1374991-75-9

Upstream product

• 1261154-81-7 (2S,3S)-4-(tert-butyldiphenylsilyloxy)-2-methylbutane-1,3-diol 
• 26291-75-8 (R)-1-((3aR,5S,6R,6aR)-2,2,6-trimethyl-3a,5,6,6a-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)ethane-1,2-diol 
• 1374991-67-9 (6S,7S)-6-(methoxymethoxy)-2,2,7,10,10,11,11-heptamethyl-3,3-diphenyl-4,9-dioxa-3,10-disiladodecane 
• 1374991-68-0 (2S,3S)-4-(tert-butyldiphenylsilyloxy)-3-(methoxymethoxy)-2-methylbutyl 4-methylbenzenesulfonate 
• 78785-15-6 3-deoxy-1,2-O-isopropylidene-3-C-methyl-α-D-ribo-pentodialdo-1,4-furanose 
• 30080-45-6 ((3aR,5S,6R,6aR)-2,2,6-trimethyl-tetrahydrofuro[2,3-d][1,3]dioxol-5-yl)methanol 
• 1374991-74-8 C₂₃H₃₄O₄Si 
• 1374991-73-7 C₂₇H₄₄O₃Si₂ 

Downstream Products

• 1374991-76-0 C₁₇H₂₂N₄O₂S 

Relevant academic research and scientific papers

A carbohydrate approach for the formal total synthesis of the prostacyclin analogue (16S)-iloprost

The formal total synthesis of the synthetic and stable analogue of prostacyclin, (16S)- iloprost is described via a convergent synthesis starting from readily available d-glucose. Julia olefination and the aldol reaction are the key steps involved in the synthesis.