C-Glycosides V- Synthesis of Aryl 2-Deoxy-α-D-C-Hexopyranosides by Reduction of Aryl 2-Oeoxy-α-D-C-Hex-2-Enopyranosioes
- 1 March 1988
- journal article
- research article
- Published by Taylor & Francis in Journal of Carbohydrate Chemistry
- Vol. 7 (1) , 141-149
- https://doi.org/10.1080/07328308808058909
Abstract
The reduction of two peracetylated aryl 2-deoxy-α-D-C-hex-2-enopyranosides by several reagents is described. The steric course of the reaction is discussed.Keywords
This publication has 7 references indexed in Scilit:
- On the steric course of the reduction of 2-alkoxy-4-pyranones: a remarkable demonstration of anomeric controlThe Journal of Organic Chemistry, 1985
- 1 The Chemistry and Biochemistry of C-Nucleosides and C-ArylglycosidesPublished by Elsevier ,1985
- Arylation de glycals catalysée par les sels de palladium: nouvelle synthèse de C-glycosidesCanadian Journal of Chemistry, 1983
- β-Elimination in aldonolactones. Synthesis of 3,6-dideoxy L-arabino-hexose (ascarylose)Carbohydrate Research, 1979
- Unsaturated ketonucleosides. Synthesis and properties of 7-(3,6-di-O-acetyl,2-deoxy-β-d-glycero-hex-2-enopyranosyl-4-ulose)theophyllineCarbohydrate Research, 1979
- Stereochemistry and mechanism of ketone reductions by hydride reagentsTetrahedron, 1979
- Reduction of ketones with incorporation of deuterium at the .alpha. position. Anomalous reduction of keto sugar derivativesThe Journal of Organic Chemistry, 1976