78329-39-2Relevant academic research and scientific papers
An efficient new route towards biologically active isocryptolepine and γ-carboline derivatives using an intramolecular thermal electrocyclization strategy
Hingane, Dattatray G.,Kusurkar, Radhika S.
scheme or table, p. 3686 - 3688 (2011/07/31)
An efficient and short route is established for biologically active 11H-indolo[3,2-c]quinoline 1, naturally occurring antiplasmodial isocryptolepine 2 and 5-methyl-11H-indolo[3,2-c]quinoline-5-inium iodide 3 using intramolecular thermal electrocyclization
Synthesis of Carbazole Alkaloids Hyellazole and 6-Chlorohyellazole
Kano, Shinzo,Sugino, Eiichi,Shibuya, Shiroshi,Hibino, Satoshi
, p. 3856 - 3859 (2007/10/02)
2-(1-Cyclohexenyl)-3-(β-methoxyvinyl)indole was heated in decalin in the presence of 5percent Pd-C to give 1,2,3,4-tetrahydro-5-methoxy-11H-benzocarbazole and 5-methoxy-11H-benzocarbazole. 3-(β-Methoxyvinyl)-2-(1-phenyl-1-propenyl)indole and 5-chloro-3-(β-methoxyvinyl)-2-(1-phenyl-1-propenyl)indole were also heated in decalin in the presence of 5percent Pd-C at 210 deg C, yielding the carbazole alkaloids hyellazole and 6-chlorohyellazole, respectively.
