Document Type
Article
Abstract
Carbohydrate oligomers remain challenging targets for chemists due to the requirement for elaborate protecting and leaving group manipulations, functionalization, tedious purification, and sophisticated characterization. Achieving high stereocontrol in glycosylation reactions is arguably the major hurdle that chemists experience. This review article overviews methods for intramolecular glycosylation reactions wherein the facial stereoselectivity is achieved by tethering of the glycosyl donor and acceptor counterparts.
Publication Date
September 2017
Publication Title
Beilstein Journal of Organic Chemistry
Volume
13
First Page
2028
Last Page
2048
DOI
10.3762/bjoc.13.201
Recommended Citation
Demchenko, Alexei and Jia, Xiao, "Intramolecular Glycosylation" (2017). Chemistry & Biochemistry Faculty Works. 34.
DOI: https://doi.org/10.3762/bjoc.13.201
Available at:
https://irl.umsl.edu/chemistry-faculty/34