Stereoselective Synthesis of β-Mannopyranosides via the Temporary Silicon Connection Method
- 1 January 1996
- journal article
- Published by American Chemical Society (ACS) in Journal of the American Chemical Society
- Vol. 118 (1) , 247-248
- https://doi.org/10.1021/ja9532291
Abstract
No abstract availableThis publication has 23 references indexed in Scilit:
- C(5)-Epimerization in Glycopyranosides during the Cyclization of anomeric Radicals: Ease of the intramolecular 1,5-Hydrogen Atom TransferSynlett, 1994
- C(5)-Epimerization in Glycopyranosides During the Cyclization of Anomeric Radicals: A Comparison with GlycofuranosidesSynlett, 1992
- The temporary silicon connection method in the control of regio- and stereochemistry. Applications to radical-mediated reactions. The stereospecific synthesis of C-glycosidesJournal of the American Chemical Society, 1991
- Stereoselective C-C Bond Formation in Carbohydrates by Radical Cyclization Reactions; V. Application for the Synthesis of α-C (2) -Branched SugarsSynlett, 1990
- Stereoselective C-C Bond Formation in Carbohydrates by Radical Cyclization Reactions; VI. Influence of the Conformation of Anomeric Radicals on the Stereoselectivity of Their CyclizationSynlett, 1990
- On the direct epoxidation of glycals: application of a reiterative strategy for the synthesis of .beta.-linked oligosaccharidesJournal of the American Chemical Society, 1989
- Stereospecific reductive methylation via a radical cyclization desilylation processJournal of the American Chemical Society, 1986
- Radical cyclization-trapping in the synthesis of natural products. A simple, stereocontrolled route to prostaglandin F2.alpha.Journal of the American Chemical Society, 1986
- Free-radical cyclization of bromo acetals. Use in the construction of bicyclic acetals and lactonesJournal of the American Chemical Society, 1983
- The Direct Synthesis of Methyl 2,4-Di-O-benzyl-α-d-xylopyranoside by the Regiospecific Benzylation of Methyl α-d-XylopyranosideBulletin of the Chemical Society of Japan, 1982