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For leading references:
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For leading references:. Bernsmann H., Van den Berg M., Hoen R., Minnaard A.J., Mehler G., Reetz M.T., De Vries J.G., and Feringa B.L. J. Org. Chem. 70 (2005) 943
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Reetz M.T., Sell T., Meiswinkel A., and Mehler G. Angew. Chem., Int. Ed. 42 (2003) 790
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Hu A.-G., Fu Y., Xie J.-H., Zhou H., Wang L.-X., and Zhou Q.-L. Angew. Chem., Int. Ed. 41 (2002) 2348
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Lee S.-G., Zhang Y.J., Song C.E., Lee J.K., and Choi J.H. Angew. Chem., Int. Ed. 41 (2002) 847
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Lee, S.-G.1
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Zhang, Z.1
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24
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0022921957
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All exceptions are with non-phenethyl systems. For a relevent example that uses alternatives to the acetate group, including a trifluoroacetamide, see:
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All exceptions are with non-phenethyl systems. For a relevent example that uses alternatives to the acetate group, including a trifluoroacetamide, see:. Noyori R., Ohta M., Hsiao Y., and Kitamura. J. Am. Chem. Soc. 108 (1986) 7117
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(1986)
J. Am. Chem. Soc.
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Noyori, R.1
Ohta, M.2
Hsiao, Y.3
Kitamura4
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25
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0012000985
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Kocienski P.J. (Ed), Thieme Medical Publishers, New York Chapter 6
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In: Kocienski P.J. (Ed). Protecting Groups (2000), Thieme Medical Publishers, New York 185 Chapter 6
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Protecting Groups
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32
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37049133190
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Boar R.B., McGhie J.F., Robinson M., Barton D.H.R., Horwell D.C., and Stick R.V. J. Chem. Soc., Perkin Trans. 1 (1975) 1237
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J. Chem. Soc., Perkin Trans. 1
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Boar, R.B.1
McGhie, J.F.2
Robinson, M.3
Barton, D.H.R.4
Horwell, D.C.5
Stick, R.V.6
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39
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0001246886
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Van den Berg M., Haak R.M., Minnaard A.J., deVries A.H.M., Vries J.G., and Feringa B.L. Adv. Synth. Catal. 344 (2002) 1003
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Adv. Synth. Catal.
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Van den Berg, M.1
Haak, R.M.2
Minnaard, A.J.3
deVries, A.H.M.4
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Feringa, B.L.6
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40
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0036003910
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Storace L., Anzalone P.N., Confalone W.P., Davis J.M., Fortunak J.M., Giangiordano M., Haley J.J., Kamholz K., Li H.-Y., Ma P., Nugent W.A., Parsons R.L., Sheeran P.J., Silverman C.E., Waltermire R.E., and Wood C.C. Org. Process Res. Dev. 6 (2002) 54
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Org. Process Res. Dev.
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Storace, L.1
Anzalone, P.N.2
Confalone, W.P.3
Davis, J.M.4
Fortunak, J.M.5
Giangiordano, M.6
Haley, J.J.7
Kamholz, K.8
Li, H.-Y.9
Ma, P.10
Nugent, W.A.11
Parsons, R.L.12
Sheeran, P.J.13
Silverman, C.E.14
Waltermire, R.E.15
Wood, C.C.16
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41
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33746600383
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note
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It is assumed that optimization of enantioselectivity and catalyst loading will be conducted on case by case basis.
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42
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0003128726
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For a review of Josiphos discovery and applications, see:
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For a review of Josiphos discovery and applications, see:. Blaser H.-U., Brieden W., Pugin B., Spindler F., Studer M., and Togni A. Top. Catal. 19 (2002) 3
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(2002)
Top. Catal.
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Blaser, H.-U.1
Brieden, W.2
Pugin, B.3
Spindler, F.4
Studer, M.5
Togni, A.6
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43
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33746598321
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For a recent example of a Josiphos ligand used for the asymmetric hydrogenation of beta-aminoamides, see:
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For a recent example of a Josiphos ligand used for the asymmetric hydrogenation of beta-aminoamides, see:. Hsiao Y., Rivera N.R., Rosner T., Krska S.W., Njolito E., Wang F., Sun Y., Armstrong III J.D., Grabowski E.J.J., Tillyer R.D., Spindler F., and Malan C. J. Am. Chem. Soc. 125 (2004) 1142
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J. Am. Chem. Soc.
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Hsiao, Y.1
Rivera, N.R.2
Rosner, T.3
Krska, S.W.4
Njolito, E.5
Wang, F.6
Sun, Y.7
Armstrong III, J.D.8
Grabowski, E.J.J.9
Tillyer, R.D.10
Spindler, F.11
Malan, C.12
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