A5003120394- Carbohydrate Chemistry and Synthesis
- Click Chemistry and Applications
- Crystallization and Solubility Studies
- Glycosylation and Glycoproteins Research
- Chemical and Physical Properties in Aqueous Solutions
- Pharmacological Effects of Natural Compounds
- Crystallography and molecular interactions
- Fluorine in Organic Chemistry
- Energetic Materials and Combustion
University of Chinese Academy of Sciences
2024
Tianjin University
2020-2021
Abstract The selective functionalization of carbohydrates holds a central position in synthetic carbohydrate chemistry, driving the ongoing quest for ideal approaches to manipulate these compounds. In this study, we introduce general strategy that enables regiodivergent saccharides. use electron‐deficient photoactive 4‐tetrafluoropyridinylthio (SPyf) fragment as an adaptable activating group, facilitated efficient across all saccharide sites. More importantly, group can be directly installed...
Abstract The selective functionalization of carbohydrates holds a central position in synthetic carbohydrate chemistry, driving the ongoing quest for ideal approaches to manipulate these compounds. In this study, we introduce general strategy that enables regiodivergent saccharides. use electron‐deficient photoactive 4‐tetrafluoropyridinylthio (SPyf) fragment as an adaptable activating group, facilitated efficient across all saccharide sites. More importantly, group can be directly installed...
The solubility of m-aminobenzoic acid (m-ABA) Form I in 12 pure solvents (methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, isobutyl alcohol, water, acetonitrile, acetone, methyl acetate, isopropyl 1,4-dioxane) was measured at temperatures from T = 283.15 to 323.15 K by a gravimetric method under atmospheric pressure. mole fraction values m-ABA these increase with increasing temperature the following order: 1,4-dioxane > acetone methanol ethanol acetate 2-propanol 1-propanol 1-butanol...
The selective functionalization of carbohydrates holds a central position in synthetic carbohydrate chemistry, driving the ongoing quest for ideal approaches to manipulate these compounds. In this study, we introduce general strategy that enables regiodivergent saccharides. use electron-deficient photoactive 4-tetrafluoropyridinylthio (SPyf) fragment as an adaptable activating group, facilitated efficient across all saccharide sites. More importantly, group can be directly installed at C1,...