154920-34-0Relevant articles and documents
Solid- and solution-phase synthesis of heparin and other glycosaminoglycans
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, (2008/06/13)
Described is a modular, general synthetic strategy for the preparation in solution and on a solid support of heparin, heparin-like glycosaminoglycans, glycosaminoglycans and non-natural analogs of each of them. Additionally, the modular strategy provides
Modular synthesis of heparin oligosaccharides
Orgueira, Hernan A.,Bartolozzi, Alessandra,Schell, Peter,Litjens, Remy E. J. N.,Palmacci, Emma R.,Seeberger, Peter H.
, p. 140 - 169 (2007/10/03)
A general, modular strategy for the first completely stereoselective synthesis of defined heparin oligosaccharides is described. Six monosaccharide building blocks (four differentially protected glucosamines, one glucuronic and one iduronic acid) were uti
Dispiroketals in synthesis (part 5): A new opportunity for oligosaccharide synthesis using differentially activated glycosyl donors and acceptors
Boons, Geert-Jan,Grice, Peter,Leslie, Ray,Ley, Steven V.,Yeung, Lam Lung
, p. 8523 - 8526 (2007/10/02)
The reactivity of dispiroketal protected thioglycosides makes them useful new precursors for oligosaccharide synthesis as is illustrated by the preparation of a protected pentasaccharide unit common to the variant surface glycoprotein of Trypanosoma bruce