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Volumn 38, Issue 11, 2008, Pages 1778-1783

Novel method for the synthesis of 6,12-dihydro-2-methylindolo[2,3- b]carbazol-6-ones

Author keywords

1 oxo 2,3,4,9 tetrahydro 1H carbazol 1 one; 6,12 Dihydro 2 methylindolo 2,3 b carbazol 6 ones; Fischer indole cyclization; Methyl 6 methyl 2 (1 oxo 2,3,4,9 tetrahydro 1H carbazol 2 yl) oxoacetate

Indexed keywords

1 OXO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; 2 HYDROXY METHYLENE 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; 4' METHYL 2 PHENYLHYDRAZONO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; 6,12 DIHYDRO 2 METHYLINDOLO[2,3 BETA]CARBAZOL 6 ONE; 6,12 DIHYDRO 2 METHYLINDOLO[2,3 BETA]CARBAZOL 6 ONES; 6,12 DIHYDRO 2,8 DIMETHYLINDOLO[2,3 BETA]CARBAZOL 6 ONE; 6,12 DIHYDRO 2,9 DIMETHYLINDOLO[2,3 BETA]CARBAZOL 6 ONE; 6,4' DIMETHYL 2 PHENYLHYDRAZONO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; 7,4' DIMETHYL 2 PHENYLHYDRAZONO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; 8,4' DIMETHYL 2 PHENYLHYDRAZONO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 1 ONE; CARBAZOLE DERIVATIVE; METHYL 6 METHYL 2 (1 OXO 2,3,4,9 TETRAHYDRO 1H CARBAZOL 2 YL)OXOACETATE;

EID: 45749124495     PISSN: 00397911     EISSN: 15322432     Source Type: Journal    
DOI: 10.1080/00397910801989535     Document Type: Article
Times cited : (4)

References (10)
  • 2
    • 0036826933 scopus 로고    scopus 로고
    • Isolation and synthesis of biologically active carbazole alkaloids
    • Knolker, H.-J.; Reddy, K. R. Isolation and synthesis of biologically active carbazole alkaloids. Chem. Rev. 2002, 102, 4303-4427.
    • (2002) Chem. Rev , vol.102 , pp. 4303-4427
    • Knolker, H.-J.1    Reddy, K.R.2
  • 4
    • 0033532124 scopus 로고    scopus 로고
    • Syntheses of 6-substituted indolo[3,2-b]carbazoles, including 6-formyindolo[3,2-b]carbazole, an extremely efficient ligand for the TCDD (Ah) receptor
    • Tholander, J.; Bergman, J. Syntheses of 6-substituted indolo[3,2-b]carbazoles, including 6-formyindolo[3,2-b]carbazole, an extremely efficient ligand for the TCDD (Ah) receptor. Tetrahedron 1999, 55, 6243-6260.
    • (1999) Tetrahedron , vol.55 , pp. 6243-6260
    • Tholander, J.1    Bergman, J.2
  • 5
    • 0033595871 scopus 로고    scopus 로고
    • Syntheses of 6,12-disubstituted 5,11-dihydroindolo[3,2-b]carbazoles, including 5,11-dihydroindolo[3,2- b]carbazole-6,12-dicarbaldehyde, an extremely efficient ligand for the TCDD (Ah) receptor
    • Tholander, J.; Bergman, J. Syntheses of 6,12-disubstituted 5,11-dihydroindolo[3,2-b]carbazoles, including 5,11-dihydroindolo[3,2- b]carbazole-6,12-dicarbaldehyde, an extremely efficient ligand for the TCDD (Ah) receptor. Tetrahedron 1999, 55, 12577-12594.
    • (1999) Tetrahedron , vol.55 , pp. 12577-12594
    • Tholander, J.1    Bergman, J.2
  • 6
    • 0037060086 scopus 로고    scopus 로고
    • Synthesis of indolocarbazole quinones, potent arylhydrocarbon receptor ligands
    • Bergman, J.; Wahlstrom, N.; Yudina, L. N.; Tholander, J.; Lidgren, G. Synthesis of indolocarbazole quinones, potent arylhydrocarbon receptor ligands. Tetrahedron 2002, 58, 1443-1452.
    • (2002) Tetrahedron , vol.58 , pp. 1443-1452
    • Bergman, J.1    Wahlstrom, N.2    Yudina, L.N.3    Tholander, J.4    Lidgren, G.5
  • 7
    • 0033595847 scopus 로고    scopus 로고
    • Thallium(III) acetate-mediated 3,3-couplings of indoles with formation of indolocarbazoles
    • Tholander, J.; Bergman. Thallium(III) acetate-mediated 3,3-couplings of indoles with formation of indolocarbazoles. Tetrahedron 1999, 55, 12595-12602.
    • (1999) Tetrahedron , vol.55 , pp. 12595-12602
    • Tholander, J.1    Bergman2
  • 8
    • 0032546220 scopus 로고    scopus 로고
    • Synthesis of 6-formylindolo[3,2-b] carbazole, an extremely potent ligand for the aryl hydrogen (Ah) receptor
    • Tholander, J.; Bergman, J. Synthesis of 6-formylindolo[3,2-b] carbazole, an extremely potent ligand for the aryl hydrogen (Ah) receptor. Tetrahedron Lett. 1998, 39, 1619-1622.
    • (1998) Tetrahedron Lett , vol.39 , pp. 1619-1622
    • Tholander, J.1    Bergman, J.2
  • 9
    • 33744810088 scopus 로고    scopus 로고
    • Sangeetha, V.; Rajendra Prasad, K. J. Synthesis of pyrimido annelated carbazoles and 2-methyl-6-oxo-bisindolo[1,2-b:5,4-b′] cyclohexanones using 2-hydroxymethylene-1-oxo-1,2,3,4-tetrahydrocarbazoles. Indian J. Chem. 2006, 45B, 1028-1033.
    • Sangeetha, V.; Rajendra Prasad, K. J. Synthesis of pyrimido annelated carbazoles and 2-methyl-6-oxo-bisindolo[1,2-b:5,4-b′] cyclohexanones using 2-hydroxymethylene-1-oxo-1,2,3,4-tetrahydrocarbazoles. Indian J. Chem. 2006, 45B, 1028-1033.
  • 10
    • 33747152754 scopus 로고    scopus 로고
    • Syntheses of methyl 4,5-dihydro-2H-pyrazolo-[3,4-a]carbazole-3-carboxylates
    • Martin, A. E.; Rajendra Prasad, K. J. Syntheses of methyl 4,5-dihydro-2H-pyrazolo-[3,4-a]carbazole-3-carboxylates. J. Chem. Res. 2006, 473-477.
    • (2006) J. Chem. Res , pp. 473-477
    • Martin, A.E.1    Rajendra Prasad, K.J.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.