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Stereoselective Synthesis of the α-Glycoside of a KDO 'C'-Disaccharide
- Source :
- Organic Letters. 2:3361-3363
- Publication Year :
- 2000
- Publisher :
- American Chemical Society (ACS), 2000.
-
Abstract
- The reaction of tert-butyl (4,5,7, 8-tetra-O-acetyl-3-deoxy-alpha-D-manno-2-octulopyranosyl chloride)onate donor 7 with the 6-formylgalactopyranoside acceptor 4 in the presence of SmI(2) provided only the KDO alpha-C-disaccharide 8. The bulky tert-butyl ester in the donor was used to reverse the stereochemical outcome of C-glycosylation, stereoselectively forming the alpha-"C"-disaccharide of KDO.
- Subjects :
- chemistry.chemical_classification
Stereochemistry
Organic Chemistry
Disaccharide
Alpha (ethology)
Glycoside
Disaccharides
Biochemistry
Acceptor
Chloride
chemistry.chemical_compound
Carbohydrate Sequence
chemistry
medicine
Stereoselectivity
Glycosides
Physical and Theoretical Chemistry
Nuclear Magnetic Resonance, Biomolecular
medicine.drug
Subjects
Details
- ISSN :
- 15237052 and 15237060
- Volume :
- 2
- Database :
- OpenAIRE
- Journal :
- Organic Letters
- Accession number :
- edsair.doi.dedup.....eb1b04b0c0bf8c1341bc26be1738a631
- Full Text :
- https://doi.org/10.1021/ol006458n