A5103108452- Chemical Synthesis and Reactions
- Catalytic C–H Functionalization Methods
- Chemical Synthesis and Analysis
- Electrochemical Analysis and Applications
- Electrochemical sensors and biosensors
- Analytical Chemistry and Sensors
- Mercury impact and mitigation studies
- Metal-Organic Frameworks: Synthesis and Applications
- Advanced Photocatalysis Techniques
- Click Chemistry and Applications
- Carbon dioxide utilization in catalysis
- Oxidative Organic Chemistry Reactions
- Sulfur-Based Synthesis Techniques
- Covalent Organic Framework Applications
Central South University
2019-2022
Hunan Institute of Engineering
2020-2022
Central South University of Forestry and Technology
2019-2022
A practical method is developed for the synthesis of oxazolidinone derivatives, an important class heterocyclic compounds. The effect bases and solvents on this cyclization reaction discussed a simple new base–solvent system (triethylamine in toluene) found to be most effective. conditions here are mild no by-products observed. Moreover, using optimized conditions, number differently substituted propargylic alcohols cyclized corresponding N-substituted-4-methylene-oxazolidinones yields up 99%.
Abstract A novel strategy to selective cleavage and esterification of C(CO)−C bonds is described. The efficient approach showed a prominent merit compared previously reported systems, without high temperature, pressure, inert gas protection, transition‐metal free. Meanwhile, rational C−C bond possible mechanism proposed by the control experiments.