Development of an Arming Participating Group for Stereoselective Glycosylation and Chemoselective Oligosaccharide Synthesis
- 31 October 2005
- journal article
- research article
- Published by Wiley in Angewandte Chemie-International Edition
- Vol. 44 (43), 7123-7126
- https://doi.org/10.1002/anie.200502694
Abstract
No abstract availableKeywords
This publication has 36 references indexed in Scilit:
- Stereoselective Glycosylation Reactions with Chiral AuxiliariesAngewandte Chemie-International Edition, 2005
- Stereoselective Glycosylation Reactions with Chiral AuxiliariesAngewandte Chemie, 2005
- Potent, Versatile, and Stable: Thiazolyl Thioglycosides as Glycosyl DonorsAngewandte Chemie, 2004
- Catalytic and Chemoselective Glycosylation between “Armed” and “Disarmed” Glycosyl p-Trifluoromethylbenzylthio-p-trifluoromethylphenyl FormimidatesChemistry Letters, 2002
- Programmable One-Pot Oligosaccharide SynthesisJournal of the American Chemical Society, 1999
- Tuning glycoside reactivity: New tool for efficient oligosaccharide synthesisJournal of the Chemical Society, Perkin Transactions 1, 1998
- Synthesis of Disaccharides by Selective Metallocene Promoted Activation of Glycosyl FluoridesSynlett, 1996
- On the controlled oxidative coupling of glycals: a new strategy for the rapid assembly of oligosaccharidesJournal of the American Chemical Society, 1989
- Armed and disarmed n-pentenyl glycosides in saccharide couplings leading to oligosaccharidesJournal of the American Chemical Society, 1988
- A study of 13CH coupling constants in hexopyranosesJournal of the Chemical Society, Perkin Transactions 2, 1974