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3
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0027972828
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2. For recent enantioselective syntheses of α-amino acids, see: (a) Lander, P. A.; Hegedus, L. S. J. Am. Chem. Soc. 1994, 116, 8126-8132;
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(b) Myers, A. G.; Gleason, J. L.; Yoon, T. J. Am. Chem. Soc. 1995, 117, 8488-8489;
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(d) Calmes, M.; Daunis, J.; Mai, N.; Natt, F. Tetrahedron Lett. 1996, 37, 379-380;
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(f) Ferey, V.; Toupet, L.; Le Gall, T.; Mioskowski, C. Angew. Chem. Int. Ed. Engl. 1996, 35, 430-432;
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(g) Ferey, V.; Vedrenne, P.; Toupet, L.; Le Gall, T.; Mioskowski, C. J. Org. Chem. 1996, 61, 7244-7245.
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3. (a) Hirama, M.; Hioki, H.; Itô, S. Tetrahedron Lett. 1988, 29, 3125-3128;
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(b) Barrett, A. G. M.; Weipert, P. D.; Dhanak, D.; Husa, R. K.; Lebold, S. A. J. Am. Chem. Soc. 1991, 113, 9820-9824.
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14
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0010553894
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note
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3OH) to yield compound 3e (0.89 g, 89%).
-
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16
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0001285932
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8. See also: (a) Ojima, I.; Chen, H.-J. C.; Qiu, X, Tetrahedron 1988, 44, 5307-5318;
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Ojima, I.1
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18
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0010624126
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reference 4
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(c) reference 4.
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19
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0027209519
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9. Fisher, J. W.; Dunigan, J. M.; Hatfield, L. D.; Hoying, R. C.; Ray, J. E.; Thomas, K. L. Tetrahedron Lett. 1993, 34, 4755-4758.
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21
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0010625547
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note
-
f = 0.65). D-tert-Leucine 4e was obtained as a white solid (0.145 g; 88%).
-
-
-
-
22
-
-
0010588265
-
-
note
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D -31.4 (c 1, AcOH).
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23
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13. (a) Eguchi, T.; Koudate, T.; Kakinuma, K. Tetrahedron 1993, 49, 4527-4540;
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(e) Diner, U. E.; Worsley, M.; Lown, J. W.; Forsythe, J.-A. Tetrahedron Lett. 1986, 3145-3148;
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Diner, U.E.1
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29
-
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0010555429
-
-
note
-
t(L-enantiomer) = 3.7 min / 4.8 min (alanine); 5.9 min / 9.2 min (norvaline); 3.9 min / 4.9 min (serine); 5.8 min / 7.4 min (valine).
-
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-
-
30
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0000751250
-
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Paquette, L. A. Ed.; Wiley: New York
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15. Recent accounts on the use of chiral oxazolidinones in asymmetric synthesis: (a) Evans, D. A.; Kim, A. S. In Encyclopedia of Reagents for Organic Synthesis, Vol. 1; Paquette, L. A. Ed.; Wiley: New York, 1995; pp. 345-356;
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