184025-35-2

Upstream product

• 184025-97-6 C₂₀H₂₄O₃Se 
• 184025-27-2 ((1S,6S)-6-Benzyloxymethyl-cyclohex-2-enyl)-acetic acid ethyl ester 
• 163812-77-9 (1R,2R,4S)-4-(benzyloxymethyl)-2-(phenylseleno)-1-cyclohexanol 
• 163956-42-1 (1R,2S,4S)-4-(benzyloxymethyl)-1,2-epoxycyclohexane 
• 163812-76-8 (1S,2S,4S)-4-(hydroxymethyl)-1-iodo-2-cyclohexanol 
• 100-39-0 benzyl bromide 
• 5708-19-0 (1S)-3-cyclohexenecarboxylic acid 
• 179091-38-4 (1S,4S)-4-Benzyloxymethyl-cyclohex-2-enol 
• 163812-78-0 (1R,4S)-4-(benzyloxymethyl)-2-cyclohexen-1-ol 
• 178945-61-4 (1'S,6'S)-2-(6'-benzyloxymethyl-2'-cyclohexenyl)ethanol 

Downstream Products

• 178945-62-5 (3aS,4S,7aS)-4-Benzyloxymethyl-1-methylene-octahydro-indene 
• 179091-39-5 ((1S,2S)-2-But-3-ynyl-cyclohex-3-enylmethoxymethyl)-benzene 

Relevant academic research and scientific papers

Palladium catlyzed reductive cyclization reaction in alkaloid synthesis - an enantioselective total synthetic route to (+)-pumiliotoxin C

Beginning with the chirally homogeneous cyclohexenol 3, an enantioselective total synthetic route to (+)-pumiliotoxin C (1) has been described. Palladium catalyzed reductive cyclization reaction was employed to prepare a key component in the synthesis. Co