@article { WOS:000308978800001,
	title = {Automated synthesis of sialylated oligosaccharides},
	journal = {BEILSTEIN JOURNAL OF ORGANIC CHEMISTRY},
	volume = {8},
	year = {2012},
	month = {SEP 21},
	pages = {1601-1609},
	abstract = {Sialic acid-containing glycans play a major role in cell-surface interactions with external partners such as cells and viruses. Straightforward access to sialosides is required in order to study their biological functions on a molecular level. Here, automated oligosaccharide synthesis was used to facilitate the preparation of this class of biomolecules. Our strategy relies on novel sialyl alpha-(2 -\&gt; 3) and alpha-(2 -\&gt; 6) galactosyl imidates, which, used in combination with the automated platform, provided rapid access to a small library of conjugation-ready sialosides of biological relevance.},
	issn = {1860-5397},
	doi = {10.3762/bjoc.8.183},
	url = {https://www.beilstein-journals.org/bjoc/articles/8/183},
	author = {Esposito, Davide and Mattan Hurevich and Castagner, Bastien and Wang, Cheng-Chung and Seeberger, Peter H.}
}
