A5080687169- Multicomponent Synthesis of Heterocycles
- Synthesis and Biological Evaluation
- Synthesis and Biological Activity
- Marine Sponges and Natural Products
- Supercapacitor Materials and Fabrication
- Chemical Synthesis and Analysis
- Synthetic Organic Chemistry Methods
- Synthesis and Catalytic Reactions
- Synthesis and biological activity
- Advancements in Battery Materials
- Synthesis of Organic Compounds
- Multiferroics and related materials
- Chemical synthesis and alkaloids
- Electronic and Structural Properties of Oxides
- TiO2 Photocatalysis and Solar Cells
- Microwave-Assisted Synthesis and Applications
- Advanced Photocatalysis Techniques
- Catalytic C–H Functionalization Methods
- Oxidative Organic Chemistry Reactions
- Catalytic Cross-Coupling Reactions
- Bioactive Compounds and Antitumor Agents
- Interconnection Networks and Systems
- Innovative Microfluidic and Catalytic Techniques Innovation
- Religious Studies and Spiritual Practices
- Traditional and Medicinal Uses of Annonaceae
Korea Basic Science Institute
2012-2016
Busan Medical Center
2014-2015
Vellore Institute of Technology University
2015
Tetrahydroacridine-1,8-(2<italic>H</italic>,5<italic>H</italic>,9<italic>H</italic>,10<italic>H</italic>)-diones<bold>4</bold>from 1,3-cyclohexanedione and/or dimedone 1,2-chloro-3-formylquinoline<bold>2</bold>and anilines<bold>3</bold>in water at 90 °C were obtained by domino reaction approach.
TiO<sub>2</sub> nanoparticles was effectively applied in the microwave assisted synthesis of quinolines and quinolones.
Intramolecular C–N bond formation is achieved through oxidative cyclization of 1-(3-arylisoquinolin-1-yl)-2-(arylmethylene)hydrazines,<bold>3</bold>, in the presence hypervalent iodine oxidant and dichloromethane at ambient temperature.
C–C bond formation of tautomerizable quinolinones. C–OH activation using BOP reagent and boronic acids.
Microwave supported, water intervened, nano crystalline TiO<sub>2</sub> catalyzed synthesis of 3-(1,5-dioxo-1,5-diphenylpentan-3-yl)quinolin-2(1<italic>H</italic>)-ones, is described.
Various surface modifications have been applied to improve the adhesion properties of aluminum for cap plate and sealing quality electrolyte on Li ion batteries. In this study, we tried find effective condition polymerization triazine thiols (TT) modified surfaces by anodic oxide. Characterization polymerized films was explored scanning electron microscopy, X-ray photoelectron spectroscopy, secondary mass spectroscopy analysis. Scanning microscopy results reveal that meaningful roughness...
It has been reported that improving electrical conductivity and maintaining stable structure during discharge/charge process are challenge for Si to be used as an anode lithium ion batteries (LIB). To address this problem, milkweed (MW) was carbonized prepare hollow carbon microtubes (HCMT) derived from biomass template LIB. In order improve conductivity, various materials such chitosan (CTS), agarose, polyvinylidene fluoride (PVDF) source (C1, C2, C3) by carbonization. Carbon coated HCMT@Si...
Recently Li-ion battery has been used extensively as a portable power source for small electronic devices, electric vehicles and an attractive option energy storage. Artificial graphite, natural hard carbon, such carbon-based materials anode active material have applied, According to the requirements of high capacity, theoretical capacity Si (ca. 4200mAh/g) which is 5 times higher than mateirlas actively studied in recent years. There are several problems overcome despite advantages values...
A Silicon/Porous-Carbon (Si/Porous-C) composite with Ag nanoparticles was prepared by the co-assembly of polyvinylidene fluoride (PVdF), nano-SiO 2 (~20 nm), AgNO 3 and Si (~ 50 nm) followed a carbonizing process subsequent removal SiO template. The Si/Porous-C Ag/Si/Porous-C were characterized scanning transmission electron microscopy (STEM), X-ray photoelectron spectroscopy (XPS), diffraction (XRD). remained even after heat treatment at high temperature hydrofluoric acid etching. electrode...
Abstract 23 examples
Abstract The title sequence allows the synthesis of highly functionalized quinolines via three‐ component reaction 2‐chloro‐3‐formylquinolines, acetophenones, and boronic acids.