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For some total syntheses of natural michellamines, see (a)
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For some total syntheses of natural michellamines, see (a) Bringmann G., Harmsen S., Holenz J., Geuder T., Götz R., Keller P.A., Walter R. Tetrahedron. 50:1994;9643-9648 (b) Kelly T.R., Garcia A., Lang F., Walsh J., Bhaskar K.V., Boyd M.R., Götz R., Keller P.A., Walter R., Bringmann G. Tetrahedron Lett. 35:1994;7621-7624 (c) Bringmann G., Götz R., Harmsen S., Holenz J., Walter R. Liebigs Ann. 1996;2045-2058 (d) Bringmann G., Götz R., Keller P.A., Walter R., Boyd M.R., Lang F., Garcia A., Walsh J.J., Tellitu I., Bhaskar K.V., Kelly T.R. J. Org. Chem. 63:1998;1090-1097 (e) Hoye T.R., Chen M., Mi L., Priest O.P. Tetrahedron Lett. 35:1994;8747-8750 (f) Hoye T.R., Chen M., Hoang B., Mi L., Priest M.P. J. Org. Chem. 64:1999;7184-7201 (g) Hobbs P.D., Upender V., Liu J., Pollart D.J., Thomas D.W., Dawson M.I. J. Chem. Soc., Chem. Commun. 8:1996;923-924 (h) Hobbs P.D., Upender V., Dawson M.I. Synlett. 8:1997;965-967.
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For the synthesis of bioactive michellamine analogs, see (a)
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For the synthesis of bioactive michellamine analogs, see (a) Bringmann G., Saeb W., Koppler D., François G. Tetrahedron. 52:1996;13409-13418 (b) Bringmann G., Götz R., François G. Tetrahedron. 1996;13419-13426 (c) Upender V., Pollart D.J., Liu J., Hobbs P.D., Olsen C., Chao W., Bowden B., Crase J.L., Thomas D.W., Pandey A., Lawson J.A., Dawson M.I. J. Heterocycl. Chem. 33:1996;1371-1384 (d) Zhang H., Zembower D.E., Chen Z. Bioorg. Med. Chem. Lett. 7:1997;2687-2690 (e) Bringmann G., Holenz J., Weirich R., Rübenacker M., Funke C., Boyd M.R., Gulakowski R.J., François G. Tetrahedron. 54:1998;497-512 (f) Bringmann G., Wenzel M., Kelly T.R., Boyd M.R., Gulakowski R.J., Kaminsky R. Tetrahedron. 55:1999;1731-1740 (g) de Konig C.B., Michael J.P., van Otterlo W.A.L. Tetrahedron Lett. 40:1999;3037-3040 (h) Bringmann G., Saeb W., Kraus J., Brun R., François G. Tetrahedron. 56:2000;3523-3531 (i) Bringmann G., Saeb W., Wohlfarth M., Messer K., Brun R. Tetrahedron. 56:2000;5871-5875.
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For the first (and as yet only) dimeric naphthylisoquinoline alkaloid detected in another Ancistrocladus species, ancistrogriffithine A from the South-East Asian liana A. griffithii, see
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For the first (and as yet only) dimeric naphthylisoquinoline alkaloid detected in another Ancistrocladus species, ancistrogriffithine A from the South-East Asian liana A. griffithii, see Bringmann G., Schlauer J., Rischer H., Wohlfarth M., Heubes M., Saeb W., Diem S., Herderich M. Anal. Chem. 73:2001;2571-2577.
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Strictly speaking, these compounds should be addressed as dehydro dimers; still, for reasons of simplicity, the term 'dimers' will be used throughout this paper
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Strictly speaking, these compounds should be addressed as dehydro dimers; still, for reasons of simplicity, the term 'dimers' will be used throughout this paper.
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this program package is available at: Oxford Molecular Limited, The Magdalen Centre, Oxford Science Park, Sandford on Thames, Oxford OX4 4GA, England
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Erlangen. VAMP 5.0
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Rauhut, G.1
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0004303991
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Department of Chemistry and Biochemistry, University of Colorado, Boulder, USA; modified by Fleischhauer, J.; Schleker, W.; Kramer, B. ported to Linux by Gulden, K.-P.
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Downing, J. W. Program package BDZDO/MCDSPD, Department of Chemistry and Biochemistry, University of Colorado, Boulder, USA; modified by Fleischhauer, J.; Schleker, W.; Kramer, B. ported to Linux by Gulden, K.-P.
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Program Package BDZDO/MCDSPD
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Downing, J.W.1
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