81127-24-4

Upstream product

• 81127-23-3 5-[1,3]Dioxolan-2-ylmethyl-piperidin-3-ol 
• 501-53-1 benzyl chloroformate 
• 87499-81-8 benzyl 3-(1,3-dioxolan-2-ylmethyl)-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 81127-22-2 ethyl 5-(2-ethylenedioxyethyl)-3-hydroxypiperidine-1-carboxylate 
• 76525-44-5 ethyl 3-(1,3-dioxolan-2-ylmethyl)-1,2,3,6-tetrahydropyridine-1-carboxylate 
• 87499-79-4 benzyl 5-(1,3-dioxolan-2-ylmethyl)-3,4-epoxypiperidine-1-carboxylate 

Downstream Products

• 81127-26-6 benzyl (E)-5-(3-ethoxycarbonyl-2-propenyl)-3-hydroxypiperidine-1-carboxylate 
• 81127-27-7 benzyl (E)-5-(3-ethoxycarbonyl-2-propenyl)-3-oxopiperidine-1-carboxylate 
• 19508-69-1 C₂₆H₂₈N₂O₄S 
• 19508-69-1 C₂₆H₂₈N₂O₄S 
• 81127-37-9 (1R,4S,7R)-7-(2-Methanesulfonyloxy-ethyl)-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-37-9 (1R,4S,7S)-7-(2-Methanesulfonyloxy-ethyl)-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-35-7 (1R,4S,7R)-7-Ethoxycarbonylmethyl-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-35-7 (1R,4S,7S)-7-Ethoxycarbonylmethyl-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-34-6 (1R,4S,6R)-6-Ethoxycarbonylmethyl-7-oxo-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-34-6 (1R,4S,6S)-6-Ethoxycarbonylmethyl-7-oxo-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-36-8 (1R,4S,7R)-7-(2-Hydroxy-ethyl)-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-36-8 (1R,4S,7S)-7-(2-Hydroxy-ethyl)-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-38-0 (1R,4S,7S)-7-Ethyl-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 
• 81127-38-0 (1R,4S,7R)-7-Ethyl-6,6-dimethoxy-2-aza-bicyclo[2.2.2]octane-2-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

1,6-dihydro-3(2H)-pyridinones. X. 2-azabicyclooctane Ring Formation via Intramolecular Michael reaction: Total synthesis of (+/-)-Ibogamine and (+/-)-Epiibogamine

A new elaboration method for the 2-azabicyclooctane ring via an intramolecular Michael reaction has been developed and applied to the total synthesis of (+/-)-ibogamine (1) and (+/-)-epiibogamine (2).The unsaturated estert (9) derived from ethyl 1,