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Organic Letters|October 6, 2006
1-naphthylpropargyl ether group: a readily cleaved and sterically minimal protecting system for stereoselective glycosylationDavid Crich, Baolin WuChimia|April 8, 2011
Synthesis of the beta-rhamnopyranosides and the 6-deoxy-beta-mannoheptopyranosidesSébastien Picard, David CrichOrganic Letters|October 2, 2008
Is donor-acceptor hydrogen bonding necessary for 4,6-O-benzylidene-directed beta-mannopyranosylation? Stereoselective synthesis of beta-C-mannopyranosides and alpha-C-glucopyranosidesDavid Crich, Indrajeet SharmaOrganic Letters|September 2, 2009
Reaction of thioacids with isocyanates and isothiocyanates: a convenient amide ligation processDavid Crich, Kaname SasakiOrganic Letters|August 22, 2008
Stereoselective iterative one-pot synthesis of N-glycolylneuraminic acid-containing oligosaccharidesDavid Crich, Baolin WuOrganic Letters|September 25, 2007
Revisiting the armed-disarmed concept: the importance of anomeric configuration in the activation of S-benzoxazolyl glycosidesDavid Crich, Ming LiAngewandte Chemie (International Ed. in English)|September 17, 2013
Chemical diversification of sialic acid glycosides by stereospecific, chemoselective deaminationChandrasekhar Navuluri, David CrichCarbohydrate Research|December 27, 2021
Unusual C-C bond cleavage of an α-trifloxy Sialic acid hemiacetal under Lattrell-Dax conditionsSantanu Jana, David CrichJournal of the American Chemical Society|October 24, 2018
Synthesis and Stereocontrolled Equatorially Selective Glycosylation Reactions of a Pseudaminic Acid Donor: Importance of the Side-Chain Conformation and Regioselective Reduction of Azide Protecting GroupsBibek Dhakal, David CrichPageof 28