385374-39-0Relevant articles and documents
Thiosugars. VIII. Preparation of new 4′-thio-L-lyxo pyrimidine nucleoside analogues
Wirsching, Joern,Voss, Juergen,Adiwidjaja, Gunadi,Balzarini, Jan,De Clercq, Erik
, p. 1625 - 1645 (2001)
Reaction of 1-O-acetyl-2,3,5-tri-O-benzyl-4-thio-L-lyxofuranose with silylated pyrimidine bases and subsequent deprotection with boron tribromide led to 4′-thio-L-lyxo pyrimidine nucleosides. The 5-bromo-6-methyl derivative was prepared from methyl 2,3,5-
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.