678183-45-4

Upstream product

• 678183-46-5 1-(2-bromobenzyl)-3a-methyl-1,3,3a,4,5,6-hexahydroindol-2-one 
• 100-46-9 benzylamine 
• 3959-05-5 2-bromobenzylamine 
• 58711-31-2 (1-methyl-2-oxo-cyclohexyl)-acetic acid 
• 203244-99-9 1-benzyl-3a-methyl-1,3,3a,4,5,6-hexahydroindol-2-one 

Relevant academic research and scientific papers

A study of vinyl radical cyclization using N-alkenyl-7-bromo-substituted hexahydroindolinones

(Chemical Equation Presented) A new method for the synthesis of the octahydropyrrolo[3,2,1-ij]quinoline ring system that possesses the characteristic skeleton of the aspidosperma family of alkaloids has been developed. The method utilizes an intramolecula

Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones

(Equation presented) Radical cyclization of N-allyl-7-bromo-3a-methyl- hexahydroindol-2-one affords a six-membered ring product that prevails over the isomeric five-membered compound. The former product is generated through two reaction pathways: (a) 6-en