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5
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G. Wilkinson, F.G.A. Stone, E.W. Abel, Hegedus L.S. New York: Pergamon. Chapter 11.1
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Jacobsen E.N. Wilkinson G., Stone F.G.A., Abel E.W., Hegedus L.S. Comprehensive Organometallic Chemistry II. Vol. 12:1995;Pergamon, New York. Chapter 11.1.
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Ruffo, F.5
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9
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0037423130
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A few examples of nitrogen ligands based on carbohydrates have been described by other authors. For recent examples, see:
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A few examples of nitrogen ligands based on carbohydrates have been described by other authors. For recent examples, see: Huang H., Chen H., Hu X., Bai C., Zheng Z. Tetrahedron: Asymmetry. 14:2003;297-304.
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11
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0042564613
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14
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Klemm, D.5
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15
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0037069709
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Several examples of phosphorous ligands based on carbohydrates are known. For recent examples, see:
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Several examples of phosphorous ligands based on carbohydrates are known. For recent examples, see: Liu D., Li W., Zhang X. Org. Lett. 4:2002;4471-4474.
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Liu, D.1
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26
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33750368763
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Jacobsen E.N., Larrou J.F., Gao Y., Hong Y., Nie X., Zepp C.M. J. Org. Chem. 59:1994;1939-1942.
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30
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85030900827
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note
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We also estimate that the enantiomeric excess of the trans-epoxide is substantial. In fact, in the presence of the shift reagent, the signals of the major enantiomer are clear and well resolved, while those of the minor enantiomer fall within the noise.
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31
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85030899023
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note
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Actually, it should be noted that according to the stereochemical rules, the configurations at C2 and C3 are (R,R) and (S,R) for 2,3-D-gluco-diamines and 2,3-D-manno-diamines, respectively.
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32
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85030903300
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note
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10.
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