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For recent reviews on asymmetric Michael addition reactions, see:. Tsogoeva S.B. Eur. J. Org. Chem. (2007) 1701-1716
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For selected examples, see:. Vishnumaya, and Singh V.K. Org. Lett. 9 (2007) 1117-1119
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Luo, S.Z.1
Mi, X.L.2
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Hayashi, Y.1
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33748791724
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Palomo C., Vera S., Mielgo A., and Gomez-Bengoa E. Angew. Chem., Int. Ed. 45 (2006) 5984-5987
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Palomo, C.1
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Diez D., Jose Gil M., Moro R.F., Marcos I.S., Garcia P., Basabe P., Garrido N.M., Broughton H.B., and Urones J.G. Tetrahedron 63 (2007) 740-747
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For other types of organocatalytic Michael addition reactions, see:
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For other types of organocatalytic Michael addition reactions, see:. Zhang F.-Y., and Corey E.J. Org. Lett. 2 (2000) 1097-1100
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For asymmetric aldol reaction using immobilized proline and its analogous, see:
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For asymmetric aldol reaction using immobilized proline and its analogous, see:. Benaglia M., Celentano G., and Cozzi F. Adv. Synth. Catal. 343 (2001) 171-173
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Adv. Synth. Catal.
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Adv. Synth. Catal.
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Benaglia, M.1
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Luo S., Li J., Xu H., Zhang L., and Cheng J.-P. Org. Lett. 9 (2007) 3675-3678
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For immobilized Michael catalysts, see:
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For immobilized Michael catalysts, see:. Benaglia M., Cinquini M., Cozzi F., Puglisi A., and Celentano G. J. Mol. Catal. A: Chem. 204 (2003) 157-163
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Luo, S.; Li, J.; Zhang, L.; Xu, H.; Cheng, J.-P. Chem. Eur. J. 2007. doi:10.1002/chem.200701129.
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34249297939
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For enantioselective α-aminoxylation of aldehydes and ketones with a polymer-supported organocatalyst, see:
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For enantioselective α-aminoxylation of aldehydes and ketones with a polymer-supported organocatalyst, see:. Font D., Bastero A., Sayalero S., Jimeno C., and Pericas M.A. Org. Lett. 9 (2007) 1943-1946
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Org. Lett.
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Shi L.-X., Sun Q., Ge Z.-M., Zhu Y.-Q., Cheng T.-M., and Li R.-T. Synlett (2004) 2215-2217
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Synlett
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Shi, L.-X.1
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Ge, Z.-M.3
Zhu, Y.-Q.4
Cheng, T.-M.5
Li, R.-T.6
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52
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39649089671
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This kind of organocatalyst and its analogous were reported by our group in the abstract of Chinese Journal of Organic Chemistry, see: Yan, J.; Zhou, L.; Miao, T.; Li, P.; Wang, L. Chin. J. Org. Chem. 2007, 27, 260 (ISSN 0253-2786).
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This kind of organocatalyst and its analogous were reported by our group in the abstract of Chinese Journal of Organic Chemistry, see: Yan, J.; Zhou, L.; Miao, T.; Li, P.; Wang, L. Chin. J. Org. Chem. 2007, 27, 260 (ISSN 0253-2786).
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During the preparation of this manuscript, a similar catalyst was reported to be a good catalyst for asymmetric Michael addition of cyclohexanone to nitroolefins, see:
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During the preparation of this manuscript, a similar catalyst was reported to be a good catalyst for asymmetric Michael addition of cyclohexanone to nitroolefins, see:. Alza E., Cambeiro X.C., Jimeno C., and Pericás M.A. Org. Lett. 9 (2007) 3717-3720
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(2007)
Org. Lett.
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Alza, E.1
Cambeiro, X.C.2
Jimeno, C.3
Pericás, M.A.4
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