One-Pot Synthesis of Glucosamine Oligosaccharides Micha Fridman Dmitry Solomon Shay Yogev Timor Baasov 10.1021/ol017054d.s002 https://acs.figshare.com/articles/journal_contribution/One-Pot_Synthesis_of_Glucosamine_Oligosaccharides/3741252 Tuning the reactivity of glycosyl donors derived from 2-amino-2-deoxy glucose by selective introduction of different N-protecting (NPhth and NHTroc) and anomeric leaving groups (ethylthio and phenylthio) enabled highly efficient oligosaccharide synthesis in a one-pot manner. One-pot sequential glycosylation of three and four units of 2-amino-2-deoxy glucose gave trisaccharides and tetrasaccharide in 50−81% yields. 2001-12-29 00:00:00 glycosyl donors manner ethylthio anomeric NPhth glycosylation introduction reactivity sequential tetrasaccharide glucose yield phenylthio trisaccharide NHTroc oligosaccharide synthesis Glucosamine Oligosaccharides Tuning Synthesi