103557-92-2

Upstream product

• 100-51-6 benzyl alcohol 
• 103558-83-4 (3aR,4R,11aR,11bR)-11a-Ethyl-10-oxo-1,2,3,3a,4,5,10,11,11a,11b-decahydro-9b-aza-benzo[cd]fluoranthene-4-carboxylic acid allyl ester 
• 103580-94-5 (E)-3-{1-[2-(1-Ethyl-cyclohex-2-enyl)-acetyl]-1H-indol-3-yl}-acrylic acid allyl ester 
• 103581-30-2 (3aα,12α,12aα,12bα)-1,2,3,3a,4,5,11,12,12a,12b-decahydro-3aα-ethyl-5-oxoisoquino<2,1,8,-lma>carbazole-12-carboxylic acid 
• 103580-93-4 2-(1-ethyl-2-cyclohexen-1-yl)acetyl chloride 
• 103557-55-7 methyl (3aα,12α,12aα,12bα)-1,2,3,3a,4,5,11,12,12a,12b-decahydro-3aα-ethyl-5-oxoisoquino<2,1,8,-lma>carbazole-12-carboxylate 
• 103581-16-4 methyl (3aα,12α,12aα,12bα,12cβ)-1,2,3,3a,4,5,12,12a,12b,12c-decahydro-3aα-ethyl-5-oxoisoquino<2,1,8,-lma>carbazole-12-carboxylate 
• 128505-27-1 methyl (E)-3-<1-<2-(1-ethyl-2-cyclohexen-1-yl)acetyl>-1H-indol-3-yl>-2-propenoate 
• 142467-28-5 ethyl (1-ethyl-2-cyclohexen-1-yl)acetate 
• 142467-29-6 (+/-)-1-ethyl-2-cyclohexene-1-acetic acid 
• 19626-92-7 trans-3-(3-indolyl)acrylsaeuremethylester 

Relevant academic research and scientific papers

Synthesis and biological action of the aminotetrahydroisoquinocarbazoles and related compounds: A new class of compounds with antiarrhythmic activity

A series of 12-aminotetrahydroisoquinocarbazoles and related compounds were synthesized using an intramolecular Diels-Alder reaction and screened for antiarrhythmic activity in chloroform-induced ventricular arrhythmias in mice. Several compounds showed m

SYNTHESIS OF FUSED AMINOTETRAHYDROCARBAZOLE COMPOUNDS

Intramolecular Diels-Alder reaction of 3-(1H-indol-3-yl)-2-propenoates having olefinic substituents at the 1-position of the indole ring gave stereoselectively pentacyclic fused indole compounds in good yield.Aminotetrahydrocarbazoles derivatives (8, 21,