Sequential One-Pot Glycosylations Using 1-Hydroxyl and 1-Thiodonors
- 1 May 2003
- journal article
- research article
- Published by American Chemical Society (ACS) in Organic Letters
- Vol. 5 (11) , 1947-1950
- https://doi.org/10.1021/ol034528v
Abstract
No abstract availableKeywords
This publication has 13 references indexed in Scilit:
- S-Benzoxazolyl (SBox) Glycosides as Novel, Versatile Glycosyl Donors for Stereoselective 1,2-Cis GlycosylationOrganic Letters, 2003
- Concise and Efficient Total Synthesis of Lycopodium Alkaloid MagellanineAngewandte Chemie International Edition in English, 2002
- A New, Iterative Strategy of Oligosaccharide Synthesis Based on Highly Reactive β-Bromoglycosides Derived from SelenoglycosidesOrganic Letters, 2001
- Rapid assembly of oligosaccharides: 1,2-diacetal-mediated reactivity tuning in the coupling of glycosyl fluoridesTetrahedron: Asymmetry, 2000
- Direct Glycosylations with 1-Hydroxy Glycosyl Donors using Trifluoromethanesulfonic Anhydride and Diphenyl SulfoxideJournal of the American Chemical Society, 1997
- Glycals in Organic Synthesis: The Evolution of Comprehensive Strategies for the Assembly of Oligosaccharides and Glycoconjugates of Biological ConsequenceAngewandte Chemie International Edition in English, 1996
- Synthesis of Methyl (Ethyl 2-O-acyl-3,4-di-O-benzyl-1-thio-.beta.-D-glucopyranosid)uronates and Evaluation of Their Use as Reactive .beta.-Selective Glucuronic Acid DonorsThe Journal of Organic Chemistry, 1995
- Recent progress in O-glycosylation methods and its application to natural products synthesisChemical Reviews, 1993
- Armed/disarmed effects in glycosyl donors: rationalization and sidetrackingThe Journal of Organic Chemistry, 1990
- On the controlled oxidative coupling of glycals: a new strategy for the rapid assembly of oligosaccharidesJournal of the American Chemical Society, 1989