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Mild Cu(OTf)2-Mediated C-Glycosylation with Chelation-Assisted Picolinate as a Leaving Group
- Source :
- J Org Chem
- Publication Year :
- 2020
- Publisher :
- American Chemical Society (ACS), 2020.
-
Abstract
- C-glycosylation reactions of glycosyl picolinates with allyltrimethylsilane or silyl enol ethers were developed. Picolinate as a chelation-assisted leaving group could be activated by Cu(OTf)(2) and avoided the use of harsh Lewis acids. The glycosylations were operated under mild neutral conditions and gave the corresponding C-glycosides in up to 95% yield with moderate to excellent stereoselectivities.
- Subjects :
- Glycosylation
animal structures
Silylation
010405 organic chemistry
Organic Chemistry
Leaving group
macromolecular substances
010402 general chemistry
01 natural sciences
Enol
Medicinal chemistry
Article
0104 chemical sciences
carbohydrates (lipids)
chemistry.chemical_compound
chemistry
Yield (chemistry)
lipids (amino acids, peptides, and proteins)
Glycosyl
Chelation
Glycosides
Lewis acids and bases
Picolinic Acids
Lewis Acids
Subjects
Details
- ISSN :
- 15206904 and 00223263
- Volume :
- 85
- Database :
- OpenAIRE
- Journal :
- The Journal of Organic Chemistry
- Accession number :
- edsair.doi.dedup.....096963d3912abc32b903edaaf9089af1