| Literature DB >> 28741787 |
Rens A Mensink1, Thomas J Boltje1.
Abstract
The control of stereoselectivity in a glycosylation reaction remains one of the most challenging aspects of oligosaccharide synthesis. Especially the synthesis of 1,2-cis-glycosides is challenging and generally applicable methodology to prepare this linkage is needed to standardize oligosaccharide synthesis. This review highlights the recent development of an elegant strategy employing a C-2 auxiliary to control the anomeric stereoselectivity in glycosylations. The various auxiliaries developed to date, their compatibility with protecting groups and monosaccharide types as well as mechanistic aspects are summarized. Furthermore, the application, advantages and limitations of C-2 auxiliaries in oligosaccharide synthesis are discussed.Entities:
Keywords: chiral auxiliary; glycosylation; oligosaccharides; stereoselectivity; sulfonium ion
Year: 2017 PMID: 28741787 DOI: 10.1002/chem.201700908
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236