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Transition metal catalyzed reactions
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3. H. Brunner, Transition Metal Catalyzed Reactions in Houben-Weyl, Vol. E 21d, Stereoselective Synthesis (Eds.: G. Helmchen, R. W. Hoffmann, J. Mulzer, E. Schaumann), Thieme, Stuttgart, New York 1995, 4074-4081 and references therein.
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Brunner, H.1
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4
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0003394736
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VCH, Weinheim
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4. H. Brunner, W. Zettlmeier, Handbook of Enantioselective Catalysis, Vol. I & II, VCH, Weinheim 1993.
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Brunner, H.1
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5. H. Nishiyama, H. Sakaguchi, T. Nakamura, M. Horihata, M. Kondo, K. Itoh, Organometallics 1989, 8, 846-848.
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Nishiyama, H.1
Sakaguchi, H.2
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Kondo, M.5
Itoh, K.6
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6
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0000011537
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6. H. Nishiyama, M. Kondo, T. Nakamura, K. Itoh, Organometallics 1991, 10, 500-508.
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Nishiyama, H.1
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7
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7. H. Nishiyama, S. Yamaguchi, S.-B. Park, K. Itoh, Tetrahedron: Asymmetry 1993, 4, 143-150.
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Nishiyama, H.1
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Park, S.-B.3
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8
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85008090337
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8. D. A. Evans, K. A. Woerpel, M. M. Hinman, M. M. Faul, J. Am. Chem. Soc. 1991, 113, 726-728.
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Evans, D.A.1
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Hinman, M.M.3
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9
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84940909672
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9. C. Bolm, K. Weickhardt, M. Zehnder, T. Ranff, Chem. Ber. 1991, 124, 1173-1180.
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Bolm, C.1
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Ranff, T.4
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12
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0030847032
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and references therein
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12. G. Chelucci, G. A. Pinna, A. Saba, Tetrahedron: Asymmetry 1997, 8, 2571-2578 and references therein.
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Tetrahedron: Asymmetry
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Chelucci, G.1
Pinna, G.A.2
Saba, A.3
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14
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0001485412
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14. P. Hayoz, A. von Zelewsky, H. Stoeckli-Evans, J. Am. Chem. Soc. 1993, 115, 5111-5114.
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Hayoz, P.1
Von Zelewsky, A.2
Stoeckli-Evans, H.3
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16
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0010339791
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-
Since (+)-pinocarvone was prepared from (-)-α-pinene (ca. 80% ee) 10% of the other enantiomer was present. Hence, after synthesis of the chiral oxazoline 9 there might be a mixture of diastereomers
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16. Since (+)-pinocarvone was prepared from (-)-α-pinene (ca. 80% ee) 10% of the other enantiomer was present. Hence, after synthesis of the chiral oxazoline 9 there might be a mixture of diastereomers.
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-
-
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17
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-
0010388058
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-
In this paper L-menthyl-represents [(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]-and D-menthyl-represents [(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl]-
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17. In this paper L-menthyl-represents [(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]-and D-menthyl-represents [(1S,2R,5S)-2-isopropyl-5-methylcyclohexyl]-.
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-
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20
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0010418367
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Ph.D. Thesis, Stanford University
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20. S. G. Hentges, Ph.D. Thesis, Stanford University 1980.
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Hentges, S.G.1
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21
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49149142406
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21. T. Hayashi, M. Konishi, M. Kumada, Tetrahedron Lett. 1979, 21, 1871-1874.
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Hayashi, T.1
Konishi, M.2
Kumada, M.3
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24
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0000730350
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24. T. W. Bell, L.-Y. Hu, S. V. Patel, J. Org. Chem. 1987, 52, 3847-3850.
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Bell, T.W.1
Hu, L.-Y.2
Patel, S.V.3
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25
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33845550434
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25. General procedure: W. K. Fife, J. Org. Chem. 1983, 48, 1375-1377.
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Fife, W.K.1
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27
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0001542678
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27. K. Nordström, E. Macedo, C. Moberg, J. Org. Chem. 1997, 62, 1604-1609.
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Nordström, K.1
Macedo, E.2
Moberg, C.3
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30
-
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0010383174
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-
We thank Prof. A. von Zelewsky, University of Fribourg (Switzerland) for providing this compound
-
30. We thank Prof. A. von Zelewsky, University of Fribourg (Switzerland) for providing this compound.
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-
-
-
33
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0010341897
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-
4 to improve the performance of Rh-catalysed asymmetric hydrosilylations has been reported (e.g. Refs. 6 and 7)
-
4 to improve the performance of Rh-catalysed asymmetric hydrosilylations has been reported (e.g. Refs. 6 and 7).
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-
-
-
35
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0029965916
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35. The CIP-nomenclature of related compounds (e.g. Ref. 12 and G. Chelucci, M. A. Cabras, Tetrahedron: Asymmetry 1996, 7, 965-966) is in error. The correct configuration of 3-9 at C-5 is R (C-4a/C-8a has priority with respect to C-9/C-7) and at C-7 also R (priority sequence: C-9>C-8/C-8a>C-6/C-5).
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(1996)
Tetrahedron: Asymmetry
, vol.7
, pp. 965-966
-
-
Chelucci, G.1
Cabras, M.A.2
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