-
1
-
-
0018347070
-
-
[1a] H. G. W. Leuenberger, W. Boguth, R. Barner, M. Schmid, R. Zell, Helv. Chim. Acta 1979, 62, 455-463.
-
(1979)
Helv. Chim. Acta
, vol.62
, pp. 455-463
-
-
Leuenberger, H.G.W.1
Boguth, W.2
Barner, R.3
Schmid, M.4
Zell, R.5
-
4
-
-
0024990816
-
-
R. Schmid, S. Antoulas, A. Rüttimann, M. Schmid, M. Vecchi, H. Weiser, Helv. Chim. Acta 1990, 73, 1276-1299.
-
(1990)
Helv. Chim. Acta
, vol.73
, pp. 1276-1299
-
-
Schmid, R.1
Antoulas, S.2
Rüttimann, A.3
Schmid, M.4
Vecchi, M.5
Weiser, H.6
-
5
-
-
0043231033
-
-
S. Suzuki, F. Mori, T. Takigawa, K. Ibata, Y. Ninagawa, T. Nishida, M. Mizuno, Y. Tanaka, Tetrahedron Lett. 1983, 24, 5103-5106.
-
(1983)
Tetrahedron Lett.
, vol.24
, pp. 5103-5106
-
-
Suzuki, S.1
Mori, F.2
Takigawa, T.3
Ibata, K.4
Ninagawa, Y.5
Nishida, T.6
Mizuno, M.7
Tanaka, Y.8
-
6
-
-
0030920075
-
-
T. Eguchi, K. Arakawa, T. Terachi, K. Kakinuma, J. Org. Chem. 1997, 62, 1924-1933.
-
(1997)
J. Org. Chem.
, vol.62
, pp. 1924-1933
-
-
Eguchi, T.1
Arakawa, K.2
Terachi, T.3
Kakinuma, K.4
-
7
-
-
37049070870
-
-
P. Ferraboschi, A. Fiecchi, P. Grisenti, E. Santaniello, J. Chem. Soc., Perkin Trans. 1 1987, 1749-1752.
-
(1987)
J. Chem. Soc., Perkin Trans. 1
, pp. 1749-1752
-
-
Ferraboschi, P.1
Fiecchi, A.2
Grisenti, P.3
Santaniello, E.4
-
8
-
-
0011779243
-
-
F. E. Ziegler, E. P. Stirchak, R. T. Wester, Tetrahedron Lett. 1986, 27, 1229-1232.
-
(1986)
Tetrahedron Lett.
, vol.27
, pp. 1229-1232
-
-
Ziegler, F.E.1
Stirchak, E.P.2
Wester, R.T.3
-
9
-
-
46549101647
-
-
F. van Middelsworth, Y. F. Wang, B.-N. Zhou, D. DiTullio, C. J. Sih, Tetrahedron Lett. 1985, 961-964.
-
(1985)
Tetrahedron Lett.
, pp. 961-964
-
-
Van Middelsworth, F.1
Wang, Y.F.2
Zhou, B.-N.3
DiTullio, D.4
Sih, C.J.5
-
10
-
-
37049085665
-
-
C. Funganti, P. Grasselli, S. Servi, H.-E. Högberg, J. Chem. Soc., Perkin Trans. 1 1988, 3061-3065.
-
(1988)
J. Chem. Soc., Perkin Trans. 1
, pp. 3061-3065
-
-
Funganti, C.1
Grasselli, P.2
Servi, S.3
Högberg, H.-E.4
-
11
-
-
0020634913
-
-
K. Mori, Tetrahedron 1983, 39, 3107-3109.
-
(1983)
Tetrahedron
, vol.39
, pp. 3107-3109
-
-
Mori, K.1
-
14
-
-
0035861011
-
-
and references cited therein
-
Base-catalyzed mono esterification of methylsuccinic anhydride is an additional possibility: Y. Chen, L. Deng, J. Am. Chem. Soc. 2001, 123, 11302-11303 and references cited therein.
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 11302-11303
-
-
Chen, Y.1
Deng, L.2
-
15
-
-
0003544583
-
-
(Ed.: I. Ojima), John Wiley & Sons, New York
-
Survey: T. Ohkuma, M. Kitamura, R. Noyori in Catalytic Asymmetric Synthesis, 2nd ed. (Ed.: I. Ojima), John Wiley & Sons, New York, 2000, pp. 1-94.
-
(2000)
Catalytic Asymmetric Synthesis, 2nd Ed.
, pp. 1-94
-
-
Ohkuma, T.1
Kitamura, M.2
Noyori, R.3
-
16
-
-
0000077559
-
-
I. Komarov, A. Börner, Angew. Chem. 2001, 113, 1237-1240; Angew. Chem. Int. Ed. 2001, 40, 1197-1200, and references cited therein.
-
(2001)
Angew. Chem.
, vol.113
, pp. 1237-1240
-
-
Komarov, I.1
Börner, A.2
-
17
-
-
0035794970
-
-
and references cited therein
-
I. Komarov, A. Börner, Angew. Chem. 2001, 113, 1237-1240; Angew. Chem. Int. Ed. 2001, 40, 1197-1200, and references cited therein.
-
(2001)
Angew. Chem. Int. Ed.
, vol.40
, pp. 1197-1200
-
-
-
18
-
-
0000550393
-
-
M. T. Reetz, G. Mehler, Angew. Chem. 2000, 112, 4047-4049; Angew. Chem. Int. Ed. 2000, 39, 3889-3890.
-
(2000)
Angew. Chem.
, vol.112
, pp. 4047-4049
-
-
Reetz, M.T.1
Mehler, G.2
-
19
-
-
0034602040
-
-
M. T. Reetz, G. Mehler, Angew. Chem. 2000, 112, 4047-4049; Angew. Chem. Int. Ed. 2000, 39, 3889-3890.
-
(2000)
Angew. Chem. Int. Ed.
, vol.39
, pp. 3889-3890
-
-
-
20
-
-
29044437476
-
-
WO-0194278, 2001
-
M. T. Reetz, G. Mehler, A. Meiswinkel, WO-0194278, 2001 [Chem. Abstr. 2001, 136, 20159].
-
(2001)
Chem. Abstr.
, vol.136
, pp. 20159
-
-
Reetz, M.T.1
Mehler, G.2
Meiswinkel, A.3
-
21
-
-
0001181461
-
-
Hydrogenation of Stobbe condensation products derived from aromatic aldehydes gave enantiomeric excess of up to 96% ee and 94% ee with MOD-DIOP and XYL-DIOP, respectively, as ligands: K. Yoshikawa, K. Inoguchi, T. Morimoto, K. Achiwa, Heterocycles 1990, 31, 1413-1416, and literature cited. With Et-DuPHOS as ligand hydrogenation of Stobbe condensatation products derived from aliphatic aldehydes was achieved with up to 99% ee: M. J. Burk, F. Bienewald, M. Harris, A. Zanotti-Gerosa, Angew. Chem. 1998, 110, 2034-2037; Angew. Chem. Int. Ed. 1998, 37, 1931-1933.
-
(1990)
Heterocycles
, vol.31
, pp. 1413-1416
-
-
Yoshikawa, K.1
Inoguchi, K.2
Morimoto, T.3
Achiwa, K.4
-
22
-
-
0001181461
-
-
Hydrogenation of Stobbe condensation products derived from aromatic aldehydes gave enantiomeric excess of up to 96% ee and 94% ee with MOD-DIOP and XYL-DIOP, respectively, as ligands: K. Yoshikawa, K. Inoguchi, T. Morimoto, K. Achiwa, Heterocycles 1990, 31, 1413-1416, and literature cited. With Et-DuPHOS as ligand hydrogenation of Stobbe condensatation products derived from aliphatic aldehydes was achieved with up to 99% ee: M. J. Burk, F. Bienewald, M. Harris, A. Zanotti-Gerosa, Angew. Chem. 1998, 110, 2034-2037; Angew. Chem. Int. Ed. 1998, 37, 1931-1933.
-
(1998)
Angew. Chem.
, vol.110
, pp. 2034-2037
-
-
Burk, M.J.1
Bienewald, F.2
Harris, M.3
Zanotti-Gerosa, A.4
-
23
-
-
0032479758
-
-
Hydrogenation of Stobbe condensation products derived from aromatic aldehydes gave enantiomeric excess of up to 96% ee and 94% ee with MOD-DIOP and XYL-DIOP, respectively, as ligands: K. Yoshikawa, K. Inoguchi, T. Morimoto, K. Achiwa, Heterocycles 1990, 31, 1413-1416, and literature cited. With Et-DuPHOS as ligand hydrogenation of Stobbe condensatation products derived from aliphatic aldehydes was achieved with up to 99% ee: M. J. Burk, F. Bienewald, M. Harris, A. Zanotti-Gerosa, Angew. Chem. 1998, 110, 2034-2037; Angew. Chem. Int. Ed. 1998, 37, 1931-1933.
-
(1998)
Angew. Chem. Int. Ed.
, vol.37
, pp. 1931-1933
-
-
-
24
-
-
0033531366
-
-
[17a] D. Carmichael, H. Doucet, J. M. Brown, Chem. Commun. 1999, 3, 261-262.
-
(1999)
Chem. Commun.
, vol.3
, pp. 261-262
-
-
Carmichael, D.1
Doucet, H.2
Brown, J.M.3
-
25
-
-
0042729764
-
-
[17b] J. M. Brown, D. Carmichael, H. Doucet, WO-0026220, 2000 [Chem. Abstr. 2000, 132, 3321987].
-
(2000)
Chem. Abstr.
, vol.132
, pp. 3321987
-
-
Brown, J.M.1
Carmichael, D.2
Doucet, H.3
-
26
-
-
0042228861
-
-
WO-0027855, 2000
-
U. Berens (Chirotech Technology Ltd.), WO-0027855, 2000 [Chem. Abstr. 2000, 132, 334630].
-
(2000)
Chem. Abstr.
, vol.132
, pp. 334630
-
-
Berens, U.1
-
27
-
-
0000294061
-
-
B. R. Baker, R. E. Schaub, J. H. Williams, J. Org. Chem. 1952, 17, 116-131.
-
(1952)
J. Org. Chem.
, vol.17
, pp. 116-131
-
-
Baker, B.R.1
Schaub, R.E.2
Williams, J.H.3
-
28
-
-
0010983075
-
-
M. Ostermeier, J. Prieß, G. Helmchen, Angew. Chem. 2002, 114, 625-628; Angew. Chem. Int. Ed. 2002, 41, 612-614.
-
(2002)
Angew. Chem.
, vol.114
, pp. 625-628
-
-
Ostermeier, M.1
Prieß, J.2
Helmchen, G.3
-
29
-
-
0037084183
-
-
M. Ostermeier, J. Prieß, G. Helmchen, Angew. Chem. 2002, 114, 625-628; Angew. Chem. Int. Ed. 2002, 41, 612-614.
-
(2002)
Angew. Chem. Int. Ed.
, vol.41
, pp. 612-614
-
-
-
34
-
-
0001628139
-
-
A. Miyashita, H. Takaya, T. Souchi, R. Noyori, Tetrahedron 1984, 40, 1245-1253.
-
(1984)
Tetrahedron
, vol.40
, pp. 1245-1253
-
-
Miyashita, A.1
Takaya, H.2
Souchi, T.3
Noyori, R.4
-
35
-
-
0042228859
-
-
note
-
Hydrogenation of N-acetyl-dehydroalanine and its methyl ester was accomplished with 97.3 and 95.7% ee, respectively. For N-acetyl-dehydrophenylalanine and its methyl ester only 81.7 and 86.9% ee, respectively, were obtained.
-
-
-
-
36
-
-
37049086765
-
-
E. Guibe-Jampel, G. Rousseau, J. Salaün, J. Chem. Soc., Chem. Commun. 1987, 1080-1081.
-
(1987)
J. Chem. Soc., Chem. Commun.
, pp. 1080-1081
-
-
Guibe-Jampel, E.1
Rousseau, G.2
Salaün, J.3
-
38
-
-
0001338605
-
-
K. Achiwa, P. A. Chaloner, D. Parker, J. Organomet. Chem. 1981, 218, 249-260.
-
(1981)
J. Organomet. Chem.
, vol.218
, pp. 249-260
-
-
Achiwa, K.1
Chaloner, P.A.2
Parker, D.3
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