144217-03-8Relevant articles and documents
4-Deoxy-4-fluoro-xyloside derivatives as inhibitors of glycosaminoglycan biosynthesis
Tsuzuki, Yasuhiro,Nguyen, Thao Kim Nu,Garud, Dinesh R.,Kuberan, Balagurunathan,Koketsu, Mamoru
supporting information; experimental part, p. 7269 - 7273 (2011/01/12)
Various 4-deoxy-4-fluoro-xylosides were prepared using click chemistry for evaluating their potential utility as inhibitors of glycosaminoglycan biosynthesis. 2,3-Di-O-benzoyl-4-deoxy-4-fluoro-β-d-xylopyranosylazide, obtained from l-arabinopyranose by six
Potential Antiviral Agents. Stereospecific Synthesis of Purines and Pyrimidines Substituted with Chiral Acyclic Chains by Sugar-Ring Opening of &α-L-Arabinopyranosyl Nucleosides
Perigaud, Christian,Gosselin, Gilles,Imbach, Jean-Louis
, p. 1943 - 1952 (2007/10/02)
3',4'-Seco-nucleosides as well as their derivatives lacking C-3', all retain the carbon framework and chirality of the β-D-ribofuranosyl moiety of the nucleosides occurring in nucleic acids, have been synthesized and their antiviral properties examined.Mo