168424-13-3

Upstream product

• 67-56-1 methanol 
• 82267-01-4 (2S,3S,4R,5R)-3,4-bis(benzyloxy)-5-((benzyloxy)methyl)tetrahydrofuran-2-carbonitrile 
• 75172-84-8 2,3,5-tri-O-benzyl-1-O-(p-nitrobenzoyl)-α,β-D-ribofuranose 

Downstream Products

• 168424-15-5 5-(2',3',5'-Tri-O-benzyl-β-D-ribofuranosyl)-3,6-bis(trifluormethyl)-1,2,4-triazin 

Relevant academic research and scientific papers

Synthesis of the first 1,2,4-triazine C-nucleoside and its transformation to novel pyridine C-nucleosides by 'inverse' [4 + 2]-cycloaddition reactions

The anomeric C-glycosyl precursors 6 and 7, appropriate for C-nucleoside synthesis and functionalized by an imidate group, were prepared. They were utilized as heterodienophiles in a Diels-Alder reaction with inverse electron demand to yield the O-benzyl

A new C-nucleoside analogue of tiazofurin: Synthesis and biological evaluation of 2-β-D-ribofuranosylimidazole-4-carboxamide (imidazofurin)

2-β-D-Ribofuranosylimidazole-4-carboxamide, an imidazole analogue of the antitumor agent tiazofurin, was synthesized and evaluated for the growth inhibitory activity of human myelogenous leukemia K562 cells. (C) 2000 Elsevier Science Ltd.