V. Pejanovic, Zdenka Stokić, B. Stojanović
Jun 2, 2003
Citations
1
Influential Citations
10
Citations
Quality indicators
Journal
Bioorganic & medicinal chemistry letters
Abstract
1,2,3,5-tetra-O-acetyl-4-thio-beta-L-ribofuranose (13) was synthesized by an improved five-step sequence starting from methyl alpha-D-lyxopyranoside. Compound 13 was then converted to the corresponding L-4'-thionucleosides 4-6 and 19 by a modified Vorbrüggen procedure. All of these nucleoside analogues were tested for their antitumour activity in vitro.