114201-07-9

Upstream product

• 123-75-1 pyrrolidine 
• 114201-02-4 3-bromo-1,4-dihydro-1,4-dioxo-α-(phenylmethylene)-2-naphthaleneacetonitrile 
• 114200-93-0 (E/Z)-3-bromo-1,4-dimethoxy-α-(phenylmethylene)-2-naphthaleneacetonitrile 
• 86489-90-9 2-bromo-3-(2-bromomethyl)-1,4-dimethoxynaphthalene 
• 114200-92-9 3-bromo-1,4-dimethoxy-2-naphthaleneacetonitrile 

Downstream Products

• 114201-14-8 (E/Z)-1,4-dimethoxy-α-(phenylmethylene)-3-(1-pyrrolidinyl)-2-naphthaleneacetonitrile 
• 114201-22-8 (11R,11aR)-11-Benzyl-5,10-dioxo-2,3,5,10,11,11a-hexahydro-1H-benzo[f]pyrrolo[1,2-a]indole-11-carbonitrile 

Relevant academic research and scientific papers

"tert-Amino Effect" in Heterocyclic Synthesis. The Effect of a p-Quinone Moiety on the H-Transfer and 1,5-Electrocyclization Reactions

(Dialkylamino)benzoquinone 15 and (dialkylamino)naphthoquinones 32 and 34-37 undergo a thermal cyclization to the corresponding pyrroloindoles 41, 43, and 45-47 and to the pyridoindole 44, respectively.A corresponding hydroquinone, viz. (E/Z