Radical intermediates in the stereoselective synthesis of C-glycosides
- 1 January 1999
- book chapter
- Published by Elsevier
Abstract
No abstract availableThis publication has 70 references indexed in Scilit:
- Samarium Diiodide PromotedC-Glycosylation: An Application to the Stereospecific Synthesis ofα-1,2-C-Mannobioside and Its DerivativesChemistry – A European Journal, 1999
- A General Approach to 1,2-trans-C-Glycosides via Glycosyl Samarium(III) CompoundsChemistry – A European Journal, 1998
- Stereocontrolled Synthesis of α-C-Galactosamine Derivatives via Chelation-Controlled C-GlycosylationThe Journal of Organic Chemistry, 1998
- An Unusual Route to Deoxysugars by Hydrogen Atom Transfer from Cyclohexane. Possible Manifestation of Polar Effects in a Radical ProcessJournal of the American Chemical Society, 1996
- Sequenced Reactions with Samarium(II) Iodide. Tandem Nucleophilic Acyl Substitution/Ketyl−Olefin Coupling ReactionsJournal of the American Chemical Society, 1996
- Conformation and reactivity of anomeric radicalsJournal of the American Chemical Society, 1992
- Application of lanthanide reagents in organic synthesisChemical Reviews, 1992
- Kinetics and mechanism of the exo cyclizations of .omega.-formylalkyl radicalsJournal of the American Chemical Society, 1989
- Surprisingly efficient intramolecular addition of carbon radicals to carbonyl groups: a ready route to cycloalkanolsJournal of the American Chemical Society, 1986
- A general preparative method for .alpha.-lithioethers and its application to a concise, practical synthesis of brevicominJournal of the American Chemical Society, 1980