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Volumn 40, Issue 2, 2003, Pages 297-302

Synthesis and reactions of 11H-benzo[b]pyrano[3,2-f]indolizines and pyrrolo[3,2,1-ij]pyrano[3,2-c]quinolines [1]

Author keywords

[No Author keywords available]

Indexed keywords

2 CHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 2,3,3 TRIMETHYL 2,3 DIHYDRO 1H INDOLE; 2,3,3 TRIMETHYL 3H INDOLE; 2,9 DICHLORO 7 DICHLOROACETYL 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 2,9 DICHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 4 HYDROXY 11,11 DIMETHYL 11H BENZO[B]PYRANO[3,2 F]INDOLIZINE 2,5 DIONE; 5 ACETYL 6 HYDROXY 1,1,2 TRIMETHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 5 ACETYL 6 HYDROXY 2 METHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 5 CHLORO 2,3,3 TRIMETHYL 3H INDOLE; 5 DICHLOROACETYL 6 HYDROXY 1,1,2 TRIMETHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 5 DICHLOROACETYL 6 HYDROXY 2 METHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 6 HYDROXY 1,1,2 TRIMETHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 6 HYDROXY 1,1,2 TRIMETHYL 5 (1H TETRAZOL 5 YLCARBONYL) 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 6 HYDROXY 2 METHYL 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 6 HYDROXY 2 METHYL 5 (1H TETRAZOL 5 YLCARBONYL) 1,2 DIHYDRO 4H PYRROLO[3,2,1 IJ]QUINOLIN 4 ONE; 7 ACETYL 2 CHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 7 ACETYL 2,9 DICHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 7 ACETYL 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 7 ACETYL 9 CHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 8 HYDROXY 4,4,5 TRIMETHYL 4,5 DIHYDROPYRROLO[3,2,1 IJ]PYRANO[3,2 C]QUINOLINE 7,10 DIONE; 8 HYDROXY 5 METHYL 4,5 DIHYDROPYRROLO[3,2,1 IJ]PYRANO[3,2 C]QUINOLINE 7,10 DIONE; 9 CHLORO 4 HYDROXY 11,11 DIMETHYL 11H BENZO[B]PYRANO[3,2 F]INDOZILIN 2,5 DIONE; 9 CHLORO 7 DICHLOROACETYL 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; 9 CHLORO 8 HYDROXY 10,10 DIMETHYL 10H PYRIDO[1,2 A]INDOL 6 ONE; ACETIC ACID DERIVATIVE; DIETHYLMALONATE; INDOLIZINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG; UNINDEXED DRUG;

EID: 0038710914     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570400215     Document Type: Article
Times cited : (8)

References (17)
  • 10
    • 0021738869 scopus 로고
    • K. Faber and T. Kappe, J. Heterocyclic Chem., 21, 1881 (1984); T. Kappe and C. O. Kappe in "Progress in Heterocyclic Chemistry" (H. Suschitzky and G. W. Gribble, eds), vol. 8, Pergamon, Oxford, UK, 1996, pp 1-13.
    • (1984) J. Heterocyclic Chem. , vol.21 , pp. 1881
    • Faber, K.1    Kappe, T.2
  • 11
    • 2842587710 scopus 로고    scopus 로고
    • H. Suschitzky and G. W. Gribble, eds, Pergamon, Oxford, UK
    • K. Faber and T. Kappe, J. Heterocyclic Chem., 21, 1881 (1984); T. Kappe and C. O. Kappe in "Progress in Heterocyclic Chemistry" (H. Suschitzky and G. W. Gribble, eds), vol. 8, Pergamon, Oxford, UK, 1996, pp 1-13.
    • (1996) Progress in Heterocyclic Chemistry , vol.8 , pp. 1-13
    • Kappe, T.1    Kappe, C.O.2
  • 12
    • 0038268781 scopus 로고    scopus 로고
    • Dissertation, University of Graz
    • T. Krivitchenko, Dissertation, University of Graz, 1999.
    • (1999)
    • Krivitchenko, T.1
  • 14
    • 0037593607 scopus 로고
    • N. P. Buu-Hoi, P. Jaquinon and T. B. Loc, J. Chem. Soc., 738 (1958); S. Sakai, M. Wakabayashi and M. Nishina, Yakugaku Zasshi, 89, 1061 (1969); Chem. Abstr., 72, 3308d (1970).
    • (1958) J. Chem. Soc. , pp. 738
    • Buu-Hoi, N.P.1    Jaquinon, P.2    Loc, T.B.3
  • 15
    • 0014559708 scopus 로고
    • N. P. Buu-Hoi, P. Jaquinon and T. B. Loc, J. Chem. Soc., 738 (1958); S. Sakai, M. Wakabayashi and M. Nishina, Yakugaku Zasshi, 89, 1061 (1969); Chem. Abstr., 72, 3308d (1970).
    • (1969) Yakugaku Zasshi , vol.89 , pp. 1061
    • Sakai, S.1    Wakabayashi, M.2    Nishina, M.3
  • 16
    • 4243335685 scopus 로고
    • N. P. Buu-Hoi, P. Jaquinon and T. B. Loc, J. Chem. Soc., 738 (1958); S. Sakai, M. Wakabayashi and M. Nishina, Yakugaku Zasshi, 89, 1061 (1969); Chem. Abstr., 72, 3308d (1970).
    • (1970) Chem. Abstr. , vol.72


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.