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Volumn 53, Issue 33, 1997, Pages 11465-11480

Hetero Diels-Alder reactions of 4,5,8(1H)-quinolinetriones

Author keywords

[No Author keywords available]

Indexed keywords

1,5 DIAZAANTHRACENE 4,9,10 TRIONE; 1,8 DIAZAANTHRACENE 4,9,10 TRIONE; 2,5,8(1H) QUINOLINETRIONE; 4,5,8(1H) QUINOLINETRIONE DERIVATIVE; 9,10 DIHYDROXY 1,8 DIAZAANTHRACENE 4,9,10 TRIONE; DIMETHYLAMINOAZADIENE; FURO[2,3 F]QUINOLINE DERIVATIVE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0000506271     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(97)00726-6     Document Type: Article
Times cited : (12)

References (43)
  • 1
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    • Sammes, P. G. (ed.). (Hansch, C.; Sammes, P. G.; Taylor, J. B., general editors). Pergamon Press
    • Hertzberg, R. P., in Sammes, P. G. (ed.). Comprehensive Medicinal Chemistry, vol. 2, p.753 (Hansch, C.; Sammes, P. G.; Taylor, J. B., general editors). Pergamon Press, 1990.
    • (1990) Comprehensive Medicinal Chemistry , vol.2 , pp. 753
    • Hertzberg, R.P.1
  • 4
    • 0000536536 scopus 로고
    • Atta-ur Rahman (ed.), Elsevier
    • For a review on synthetic work in this area, see: c) Su, T.-L.; Watanabe, K. A. in Atta-ur Rahman (ed.), Studies in Natural Products Chemistry vol. 13, p. 347. Elsevier, 1993.
    • (1993) Studies in Natural Products Chemistry , vol.13 , pp. 347
    • Su, T.-L.1    Watanabe, K.A.2
  • 8
    • 0001078943 scopus 로고
    • Reviews on marine, nitrogen containing natural products: a) Álvarez, M.; Salas, M. Heterocycles 1991, 32, 759.
    • (1991) Heterocycles , vol.32 , pp. 759
    • Álvarez, M.1    Salas, M.2
  • 15
    • 0023588127 scopus 로고
    • Halogenation of the 5 and 6 positions of 4-hydroxyquinolinequinones leads to slight improvements in the yields of their Diels-Alder reactions, as shown during the total synthesis of phomazarin analogues. See; Guay, V.; Brassard, P. J. Heterocycl. Chem. 1987, 24, 1649.
    • (1987) J. Heterocycl. Chem. , vol.24 , pp. 1649
    • Guay, V.1    Brassard, P.2
  • 29
    • 84986366191 scopus 로고
    • These 1-azadienes were prepared using the method described in: Waldner, A. Helv. Chim. Acta 1988, 71, 486.
    • (1988) Helv. Chim. Acta , vol.71 , pp. 486
    • Waldner, A.1
  • 35
    • 0001240792 scopus 로고
    • For other examples of the lower reactivity of 4-substituted 1-dimethylamino-1-azadienes in comparison to their 3-substituted isomers, see: Echavarren, A. M. Advances in Nitrogen Heterocycles, 1995, 2, 211.
    • (1995) Advances in Nitrogen Heterocycles , vol.2 , pp. 211
    • Echavarren, A.M.1
  • 37
    • 0342548132 scopus 로고    scopus 로고
    • note
    • 12d


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.