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Asymmetric synthesis via chiral oxazolines
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(b) Lutomski, K. A.; Meyers, A. I. "Asymmetric Synthesis via Chiral Oxazolines". In Asymmetric Synthesis; Morison, J. D.; Ed.; Academic Press, Inc.: New York, 1984, Vol. 3, pp. 213-274.
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2 For representative references: (a) Hattori, T.; Hotta, H.; Suzuki, T.; Miyano, S. J. Bull. Chem. Soc. Jpn. 1993, 66, 613-622.
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(c) Hattori, T.; Sakamoto, J.; Hayashizaka, N.; Miyano, S. Synthesis 1994, 199-202.
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Baker, R.W.1
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(g) Shindo, M.; Koga, K.; Tomioka, K. J. Am. Chem. Soc. 1992, 114, 8732-8733.
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Wilkinsons, G.; Stone, P. G. A.; Abel, E. W. Eds.; Pergamon Press: Oxford
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3 (a) Semmelhack, M. F. In "Comprehensive Organometallic Chemistry II", Wilkinsons, G.; Stone, P. G. A.; Abel, E. W. Eds.; Pergamon Press: Oxford, 1995, Vol. 12, pp. 979-1015.
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(b) Collman, J. P.; Hegedus, L. S.; Norton, J. R.; Finke, R. G. Principles and Applications of Organotransition Metal Chemistry, University Science Books, Mill Valley, Calf., 1987, pp. 921-940.
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(b) Watanabe, T.; Kamikawa, K.; Uemura, M. Tetrahedron Lett. 1995, 36, 6695-6698.
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(c) Kamikawa, K.; Watanabe, T.; Uemura, M. J. Org. Chem. 1996, 61, 1375-1384.
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Kamikawa, K.1
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0030010394
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5 Planar chirality of cyclophane is converted to axial chirality of binaphthyls by nucleophilic addition of aryl Grignard: Hattori, T.; Koike, N.; Okaishi, Y.; Miyano, S. Tetrahedron Lett. 1996, 37, 2057-2060.
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Hattori, T.1
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Miyano, S.4
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17
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85030270666
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note
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3) δ 1.88 (3H, s), 1.96 (6H, s), 2.08 (3H, s), 2.19 (3H, s), 5.36 (1H, d, J = 6.4 Hz), 5.67 (1H, t, J = 6.4 Hz), 5.97 (1H, d, J = 6.4 Hz), 6.77 (2H, s), 7.16-7.26 (3H, m), 7.49 (1H, dd, J = 6.3, 7.1 Hz).
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18
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0002356610
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7 (a) Uemura, M.; Nishimura, H.; Kamikawa, K.; Shiro, M. Inorg. Chim. Acta 1994, 222, 63-70.
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Inorg. Chim. Acta
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Uemura, M.1
Nishimura, H.2
Kamikawa, K.3
Shiro, M.4
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19
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0000291857
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(b) Bringmann, G.; Göbel, L.; Peters, K.; Peters, E.-M.; Schnering, H. G. Inorg. Chim. Acta 1994, 222, 255-260.
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Inorg. Chim. Acta
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Bringmann, G.1
Göbel, L.2
Peters, K.3
Peters, E.-M.4
Schnering, H.G.5
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20
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0039202559
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(c) Kalchauser, H.; Schögl, K.; Weissensteiner, W.; Werner, A. J. Chem. Soc. Perkin Trans 1 1983, 1723-1729.
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Kalchauser, H.1
Schögl, K.2
Weissensteiner, W.3
Werner, A.4
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23
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0027458113
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and references cited there in
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9 It is well known that the ortho oxygen on aryl Grignards can easily coordinate with magnesium in the enolate intermediate of the reaction with chiral aryloxazolines: Moorlag, H.; Meyers, A. I. Tetrahedron Lett. 1993, 34, 6989-6992 and references cited there in.
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Tetrahedron Lett.
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Moorlag, H.1
Meyers, A.I.2
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24
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0000160409
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10 (a) Price, D. A.; Simpkins, N. S.; MacLeod, A. M.; Watt, A. P. J. Org. Chem. 1994, 59, 1961-1962.
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J. Org. Chem.
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Price, D.A.1
Simpkins, N.S.2
MacLeod, A.M.3
Watt, A.P.4
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25
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0028086437
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(b) Price, D. A.; Simpkins, N. S.; MacLeod, A. M.; Watt, A. P. Tetrahedron Lett. 1994, 35, 6159-6162.
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Tetrahedron Lett.
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Price, D.A.1
Simpkins, N.S.2
MacLeod, A.M.3
Watt, A.P.4
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27
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85030279951
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