1627-29-8Relevant academic research and scientific papers
4-alkylated 2-(2,3,5-tri-O-acyl-β-D-ribofuranosyl)- and 2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-1,2,4-triazine-3,5-diones
Harutyunyan,Panosyan,Tamazyan,Aivazyan,Danagulyan
, p. 573 - 576 (2017)
The alkylation of 2-(2,3,5-tri-O-acyl-β-D-ribofuranosyl)- and 2-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)- 1,2,4-triazine-3,5-diones with benzyl halides afforded the corresponding 4-benzyl derivatives whose structure was determined by spectral methods, including X-ray analysis. Some of the synthesized compounds were tested for antibacterial and antitumor activity.
An economical synthesis of D- and L-pyrimidine arabinoand ribonucleosides
Lazrek, Hassan B.,Ouzebla, Driss,Faraj, Abdesslem
experimental part, p. 227 - 234 (2012/04/18)
The one-step synthesis of several β-D/L-arabino- and ribonucleosides was performed in good yields under reflux or microwave-assisted fusion method. A comparison of the two methods showed that better yields were obtained using the reflux conditions. Copyright Taylor and Francis Group, LLC.
TRIMETHYLIODOSILANE IN THE GLYCOSYLATION OF 5-SUBSTITUTED 6-AZAURACILS
Kobylinskaya, V. I.,Dashevskaya, T. A.,Shalamai, A. S.,Levitskaya, Z. V.
, p. 912 - 915 (2007/10/02)
Intermediate quaternary salts of heterocycles with trimethyliodosilane are formed in glycosylation of 2,4-bistrimethylsilylized 5-substituted 6-azauracils with the participation of trimethyliodosilane as condensing medium.
