-
4
-
-
0001226919
-
-
For other early contributions in this field, see:
-
For other early contributions in this field, see:. Kira M., Kobayashi M., and Sakurai H. Tetrahedron Lett. 28 (1987) 4081
-
(1987)
Tetrahedron Lett.
, vol.28
, pp. 4081
-
-
Kira, M.1
Kobayashi, M.2
Sakurai, H.3
-
6
-
-
0041878778
-
-
For reviews on Lewis base-catalyzed asymmetric allylations, see:
-
For reviews on Lewis base-catalyzed asymmetric allylations, see:. Denmark S.E., and Fu J. Chem. Rev. 103 (2003) 2763
-
(2003)
Chem. Rev.
, vol.103
, pp. 2763
-
-
Denmark, S.E.1
Fu, J.2
-
11
-
-
29244443974
-
-
For reviews on Lewis acid-Lewis base bifunctional asymmetric catalysis, see:
-
For reviews on Lewis acid-Lewis base bifunctional asymmetric catalysis, see:. Kanai M., Kato N., Ichikawa E., and Shibasaki M. Pure Appl. Chem. 77 (2005) 2047
-
(2005)
Pure Appl. Chem.
, vol.77
, pp. 2047
-
-
Kanai, M.1
Kato, N.2
Ichikawa, E.3
Shibasaki, M.4
-
19
-
-
33644532245
-
-
Denmark S.E., Fu J., Coe D.M., Su X., Pratt N.E., and Griedel B.D. J. Org. Chem. 71 (2006) 1523
-
(2006)
J. Org. Chem.
, vol.71
, pp. 1523
-
-
Denmark, S.E.1
Fu, J.2
Coe, D.M.3
Su, X.4
Pratt, N.E.5
Griedel, B.D.6
-
21
-
-
0031562483
-
-
Iseki K., Kuroki Y., Takahashi M., Kishimoto S., and Kobayashi Y. Tetrahedron 53 (1997) 3513
-
(1997)
Tetrahedron
, vol.53
, pp. 3513
-
-
Iseki, K.1
Kuroki, Y.2
Takahashi, M.3
Kishimoto, S.4
Kobayashi, Y.5
-
28
-
-
0001056484
-
-
Malkov A.V., Orsini M., Pernazza D., Muir K.W., Langer V., Meghani P., and Kocovsky P. Org. Lett. 4 (2002) 1047
-
(2002)
Org. Lett.
, vol.4
, pp. 1047
-
-
Malkov, A.V.1
Orsini, M.2
Pernazza, D.3
Muir, K.W.4
Langer, V.5
Meghani, P.6
Kocovsky, P.7
-
29
-
-
0041967639
-
-
Malkov A.V., Dufková D., Farrugia P., and Kocovsky P. Angew. Chem., Int. Ed. 42 (2003) 3674
-
(2003)
Angew. Chem., Int. Ed.
, vol.42
, pp. 3674
-
-
Malkov, A.V.1
Dufková, D.2
Farrugia, P.3
Kocovsky, P.4
-
39
-
-
1642291312
-
-
For Pd-catalyzed asymmetric reactions, see:
-
For Pd-catalyzed asymmetric reactions, see:. Nemoto T., Matsumoto T., Masuda T., Hitomi T., Hatano K., and Hamada Y. J. Am. Chem. Soc. 126 (2004) 3690
-
(2004)
J. Am. Chem. Soc.
, vol.126
, pp. 3690
-
-
Nemoto, T.1
Matsumoto, T.2
Masuda, T.3
Hitomi, T.4
Hatano, K.5
Hamada, Y.6
-
41
-
-
27644507981
-
-
Nemoto T., Fukuda T., Matsumoto T., Hitomi T., and Hamada Y. Adv. Synth. Catal. 347 (2005) 1504
-
(2005)
Adv. Synth. Catal.
, vol.347
, pp. 1504
-
-
Nemoto, T.1
Fukuda, T.2
Matsumoto, T.3
Hitomi, T.4
Hamada, Y.5
-
42
-
-
26444603763
-
-
Nemoto T., Masuda T., Akimoto Y., Fukuyama T., and Hamada Y. Org. Lett. 7 (2005) 4447
-
(2005)
Org. Lett.
, vol.7
, pp. 4447
-
-
Nemoto, T.1
Masuda, T.2
Akimoto, Y.3
Fukuyama, T.4
Hamada, Y.5
-
44
-
-
33947148640
-
-
Nemoto T., Fukuyama T., Yamamoto E., Tamura S., Fukuda T., Matsumoto T., Akimoto Y., and Hamada Y. Org. Lett. 9 (2007) 927
-
(2007)
Org. Lett.
, vol.9
, pp. 927
-
-
Nemoto, T.1
Fukuyama, T.2
Yamamoto, E.3
Tamura, S.4
Fukuda, T.5
Matsumoto, T.6
Akimoto, Y.7
Hamada, Y.8
-
46
-
-
33750471192
-
-
For Ir-catalyzed asymmetric reactions, see:
-
For Ir-catalyzed asymmetric reactions, see:. Nemoto T., Sakamoto T., Matsumoto T., and Hamada Y. Tetrahedron Lett. 47 (2006) 8737
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 8737
-
-
Nemoto, T.1
Sakamoto, T.2
Matsumoto, T.3
Hamada, Y.4
-
49
-
-
34548385158
-
-
note
-
There was no improvement in the chemical yield when the reaction time was increased.
-
-
-
-
50
-
-
34548403715
-
-
note
-
Enantioselectivity was not increased when the reaction was performed at a temperature below -40 °C.
-
-
-
|