85203-07-2

Upstream product

• 75-03-6 ethyl iodide 
• 85203-06-1 3-(benzyl(phenyl)amino)cyclohex-2-en-1-one 
• 504-02-9 1,3-cylohexanedione 
• 758640-21-0 N-Benzylaniline 

Downstream Products

• 85203-08-3 3-(N-benzylanilino)-6-(3-chloropropyl)-6-ethylcyclohex-2-en-1-one 
• 73367-84-7 6-(3-azidopropyl)-6-ethyl-3-(N-(methoxycarbonyl)anilino)cyclohexa-2,4-dien-1-one 
• 73367-82-5 6-(3-azidopropyl)-6-ethyl-3-(N-(methoxycarbonyl)anilino)cyclohex-2-en-1-one 
• 73367-83-6 6-(3-azidopropyl)-4-bromo-6-ethyl-3-(N-(methoxycarbonyl)anilino)cyclohex-2-en-1-one 
• 85203-09-4 3-anilino-6-(3-chloropropyl)-6-ethylcyclohex-2-en-1-one 
• 85203-11-8 6-(3-azidopropyl)-6-ethyl-3-anilinocyclohexa-2,4-dien-1-one 
• 85220-70-8 6a-Ethyl-9-phenylamino-4,5,6,6a,9a,9b-hexahydro-[1,2,3]triazolo[4,5,1-ij]quinolin-7-one 
• 85203-10-7 6-(3-chloropropyl)-6-ethyl-3-(N-(methoxycarbonyl)anilino)cyclohex-2-en-1-one 
• 73367-85-8 6a-ethyl-5,6,6a,7,9a,9b-hexahydro-9-(N-(methoxycarbonyl)anilino)-7-oxo-4H-1,2,3-triazolo<4,5,1-ij>quinoline 
• 129574-45-4 (3S,4aR,9aR)-9-Benzyl-3-ethyl-4a-methyl-1,2,3,4a,9,9a-hexahydro-carbazol-4-one 

Relevant academic research and scientific papers

Regioselective control of N-aryl enaminone alkylation

The regioselectivity of the C-alkylation of unsubstituted N-aryl enaminones prepared from cyclohexane-1,3-dione may be controlled by the nature of the base used.Our results indicate that monoalkylation is completely regioselective; lithium diisopropylamid

A Short Synthesis of (+/-) N-Benzyl Aspidospermidine

(+/-) N-Benzyl aspidospermidine is synthesized in seven steps via the trisubstituted hexahydrocarbazolone 4; reductive cyclization of this intermediate which is obtained by photocyclization and Michael reaction with nitroethylene, creates simulteanously b

Triazoline Photochemistry. Pyrrole Formation by Retro-Diels-Alder Synthesis

Irradiation of triazoline 3, prepared by intramolecular azide-olefin cycloaddition, in methanol solution gives pyrrole methyl ester 4.