-
1
-
-
78650121952
-
-
Recent reviews on asymmetric aminocatalysis
-
Recent reviews on asymmetric aminocatalysis
-
-
-
-
4
-
-
53549121402
-
-
Melchiorre, P., Marigo, M., Carlone, A., and Bartoli, G. Angew. Chem., Int. Ed. 2008, 47, 6138
-
(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 6138
-
-
Melchiorre, P.1
Marigo, M.2
Carlone, A.3
Bartoli, G.4
-
6
-
-
0034750244
-
-
List, B. Synlett 2001, 11, 1675
-
(2001)
Synlett
, vol.11
, pp. 1675
-
-
List, B.1
-
7
-
-
78650109491
-
-
Reviews on asymmetric aminocatalysis by primary amino acids
-
Reviews on asymmetric aminocatalysis by primary amino acids
-
-
-
-
8
-
-
67549137639
-
-
Xu, L.-W., Luo, J., and Lu, Y. Chem. Commun. 2009, 14, 1807
-
(2009)
Chem. Commun.
, vol.14
, pp. 1807
-
-
Xu, L.-W.1
Luo, J.2
Lu, Y.3
-
11
-
-
0001002139
-
-
See also: Angew. Chem., Int. Ed. 2009, 48, 9848
-
Bennani, Y. L. and Hanessian, S. Chem. Rev. 1997, 97, 3161 See also: Uehara, H. and Barbas, C. F., III. Angew. Chem., Int. Ed. 2009, 48, 9848
-
(1997)
Chem. Rev.
, vol.97
, pp. 3161
-
-
Bennani, Y.L.1
Hanessian, S.2
Uehara, H.3
Barbas III, C.F.4
-
12
-
-
62949181205
-
-
Zhang, X.-J., Liu, S.-P., Li, X.-M., Yan, M., and Chan, A. S. C. Chem. Commun. 2009, 833
-
(2009)
Chem. Commun.
, pp. 833
-
-
Zhang, X.-J.1
Liu, S.-P.2
Li, X.-M.3
Yan, M.4
Chan, A.S.C.5
-
13
-
-
48849100191
-
-
Luo, S., Xu, H., Chen, L., and Cheng, J.-P. Org. Lett. 2008, 10, 1775
-
(2008)
Org. Lett.
, vol.10
, pp. 1775
-
-
Luo, S.1
Xu, H.2
Chen, L.3
Cheng, J.-P.4
-
15
-
-
33749340635
-
-
Lalonde, M. P., Chen, Y., and Jacobsen, E. N. Angew. Chem., Int. Ed. 2006, 45, 6366
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 6366
-
-
Lalonde, M.P.1
Chen, Y.2
Jacobsen, E.N.3
-
17
-
-
78650102583
-
-
Recent reviews on α,α-dialkylated amino acids
-
Recent reviews on α,α-dialkylated amino acids
-
-
-
-
21
-
-
0038391041
-
-
Previous examples of chiral α,α-dialkylamino aldehyde synthesis:, Eur. J. Org. Chem. 2008, 13, 2207
-
Ohfune, Y. and Shinada, T. Bull. Chem. Soc. Jpn. 2003, 76, 1115 Previous examples of chiral α,α-dialkylamino aldehyde synthesis: Baumann, T., Baechle, M., Hartmann, C., and Braese, S. Eur. J. Org. Chem. 2008, 13, 2207
-
(2003)
Bull. Chem. Soc. Jpn.
, vol.76
, pp. 1115
-
-
Ohfune, Y.1
Shinada, T.2
Baumann, T.3
Baechle, M.4
Hartmann, C.5
Braese, S.6
-
22
-
-
33846464171
-
-
Baumann, T., Vogt, H., and Braese, S. Eur. J. Org. Chem. 2007, 2, 266
-
(2007)
Eur. J. Org. Chem.
, vol.2
, pp. 266
-
-
Baumann, T.1
Vogt, H.2
Braese, S.3
-
24
-
-
33645454252
-
-
Guo, H.-M., Cheng, L., Cun, L.-F., Gong, L.-Z., Mi, A.-Q., and Jiang, Y.-Z. Chem. Commun. 2006, 429
-
(2006)
Chem. Commun.
, pp. 429
-
-
Guo, H.-M.1
Cheng, L.2
Cun, L.-F.3
Gong, L.-Z.4
Mi, A.-Q.5
Jiang, Y.-Z.6
-
25
-
-
24944569764
-
-
Suri, J. T., Steiner, D. D., and Barbas, C. F., III. Org. Lett. 2005, 7, 3885
-
(2005)
Org. Lett.
, vol.7
, pp. 3885
-
-
Suri, J.T.1
Steiner, D.D.2
Barbas III, C.F.3
-
27
-
-
0142074715
-
-
Vogt, H., Vanderheiden, S., and Braese, S. Chem. Commun. 2003, 2448
-
(2003)
Chem. Commun.
, pp. 2448
-
-
Vogt, H.1
Vanderheiden, S.2
Braese, S.3
-
30
-
-
78650160199
-
-
For preparation of (S, S)- 3, see
-
For preparation of (S, S)- 3, see
-
-
-
-
31
-
-
29044434572
-
-
Fox, M. E., Gerlach, A., Lennon, I. C., Meek, G., and Praquin, C. Synthesis 2005, 19, 3196
-
(2005)
Synthesis
, vol.19
, pp. 3196
-
-
Fox, M.E.1
Gerlach, A.2
Lennon, I.C.3
Meek, G.4
Praquin, C.5
-
32
-
-
0034622909
-
-
Allenmark, S., Skogsberg, U., and Thunberg, L. Tetrahedron: Asymmetry 2000, 11, 3527
-
(2000)
Tetrahedron: Asymmetry
, vol.11
, pp. 3527
-
-
Allenmark, S.1
Skogsberg, U.2
Thunberg, L.3
-
33
-
-
78650132149
-
-
Preparation of α-amino-substituted aldehydes 5a - i
-
Preparation of α-amino-substituted aldehydes 5a - i
-
-
-
-
34
-
-
57049159781
-
-
Alfaro, R., Yuste, F., Ortiz, B., Sanchez-Obregon, R., and Garcia Ruano, J. L. Tetrahedron 2009, 65, 357
-
(2009)
Tetrahedron
, vol.65
, pp. 357
-
-
Alfaro, R.1
Yuste, F.2
Ortiz, B.3
Sanchez-Obregon, R.4
Garcia Ruano, J.L.5
-
35
-
-
0028814351
-
-
Methoxyphenylacetaldehyde 5f:, J. Am. Chem. Soc. 2005, 127, 1002
-
Dondoni, A., Perrone, D., and Semola, T. Synthesis 1995, 2, 181. α-Methoxyphenylacetaldehyde 5f: Trost, B. M., Ball, Z. T., and Laemmerhold, K. M. J. Am. Chem. Soc. 2005, 127, 1002
-
(1995)
Synthesis
, vol.2
, pp. 181
-
-
Dondoni, A.1
Perrone, D.2
Semola, T.3
Trost, B.M.4
Ball, Z.T.5
Laemmerhold, K.M.6
-
36
-
-
78650119960
-
-
Use of 1,1-bis(benzenesulfonyl)ethylene for the generation of quaternary carbon centers
-
Use of 1,1-bis(benzenesulfonyl)ethylene for the generation of quaternary carbon centers
-
-
-
-
37
-
-
77951946549
-
-
Alba, A.-N. R., Companyo, X., Valero, G., Moyano, A., and Rios, R. Chem.-Eur. J. 2010, 16, 5354
-
(2010)
Chem.-Eur. J.
, vol.16
, pp. 5354
-
-
Alba, A.-N.R.1
Companyo, X.2
Valero, G.3
Moyano, A.4
Rios, R.5
-
39
-
-
33744823336
-
-
For other examples of Michael addition of aldehydes to vinyl sulfones, see:, Eur. J. Org. Chem. 2010, 5, 927
-
Liu, T.-Y., Long, J., Li, B.-J., Jiang, L., Li, R., Wu, Y., Ding, L.-S., and Chen, Y.-C. Org. Biomol. Chem 2006, 4, 2097 For other examples of Michael addition of aldehydes to vinyl sulfones, see: Quintard, A., Belot, S., Marchal, E., and Alexakis, A. Eur. J. Org. Chem. 2010, 5, 927
-
(2006)
Org. Biomol. Chem
, vol.4
, pp. 2097
-
-
Liu, T.-Y.1
Long, J.2
Li, B.-J.3
Jiang, L.4
Li, R.5
Wu, Y.6
Ding, L.-S.7
Chen, Y.-C.8
Quintard, A.9
Belot, S.10
Marchal, E.11
Alexakis, A.12
-
41
-
-
63749095504
-
-
Sulzer-Mosse, S., Alexakis, A., Mareda, J., Bollot, G., Bernardinelli, G., and Filinchuk, Y. Chem.-Eur. J. 2009, 15, 3204
-
(2009)
Chem.-Eur. J.
, vol.15
, pp. 3204
-
-
Sulzer-Mosse, S.1
Alexakis, A.2
Mareda, J.3
Bollot, G.4
Bernardinelli, G.5
Filinchuk, Y.6
-
42
-
-
60749134052
-
-
Landa, A., Maestro, M., Masdeu, C., Puente, A., Vera, S., Oiarbide, M., and Palomo, C. Chem.-Eur. J. 2009, 15, 1562
-
(2009)
Chem.-Eur. J.
, vol.15
, pp. 1562
-
-
Landa, A.1
Maestro, M.2
Masdeu, C.3
Puente, A.4
Vera, S.5
Oiarbide, M.6
Palomo, C.7
-
45
-
-
78650153852
-
-
Asymmetric conjugate addition of 5i at -20 °C for 72 h gave 6i in 98% yield with 80% ee
-
Asymmetric conjugate addition of 5i at -20 °C for 72 h gave 6i in 98% yield with 80% ee.
-
-
-
-
46
-
-
22744434029
-
-
Leuser, H., Perrone, S., Liron, F., Kneisel, F. F., and Knochel, P. Angew. Chem., Int. Ed. 2005, 44, 4627
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 4627
-
-
Leuser, H.1
Perrone, S.2
Liron, F.3
Kneisel, F.F.4
Knochel, P.5
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