A5048428307- Asymmetric Hydrogenation and Catalysis
- Synthesis and Catalytic Reactions
- Nanomaterials for catalytic reactions
- Chemical Synthesis and Analysis
- Catalytic C–H Functionalization Methods
- Cancer, Hypoxia, and Metabolism
- Surface Chemistry and Catalysis
- Catalysis for Biomass Conversion
- Oxidative Organic Chemistry Reactions
- Advanced Physical and Chemical Molecular Interactions
- Carbohydrate Chemistry and Synthesis
- Lymphoma Diagnosis and Treatment
- Inorganic and Organometallic Chemistry
- Various Chemistry Research Topics
- RNA and protein synthesis mechanisms
- Advanced biosensing and bioanalysis techniques
- Phenothiazines and Benzothiazines Synthesis and Activities
- Metabolism, Diabetes, and Cancer
- Innovative Microfluidic and Catalytic Techniques Innovation
- Carbon dioxide utilization in catalysis
Lishui Central Hospital
2024
Chongqing University
2024
Georgetown University
2012-2016
K 2 RuO 4 -mediated oxidation offers a DNA-compatible method for functional group transformations, enabling alcohol-to-carboxylic acid and amine-to-nitrile conversions valuable DNA-encoded library synthesis.
Introduction The effectiveness of Fragment-based drug design (FBDD) for targeting challenging therapeutic targets has been hindered by two factors: the small library size and complexity fragment-to-hit optimization process. DNA-encoded (DEL) technology offers a compelling robust high-throughput selection approach to potentially address these limitations.
Substrate (I) is insoluble in water at room temperature, but becomes more soluble higher temperature.