O-Picoloyl groups at remote positions can mediate the course of glycosylation reactions by providing high facial selectivity for the H-bond-mediated attack of the glycosyl acceptor. A new practical method for the stereoselective synthesis of β-mannosides at ambient temperature is presented.
Download full-text PDF |
Source |
|---|---|
| http://dx.doi.org/10.1021/ol403396j | DOI Listing |
Publication Analysis
Top Keywords
hydrogen-bond-mediated aglycone
4
aglycone delivery
4
delivery focus
4
focus β-mannosylation
4
β-mannosylation o-picoloyl
4
o-picoloyl groups
4
groups remote
4
remote positions
4
positions mediate
4
mediate course
4
Similar Publications
Want AI Summaries of new PubMed Abstracts delivered to your In-box?
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!