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G. C. Fu, Acc. Chem. Res., 33, 412 (2000) and references therein.
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Fu, G.C.1
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3
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b) T. Kawabata, K. Yamamoto, Y. Momose, H. Yoshida, Y. Nagaoka, and K. Fuji, Chem. Commun., 2001, 2700.
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Chem. Commun.
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4
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5
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b) T. Oriyama, K. Imai, T. Sano, and T. Hosoya, Tetrahedron Lett., 39, 3529 (1998).
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6
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10
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14
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33748216006
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c) K.-S. Jeong, K. Parris, P. Ballester, and J. Rebek, Jr., Angew. Chem., Int. Ed. Engl., 29, 555 (1990).
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15
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0012980793
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note
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4: C, 73.74; H, 6.19; N, 10.49. Found: C, 73.72; H, 6.23; N, 10.53%.
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16
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0012984776
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note
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The conversion rate of the reaction between 1-phenylethanol and acetic anhydride with the catalyst 1 was nearly equal to or slightly slower than that with the DMAP itself under similar reaction conditions. This is possibly because the reaction center (ring nitrogen) of 1 is sterically more congested than the DMAP.
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18
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0001647560
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For a similar trend of solvent effects on the kinetic resolution, see: J. C. Ruble, J. Tweddell, and G. C. Fu, J. Org. Chem., 63, 2794 (1998).
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Ruble, J.C.1
Tweddell, J.2
Fu, G.C.3
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19
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0033516290
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For the same observation, see: B. Tao, J. C. Ruble, D. A. Hoic, and G. C. Fu, J. Am. Chem. Soc., 121, 5901 (1999).
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J. Am. Chem. Soc.
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Tao, B.1
Ruble, J.C.2
Hoic, D.A.3
Fu, G.C.4
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