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37449015782
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Even if enrichment during crystallization were taking place, an initial enantiomeric excess of more than 35% must be assumed
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Even if enrichment during crystallization were taking place, an initial enantiomeric excess of more than 35% must be assumed.
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86
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0038445374
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77954094031
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We found one unsuccessful contemporary attempt to apply the CSA method: H. Brockmann, K. Maier, Justus Liebigs Ann. Chem. 1938, 535, 149-175.
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37049172761
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Early example of asymmetric catalysis with camphorsulfonic acid: P. Maitland, W. H. Mills, J. Chem. Soc. 1936, 987-998.
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Angew. Chem. Int. Ed. 2004, 43, 1566-1568 and subsequent works;
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Angew. Chem. Int. Ed. 2005, 44, 7424-7427 and subsequent works;
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30744477746
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37449024615
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S are not equal, the reaction progress curve assumes a different shape, which will be discussed elsewhere.
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S are not equal, the reaction progress curve assumes a different shape, which will be discussed elsewhere.
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104
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37449023468
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eq = 3.5 was found in an aqueous alcoholic buffer at pH 7 and 80°C: A. Grouiller, P. Thomassery, H. Pacheco, Bull. Soc. Chim. Fr. 1973, 3448-3451.
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eq = 3.5 was found in an aqueous alcoholic buffer at pH 7 and 80°C: A. Grouiller, P. Thomassery, H. Pacheco, Bull. Soc. Chim. Fr. 1973, 3448-3451.
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106
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37449011358
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(Chem. Abstr. 1924, 18, 13671).
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(Chem. Abstr. 1924, 18, 13671).
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109
-
-
37449015025
-
-
(Chem. Abstr. 1930, 24, 30312)
-
(Chem. Abstr. 1930, 24, 30312)
-
-
-
-
110
-
-
37449004552
-
-
b
-
; b) J. Xie, L. Wang, C. Liu, D. Ge, C. A 1988, 108, 204365;
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C. A
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-
-
Xie, J.1
Wang, L.2
Liu, C.3
Ge, D.4
-
112
-
-
33749155661
-
-
M. Hauteville, R. Stromberg, P. Gaillard, M.-C. Duclos, Liebigs Ann. 1995, 1707-1709.
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(1995)
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-
-
Hauteville, M.1
Stromberg, R.2
Gaillard, P.3
Duclos, M.-C.4
-
118
-
-
2042436857
-
-
a) W. Riedl, J. Nicki, K. H. Risse, R. Mitteldorf, Chem. Ber. 1956, 89, 1849-1863;
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Chem. Ber
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-
Riedl, W.1
Nicki, J.2
Risse, K.H.3
Mitteldorf, R.4
-
128
-
-
37449000227
-
-
Determinations of ee values are more accurate at higher conversions because of the better signal to noise ratio.
-
Determinations of ee values are more accurate at higher conversions because of the better signal to noise ratio.
-
-
-
-
129
-
-
0001063772
-
-
C. O. Miles, L. Main, B. K. Nicholson, Aust. J. Chem. 1989, 42, 1103-1113.
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(1989)
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-
Miles, C.O.1
Main, L.2
Nicholson, B.K.3
-
131
-
-
37448999831
-
-
(Chem. Abstr. 1950, 44, 7577).
-
(Chem. Abstr. 1950, 44, 7577).
-
-
-
-
132
-
-
17144365401
-
-
Naringenin 4′,7-dimethyl ether: T. A. Geissman, R. O. Clinton, J. Am. Chem. Soc. 1946, 68, 697-700;
-
a) Naringenin 4′,7-dimethyl ether: T. A. Geissman, R. O. Clinton, J. Am. Chem. Soc. 1946, 68, 697-700;
-
-
-
-
133
-
-
37449029261
-
-
For conversion into chalcone, see ref.[8i
-
[8i].
-
-
-
-
136
-
-
0003154477
-
-
For examples, see: a
-
For examples, see: a) C. A. Mead, A. Moscowitz, J. Am. Chem. Soc. 1980, 102, 7301-7302;
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J. Am. Chem. Soc
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-
Mead, C.A.1
Moscowitz, A.2
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138
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0038106164
-
-
c) J. W. Cornforth, R. H. Cornforth, M. J. S. Dewar, Nature 1944, 153, 317-317.
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Nature
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, pp. 317-317
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-
Cornforth, J.W.1
Cornforth, R.H.2
Dewar, M.J.S.3
-
139
-
-
37449007653
-
-
D = -182° (solvent not available) and has therefore the S configuration: G. P. Kononenko, S. A. Popravko, N. S. Vul'fson, Bioorg. Khim. 1975, 1, 506-511
-
D = -182° (solvent not available) and has therefore the S configuration: G. P. Kononenko, S. A. Popravko, N. S. Vul'fson, Bioorg. Khim. 1975, 1, 506-511
-
-
-
-
140
-
-
37449011551
-
-
(Chem. Abstr. 1975, 83, 128765).
-
(Chem. Abstr. 1975, 83, 128765).
-
-
-
-
142
-
-
0014352659
-
-
E. B. Lee, K. H. Shin, W. S. Woo, J. Med. Chem. 1968, 11, 1262-1263.
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J. Med. Chem
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Lee, E.B.1
Shin, K.H.2
Woo, W.S.3
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0027133428
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a) S. Sogawa, Y. Nihro, H. Ueda, A. Izumi, T. Miki, H. Matsumoto, T. Satoh, J. Med. Chem. 1993, 36, 3904-3909;
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Miki, T.5
Matsumoto, H.6
Satoh, T.7
-
144
-
-
37449022517
-
-
U. S. Patent 5068364
-
b) H. Takagaki, S. Nakanishi, M. Abe, H. Ohki, Y. Sano, U. S. Patent 5068364, 1991.
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(1991)
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-
Takagaki, H.1
Nakanishi, S.2
Abe, M.3
Ohki, H.4
Sano, Y.5
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146
-
-
84948870203
-
-
b) L. Reichel, W. Burkart, K. Müller, Justus Liebigs Ann. Chem. 1942, 550, 146-151.
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(1942)
Justus Liebigs Ann. Chem
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, pp. 146-151
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-
Reichel, L.1
Burkart, W.2
Müller, K.3
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150
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-
1342302800
-
-
b) H. Chu, H. Wu, Y. Lee, Tetrahedron 2004, 60, 2647-2656.
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Tetrahedron
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Chu, H.1
Wu, H.2
Lee, Y.3
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152
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33750958316
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-
a) M. do. C. M. Miraglia, A. P. de Padua, A. A. L. Mesquita, O. R. Gottlieb, Phytochemistry 1985, 24, 1120-1120;
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(1985)
Phytochemistry
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-
do, M.1
Miraglia, C.M.2
de Padua, A.P.3
Mesquita, A.A.L.4
Gottlieb, O.R.5
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153
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85024244443
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b) N. Tanaka, T. Murakami, H. Wada, A. B. Gutierrez, Y. Saiki, C. Chen, Chem. Pharm. Bull. 1985, 33, 5231-5238.
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Tanaka, N.1
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Chen, C.6
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