98206-34-9

Upstream product

• 85203-06-1 3-(benzyl(phenyl)amino)cyclohex-2-en-1-one 
• 504-02-9 1,3-cylohexanedione 
• 134256-34-1 2-Methyl-3-phenylamino-cyclohex-2-enone 
• 99459-02-6 9-benzyl-1,2,3,4a,9,9a-hexahydrocarbazol-4-one 
• 74-88-4 methyl iodide 
• 758640-21-0 N-Benzylaniline 

Downstream Products

• 98206-37-2 (4aR,9aS)-9-Benzyl-4a-methyl-1,2,3,4a,9,9a-hexahydro-carbazol-4-one 

Relevant academic research and scientific papers

A Novel and Efficient Synthesis of the Aspidosperma Alkaloid Ring System: N(a)-Benzyldeethylaspidospermidine

Nonoxidative photocyclization of the aryl enaminone 3 led to the formation of the hexahydrocarbazol-4-one 4.Alkylation of the anion derived from 4 with iodoacetamide and dehydration gave the tetracyclic enamide 9, which was reduced to the imine 10 with Li

SYNTHESE STEREOSPECIFIQUE PAR VOIE PHOTOCHIMIQUE DE TRANS HEXAHYDRO-1,2,3,4,4a,9a CARBAZOLONES-4 SUBSTITUEES EN 4a

Trans hexahydrocarbazol-4-ones substituted in 4a position were obtained quantitatively and stereospecifically by photocyclisation of tertiary aryl enaminones.