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5
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33747165991
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Gobert, J.; Greets, J. P.; Bodson, G. Eur. Pat. Appl. E0162036; Chem. Abstr. 105, 018467.
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6
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Dolityzky, B. Z. PCT Int. Appl. WO 2004/069796; Chem. Abstr. 133, 183002.
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Ates, C.; Surtees, J.; Burteau, A. C.; Marmon, V.; Cavoy, E. PCT Int. Appl. WO 2003/014080; Chem. Abstr. 138, 170071.
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Futagawa, T.; Canvat, J. P.; Cavoy, E.; Deleers, M.; Hamende, M.; Zimmermann, V. US Patent 2000/6107492; Chem. Abstr., 133, 183002.
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Cavoy, E.; Hamende, M.; Deleers, M.; Canvat, J. P.; Zimmermann, V. US Patent 2000/6124473; Chem. Abstr. 133, 268549.
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Surtees, J.; Marmon, V; Differding, E.; Zimmermann, V. PCT Int. Appl. WO 2001/64367.
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33747201771
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Boaz, N. W.; Debenham, S. D. PCT Int. Appl. WO 2002/26705; Chem. Abstr. 136, 279566.
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13
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27944472739
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Boschi F., Camps P., Comes-Franchini M., Munoz-Torrero D., Riccib A., and Sancheza L. Tetrahedron: Asymmetry 16 (2005) 3739
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Boschi, F.1
Camps, P.2
Comes-Franchini, M.3
Munoz-Torrero, D.4
Riccib, A.5
Sancheza, L.6
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Sayyed I.A., Thakur V.V., Nikalje M.D., Dewkar G.K., Kotkar S.P., and Sudalai A. Tetrahedron 61 (2005) 2831
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Sayyed, I.A.1
Thakur, V.V.2
Nikalje, M.D.3
Dewkar, G.K.4
Kotkar, S.P.5
Sudalai, A.6
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22
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Hayashi, Y.1
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Cordova, A.1
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Himo, F.5
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27
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4143094833
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Houk K.N., and List B. (Eds)
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In: Houk K.N., and List B. (Eds). Acc. Chem. Res. 37 (2004) 487
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28
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33747183208
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List B., and Bolm C. (Eds)
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In: List B., and Bolm C. (Eds). Adv. Synth. Catal. (2004) 346
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(2004)
Adv. Synth. Catal.
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30
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0037043180
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For a review of proline-catalyzed asymmetric reactions, see:
-
For a review of proline-catalyzed asymmetric reactions, see:. List B. Tetrahedron 58 (2002) 5573
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List, B.1
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31
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33747178249
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note
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2 requires C, 72.84; H, 8.56; N, 5.66. Found: C, 72.88; H, 8.55; N, 5.63.
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32
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0033515510
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Zhao M.L., Mano E., Song Z., Tschaen D.M., Grabowski E.J., and Reider P.J. J. Org. Chem. 64 (1999) 2564
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Reider, P.J.6
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33
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33747194261
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-
note
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2 requires C, 56.45; H, 8.29; N, 16.46. Found: C, 56.49; H, 8.34; N, 16.44.
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34
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4344692607
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HPLC conditions: Chiral OD-H column; hexane: i-PrOH (90:10 v/v); flow rate 1.0 mL/min; UV - 210 nm; column temperature 25 °C; retention time: 10.3 min (R-isomer) and 16.3 min (S-isomer). Compared with reported conditions:
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HPLC conditions: Chiral OD-H column; hexane: i-PrOH (90:10 v/v); flow rate 1.0 mL/min; UV - 210 nm; column temperature 25 °C; retention time: 10.3 min (R-isomer) and 16.3 min (S-isomer). Compared with reported conditions:. Rao B.M., Ravi R., Reddy B.S., Sivakumar S., Gopi Chand I., Praveen Kumar K., Acharyulu P.V.R., Om Reddy G., and Srinivasu M.K. J. Pharm. Biomed. Anal. 35 (2004) 1017
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, pp. 1017
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Rao, B.M.1
Ravi, R.2
Reddy, B.S.3
Sivakumar, S.4
Gopi Chand, I.5
Praveen Kumar, K.6
Acharyulu, P.V.R.7
Om Reddy, G.8
Srinivasu, M.K.9
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