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For a recent review see G. Bringmann, S. Busemann, in Natural Product Analysis (Eds.: P. Schreier, M. Herderich, H. U. Humpf, W. Schwab), Vieweg, Braunschweig, 1998, pp. 195-212.
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For selected examples involving axial chirality: a) G. Bringmann, K.-P. Gulden, H. Busse, J. Fleischhauer, B. Kramer, E. Zobel, Tetrahedron 1993, 49, 3305-3312; b) G. Bringmann, K.-P. Gulden, Y. F. Hallock, K. P. Manfredi, J. H. Cardellina, II, M. R. Boyd, B. Kramer, J. Fleischhauer, Tetrahedron 1994, 50, 7807-7814; c) G. Bringmann, M. Stahl, K.-P. Gulden, Tetrahedron 1997, 53, 2817-2822; d) G. Bringmann, C. Günther, S. Busemann, M. Schäffer, J. D. Olowokudejo, B. Alo, Phytochemistry 1998, 47, 37-43.
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34
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0031584896
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For selected examples involving axial chirality: a) G. Bringmann, K.-P. Gulden, H. Busse, J. Fleischhauer, B. Kramer, E. Zobel, Tetrahedron 1993, 49, 3305-3312; b) G. Bringmann, K.-P. Gulden, Y. F. Hallock, K. P. Manfredi, J. H. Cardellina, II, M. R. Boyd, B. Kramer, J. Fleischhauer, Tetrahedron 1994, 50, 7807-7814; c) G. Bringmann, M. Stahl, K.-P. Gulden, Tetrahedron 1997, 53, 2817-2822; d) G. Bringmann, C. Günther, S. Busemann, M. Schäffer, J. D. Olowokudejo, B. Alo, Phytochemistry 1998, 47, 37-43.
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For selected examples involving axial chirality: a) G. Bringmann, K.-P. Gulden, H. Busse, J. Fleischhauer, B. Kramer, E. Zobel, Tetrahedron 1993, 49, 3305-3312; b) G. Bringmann, K.-P. Gulden, Y. F. Hallock, K. P. Manfredi, J. H. Cardellina, II, M. R. Boyd, B. Kramer, J. Fleischhauer, Tetrahedron 1994, 50, 7807-7814; c) G. Bringmann, M. Stahl, K.-P. Gulden, Tetrahedron 1997, 53, 2817-2822; d) G. Bringmann, C. Günther, S. Busemann, M. Schäffer, J. D. Olowokudejo, B. Alo, Phytochemistry 1998, 47, 37-43.
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0031550603
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For a selected example involving related (hydro)naphthalene epoxides, see: G. Bringmann, S. Busemann, K. Krohn, K. Beckmann, Tetrahedron 1997, 53, 1655-1664.
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39
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0344909761
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note
-
The PM3 results achieved were very similar to those obtained with AM1 and are therefore not explicitly presented in the text.
-
-
-
-
40
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0000134041
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For a recent discussion of the mechanism of the Jacobsen - Katsuki epoxidation see: T. Linker, Angew. Chem. 1997, 109, 2150-2152; Angew. Chem. Int. Ed. Engl. 1997, 36, 2060-2062.
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0030726868
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For a recent discussion of the mechanism of the Jacobsen - Katsuki epoxidation see: T. Linker, Angew. Chem. 1997, 109, 2150-2152; Angew. Chem. Int. Ed. Engl. 1997, 36, 2060-2062.
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0345340903
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The Medawar Centre, Oxford Science Park, Sandford-on-Thames, Oxford, OX4 4GA (England)
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G. Rauhut, J. Chandrasekhar, A. Alex, B. Beck, W. Sauer, T. Clark, VAMP 6.1, Oxford Molecular. The Medawar Centre, Oxford Science Park, Sandford-on-Thames, Oxford, OX4 4GA (England).
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VAMP 6.1, Oxford Molecular
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43
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0344909760
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SYBYL: Tripos Associates, 1699 St. Hanley Road, Suite 303, St. Louis, MO 63144 (USA)
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SYBYL: Tripos Associates, 1699 St. Hanley Road, Suite 303, St. Louis, MO 63144 (USA).
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45
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0004303991
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Department of Chemistry and Biochemistry, University of Colorado, Boulder (USA); modified by J. Fleischhauer, W. Schleker, B. Kramer; transported to LinuX by K.-P. Gulden
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J. W. Downing, Program Packet BDZDO/MCDSPD, Department of Chemistry and Biochemistry, University of Colorado, Boulder (USA); modified by J. Fleischhauer, W. Schleker, B. Kramer; transported to LinuX by K.-P. Gulden.
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Program Packet BDZDO/MCDSPD
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Downing, J.W.1
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