Document Type
Article
Keywords
Carbohydrates, Glycosylation, Intramolecular reactions, Oligosaccharides
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
9-29-2017
Publication Title
Beilstein Journal of Organic Chemistry
E-ISSN
18605397
Volume
13
First Page
2028
Last Page
2048
Rights
CC BY
DOI
10.3762/bjoc.13.201
Funding Number
GM111835
Funding Sponsor
National Institute of General Medical Sciences
Recommended Citation
Jia, Xiao G. and Demchenko, Alexei V., "Intramolecular glycosylation" (2017). Chemistry & Biochemistry Faculty Works. 106.
DOI: https://doi.org/10.3762/bjoc.13.201
Available at:
https://irl.umsl.edu/chemistry-faculty/106