102728-49-4Relevant articles and documents
An easy and versatile approach for the regioselective De-O-benzylation of protected sugars based on the I2/Et3SiH combined system
Pastore, Antonello,Valerio, Silvia,Adinolfi, Matteo,Iadonisi, Alfonso
experimental part, p. 5881 - 5889 (2011/06/24)
The use of cheap and easy to handle reagents, such as I2 and Et3SiH, at low temperature allows the regioselective removal of benzyl protecting groups from highly O-benzylated carbohydrates. The observed regioselectivity is dependent
Synthesis of a branched pentasaccharide sequence of "bisected" structure of N-glycoproteins
Paulsen,Heume,Gyoergydeak,Lebuhn
, p. 57 - 70 (2007/10/02)
For the synthesis of the threefold-branched pentasaccharide, O-alpha-D-mannopyranosyl-(1----3)-O-[(2-acetamido-2-deoxy-beta-D- glucopyranosyl)-(1----4)]-O-[alpha-D-mannopyranosyl-(1----6)]-O-beta-D- mannopyranosyl-(1----4)-2-acetamido-2-deoxy-D-glucopyran