A new route to C-glycosyl compounds. Wittig-type reaction promoted by zinc
- 1 February 1992
- journal article
- research article
- Published by Elsevier in Carbohydrate Research
- Vol. 224, 301-306
- https://doi.org/10.1016/0008-6215(92)84116-a
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- The Wittig-Horner reaction on 2,3,4,6-tetra-O-benzyl-D-mannopyranose and 2,3,4,6-tetra -O-benzyl-D-glucopyranoseJournal of the Chemical Society, Perkin Transactions 1, 1989
- Synthesis of C-glycosyl compounds by the wittig iodocyclization procedure. Differences from mercuriocyclizationCarbohydrate Research, 1987
- Stereocontrolled routes to functionalized C-glycopyranosidesThe Journal of Organic Chemistry, 1984
- Synthesis of saccharides and related polyhydroxylated natural products. 4. .alpha.-D- and .beta.-D-C-Glycopyranosides (2,6-dialkyl-substituted tetrahydropyrans)Journal of the American Chemical Society, 1982
- Highly stereoselective approaches to .alpha.- and .beta.-C-glycopyranosidesJournal of the American Chemical Society, 1982
- Synthesis of phosphonate analogs of α-d-glucopyranosyl and α-d-galactopyranosyl phosphateCarbohydrate Research, 1981
- Mercuricyclisation in carbohydrate chemistry: a highly stereoselective route to α-D-C-glucopyranosyl derivativesJournal of the Chemical Society, Chemical Communications, 1981
- Stereoselective routes to some unsaturated α- and β-C-glycopyranosidesCanadian Journal of Chemistry, 1979
- C-Glycosyl nucleosides. V. Unexpected observations on the relative stabilities of compounds containing fused five-membered rings with epimerizable substituentsJournal of the American Chemical Society, 1975
- The Wittig Reaction in Carbohydrate ChemistryPublished by Elsevier ,1972