163592-77-6

Upstream product

• 190733-40-5 (3aR,5S,6S,6aR)-6-Benzyloxy-2,2-dimethyl-5-((R)-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-yl)-tetrahydro-furo[2,3-d][1,3]dioxole 
• 158946-12-4 3-O-benzyl 1,2-O-isopropylidene-5,6-O-sulfuryl-α-D-glucofuranose 
• 22529-61-9 (1R)-1-((3aR,6S,6aR)-6-(benzyloxy)-2,2-dimethyltetrahydrofuro(2,3-d)(1,3)dioxol-5-yl)ethane-1,2-diol 

Downstream Products

• 190599-82-7 6-O-acetyl-5-S-acetyl-3-O-benzyl-1,2-O-isopropylidene-5-thio-β-L-idofuranose 
• 190599-86-1 5-S-acetyl-3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-thio-β-L-idofuranose 
• 190599-84-9 3-O-benzyl-6-deoxy-1,2-O-isopropylidene-5-thio-β-L-idofuranose 

Relevant academic research and scientific papers

Synthesis of Sugar Episulfides and Olefins from vic-Diols via Cyclic Sulfates

Cyclic sulfates of vic-diols are transformed in one-pot into sugar episulfides by treatment with potassium thioacetate or thiourea followed by reaction with sodium methoxide; reaction of these cyclic sulfates with potassium selenocyanate followed by treat

Applications of Cyclic Sulfates of vic-Diols: Synthesis of Episulfides, Olefins, and Thio Sugars

A new efficient and expeditious one-pot synthesis of thiiranes and olefins from cyclic sulfates of inc-diols is described. Opening of cyclic sulfates with potassium thioacetate or potassium thiocyanate followed by treatment with sodium methoxide led to ep