95475-35-7Relevant 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
Glycosylation using hemiacetal sugar derivatives: Synthesis of O-α-D-rhamnosyl-(1 → 3)-O-α-D-rhamnosyl-(1 → 2) -D-rhamnose and O-α-D-tyvelosyl-(1 → 3)-O-α-D-mannosyl-(1 → 4)-L-rhamnose
Hirooka, Motoko,Yoshimura, Asako,Saito, Izumi,Ikawa, Fumio,Uemoto, Yoko,Koto, Shinkiti,Takabatake, Ayano,Taniguchi, Aya,Shinoda, Yoshika,Morinaga, Aya
, p. 1409 - 1421 (2007/10/03)
O-α-D-Rhamnopyranosyl-(1 → 3)-O-α-D-rhamnopyranosyl-(1 → 2)-D-rhamnopyranose, a repeating trisaccharide of the O-specific polysaccharides (OPSs) of Pseudomonades, and O-α-D-tyvelopyranosyl-(1 → 3)-O-α-D-mannopyranosyl-(1 → 4)-L-rhamnopyranose, a trisaccha
A Simple Synthesis of Methyl 2,3,6- and 2,4,6-Tri-O-benzyl-α-D-mannosides
Koto, Shinkiti,Takenaka, Kazuhiro,Morishima, Naohiko,Sugimoto, Akiko,Zen, Shonosuke
, p. 3603 - 3604 (2007/10/02)
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