170935-56-5

Upstream product

• 67-56-1 methanol 
• 170935-55-4 5-O-benzoyl-2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 
• 1207872-17-0 C₁₀H₂₀O₃S₂ 
• 98-88-4 benzoyl chloride 
• 77735-30-9 4,5-di-O-acetyl-2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 
• 77735-33-2 2,3-di-S-ethyl-2,3-dithio-D-ribose diethyl dithioacetal 

Downstream Products

• 17081-07-1 methyl 5-O-benzoyl-2,3-dideoxy-β-D-erythro-pentofuranoside 
• 132575-43-0 5-O-benzoyl-2,3-dideoxy-D-glycero-pentofuranose 
• 1207872-24-9 C₁₆H₂₁N₃O₃S₂ 

Relevant academic research and scientific papers

Synthesis and antitumor activity of novel 2′,3′-dideoxy-2′,3′-diethanethionucleosides bearing 1,2,3-triazole residues

A series of novel 2′,3′-dideoxy-2′,3′-diethanethioribonucleosides and those modified with a triazole ring were prepared in excellent yields and their antitumor activity was evaluated. Nucleosides with a triazole ring, 16a-16c, showed significantly improved activity towards a broad range of tumor cell lines.

Fischer indole synthesis with selected 2,3-dideoxy-D-glycero-aldopentose derivatives. Conversion of d-xylose to (2S)-3-(indol-3-YL)propane-1,2-diol

Two independent routes towards (2S)-3-(indol-3-yl)propane-1,2-diol (11) were achieved starting from 3,5-di-O-acetyl-1,2-O-cyclohexylidene-α-D-xylofuranose (1). Ethanethiolysis of 1 afforded acyclic diethyl dithioacetal 2 which was further O-deacetylated t