862563-56-2

Upstream product

• 1655-07-8 ethyl 2-oxocyclohexane carboxylate 
• 108-98-5 thiophenol 
• 104316-13-4 2-(1-tert-butoxycarbonyl-2-methyl-propylamino)-cyclohex-1-enecarboxylic acid ethyl ester 
• 862563-53-9 2-benzenesulfonyl-1-methyl-cyclohex-2-enecarbaldehyde 
• 862563-60-8 (1-methyl-2-phenylsulfanyl-cyclohex-2-enyl)-methanol 
• 172825-16-0 (1R)-1-methyl-2-oxo-cyclohexanecarboxylic acid ethyl ester 
• 862563-55-1 C₁₉H₂₁NO₃S 
• 862563-51-7 1-methyl-2-phenylsulfanyl-cyclohex-2-enecarboxylic acid ethyl ester 
• 862563-54-0 (2-benzenesulfonyl-1-methyl-cyclohex-2-enylmethyl)-furan-2-ylmethyl-amine 
• 862563-52-8 1-methyl-2-phenylsulfanyl-cyclohex-2-enecarbaldehyde 

Downstream Products

• 862563-57-3 C₁₉H₂₃NO₂S 
• 862563-61-9 C₂₀H₂₂F₃NO₅S₂ 

Relevant academic research and scientific papers

Enantioselective approach to the hetisine alkaloids. Synthesis of the 3-methyl-1-aza-tricyclo[5.2.1.03,8]decane core via intramolecular dipolar cycloaddition

(Chemical Equation Presented) An efficient, enantioselective approach to the hetisine class of the C20-diterpenoid alkaloids is described. The strategy involves an intramolecular oxidopyridinium dipolar cycloaddition as the key transformation,