82659-55-0Relevant articles and documents
Highly Stereoselective Approaches to α- and β-C-Glycopyranosides
Lewis, Michael D.,Cha, Jin Kun,Kishi, Yoshito
, p. 4976 - 4978 (1982)
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Adaptable synthesis of C-glycosidic multivalent carbohydrates and succinamide-linked derivatization
Miller, Gavin J.,Gardiner, John M.
supporting information; experimental part, p. 5262 - 5265 (2011/02/24)
A modular approach to the synthesis of trivalent C-glycosidic carbohydrates is described. The approach is illustrated employing carboxylate-terminated C-glycosidic d-mannose, d-glucose, and d-galactose derivatives with different length C1-linked spacer un
Studies on the stereoselective synthesis of C-allyl glycosides
McGarvey, Glenn J.,Leclair, Christopher A.,Schmidtmann, Bahar A.
supporting information; experimental part, p. 4727 - 4730 (2009/06/05)
(Equation Presented) An investigation was carried out to explore the use of sulfoxide donors as common precursors to stereoisomeric C-glycoconjugates of glycoprotein and glycolipid tumor antigens. A study focusing on the effects of reaction conditions and substrate structure on the stereoselectivity of allylation was carried out. Although conditions were realized to selectively afford α-allylation products in good to excellent yields, the search for conditions favoring β-selectivity proved less successful.