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1
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0031748981
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For recent reviews see: (a) Steenwinkel, P.; Gossage, R. A.; van Koten, G. Chem. Eur. J. 1998, 4, 759; (b) Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. Engl. 2001, 40, 3750.
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Steenwinkel, P.1
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0035886138
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For recent reviews see: (a) Steenwinkel, P.; Gossage, R. A.; van Koten, G. Chem. Eur. J. 1998, 4, 759; (b) Albrecht, M.; van Koten, G. Angew. Chem., Int. Ed. Engl. 2001, 40, 3750.
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Albrecht, M.1
Van Koten, G.2
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6
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0001060597
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submitted for publication
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Stark M.A., Jones G., Richards C.J. Organometallics. 19:2000;1282 Fossey, J. S.; Richards, C. J. submitted for publication.
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Fossey, J.S.1
Richards, C.J.2
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Motoyama Y., Makihara N., Mikami Y., Aoki K., Nishiyama H. Chem. Lett. 1997;951.
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Motoyama Y., Mikami Y., Kawakami H., Aoki K., Nishiyama H. Organometallics. 18:1999;3584.
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0037449629
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For a recent review see:
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For a recent review see: North M. Tetrahedron: Asymmetry. 14:2003;147.
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North, M.1
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16
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0035828882
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13C NMR data consistent with that previously reported: Gerrits, P. J.; Zumbrägel, F.; Marcus, J. Tetrahedron 2001, 57, 8691
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13C NMR data consistent with that previously reported: Gerrits, P. J.; Zumbrägel, F.; Marcus, J. Tetrahedron 2001, 57, 8691.
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17
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85030951921
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Crystallographic data (excluding structure factors) for the structure in this paper, have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 217546. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.com.ac.uk)
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Crystallographic data (excluding structure factors) for the structure in this paper, have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication number CCDC 217546. Copies of the data can be obtained, free of charge, on application to CCDC, 12 Union Road, Cambridge CB2 1EZ, UK (Fax: +44(0)-1223-336033 or e-mail: deposit@ccdc.com.ac.uk).
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22
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0033477986
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Bunegar M.J., Dyer U.C., Evans G.R., Hewitt R.P., Jones S.W., Henderson N., Richards C.J., Sivaprasad S., Skead B.M., Stark M.A., Teale E. Org. Pro. R. & D. 3:1999;442.
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Bunegar, M.J.1
Dyer, U.C.2
Evans, G.R.3
Hewitt, R.P.4
Jones, S.W.5
Henderson, N.6
Richards, C.J.7
Sivaprasad, S.8
Skead, B.M.9
Stark, M.A.10
Teale, E.11
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23
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85030934979
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2. Column=CP-Chirasil-Dex CB: Initial temperature 75°C, initial time 1 min, ramp 1.5 deg./min to 195°C. 38.5 and 39.0 min corresponding to enantiomers of silylated 5 and 66.3 and 67.5 min corresponding to 5
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2. Column=CP-Chirasil-Dex CB: Initial temperature 75°C, initial time 1 min, ramp 1.5 deg./min to 195°C. 38.5 and 39.0 min corresponding to enantiomers of silylated 5 and 66.3 and 67.5 min corresponding to 5.
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