2. 您的位置
3. 首页
4. 会议论文
5. Natural Berberine-derived Azoles Synthesis and Antimicrobial Activities

Natural Berberine-derived Azoles Synthesis and Antimicrobial Activities

来源 :中国化学会第十三届全国有机合成化学学术研讨会 | 被引量 : 0次 | 上传用户：jiaxianczy

【摘 要】

：

　　A series of natural berberine-derived azoles as potential mulri-targeting antimicrobial agents were designed,synthesized and characterized by modern spectra

【作 者】

：

Zhou Cheng-He 

【机 构】

：

SchoolofChemistryandChemicalEngineering,SouthwestUniversity,Chongqing400715

【出 处】

：

中国化学会第十三届全国有机合成化学学术研讨会

【发表日期】

：

2016年10期

【关键词】

：

berberine imidazole triazole antibacterial antifungal 

下载到本地 , 更方便阅读

下载此文 赞助VIP

声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架

论文部分内容阅读

　　A series of natural berberine-derived azoles as potential mulri-targeting antimicrobial agents were designed,synthesized and characterized by modern spectra.Their antimicrobial activities were evaluated,and antimicrobial action mechanisms were explored.

其他文献

Cylization Reactions with Electrophilic Diaryliodonium Salts

　　Over the past few decades,theres an explosive increase of interest in electrophilic cyclization to synthesize carbocycles or heterocycles took place.However

会议

organic azidesolefinstriazolesenaminonitriles

磷自由基参与的烯烃双官能团化反应研究

　　烯烃的双官能团化反应已经成为现代有机合成中一种重要的方法.1本课题组在该领域作了一些探索.2本文报道了磷自由基参与的几个烯烃双官能团化反应,包括以下内容：1、二苯氧

会议

烯烃双官能团化自由基反应

以NBS(P)做氮源的胺化反应

　　N-溴代丁二酰亚胺(NBS)在有机合成中通常作为溴代试剂和弱氧化剂使用。最近几年,我们课题组开展了用NBS (P)作为氮源的胺化反应研究。利用NBS(P)/DBU组合策略,我们成功实

会议

NBS(P)卤键活化胺化

Synthesis of Benzo-fused Cyclic Compounds via Intramolecular Cyclization of Aryltriazenes

　　The rapid and convenient construction ofbenzo-fused cyclic compounds has attracted significant attention due to their wide applications in various fields.As

会议

aryltriazeneheterocyclesorganic synthesis

Trisulfur Radical Anion and Electron Catalysis

会议

Metal-Free Selective Functionalization of 8-amidoquinolines on the C-5 Position

　　Quinoline is an important scaffold in various natural products and synthetic compounds with wide applications in medicinal and materials chemistry.In the re

会议

8-amidoquinolineshypervalentiodine compoundsC-H functionalizationmetal-free

利用阻止芳构化策略构建具有季碳中心的喹啉-3(4H)-酮骨架

　　利用C-H键的直接官能团化,高效、高选择性的合成C-C键已成为一种广泛应用的方法。相比于过渡金属催化的方法,经由自由基中间体的C-H键活化对C(sp3)-H的直接官能团化具有

会议

N-芳基甘氨酸酯喹啉-3(4H)-酮自由基正离子C-H键官能团化

Drug Discovery Based on Natural Product Artemisinin

　　Compared to the great achievement in the development of anti-malarial drugs based on the natural product artemisinin,limited success has been accomplished i

会议

artemisininanticancerdrug targetstructural modification

Natural Products Directed Asymmetric Catalysis Total Synthesis

　　Described here is the work on the development of new catalytic asymmetric reactions and application in the synthesis of natural products and drugs.

会议

asymmetric Catalysistotal synthesis

A reversible turn-on fluorescent recognition of Hg(Ⅱ) and colorimetric detection of Cu(Ⅱ) by a singl

　　The design and synthesis of selective and sensitive probes capable of monitoring metal ions has attracted interest because heavy transition-metal ions are u

会议

ferrocenylcarbazolemetal-free conditionsmultisignaling sensoraqueous environ