105880-45-3

Upstream product

• 18162-48-6 tert-butyldimethylsilyl chloride 
• 2043-61-0 cyclohexanecarbaldehyde 
• 108104-19-4 (+/-)-spiro(bicyclo<4.2.0>oct-2-ene-7,2'-<1,3>dioxolane) 
• 31996-68-6 bicyclo[4.2.0]-oct-2-en-7-one 
• 7560-69-2 1-cyclohexyl-2-propyn-1-one 
• 97563-45-6 1-cyclohexylprop-2-yn-1-ol 
• 105803-39-2 (S)-3-<(tert-Butyldimethylsilyl)oxy>-3-cyclohexyl-1-propyne 
• 108147-26-8 (1SR,2SR,4RS,7SR)-spiro(3-oxatricyclo<5.2.0.0>nonane-8,2'-<1,3>dioxolane) 
• 91098-88-3 (3S)-3-(tert-butyldimethyl-siloxy)-3-cyclohexylprop-1-yne 
• 105880-38-4 (1S)-1-cyclohexyl-2-propyn-1-ol 

Downstream Products

• 105880-66-8 RS₉₃₅₂₀ 
• 108147-34-8 (1S,2R,3S,6R)-2-((S)-3-Cyclohexyl-3-hydroxy-prop-1-ynyl)-3-hydroxy-bicyclo[4.2.0]octan-7-one 
• 108147-33-7 (1R,2S,3R,6S)-2-((R)-3-Cyclohexyl-3-hydroxy-prop-1-ynyl)-3-hydroxy-bicyclo[4.2.0]octan-7-one 
• 105880-46-4 C₃₈H₅₃NO₅Si 
• 105880-47-5 C₃₈H₅₃NO₅Si 

Relevant academic research and scientific papers

Potent Prostacyclin Analogues Based on the Bicyclooctane Ring System

The novel and biologically active prostacyclin mimetics 2 and 29 were prepared in a sequence based on the regioselective opening of epoxide 7 with a lithium acetylide in the presence of boron trifluoride etherate.The regioselectivity of epoxide opening wa