681811-55-2

Upstream product

• 681811-54-1 (+)-N-[1-((2S,3R,4R)-3-benzyloxy-4-benzyloxymethyltetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl]benzamide 
• 681811-49-4 (3R,4R)-4-benzyloxymethyl-2-methoxytetrahydrofuran-3-ol 
• 14048-38-5 (3aR,6aR)-2,2-dimethyl-6-methylenetetrahydrofuro[2,3-d][1,3]dioxole 
• 25904-08-9 (-)-((3aR,6R,6aR)-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxol-6-yl)methanol 
• 681811-52-9 acetic acid (3R,4R)-3-benzyloxy-4-benzyloxymethyltetrahydrofuran-2-yl ester 
• 681811-50-7 (3R,4R)-3-benzyloxy-4-benzyloxymethyl-2-methoxytetrahydrofuran 
• 681811-48-3 (-)-(3aR,6R,6aR)-6-benzyloxymethyl-2,2-dimethyltetrahydrofuro[2,3-d][1,3]dioxole 

Relevant academic research and scientific papers

Synthesis of D- and L-apio nucleoside analogues with 2′-hydroxyl group as potential anti-HIV agents

The present work describes the asymmetric synthesis of D- and L-apio-2′,3′-dideoxynucleoside analogues, 4 and 5 with 2′-hydroxyl group via a common intermediate 9, starting from D-galactose. Stereoselective dihydroxylation and deoxygenation through radica