A facile synthesis of 6,12-disubstituted 5,7-dihydroindolo[2,3-b] carbazoles from the reaction of 1H-indole and aldehydes catalyzed by molecular iodine

Synthesis

Volumn , Issue 2, 2008, Pages 286-292

  Deb, Mohit L ^a   Baruah, Biswajita ^a   Bhuyan, Pulak J ^a  

^a CSIR NORTH EAST INSTITUTE OF SCIENCE AND TECHNOLOGY   (India)

Author keywords

Aldehyde; Antitumor; Indole; Indolo 2,3 b carbazole; Molecular iodine

Indexed keywords

INDOLES; MOLECULAR IODINE;

ACETONITRILE; IODINE; REACTION KINETICS; SYNTHESIS (CHEMICAL);

NITROGEN COMPOUNDS;

12 (2 CHLOROQUINOLIN 3 YL) 6 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 12 (4 METHOXYPHENYL) 6 (4 METHYLPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 12 (4 METHOXYPHENYL) 6 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 12 (4 METHYLPHENYL) 6 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 12 METHYL 6 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6 (4 METHIXYPHENYL) 12 (4 METHYLPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6 (4 METHOXYPHENYL) 12 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6 (4 METHYLPHENYL) 12 PHENYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(2 CHLOROPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(2 HYDROXYPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(3,4,5 TRIMETHOXYPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(4 CHLOROPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(4 HYDROXY 3 METHOXYPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(4 HYDROXYPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(4 METHOXYPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS(4 METHYLPHENYL) 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 BIS[4 (BENZOYLOXY)PHENYL] 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 DIALKYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 DIARYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 DIETHYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 DIMETHYL 5,7 DIHYDROINDOLO[2,3 B]CARBAZOLE; 6,12 DIPHENYL 5,7 DIHYDROINDOLOL[2,3 B]CARBAZOLE; ALDEHYDE DERIVATIVE; CARBAZOLE DERIVATIVE; INDOLE DERIVATIVE; IODINE; UNCLASSIFIED DRUG;

ARTICLE; CATALYST; CHEMICAL STRUCTURE; CONJUGATION; PROTON NUCLEAR MAGNETIC RESONANCE; SUBSTITUTION REACTION;

EID: 38849154166     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2008-1000849     Document Type: Article

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