39506-08-6

Upstream product

• 42543-45-3 3,4,5-trimethoxybenzoyl azide 
• 64-17-5 ethanol 
• 541-41-3 chloroformic acid ethyl ester 
• 24313-88-0 3,4,5-Trimethoxyaniline 
• 118-41-2 Eudesmic acid 

Downstream Products

• 950508-46-0 N-allyl-N-carbethoxy-3,4,5-trimethoxy-benzenamine 
• 124346-71-0 N-methyl-3,4,5-trimethoxyaniline 
• 950508-55-1 (αR,3aS,9bS)-5-carbethoxy-1-(1-phenyl-2-hydroxyethyl)-7,8,9-trimethoxy-1,3a,4,9b-tetrahydro-3H-isoxazolo[4,3-c]quinoline 
• 950508-54-0 (αR,3aR,9bR)-5-carbethoxy-1-(1-phenyl-2-hydroxyethyl)-7,8,9-trimethoxy-1,3a,4,9b-tetrahydro-3H-isoxazolo[4,3-c]quinoline 
• 950508-51-7 N-allyl-N-carbethoxy-2-formyl-3,4,5-trimethoxy-benzenamine 

Relevant academic research and scientific papers

Synthesis of enantiopure 4-amino-3-hydroxymethyl-tetrahydroquinolines via an intramolecular nitrone cycloaddition

Enantiopure 4-amino-3-hydroxymethyl-1,2,3,4-tetrahydroquinolines are synthesized by using an intramolecular cycloaddition of chiral nitrones prepared from aldehydes 5 and (R)-α-(hydroxymethyl)benzylhydroxylamine. Reaction times of the nitrone cycloadditio