147103-50-2Relevant academic research and scientific papers
A stereoselective approach to nucleosides and 4′-thioanalogues from acyclic precursors
Chapdelaine, Daniel,Cardinal-David, Benoit,Prevost, Michel,Gagnon, Marc,Thumin, Isabelle,Guindon, Yvan
supporting information; experimental part, p. 17242 - 17245 (2010/03/25)
D- and L-nucleosides and analogues thereof, including the 4′-thionucleoside series, are one of the most important biological and pharmaceutically active classes of compounds. A novel approach to their synthesis from chiral acyclic thioaminal, bearing the nucleobase, is described.
THE STEREOCONTROLLED SYNTHESIS OF 1,2-CIS FURANOSYL NUCLEOSIDES VIA A NOVEL ANOMERIC ACTIVATION
Hanessian, Stephen,Conde, Jose J.,Lou, Boliang
, p. 5865 - 5868 (2007/10/02)
The coupling of 2-(2',3',5'-tri-O-benzyl-D-ribofuranosyloxy)-3-methoxypyridine as well as 2-(2',3',5'-tri-O-benzyl-D-ribofuranosyl)-thiopyridylcarbonate, with silylated pyrimidine bases by activation with trimethylsilyl trifluoromethanesulfonate and silve
Stereoselective Synthesis of 1,2-cis-N-Glycosides by the N-Bromosuccinimide Promoted Reaction of Thioglycosides with Silylated Pyrimidine Bases
Sugimura, Hideyuki,Muramoto, Ikuyo,Nakamura, Tadashi,Osumi, Kenji
, p. 169 - 172 (2007/10/02)
The coupling of O-benzylated 1-thioglycosides, derived from D-glucose, D-mannose, D-ribose, D-xylose, and D-arabinose, with silylated pyrimidine bases by activation with N-bromosuccinimide uniformly afforded the corresponding 1,2-cis-N-glycosides with good selectivity.
