-
4
-
-
0003445429
-
-
For leading references, see:. Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds), Springer, Heidelberg
-
For leading references, see:. In: Jacobsen E.N., Pfaltz A., and Yamamoto H. (Eds). Comprehensive Asymmetric Catalysis (1999), Springer, Heidelberg
-
(1999)
Comprehensive Asymmetric Catalysis
-
-
-
7
-
-
0036105107
-
-
For a recent review, see: and references therein
-
For a recent review, see:. Kobayashi S., and Manabe K. Acc. Chem. Res. 35 (2002) 209 and references therein
-
(2002)
Acc. Chem. Res.
, vol.35
, pp. 209
-
-
Kobayashi, S.1
Manabe, K.2
-
8
-
-
0035886887
-
-
Selected reviews for organocatalysis, see:
-
Selected reviews for organocatalysis, see:. Dalko P.I., and Moisan L. Angew. Chem., Int. Ed. 40 (2001) 3726
-
(2001)
Angew. Chem., Int. Ed.
, vol.40
, pp. 3726
-
-
Dalko, P.I.1
Moisan, L.2
-
15
-
-
2942641357
-
-
For notable examples of organocatalytic reactions in aqueous media, see:
-
For notable examples of organocatalytic reactions in aqueous media, see:. Torii H., Nakadai M., Ishihara K., Saito S., and Yamamoto H. Angew. Chem., Int. Ed. 43 (2004) 1983
-
(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1983
-
-
Torii, H.1
Nakadai, M.2
Ishihara, K.3
Saito, S.4
Yamamoto, H.5
-
18
-
-
32044463187
-
-
Hayashi Y., Sumiya T., Takahashi J., Gotoh H., Urushima T., and Shoji M. Angew. Chem., Int. Ed. 45 (2006) 958
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 958
-
-
Hayashi, Y.1
Sumiya, T.2
Takahashi, J.3
Gotoh, H.4
Urushima, T.5
Shoji, M.6
-
19
-
-
31444456557
-
-
Mase N., Nakai Y., Ohara N., Yoda H., Takabe K., Tanaka F., and Barbas III C.F. J. Am. Chem. Soc. 128 (2006) 734
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 734
-
-
Mase, N.1
Nakai, Y.2
Ohara, N.3
Yoda, H.4
Takabe, K.5
Tanaka, F.6
Barbas III, C.F.7
-
20
-
-
33646142092
-
-
Mase N., Watanable K., Yoda H., Takabe K., Tanaka F., and Barbas III C.F. J. Am. Chem. Soc. 128 (2006) 4966
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 4966
-
-
Mase, N.1
Watanable, K.2
Yoda, H.3
Takabe, K.4
Tanaka, F.5
Barbas III, C.F.6
-
24
-
-
33645454569
-
-
Cheng C., Sun J., Wang C., Zhang Y., Wei S., Jiang F., and Wu Y. Chem. Commun. (2006) 215
-
(2006)
Chem. Commun.
, pp. 215
-
-
Cheng, C.1
Sun, J.2
Wang, C.3
Zhang, Y.4
Wei, S.5
Jiang, F.6
Wu, Y.7
-
27
-
-
0006714024
-
-
Selected reviews for Michael reaction, see:
-
Selected reviews for Michael reaction, see:. Krause N., and Roder H. Synthesis (2001) 171
-
(2001)
Synthesis
, pp. 171
-
-
Krause, N.1
Roder, H.2
-
30
-
-
4644317493
-
-
For selected examples of organocatalytic asymmetric Michael additions of ketones to nitroolefins, see:
-
For selected examples of organocatalytic asymmetric Michael additions of ketones to nitroolefins, see:. Cobb A.J.A., Longbottom D.A., Shaw D.M., and Ley S.V. Chem. Commun. (2004) 1808
-
(2004)
Chem. Commun.
, pp. 1808
-
-
Cobb, A.J.A.1
Longbottom, D.A.2
Shaw, D.M.3
Ley, S.V.4
-
33
-
-
33645909878
-
-
Xu Y.-M., Zou W.-B., Sundén H., Ibrahem I., and Córdova A. Adv. Synth. Catal. 348 (2006) 418
-
(2006)
Adv. Synth. Catal.
, vol.348
, pp. 418
-
-
Xu, Y.-M.1
Zou, W.-B.2
Sundén, H.3
Ibrahem, I.4
Córdova, A.5
-
34
-
-
33746216402
-
-
Luo S.-Z., Mi X.-L., Zhang L., Liu S., Xu H., and Cheng J.-P. Angew. Chem., Int. Ed. 45 (2006) 3093
-
(2006)
Angew. Chem., Int. Ed.
, vol.45
, pp. 3093
-
-
Luo, S.-Z.1
Mi, X.-L.2
Zhang, L.3
Liu, S.4
Xu, H.5
Cheng, J.-P.6
-
39
-
-
33745672062
-
-
Wang Y.-Q., Song J., Hong R., Li H., and Deng L. J. Am. Chem. Soc. 128 (2006) 8156
-
(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 8156
-
-
Wang, Y.-Q.1
Song, J.2
Hong, R.3
Li, H.4
Deng, L.5
-
40
-
-
33746643770
-
-
During the proceeding of our work, Tang et al. has reported a secondary amine-(thio)urea catalyst, see:
-
During the proceeding of our work, Tang et al. has reported a secondary amine-(thio)urea catalyst, see:. Cao C.-L., Ye M.-C., Sun X.-L., Tang Y. Org. Lett. 8 (2006) 2901
-
(2006)
Org. Lett.
, vol.8
, pp. 2901
-
-
Cao, C.-L.1
Ye, M.-C.2
Sun, X.-L.3
Tang, Y.4
-
41
-
-
26444501999
-
-
Chen J.-R., Lu H.-H., Li X.-Y., Cheng L., Wan J., and Xiao W.-J. Org. Lett. 7 (2005) 4543
-
(2005)
Org. Lett.
, vol.7
, pp. 4543
-
-
Chen, J.-R.1
Lu, H.-H.2
Li, X.-Y.3
Cheng, L.4
Wan, J.5
Xiao, W.-J.6
-
45
-
-
33751421415
-
-
note
-
4, PhCOOH, and p-TsOH as the co-catalyst, and found that PhCOOH is the best one for the title reaction.
-
-
-
|