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35
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0012301660
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note
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01M Phosphate buffer, 2.7 mM KCl, 137 mM NaCl, pH = 7.4.
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-
-
36
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0012257640
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note
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2O = 10:1 (63%).
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37
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0012354128
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-
note
-
See ESI†, Table 1S.
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38
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0035860999
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See also: S. Bahmanyar and K. N. Houk, J. Am. Chem. Soc., 2001, 45, 11273; J.-F. Lin, C.-C. Wu and M.-H. Lien, J. Phys. Chem., 1995, 99, 16903.
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Bahmanyar, S.1
Houk, K.N.2
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39
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0001604129
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See also: S. Bahmanyar and K. N. Houk, J. Am. Chem. Soc., 2001, 45, 11273; J.-F. Lin, C.-C. Wu and M.-H. Lien, J. Phys. Chem., 1995, 99, 16903.
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0035850820
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A. Heine, G. Desantis, J. G. Luz, M. Mitchell, C.-H. Wong and I. A. Wilson, Science, 2001, 294, 369.
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Heine, A.1
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Wilson, I.A.6
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41
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0012348952
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note
-
The reactions also proceeded in the following organic solvents: THF, dioxane, EtOH and MeOH.
-
-
-
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42
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0012300010
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note
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The products were obtained as racemates in DMSO/PBS 1+1.
-
-
-
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43
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0001676496
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13C NMR data of the isolated 5-O-benzyl-D-xylulose were identical to that produced by rabbit muscle aldolase (RAMA)-catalysis. See: M. D. Bednarski, E. S. Simon, N. Bischofberger, W.-D. Fessner, M.-J. Kim, W. Lees, T. Saito, H. Waldmann and G. M. Whitesides, J. Am. Chem. Soc., 1989, 111, 627.
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Kim, M.-J.5
Lees, W.6
Saito, T.7
Waldmann, H.8
Whitesides, G.M.9
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