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[4a] D. Hoppe, F. Hintze, P. Tebben, Angew. Chem 1990, 102, 1457-1458; Angew. Chem. Int. Ed. Engl. 1990, 29, 1422-1423.
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0001854238
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[7a] D. Hoppe, O. Zschage, Angew. Chem. 1989, 101, 67-69; Angew. Chem. Int. Ed. Engl 1989, 28, 67-71.
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Hoppe, D.1
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[7a] D. Hoppe, O. Zschage, Angew. Chem. 1989, 101, 67-69; Angew. Chem. Int. Ed. Engl 1989, 28, 67-71.
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0344799549
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0000898481
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D. Hoppe, R. Hanko, A. Brönneke, F. Lichtenberg, E. van Hülsen, Chem. Ber. 1985, 118, 2822-2851.
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0001229447
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29
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30
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2842542195
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note
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-3, Flack parameter O 07(4), hydrogens calculated and refined as riding atoms. The data set was collected with an Enraf-Nonius MACH3 diffractometer. Programs used: data reduction: MolEN, structure solution: SHELXS-86, structure refinement: SHELXL-93, graphics: SCHAKAL-92. Crystallographic data (excluding structure factors) for the structures reported in this paper have been deposited with the Cambridge Crystallographic Data Centre as supplementary publication no. CCDC-100987. Copies of the data can be obtained free of charge on application to The Director, CCDC, 12 Union Road, Cambridge, CB2 1EZ, UK [Fax: (internat.) +44 (0)1223 336033, e-mail: deposit@ccdc.cam.ac.uk].
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0001317003
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[15b] D. Hoppe, A. Carstens, T. Krämer, Angew. Chem. 1990, 102, 1455-1456; Angew. Chem. Int. Ed. Engl. 1990, 29, 1424-1425.
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Hoppe, D.1
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33
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0343177680
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[15b] D. Hoppe, A. Carstens, T. Krämer, Angew. Chem. 1990, 102, 1455-1456; Angew. Chem. Int. Ed. Engl. 1990, 29, 1424-1425.
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37
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1542714173
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For the "gear effect" in N.N-diisopropyl groups see: A. Liden, C. Roussel, T. Liljetors, M. Chanon, R. E. Carter, J. Metzger, J. Sandström, J. Am. Chem. Soc. 1976, 98, 2853.
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Liden, A.1
Roussel, C.2
Liljetors, T.3
Chanon, M.4
Carter, R.E.5
Metzger, J.6
Sandström, J.7
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38
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0005366195
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2-symmetric ligand; for the magnesium-(-)-sparteine complexes see. G. Fraenkel, C. Cottrell, J. Ray. J. Russell, J. Chem. Soc., Chem. Commun. 1971, 273-274.
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(1971)
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Fraenkel, G.1
Cottrell, C.2
Ray, J.3
Russell, J.4
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40
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2842603180
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Melting point of the racemic compound
-
Melting point of the racemic compound.
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41
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2842589871
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Signal appears at lower field
-
Signal appears at lower field.
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42
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2842571042
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The enantiomeric excess was deduced from the hydrogenation experiment
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The enantiomeric excess was deduced from the hydrogenation experiment.
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