75622-27-4

Upstream product

• 72473-15-5 formyl-4 methoxycarbonyl-2 butanoate de methyle 
• 15741-79-4 N-benzyl tryptamine 
• 115757-56-7 2-[2-(2-Benzyl-2,3,4,9-tetrahydro-1H-β-carbolin-1-yl)-ethyl]-malonic acid dimethyl ester 

Downstream Products

• 75622-47-8 1,2,3,3a,4,5,6,7-octahydro-3-benzyl-7-oxo-azepino[1,2,3-lm]-β-carboline 
• 4802-79-3 1,2,3,4,6,7,12,12b-octahydroindolo(2,3-a)quinolizine 

Relevant academic research and scientific papers

Reduction of Lactams and Thiolactams by Sodium Borohydride: Application in the Synthesis of Some Alkaloids

Lactams 1a-8a and thiolactams 1b-8b,9a,10b-12b and 13 could be reduced to their corresponding amines in 70-98percent yield by using borohydide-tert-butyl alcohol-methanol mixtures under reflux.Even the vinylogous amide 19 underwent reduction to afford dep

Azepino [1,2,3-lm]-β-carboline compounds and pharmaceutical composition thereof

An azepino[1,2,3-lm]-β-carboline compound of the formula: STR1 wherein R1 is hydrogen, cycloalkyl of 3 to 7 carbon atoms, phenyl, hydroxy, alkoxycarbonyl of 2 or 3 carbon atoms or alkanoyl of 2 or 3 carbon atoms, and A is single bond or straigh