메뉴 건너뛰기




Volumn 35, Issue 2, 1998, Pages 279-284

Conformational Behavior on 2,2,3-Trisubstituted 1,2,3,4-Tetrahydroquinoline Alkaloids, Virantmycin, Benzastatins, and their Congeners, Evaluated by Semi-empirical Molecular Orbital Calculations

Author keywords

[No Author keywords available]

Indexed keywords

1,2,3,4 TETRAHYDROQUINOLINE DERIVATIVE; ALKALOID DERIVATIVE; BENZASTATIN C; BENZASTATIN D; UNCLASSIFIED DRUG; VIRANTMYCIN;

EID: 0031833850     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570350203     Document Type: Article
Times cited : (9)

References (31)
  • 4
    • 0000345657 scopus 로고
    • For our synthetic studies on virantmycin (1), see: [a] Y. Morimoto, K. Oda, H. Shirahama, T. Matsumoto, and S. Omura, Chem. Letters, 909 (1988); [b] Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron Letters, 31, 6031 (1990); Y. Morimoto, F. Matsuda, and H. Shirahama, Synlett, 201 (1991); Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron, 52, 10609 (1996); [e] Y. Morimoto and H. Shirahama, Tetrahedron, 52, 10631 (1996).
    • (1988) Chem. Letters , pp. 909
    • Morimoto, Y.1    Oda, K.2    Shirahama, H.3    Matsumoto, T.4    Omura, S.5
  • 5
    • 0025183188 scopus 로고
    • For our synthetic studies on virantmycin (1), see: [a] Y. Morimoto, K. Oda, H. Shirahama, T. Matsumoto, and S. Omura, Chem. Letters, 909 (1988); [b] Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron Letters, 31, 6031 (1990); Y. Morimoto, F. Matsuda, and H. Shirahama, Synlett, 201 (1991); Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron, 52, 10609 (1996); [e] Y. Morimoto and H. Shirahama, Tetrahedron, 52, 10631 (1996).
    • (1990) Tetrahedron Letters , vol.31 , pp. 6031
    • Morimoto, Y.1    Matsuda, F.2    Shirahama, H.3
  • 6
    • 0000063973 scopus 로고
    • For our synthetic studies on virantmycin (1), see: [a] Y. Morimoto, K. Oda, H. Shirahama, T. Matsumoto, and S. Omura, Chem. Letters, 909 (1988); [b] Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron Letters, 31, 6031 (1990); Y. Morimoto, F. Matsuda, and H. Shirahama, Synlett, 201 (1991); Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron, 52, 10609 (1996); [e] Y. Morimoto and H. Shirahama, Tetrahedron, 52, 10631 (1996).
    • (1991) Synlett , pp. 201
    • Morimoto, Y.1    Matsuda, F.2    Shirahama, H.3
  • 7
    • 15844409180 scopus 로고    scopus 로고
    • For our synthetic studies on virantmycin (1), see: [a] Y. Morimoto, K. Oda, H. Shirahama, T. Matsumoto, and S. Omura, Chem. Letters, 909 (1988); [b] Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron Letters, 31, 6031 (1990); Y. Morimoto, F. Matsuda, and H. Shirahama, Synlett, 201 (1991); Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron, 52, 10609 (1996); [e] Y. Morimoto and H. Shirahama, Tetrahedron, 52, 10631 (1996).
    • (1996) Tetrahedron , vol.52 , pp. 10609
    • Morimoto, Y.1    Matsuda, F.2    Shirahama, H.3
  • 8
    • 0030570874 scopus 로고    scopus 로고
    • For our synthetic studies on virantmycin (1), see: [a] Y. Morimoto, K. Oda, H. Shirahama, T. Matsumoto, and S. Omura, Chem. Letters, 909 (1988); [b] Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron Letters, 31, 6031 (1990); Y. Morimoto, F. Matsuda, and H. Shirahama, Synlett, 201 (1991); Y. Morimoto, F. Matsuda, and H. Shirahama, Tetrahedron, 52, 10609 (1996); [e] Y. Morimoto and H. Shirahama, Tetrahedron, 52, 10631 (1996).
    • (1996) Tetrahedron , vol.52 , pp. 10631
    • Morimoto, Y.1    Shirahama, H.2
  • 9
    • 0022577129 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1986) Tetrahedron Letters , vol.27 , pp. 1293
    • Hill, M.L.1    Raphael, R.A.2
  • 10
    • 0025046452 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1990) Tetrahedron , vol.46 , pp. 4587
    • Hill, M.L.1    Raphael, R.A.2
  • 11
    • 84970626943 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1990) Aust. J. Chem. , vol.43 , pp. 609
    • Raner, K.D.1    Skelton, B.W.2    Ward, A.D.3    White, A.H.4
  • 12
    • 84970579715 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1991) Aust. J. Chem. , vol.44 , pp. 1749
    • Raner, K.D.1    Ward, A.D.2
  • 13
    • 0000166661 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1993) Aust. J. Chem. , vol.46 , pp. 1657
    • De Silva, A.N.1    Francis, C.L.2    Ward, A.D.3
  • 14
    • 0028728701 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1994) Aust. J. Chem. , vol.47 , pp. 2109
    • Francis, C.F.1    Ward, A.D.2
  • 15
    • 0028785689 scopus 로고
    • For the synthetic studies on 1 from other groups, see: [a] M. L. Hill and R. A. Raphael, Tetrahedron Letters, 27, 1293 (1986); [b] M. L. Hill and R. A. Raphael, Tetrahedron, 46, 4587 (1990); K. D. Raner, B. W. Skelton, A. D. Ward, and A. H. White, Aust. J. Chem., 43, 609 (1990); K. D. Raner and A. D. Ward, Aust. J. Chem., 44, 1749 (1991); [e] A. N. De Silva, C. L. Francis, and A. D. Ward, Aust. J. Chem., 46, 1657 (1993); [f] C. F. Francis and A. D. Ward, Aust. J. Chem., 47, 2109 (1994); [g] N. M. Williamson, D. R. March, and A. D. Ward, Tetrahedron Letters, 36, 7721 (1995).
    • (1995) Tetrahedron Letters , vol.36 , pp. 7721
    • Williamson, N.M.1    March, D.R.2    Ward, A.D.3
  • 19
    • 84984929707 scopus 로고
    • and references cited therein
    • For energetic investigations on ring inversion in cyclohexene and related molecules, see: F. A. L. Anet, D. I. Freedberg, J. W. Storer, and K. N. Houk, J. Am. Chem. Soc., 114, 10969 (1992) and references cited therein.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 10969
    • Anet, F.A.L.1    Freedberg, D.I.2    Storer, J.W.3    Houk, K.N.4
  • 20
    • 85034487165 scopus 로고    scopus 로고
    • These calculations were performed on Cache system {MOPAC (version 94.1)}
    • These calculations were performed on Cache system {MOPAC (version 94.1)}.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.