Study of the stereoselectivity of 2-azido-2-deoxyglucosyl donors: protecting group effects
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2013/OB/C3OB26994A
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1. The impact of oxacarbenium ion conformers on the stereochemical outcome of glycosylations
2. Stereodirecting Effect of the Pyranosyl C-5 Substituent in Glycosylation Reactions
3. Stereochemical Reversal of Nucleophilic Substitution Reactions Depending upon Substituent: Reactions of Heteroatom-Substituted Six-Membered-Ring Oxocarbenium Ions through Pseudoaxial Conformers
4. Stereochemistry of Nucleophilic Substitution Reactions Depending upon Substituent: Evidence for Electrostatic Stabilization of Pseudoaxial Conformers of Oxocarbenium Ions by Heteroatom Substituents
5. Structural Evidence that Alkoxy Substituents Adopt Electronically Preferred Pseudoaxial Orientations in Six-Membered Ring Dioxocarbenium Ions
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