THIAZOLE相关论文
Benzobisthiazole polymer with resonance-assisted hydrogen bonds (RAHBs) has been synthesized for both organic field-effe......
Nitrogen heteroarenes widely present in naturally occurring products and synthetic bioactive molecules,and as core struc......
The emergence of multiple drug resistant microorganisms has caused major health concern worldwide....
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Design and Synthesis of Coumarin-derived Thiazolyl Diethanolamines as Novel Multi-targeting Antimicr
Coumarins have wide application in the fields of bromatology,materials and medicinal chemistry.Thiazole in a variety of ......
Thiazole and its benzothiazole is an important type of aromatic heterocycles with nitrogen and sulfur atoms.This special......
Novel Hybrids of Metronidazole and Quinolone:Synthesis, Antimicrobial Evaluation and Their Supramole
Quinolones as an important kind of synthetic antibacterial agents are widely used in clinic to treat genitourinary infec......
为了寻找新型抗肿瘤药物先导,设计合成了23个含噻唑环的天然芪类似物,其结构均经NMR和ESI-HRMS表征确证.通过Top1-介导的松散实验......
Synthesis and Biological Evaluation of Quinazolonethiazoles as New Potential Conquerors towards Pseu
Main observation and conclusionrnNovel quinazolonthiazoles were designed and synthesized as new potential antimicrobial ......
A novel chemoenzymatic one-pot multicomponent synthesis of thiazole derivatives was developed.A series of thiazole d......
蓝萼甲素(Glaucocalyxin A, GLA)是从蓝萼香茶菜中分离得到的四环二萜类活性天然产物.设计并合成了一系列基于蓝萼甲素的噻唑类衍......
Synthesis, Crystal Structure and Fungicidal Activity of Ethyl 2-(3-(4-Fluorobenzamido)phenyl)-4-((4-
本文通过对荣华二采区10...
本文通过对荣华二采区10...
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis and Biological Activities of Novel Thiophosphoryl Oximates Containing Thiazole and 1,2,3-T
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Heterocycle-bridged and Conformationally Constrained Retinoids: Synthesis of 4-(7,8,9,10-Tetrahydro-
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis of Biologically Active[4-(4-Bromophenyl)-2-thiazolyl]hydrazones and their D-Galactose Deri
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis and plant-growth regulatory activities of novel imine derivatives containing 1H-1,2,4-tria
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis, characterization and antimicrobial activity of some new biquinoline derivatives containin
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis, fluorescence properties and selective Cr(Ⅲ) recognition of tetraaryl imidazole derivative
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
为探究吕家坨井田地质构造格局,根据钻孔勘探资料,采用分形理论和趋势面分析方法,研究了井田7......
Synthesis, Characterization and Corrosion Inhibitive Properties of New Thiazole Based Polyamides Con
The present work aimed to synthesize a new interesting series of thiazole based polyamides containing diarylidenecyclohe......
N-[2-(1H-吲哚-3)乙基]-2-乙酰噻唑-4-甲酰胺是最近从海洋细菌中分离得到的一种新型的天然杀藻剂,以D-丙氨酸为原料合成了该化合物......
Novel ferrocenyl-containing thiazole derivatives have been synthesized from 2-amino-4-ferrocenyl-5-(1H-1, 2, 4-triazole-......
The title compound 2, 4-chloromethyl-3-anilino-2-(4-methyl-benzoylimido)thiazole, was prepared by the reaction of 1-p-me......
Synthesis, characterization and antimicrobial activity of some new biquinoline derivatives containin
A series of new biquinoline derivatives containing a thiazole moiety were synthesized by a one-pot,base-catalyzed cycloc......
为了寻找新型高效低毒的农药先导化合物,采用1-[(杂芳基)甲基]-5-甲基-1H-1,2,3-三唑基-4-甲酰氯与2-氨基-5-烷基-1,3,4-噻二唑的......
用串联的氮杂Wittig关环反应合成了一系列3-[取代吡啶(嘧啶)甲基]-1,2,3-三唑[4,5-d]嘧啶-7-酮.膦亚胺4和芳基异氰酸酯发生氮杂Wit......
以乙酰乙酸乙酯和苯甲醛为原料,经5步反应得到14个2-取代肉桂酰胺基-4-甲基噻唑-5-羧酸化合物,其结构经1H-NMR,13C-NMR和MS确证。......
<正> 从海洋动植物中已分离到近二十个环肽,它们结构新颖,具有强烈的生物活性,引起了广泛的研究。Ascidiacyclamide是从海鞘中分离......
对三甲基噻唑的合成工艺进行了研究，并对其在烟用香精中的应用进行了探讨，实验表明：以丁酮为起始原料，经溴代、成环缩合制备三甲基噻唑......
采用失重法和电化学方法研究了2-氨基（1-苯基-3-氧代丁基）-5-甲基-噻唑（ABT）和2-氨基（1，4-二苯基-3-氧代丁基）-5-甲基-噻唑（ADT）在1mol／L HCl......
以2-苯基-1,2,3-三唑-4-甲醛（1）为原料，与氨基硫脲缩合，生成醛缩氨基硫脲（2），分别与5种甜溴代芳基乙酮、5种α-溴代-α-（1H-1，2,4-三唑-1-基......
采用2-氯-5-（氯甲基）吡啶和2-氯-5-（氯甲基）噻唑为原料，经过叠氮化、乙酰乙酸乙酯环化、水解、酰氯化，然后与芳氧乙酰肼的缩合反应，合成了......
为进一步发展抗菌药氟喹诺酮向抗肿瘤活性转化的有效结构修饰策略,基于药效团骨架的迁越药物设计原理,用噻唑并均三唑稠环取代左氧......
合成了4个以噻唑环为母体、含有Schiff碱结构的新型二阶非线性光学（NLO）活性分子，用红外光谱、紫外光谱、核磁共振光谱和元素分析确定......
以2-氨基噻唑衍生物为重氮组分,以N,N-二取代苯胺衍生物为偶合组分,合成、提纯了一系列文题化合物。用改进的SCF-PPP-CI程序进行分......
以2-甲基-4-三氟甲基-噻唑-5-羧酸和硫代氨基脲为原料,合成了7个新型化合物,其化学结构经1H NMR、红外和元素分析确认。初步生物活......
利用交流阻抗技术和动电位极化方法研究了噻唑缓蚀剂在模拟高温高压油气井水介质中对N80油管钢的缓蚀机理.结果表明:在二氧化碳环......
为了寻找和发现高效、广谱、低毒、低生态风险并与现有杀虫剂无交互抗性的新型杀虫剂,以2-氯-5-氯甲基噻唑为原料,经多步反应制得1......
设计、合成了含羟乙基活性基团的噻唑类非线性生色分子，用IR，EA，^1H MNR，UV-Vis和DSC-TG等对其结构和性能进行了表征，用超瑞利散射技术......
噻唑类化合物是近年来发展的一个热点。噻唑基团引入到各种不同的化合物结构中,通过结构修饰能产生一系列具有广谱生物活性的化合......
采用密度泛函理论B3LYP/6-311G＊＊方法,对一系列含Schiff碱基噻唑衍生物的二阶非线性光学（NLO）性质和电子光谱进行了研究.结果表明,分子......
