative 1 3-[2-(4-hydroxy-phenyl)-ethyl]-benzo[d] isoxazole-4,6-diol (yield 63%) was synthesized from phloretin by carbonyl nucleophilic addition condensation reaction. Its structure was characterized by 1H NMR, 13C NMR and HR-MS. The phloretin, compound 1, resveratrol and acetylated resveratrol were determined by comparing them with paclitaxel. Anti-tumor activity of alcohol on SPC-A1, EC109, A549, MCF-7 and MDA-MB-231 cell lines. Compound 1 showed better antitumor activity than docetaxel against A549 tumor cells. 展开更多
关键词 3-[2-(4-Hydroxy-Phenyl)-Ethyl]-Benzo[d] isoxazole-4 6-Diol SYNTHESIS Antitumor Activity
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Role of α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor regulation in stress-induced pain chronification
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作者 Sufang Liu Feng Tao 《World Journal of Biological Chemistry》 CAS 2017年第1期1-3,共3页
Persistent postsurgical pain is a serious issue in public health, which has received increased interest in recent years. Previous studies have reported that psychological factors promote the development of chronic pos... Persistent postsurgical pain is a serious issue in public health, which has received increased interest in recent years. Previous studies have reported that psychological factors promote the development of chronic postsurgical pain. However, it is unclear how chronification of postsurgical pain occurs. The α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor(AMPA) phosphorylation in the central nervous system plays a critical role in synaptic plasticity and contributes to central sensitization and chronic pain development. Here, we discuss the role of AMPA receptor regulation in stress-induced pain chronification after surgery. 展开更多
关键词 α-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor phosphorylation Stress Pain chronification
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异噁唑类化合物中间体3′,5′-二氯-4-氟-2,2,2-三氟苯乙酮的合成研究
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作者 余磊 吴子豪 +1 位作者 刘安昌 胡勇 《广东药科大学学报》 2025年第5期32-36,共5页
目的制备高纯度的异噁唑类化合物3′,5′-二氯-4-氟-2,2,2-三氟苯乙酮。方法以4-硝基苯胺为起始原料,经氯代琥珀酰亚胺氯化得到2,6-二氯-4-硝基苯胺,然后经亚硝酸重氮化,氯化亚铜催化下得到3,4,5三氯硝基苯;在二甲亚砜溶液中,将3,4,5三... 目的制备高纯度的异噁唑类化合物3′,5′-二氯-4-氟-2,2,2-三氟苯乙酮。方法以4-硝基苯胺为起始原料,经氯代琥珀酰亚胺氯化得到2,6-二氯-4-硝基苯胺,然后经亚硝酸重氮化,氯化亚铜催化下得到3,4,5三氯硝基苯;在二甲亚砜溶液中,将3,4,5三氯硝基苯经氟化钾氟化反应得到3,5-二氯-4-氟硝基苯,再将其雷尼镍催化下加氢还原得到3,5-二氯-4-氟苯胺,并在溴化氢溶液中进一步经重氮化得到3,5-二氯-4-氟溴苯,最后将其与三氟乙酸乙酯经格氏反应得到目标产物。结果通过6步反应成功合成了3′,5′-二氯-4-氟-2,2,2-三氟苯乙酮,目标产物总收率为75%,其纯度经核磁谱图验证大于99%。结论该合成工艺简单,反应条件温和,收率较高,适合工业化生产。 展开更多
关键词 异噁唑化合物 中间体 合成
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Dipole-dipole interactions in electrolyte to facilitate Li-ion desolvation for low-temperature Li-ion batteries 被引量:1
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作者 Changlin Liu Zongjun Li +3 位作者 Lili Jiang Hao Zhu Fengchao Wang Lizhi Sheng 《Journal of Energy Chemistry》 2025年第5期678-686,共9页
Lithium-ion batteries are widely recognized as prime candidates for energy storage devices.Ethylene carbonate(EC)has become a critical component in conventional commercial electrolytes due to its exceptional film-form... Lithium-ion batteries are widely recognized as prime candidates for energy storage devices.Ethylene carbonate(EC)has become a critical component in conventional commercial electrolytes due to its exceptional film-forming properties and high dielectric constant.However,the elevated freezing point,high viscosity,and strong solvation energy of EC significantly hinder the transport rate of Li^(+)and the desolvation process at low temperatures.This leads to substantial capacity loss and even lithium plating on graphite anodes.Herein,we have developed an efficient electrolyte system specifically designed for lowtemperature conditions,which consists of 1.0 M lithium bis(fluorosulfonyl)imide(LiFSI)in isoxazole(IZ)with fluorobenzene(FB)as an uncoordinated solvent and fluoroethylene carbonate(FEC)as a filmforming co-solvent.This system effectively lowers the desolvation energy of Li^(+)through dipole-dipole interactions.The weak solvation capability allows more anions to enter the solvation sheath,promoting the formation of contact ion pairs(CIPs)and aggregates(AGGs)that enhance the transport rate of Li^(+)while maintaining high ionic conductivity across a broad temperature range.Moreover,the formation of inorganic-dominant interfacial phases on the graphite anode,induced by fluoroethylene carbonate,significantly enhances the kinetics of Li^(+)transport.At a low temperature of-20℃,this electrolyte system achieves an impressive reversible capacity of 200.9 mAh g^(-1)in graphite half-cell,which is nearly three times that observed with conventional EC-based electrolytes,demonstrating excellent stability throughout its operation. 展开更多
关键词 Lithium-ion batteries Low-temperature electrolytes isoxazole Dipole-dipole interactions Low desolvation energy
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异噁唑骨架构建及其含能化合物合成研究进展
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作者 冯心雨 毕福强 +2 位作者 薛琪 王伯周 张俊林 《兵器装备工程学报》 北大核心 2025年第1期27-37,共11页
异噁唑具有氮氧五元芳香杂环结构,其能量水平低于呋咱与氧化呋咱等氮杂五元含能骨架,是构筑含能材料的含能结构单元,目前异噁唑含能化合物已成为不敏感含能材料领域的研究热点之一。概述了2种典型的异噁唑环的构建策略,并探讨了其缩合... 异噁唑具有氮氧五元芳香杂环结构,其能量水平低于呋咱与氧化呋咱等氮杂五元含能骨架,是构筑含能材料的含能结构单元,目前异噁唑含能化合物已成为不敏感含能材料领域的研究热点之一。概述了2种典型的异噁唑环的构建策略,并探讨了其缩合环化反应机理;综述了近年来十余种异噁唑含能化合物的合成研究进展,重点介绍了典型异噁唑含能化合物的物化和爆轰性能,特别是3,3’-双异噁唑-4,4’,5,5’-四亚甲基二硝酸酯,其密度为1.585 g/cm^(3)、熔点92℃、爆速7060 m/s、爆压19.3 GPa,对冲击,摩擦和静电放电表现出低敏感性,可作为潜在含能增塑剂应用。该综述为后续设计、合成新型异噁唑含能材料提供一定的理论依据,并对该类含能化合物的未来发展前景进行了展望。 展开更多
关键词 异噁唑含能化合物 骨架构建方法 环化反应机理 合成 爆轰性能
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3-氨基苯并[d]异噁唑类大环ALK抑制剂的设计、合成及活性评价
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作者 周振 刘耀阳 +4 位作者 黎瑶 华炫智 刘洋 杨华丽 程卯生 《沈阳药科大学学报》 2025年第1期52-66,共15页
目的间变性淋巴瘤激酶(anaplastic lymphoma kinase,ALK)的活性失调与多种癌症的发生密切相关。以恩曲替尼为先导化合物,设计并合成一系列3-氨基苯并[d]异噁唑类ALK抑制剂,测试其对ALK阳性的人肺腺癌H2228细胞的抑制活性。方法以邻甲氧... 目的间变性淋巴瘤激酶(anaplastic lymphoma kinase,ALK)的活性失调与多种癌症的发生密切相关。以恩曲替尼为先导化合物,设计并合成一系列3-氨基苯并[d]异噁唑类ALK抑制剂,测试其对ALK阳性的人肺腺癌H2228细胞的抑制活性。方法以邻甲氧基苯甲醛为起始原料,经过还原性C-C偶联、杂环合成和酰胺缩合得到目标化合物A1。以间羟基苯甲酸甲酯和水杨酸甲酯为起始原料,经亲核取代、水解酸化得到中间体5a、5b、13a和13b。以水杨醛及取代水杨醛为起始原料,经过还原性C-C偶联、亲核取代、杂环合成、酰胺缩合、Boc保护与脱保护,以及分子内烯烃复分解反应最终合成得到B、C、D系列大环化合物B1-B4、C1-C4和D1-D7。以恩曲替尼为阳性对照药,使用ALK阳性人肺腺癌H2228细胞株和ALK阴性的人非小细胞肺癌A549细胞株,采用CCK-8法测试目标化合物对细胞株的抑制活性。采用Annexin V-FITC/PI双染流式细胞实验测试化合物B1对H2228肿瘤细胞的凋亡诱导情况。对目标化合物B1和D1进行了ALK酶抑制活性测试。结果与结论合成了16个3-氨基苯并[d]异噁唑类化合物,其中B、C、D系列化合物为大环结构,其结构经核磁共振氢谱和碳谱及高分辨质谱确证。体外H2228肿瘤细胞增殖抑制实验结果表明,化合物B1的抑制活性最佳,IC50=(16.55±3.79)μmol·L^(-1)。细胞凋亡实验表明B1能够浓度依赖性地诱导H2228细胞凋亡。ALK体外酶抑制活性实验中B1和D1的IC50分别为303.7 nmol·L^(-1)和288.0 nmol·L^(-1)。 展开更多
关键词 3-氨基苯并[d]异噁唑 ALK抑制剂 大环化合物
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新型酰肼类化合物的合成与杀菌活性
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作者 姜婷婷 周能婷 +2 位作者 赏欣语 马讯 杨子辉 《有机氟工业》 2025年第3期1-4,共4页
近年来,植物病原菌对杀菌剂的抗性问题日益突出,研发具有高效和低毒的杀菌剂一直是研究热点之一。基于酰肼类杀菌剂的母体结构,将异噁唑杂环引入酰肼母体结构中,设计并合成了5-甲基-4-异噁唑甲酰肼类化合物2a~2c。初步杀菌活性测试表明... 近年来,植物病原菌对杀菌剂的抗性问题日益突出,研发具有高效和低毒的杀菌剂一直是研究热点之一。基于酰肼类杀菌剂的母体结构,将异噁唑杂环引入酰肼母体结构中,设计并合成了5-甲基-4-异噁唑甲酰肼类化合物2a~2c。初步杀菌活性测试表明,化合物2a对葡萄座腔病菌抑制率达A级,优于噻呋酰胺。活体杀菌活性测试表明,化合物2a对番茄灰霉病菌的5 d保护活性抑制率为40.67%,有中等的保护活性。 展开更多
关键词 杀菌剂 酰肼 异噁唑 杀菌活性
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5-羟甲基异噁唑衍生物的合成与杀虫活性研究
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作者 马丽 钱云飞 +1 位作者 左园燕 刘根炎 《化学与生物工程》 北大核心 2025年第5期24-29,36,共7页
设计并合成了一系列5-羟甲基异噁唑衍生物(6a~6j),通过^(1)HNMR、^(13)CNMR和HRMS对目标化合物结构进行了表征,测定了目标化合物对果蝇和小菜蛾的杀虫活性。结果表明,目标化合物6a~6j对2种昆虫均表现出一定的杀虫活性,目标化合物6d~6i在... 设计并合成了一系列5-羟甲基异噁唑衍生物(6a~6j),通过^(1)HNMR、^(13)CNMR和HRMS对目标化合物结构进行了表征,测定了目标化合物对果蝇和小菜蛾的杀虫活性。结果表明,目标化合物6a~6j对2种昆虫均表现出一定的杀虫活性,目标化合物6d~6i在200 mg·L^(-1)浓度下对果蝇的杀虫活性较高,校正死亡率均超过50%,其中目标化合物6g的杀虫活性最高,校正死亡率为84.48%;目标化合物6e在300 mg·L^(-1)浓度下对小菜蛾表现出显著杀虫活性,校正死亡率为97.70%;目标化合物6g能与果蝇γ-氨基丁酸(GABA)受体的Glu146、Arg53等关键氨基酸残基形成氢键作用,为作用于GABA受体的新型杀虫剂先导化合物的研发提供了重要参考。 展开更多
关键词 GABA受体 异噁唑 有机合成 杀虫活性
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碳化钙为乙炔源与腈氧化物合成单取代异恶唑
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作者 王雪梅 王波 +1 位作者 李超 刘楠 《广州化学》 2025年第3期41-45,I0003,共6页
探究了一种原位产生的腈氧化物和碳化钙经[3+2]环加成反应合成异恶唑的新方法,反应使用固体的碳化钙替代了气态的乙炔,是一种绿色、高效的合成方法。相对乙炔而言,碳化钙安全、易于操作,且不需要专门高压设备。作为关键中间体的腈氧化物... 探究了一种原位产生的腈氧化物和碳化钙经[3+2]环加成反应合成异恶唑的新方法,反应使用固体的碳化钙替代了气态的乙炔,是一种绿色、高效的合成方法。相对乙炔而言,碳化钙安全、易于操作,且不需要专门高压设备。作为关键中间体的腈氧化物,则是通过次氯酸钠氧化醛肟原位获得的。该方法以醛肟和碳化钙为原料,三氯甲烷为溶剂,次氯酸钠溶液为氧化剂,在室温条件下反应10小时,合成了各种3-单取代异恶唑衍生物,最高的产物收率可达86%,具有反应高效、条件简单的特点。 展开更多
关键词 醛肟 乙炔 碳化钙 环加成反应 异恶唑
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5-[2,4-二(苄氧基)-5-异丙基苯基]异噁唑-3-羧酸乙酯的制备
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作者 靳清贤 刘冬 +4 位作者 张广慧 宋胜楠 孟如玉 杜星辰 方少明 《合成化学》 2025年第1期56-60,共5页
5-[2,4-二(苄氧基)-5-异丙基苯基]异噁唑-3-羧酸乙酯是一类癌细胞抑制剂的关键中间体,本文以2,4-二羟基异丙基苯为起始原料,经过傅克乙酰化、醚化、酯缩合反应、成肟反应和脱水成环5步反应,制备出5-[2,4-二(苄氧基)-5-异丙基苯基]异噁唑... 5-[2,4-二(苄氧基)-5-异丙基苯基]异噁唑-3-羧酸乙酯是一类癌细胞抑制剂的关键中间体,本文以2,4-二羟基异丙基苯为起始原料,经过傅克乙酰化、醚化、酯缩合反应、成肟反应和脱水成环5步反应,制备出5-[2,4-二(苄氧基)-5-异丙基苯基]异噁唑-3-羧酸乙酯。对已有文献的合成方法和步骤进行了优化,由原来的5步反应简化为3步反应。其中对与草酸二乙酯的酯缩合反应、与盐酸羟胺的成肟反应以及脱水成环的3步反应,采用onepot一步法,大大简化了反应流程,为HSP90系列抑制剂的研究提供了制备方法支撑。 展开更多
关键词 异噁唑 一锅法 合成 HSP90抑制剂 癌细胞 中间体
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新型甘草次酸异噁唑衍生物的合成 被引量:12
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作者 刘利军 雍建平 +3 位作者 戴小军 贾炯 王西照 王建武 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2006年第9期1669-1672,共4页
以甘草次酸(脱氧甘草次酸)和3-取代苯基-5-氨甲基-异噁唑为原料,合成了4种甘草次酸异噁唑衍生物,通过IR,1HNMR,13C NMR及FABMS等方法确定了化合物的结构.同时用L9(34)正交试验对酰胺化反应的条件进行优化,确定了酰化反应的最佳条件.
关键词 甘草次酸 异噁唑 正交试验 合成
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3-N-乙酰基-2-取代芳基-5-[5′-甲基异噁唑-3′]-Δ_3-1,3,4-噁唑啉类化合物的合成 被引量:42
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作者 钟滨 赵卫光 +1 位作者 李正名 王素华 《应用化学》 CAS CSCD 北大核心 2003年第8期719-722,共4页
由相应的酯 (1)肼解制得 5 甲基 异唑 3 甲酰肼 (2 ) ,后者与醛缩合得到酰腙 (3a~ 3h) ,3a~ 3h再进一步与乙酸酐环合 ,以良好的收率合成出了 3 N 乙酰基 2 取代芳基 5 [5′ 甲基 异唑 3′] Δ3 1,3,4 唑啉衍生物 (4a... 由相应的酯 (1)肼解制得 5 甲基 异唑 3 甲酰肼 (2 ) ,后者与醛缩合得到酰腙 (3a~ 3h) ,3a~ 3h再进一步与乙酸酐环合 ,以良好的收率合成出了 3 N 乙酰基 2 取代芳基 5 [5′ 甲基 异唑 3′] Δ3 1,3,4 唑啉衍生物 (4a~ 4h)。以上化合物的结构均经过1 HNMR、MS和元素分析的确证。 展开更多
关键词 甲基-异噁唑甲酰肼 噁唑啉 合成
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