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Polyspiranes, Part 27. For Part 26 Fitjer L., Steeneck C., Gaini-Rahimi S., Schröder U., Justus K., Puder P., Dittmer M., Hassler C., Weiser J., Noltemeyer M., Teichert M. J. Am. Chem. Soc. 120:1998;317-328.
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Fitjer L., Conia J.-M. Angew. Chem. 85:1973;832-833. Angew. Chem. Int. Ed. Engl. 1973, 12, 761-762.
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de Meijere A., Khlebnikov A.F., Kozhushkov S.I., Kostikov R.R., Schreiner P.R., Wittkopp A., Rinderspacher C., Menzel H., Yufit D.S., Howard J.A.K. Chem. Eur. J. 2002;828-842.
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Howard, J.A.K.10
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9
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0038322542
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For approaches to helical primary structures of 1,2-spiroannelated cyclopentane rings, see: (a) Kakiuchi K., Okada H., Kanehisa N., Kai Y., Kurosawa H. J. Org. Chem. 61:1996;2972-2979 (b) Gaini-Rahimi S., Steeneck C., Meyer I., Fitjer L., Pauer F., Noltemeyer M. Tetrahedron. 55:1999;3905-3916.
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0033605838
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For approaches to helical primary structures of 1,2-spiroannelated cyclopentane rings, see: (a)
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For approaches to helical primary structures of 1,2-spiroannelated cyclopentane rings, see: (a) Kakiuchi K., Okada H., Kanehisa N., Kai Y., Kurosawa H. J. Org. Chem. 61:1996;2972-2979 (b) Gaini-Rahimi S., Steeneck C., Meyer I., Fitjer L., Pauer F., Noltemeyer M. Tetrahedron. 55:1999;3905-3916.
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Tetrahedron
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Gaini-Rahimi, S.1
Steeneck, C.2
Meyer, I.3
Fitjer, L.4
Pauer, F.5
Noltemeyer, M.6
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13
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85031165615
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Serena Software, P.O. Box 3076, Bloomington, IN 47402
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The single minimum structures of (M)-1 and (M)-3 were optimized using PC-Model, Version 4.0, Serena Software, P.O. Box 3076, Bloomington, IN 47402.
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(M)-3 were optimized using PC-Model, Version 4.0
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14
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0037647049
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This finding corresponds to what is observed with aromatic [n]helicenes in going from [6]- to [7]helicene:
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This finding corresponds to what is observed with aromatic [n]helicenes in going from [6]- to [7]helicene: Meuer K.P., Vögtle F. Top. Curr. Chem. 127:1985;1-76.
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Top. Curr. Chem.
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Meuer, K.P.1
Vögtle, F.2
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0001073820
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(a) Todd D. Org. React. 4:1948;378-422
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Org. React.
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Todd, D.1
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0038661244
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For a review on enzyme-catalyzed reductions of carbonyl groups, see: G. Helmchen, R.W. Hoffmann, J. Mulzer, & E. Schaumann. Stuttgart: Georg Thieme
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For a review on enzyme-catalyzed reductions of carbonyl groups, see: Gottwald M. Helmchen G., Hoffmann R.W., Mulzer J., Schaumann E. Methods of Organic Chemistry (Houben-Weyl). Vol. E 21d:1995;4143-4197 Georg Thieme, Stuttgart.
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Gottwald, M.1
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0011725695
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For bakers' yeast reductions of cyclobutanones in bicyclic systems, see: (a) Newton R.F., Paton J., Reynolds D.P., Young S., Roberts S.M. J. Chem. Soc. Chem. Commun. 1979;908-909 (b) Dawson M.J., Lawrence G.C., Lilley G., Todd M., Noble D., Green S.M., Roberts S.M., Wallace T.W., Newton R.F., Carter M.C., Hallet P., Paton J., Reynolds D.P., Young S. J. Chem. Soc., Perkin Trans. 1. 1983;2119-2125 (c) Lowe G., Swain S. J. Chem. Soc., Perkin Trans. 1. 1985;391-398 (d) Kertesz D.J., Kluge A.F. J. Org. Chem. 53:1988;4962-4968.
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Newton, R.F.1
Paton, J.2
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Young, S.4
Roberts, S.M.5
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22
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37049095553
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For bakers' yeast reductions of cyclobutanones in bicyclic systems, see: (a) Newton R.F., Paton J., Reynolds D.P., Young S., Roberts S.M. J. Chem. Soc. Chem. Commun. 1979;908-909 (b) Dawson M.J., Lawrence G.C., Lilley G., Todd M., Noble D., Green S.M., Roberts S.M., Wallace T.W., Newton R.F., Carter M.C., Hallet P., Paton J., Reynolds D.P., Young S. J. Chem. Soc., Perkin Trans. 1. 1983;2119-2125 (c) Lowe G., Swain S. J. Chem. Soc., Perkin Trans. 1. 1985;391-398 (d) Kertesz D.J., Kluge A.F. J. Org. Chem. 53:1988;4962-4968.
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Dawson, M.J.1
Lawrence, G.C.2
Lilley, G.3
Todd, M.4
Noble, D.5
Green, S.M.6
Roberts, S.M.7
Wallace, T.W.8
Newton, R.F.9
Carter, M.C.10
Hallet, P.11
Paton, J.12
Reynolds, D.P.13
Young, S.14
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23
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37049100391
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For bakers' yeast reductions of cyclobutanones in bicyclic systems, see: (a) Newton R.F., Paton J., Reynolds D.P., Young S., Roberts S.M. J. Chem. Soc. Chem. Commun. 1979;908-909 (b) Dawson M.J., Lawrence G.C., Lilley G., Todd M., Noble D., Green S.M., Roberts S.M., Wallace T.W., Newton R.F., Carter M.C., Hallet P., Paton J., Reynolds D.P., Young S. J. Chem. Soc., Perkin Trans. 1. 1983;2119-2125 (c) Lowe G., Swain S. J. Chem. Soc., Perkin Trans. 1. 1985;391-398 (d) Kertesz D.J., Kluge A.F. J. Org. Chem. 53:1988;4962-4968.
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Lowe, G.1
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24
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0023769733
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For bakers' yeast reductions of cyclobutanones in bicyclic systems, see: (a)
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For bakers' yeast reductions of cyclobutanones in bicyclic systems, see: (a) Newton R.F., Paton J., Reynolds D.P., Young S., Roberts S.M. J. Chem. Soc. Chem. Commun. 1979;908-909 (b) Dawson M.J., Lawrence G.C., Lilley G., Todd M., Noble D., Green S.M., Roberts S.M., Wallace T.W., Newton R.F., Carter M.C., Hallet P., Paton J., Reynolds D.P., Young S. J. Chem. Soc., Perkin Trans. 1. 1983;2119-2125 (c) Lowe G., Swain S. J. Chem. Soc., Perkin Trans. 1. 1985;391-398 (d) Kertesz D.J., Kluge A.F. J. Org. Chem. 53:1988;4962-4968.
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Kertesz, D.J.1
Kluge, A.F.2
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85031176230
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(1S,5′S,10′S)-14 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 197711. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk)
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Crystallographic data (excluding structure factors) for compound (1S,5′S,10′S)-14 have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 197711. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44-1223-336033 or e-mail: deposit@ccdc.cam.ac.uk).
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