78673-97-9

Upstream product

• 78673-99-1 3-[(6-Bromo-benzo[1,3]dioxol-5-ylmethyl)-(2-chloro-ethyl)-amino]-cyclohex-2-enone 
• 78673-98-0 3-[(6-Bromo-benzo[1,3]dioxol-5-ylmethyl)-(2-bromo-ethyl)-amino]-cyclohex-2-enone 
• 15930-53-7 6-bromo-3,4-methylenedioxybenzaldehyde 
• 78673-96-8 2-{[1-(6-Bromo-benzo[1,3]dioxol-5-yl)-meth-(E)-ylidene]-amino}-ethanol 
• 78674-00-7 3-[(6-Bromo-benzo[1,3]dioxol-5-ylmethyl)-(2-hydroxy-ethyl)-amino]-cyclohex-2-enone 
• 78688-43-4 2-[(6-Bromo-benzo[1,3]dioxol-5-ylmethyl)-amino]-ethanol 

Relevant academic research and scientific papers

INTRAMOLECULAR Cα- AND Cγ-ALKYLATIONS OF TERTIARY ENAMINONES. FACILE ROUTES TO FUNCTIONALIZED INDOLE RING SYSTEMS

Under the suitably controlled conditions, the tertiary enaminones undergo intramolecular ring formation at Cα and Cγ to give 1-(2-bromo-4,5-methylenedioxybenzyl)tetra(or hexa)hydro-4(or 6)-oxoindoles which can serve as potential precursors to lycoranes.