139750-89-3

Upstream product

• 1075724-76-3 phenyl 3-[1-(benzyloxycarbonyl)-3-ethyl-1,2,5,6-tetrahydro-2-pyridyl]indole-2-carboselenoate 
• 139758-45-5 C₂₄H₂₆N₂O₂ 
• 48210-16-8 2-(1-benzyl-3-ethyl-piperidin-4-ylmethyl)-indole 
• 128350-31-2 2-(1-Benzyl-2-cyano-3-ethyl-piperidin-4-ylmethyl)-indole-1-carboxylic acid tert-butyl ester 
• 130291-34-8 (1RS,5RS,12SR)-12-ethyl-1,2,3,4,5,6-hexahydro-1,5-methanoazocino<4,3-b>indole 
• 128350-30-1 C₂₃H₂₆N₂ 

Downstream Products

• 2744-46-9 (+/-)-dasycarpinol 
• 2744-46-9 C₁₇H₂₂N₂O 
• 3620-81-3 (+/-)-nordasycarpidone 

Relevant academic research and scientific papers

A new acyl radical-based route to the 1,5-methanoazocino[4,3-b]indole framework of uleine and strychnos alkaloids

(Chemical Equation Presented) C-4 or C-12 ethyl substituted 1,5-methanoazocino[4,3-b]indoles, which constitute the tetracyclic framework of uleine alkaloids as well as the ABDE substructure of the Strychnos alkaloid family, have been synthesized by novel 6-exo and 6-endo cyclizations of selenoester-derived 2-indolylacyl radicals upon 5-ethyl-1,2,3,6- and 3-ethyl-1,2,5,6-tetrahydropyridines, respectively.