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Regioselective Dehydration of Sugar Thioacetals under Mild Conditions
- Source :
- Organic Letters
- Publication Year :
- 2021
- Publisher :
- American Chemical Society (ACS), 2021.
-
Abstract
- Pentose and hexose sugars are abundant constituents of waste biomass, making them sustainable, chiral building blocks for organic synthesis. The demand for chiral saturated heterocyclic rings from the pharmaceutical industry is increasing as they provide well-defined three-dimensional frameworks that show increased metabolic resistance. Through the formation of thioacetals, sugars may be manipulated in their straight-chain form and dehydrated selectively under basic conditions at C-2. This approach was applied to an array of sugars and extended to the production of useful chiral THFs via further selective dehydration reactions.
- Subjects :
- Green chemistry
Letter
Carbohydrates
Pentose
Biomass
Chemistry Techniques, Synthetic
010402 general chemistry
01 natural sciences
Biochemistry
chemistry.chemical_compound
Acetals
medicine
Organic chemistry
Hexose
Sulfhydryl Compounds
Dehydration
Physical and Theoretical Chemistry
Sugar
chemistry.chemical_classification
Molecular Structure
010405 organic chemistry
Organic Chemistry
food and beverages
Regioselectivity
Stereoisomerism
Ethylenes
Ketones
medicine.disease
0104 chemical sciences
chemistry
Organic synthesis
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 23
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....f41c7f09bf9f0efb82642ec9b05128f8