93451-41-3Relevant academic research and scientific papers
Automated Solution-Phase Synthesis of S-Glycosides for the Production of Oligomannopyranoside Derivatives
Kern, Mallory K.,Pohl, Nicola L. B.
, (2020/06/08)
Thioglycosides are more resistant to enzymatic hydrolysis than their O-linked counterparts, thereby becoming attractive targets for carbohydrate-based therapeutic development. We report the first development of methods for the site-selective incorporation
Total synthesis of the fully lipidated glycosylphosphatidylinositol (GPI) anchor of malarial parasite Plasmodium falciparum
Ali, Asif,Vishwakarma, Ram A.
experimental part, p. 4357 - 4369 (2010/07/06)
We report a new and convergent strategy for the total synthesis of fully lipidated glycosylphosphatidylinositol (GPI) anchor, the major pro-inflammatory factor of malarial parasite (Plasmodium falciparum). The key features of our approach include, the acc
A new approach to construct full-length glycosylphosphatidylinositols of parasitic protozoa and [4-deoxy-Man-III]-GPI analogues
Ali, Asif,Gowda, D. Channe,Vishwakarma, Ram A.
, p. 519 - 521 (2008/09/18)
A new [2 + 2 + 2] approach to construct GPI molecules through the efficient synthesis of glucosamine-inositol and tetramannose intermediates led to a total synthesis of a GPI-anchor of Trypanosoma cruzi, and also afforded a key intermediate for the synthe
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
