-
1
-
-
77951126291
-
-
For recent general reviews on organocatalysis, see
-
For recent general reviews on organocatalysis, see:
-
-
-
-
12
-
-
77951095894
-
-
For recent reviews, see
-
For recent reviews, see:
-
-
-
-
13
-
-
1242313761
-
-
Zanoni G., Castronovo F., Franzini M., Vidari G., and Giannini E. Chem. Soc. Rev. 32 (2003) 115
-
(2003)
Chem. Soc. Rev.
, vol.32
, pp. 115
-
-
Zanoni, G.1
Castronovo, F.2
Franzini, M.3
Vidari, G.4
Giannini, E.5
-
17
-
-
0346865819
-
-
For the first general review of organocatalysis through hydrogen bonding interactions, see:
-
For the first general review of organocatalysis through hydrogen bonding interactions, see:. Schreiner P.R. Chem. Soc. Rev. 32 (2003) 289
-
(2003)
Chem. Soc. Rev.
, vol.32
, pp. 289
-
-
Schreiner, P.R.1
-
18
-
-
77951104480
-
-
For recent reviews on bifunctional tertiary amine-(thio)urea organocatalysts, see
-
For recent reviews on bifunctional tertiary amine-(thio)urea organocatalysts, see:
-
-
-
-
27
-
-
77951096441
-
-
For other types of (thio)urea organocatalysts, see
-
For other types of (thio)urea organocatalysts, see:
-
-
-
-
29
-
-
33751407719
-
-
Cao Y., Lai Y., Wang X., Li Y., and Xiao W. Tetrahedron Lett. 48 (2007) 21
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 21
-
-
Cao, Y.1
Lai, Y.2
Wang, X.3
Li, Y.4
Xiao, W.5
-
31
-
-
34548556420
-
-
Sohtome Y., Takemura N., Takada K., Takagi R., Iguchi T., and Nagasawa K. Chem. Asian J. 2 (2007) 1150
-
(2007)
Chem. Asian J.
, vol.2
, pp. 1150
-
-
Sohtome, Y.1
Takemura, N.2
Takada, K.3
Takagi, R.4
Iguchi, T.5
Nagasawa, K.6
-
33
-
-
28444495969
-
-
Tsogoeva S.B., Yalalov D.A., Hateley M.J., Weckbecker C., and Huthmacher K. Eur. J. Org. Chem. (2005) 4995
-
(2005)
Eur. J. Org. Chem.
, pp. 4995
-
-
Tsogoeva, S.B.1
Yalalov, D.A.2
Hateley, M.J.3
Weckbecker, C.4
Huthmacher, K.5
-
34
-
-
77951121615
-
-
note
-
Doubly stereocontrolled asymmetric reactions here refer to the reactions that both enantiomers of a chiral product can be achieved in almost the same enantiomeric excess through the use of pseudoenantiomers not enantiomers of a chiral catalyst.
-
-
-
-
35
-
-
43049134765
-
-
For a review on chiral primary amine-mediated asymmetric organocatalytic reactions, see:
-
For a review on chiral primary amine-mediated asymmetric organocatalytic reactions, see:. Peng F., and Shao Z. J. Mol. Catal. A: Chem. 285 (2008) 1
-
(2008)
J. Mol. Catal. A: Chem.
, vol.285
, pp. 1
-
-
Peng, F.1
Shao, Z.2
-
36
-
-
77951101207
-
-
For selected contributions from our group, see
-
For selected contributions from our group, see:
-
-
-
-
38
-
-
46849103420
-
-
Peng F., Shao Z., Fan B., Song H., Li G., and Zhang H. J. Org. Chem. 73 (2008) 5202
-
(2008)
J. Org. Chem.
, vol.73
, pp. 5202
-
-
Peng, F.1
Shao, Z.2
Fan, B.3
Song, H.4
Li, G.5
Zhang, H.6
-
40
-
-
77951106822
-
-
For the recent reviews on the asymmetric conjugate addition of nitroolefins, see
-
For the recent reviews on the asymmetric conjugate addition of nitroolefins, see:
-
-
-
-
45
-
-
77951106298
-
-
For selected examples on organocatalytic asymmetric conjugate addition of 1,3-dicarbonyl compounds to nitroolefins, see
-
For selected examples on organocatalytic asymmetric conjugate addition of 1,3-dicarbonyl compounds to nitroolefins, see:
-
-
-
-
48
-
-
27144522622
-
-
Wang J., Li H., Duan W., Zu L., and Wang W. Org. Lett. 7 (2005) 4713
-
(2005)
Org. Lett.
, vol.7
, pp. 4713
-
-
Wang, J.1
Li, H.2
Duan, W.3
Zu, L.4
Wang, W.5
-
50
-
-
11244281650
-
-
Li H., Wang Y., Tang L., Wu F., Liu X., Guo C., Foxman B.M., and Deng L. Angew. Chem., Int. Ed. 44 (2005) 105
-
(2005)
Angew. Chem., Int. Ed.
, vol.44
, pp. 105
-
-
Li, H.1
Wang, Y.2
Tang, L.3
Wu, F.4
Liu, X.5
Guo, C.6
Foxman, B.M.7
Deng, L.8
-
56
-
-
58149402249
-
-
Li X., Liu K., Ma H., Nie J., and Ma J. Synlett (2008) 3242
-
(2008)
Synlett
, pp. 3242
-
-
Li, X.1
Liu, K.2
Ma, H.3
Nie, J.4
Ma, J.5
-
57
-
-
53849087875
-
-
Gao P., Wang C., Wu Y., Zhou Z., and Tang C. Eur. J. Org. Chem. (2008) 4563
-
(2008)
Eur. J. Org. Chem.
, pp. 4563
-
-
Gao, P.1
Wang, C.2
Wu, Y.3
Zhou, Z.4
Tang, C.5
-
61
-
-
64549143856
-
-
Li H., Zhang S., Yu C., Song X., and Wang W. Chem. Commun. (2009) 2136
-
(2009)
Chem. Commun.
, pp. 2136
-
-
Li, H.1
Zhang, S.2
Yu, C.3
Song, X.4
Wang, W.5
-
65
-
-
77951103416
-
-
Part of this work has been published in a preliminary form, see
-
Part of this work has been published in a preliminary form, see:
-
-
-
-
66
-
-
70349213744
-
-
Pu X., Li P., Peng F., Li X., Zhang H., and Shao Z. Eur. J. Org. Chem. (2009) 4622
-
(2009)
Eur. J. Org. Chem.
, pp. 4622
-
-
Pu, X.1
Li, P.2
Peng, F.3
Li, X.4
Zhang, H.5
Shao, Z.6
-
67
-
-
77951124923
-
-
It should be mentioned that almost simultaneously Wang et al. reported a nice asymmetric addition of 1,3-dicarbonyl compounds to nitroalkenes in a doubly stereocontrolled manner catalyzed by bifunctional rosin-derived thiourea catalysts, see
-
It should be mentioned that almost simultaneously Wang et al. reported a nice asymmetric addition of 1,3-dicarbonyl compounds to nitroalkenes in a doubly stereocontrolled manner catalyzed by bifunctional rosin-derived thiourea catalysts, see:
-
-
-
-
68
-
-
68049083712
-
-
Jiang X., Zhang Y., Liu X., Zhang G., Lai L., Wu L., Zhang J., and Wang W. J. Org. Chem. 74 (2009) 5562
-
(2009)
J. Org. Chem.
, vol.74
, pp. 5562
-
-
Jiang, X.1
Zhang, Y.2
Liu, X.3
Zhang, G.4
Lai, L.5
Wu, L.6
Zhang, J.7
Wang, W.8
-
69
-
-
77951096156
-
-
In addition, Zhou et al. reported a chiral glucose-based secondary amine-thiourea catalyst, which catalyzed highly enantio- and diastereoselective Michael addition of cyclohexanone to nitroolefins, see
-
In addition, Zhou et al. reported a chiral glucose-based secondary amine-thiourea catalyst, which catalyzed highly enantio- and diastereoselective Michael addition of cyclohexanone to nitroolefins, see:
-
-
-
-
70
-
-
68949152712
-
-
(Our Eur. J. Org. Chem. manuscript: received: May 18, 2009; published online: July 29, 2009. Wang's J. Org. Chem. manuscript: May 4, 2009; published on web: June 24, 2009. Zhou's Org. Biomol. Chem. manuscript: received: March 19, 2009, first published as an advance article on the web: June 11, 2009)
-
Lu A., Gao P., Wu Y., Wang Y., Zhou Z., and Tang C. Org. Biomol. Chem. 7 (2009) 3141 (Our Eur. J. Org. Chem. manuscript: received: May 18, 2009; published online: July 29, 2009. Wang's J. Org. Chem. manuscript: May 4, 2009; published on web: June 24, 2009. Zhou's Org. Biomol. Chem. manuscript: received: March 19, 2009, first published as an advance article on the web: June 11, 2009)
-
(2009)
Org. Biomol. Chem.
, vol.7
, pp. 3141
-
-
Lu, A.1
Gao, P.2
Wu, Y.3
Wang, Y.4
Zhou, Z.5
Tang, C.6
-
71
-
-
77951144896
-
-
For selected examples, see
-
For selected examples, see:
-
-
-
-
72
-
-
70349995077
-
-
Han X., Kwiatkowski J., Xue F., Huang K., and Lu Y. Angew. Chem., Int. Ed. 48 (2009) 7604
-
(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 7604
-
-
Han, X.1
Kwiatkowski, J.2
Xue, F.3
Huang, K.4
Lu, Y.5
-
73
-
-
42649144150
-
-
Liu J., Yang Z., Wang Z., Wang F., Chen X., Liu X., Feng X., Su Z., and Hu C. J. Am. Chem. Soc. 130 (2008) 5654
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 5654
-
-
Liu, J.1
Yang, Z.2
Wang, Z.3
Wang, F.4
Chen, X.5
Liu, X.6
Feng, X.7
Su, Z.8
Hu, C.9
-
76
-
-
35248872887
-
-
See also Ref. 5
-
Cheng L., Han X., Huang H., Wong M.W., and Lu Y. Chem. Commun. (2007) 4143 See also Ref. 5
-
(2007)
Chem. Commun.
, pp. 4143
-
-
Cheng, L.1
Han, X.2
Huang, H.3
Wong, M.W.4
Lu, Y.5
-
78
-
-
33947169944
-
-
Liu K., Cui H., Nie J., Dong K., Li X., and Ma J. Org. Lett. 9 (2007) 923
-
(2007)
Org. Lett.
, vol.9
, pp. 923
-
-
Liu, K.1
Cui, H.2
Nie, J.3
Dong, K.4
Li, X.5
Ma, J.6
-
80
-
-
48249135125
-
-
Chen J., An X., Zhu X., Wang X., and Xiao W. J. Org. Chem. 73 (2008) 6006
-
(2008)
J. Org. Chem.
, vol.73
, pp. 6006
-
-
Chen, J.1
An, X.2
Zhu, X.3
Wang, X.4
Xiao, W.5
-
81
-
-
77749255393
-
-
Chen J., Cao Y., Zou Y., Tan F., Fu L., Zhu X., and Xiao W. Org. Biomol. Chem. 8 (2010) 1275
-
(2010)
Org. Biomol. Chem.
, vol.8
, pp. 1275
-
-
Chen, J.1
Cao, Y.2
Zou, Y.3
Tan, F.4
Fu, L.5
Zhu, X.6
Xiao, W.7
-
82
-
-
34848876351
-
-
Coldham I., O'Brien P., Patel J.J., Raimbault S., Sanderson A.J., Stead D., and Whittaker D.T.E. Tetrahedron: Asymmetry 18 (2007) 2113
-
(2007)
Tetrahedron: Asymmetry
, vol.18
, pp. 2113
-
-
Coldham, I.1
O'Brien, P.2
Patel, J.J.3
Raimbault, S.4
Sanderson, A.J.5
Stead, D.6
Whittaker, D.T.E.7
-
83
-
-
85140868678
-
-
Camarasa M.J., FernandezResa P., GarciaLopez M.T., Delas Heras F.G., MendezCastrillon P.P., and Felix A.S. Synthesis (1984) 509
-
(1984)
Synthesis
, pp. 509
-
-
Camarasa, M.J.1
FernandezResa, P.2
GarciaLopez, M.T.3
Delas Heras, F.G.4
MendezCastrillon, P.P.5
Felix, A.S.6
-
84
-
-
77951136007
-
-
For recent examples, see
-
For recent examples, see:
-
-
-
-
87
-
-
77951109245
-
-
Jiang X., Zhang Y., Wu L., Zhang G., Liu X., Zhang H., Fu D., and Wang R. Adv. Synth. Catal. 351 (2009) 2449
-
(2009)
Adv. Synth. Catal.
, vol.351
, pp. 2449
-
-
Jiang, X.1
Zhang, Y.2
Wu, L.3
Zhang, G.4
Liu, X.5
Zhang, H.6
Fu, D.7
Wang, R.8
-
88
-
-
77951110592
-
-
Typically, the use of co-catalysts or additives has been employed for this purpose
-
Typically, the use of co-catalysts or additives has been employed for this purpose.
-
-
-
-
89
-
-
64149116604
-
-
Da C., Che L., Guo Q., Wu F., Ma X., and Jia Y. J. Org. Chem. 74 (2009) 2541
-
(2009)
J. Org. Chem.
, vol.74
, pp. 2541
-
-
Da, C.1
Che, L.2
Guo, Q.3
Wu, F.4
Ma, X.5
Jia, Y.6
-
90
-
-
67650333224
-
-
Companyo X., Valero G., Crovetto L., Moyano A., and Rios R. Chem.-Eur. J. 15 (2009) 6564
-
(2009)
Chem.-Eur. J.
, vol.15
, pp. 6564
-
-
Companyo, X.1
Valero, G.2
Crovetto, L.3
Moyano, A.4
Rios, R.5
-
92
-
-
77951142434
-
-
note
-
We could not ruled out participation of the solvent in the transition state. We thank one reviewer's comments on our manuscript.
-
-
-
|