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77949273614
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Reviews on chiral phosphoric-acid catalysis
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Reviews on chiral phosphoric-acid catalysis:
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8
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77949271804
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For selected examples
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For selected examples:
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9
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2342570203
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Akiyama T., Itoh J., Yokota K., and Fuchibe K. Angew. Chem., Int. Ed. 43 (2004) 1566
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(2004)
Angew. Chem., Int. Ed.
, vol.43
, pp. 1566
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Akiyama, T.1
Itoh, J.2
Yokota, K.3
Fuchibe, K.4
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11
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34247112829
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Guo Q.-X., Liu H., Guo C., Luo S.-W., Gu Y., and Gong L.-Z. J. Am. Chem. Soc. 129 (2007) 3790
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(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 3790
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Guo, Q.-X.1
Liu, H.2
Guo, C.3
Luo, S.-W.4
Gu, Y.5
Gong, L.-Z.6
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15
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77949271802
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For selected examples
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For selected examples:
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17
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34547155080
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Jia Y.-X., Zhong J., Zhu S.-F., Zhang C.-M., and Zhou Q.-L. Angew. Chem., Int. Ed. 46 (2007) 5565
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(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 5565
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Jia, Y.-X.1
Zhong, J.2
Zhu, S.-F.3
Zhang, C.-M.4
Zhou, Q.-L.5
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21
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34547487981
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Rowland G.B., Rowland E.B., Liang Y., Perman J.A., and Antilla J.C. Org. Lett. 9 (2007) 2609
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(2007)
Org. Lett.
, vol.9
, pp. 2609
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Rowland, G.B.1
Rowland, E.B.2
Liang, Y.3
Perman, J.A.4
Antilla, J.C.5
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25
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63749088972
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Sheng Y.-F., Li G.-Q., Kang Q., Zhang A.-J., and You S.-L. Chem.-Eur. J. 15 (2009) 3351
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(2009)
Chem.-Eur. J.
, vol.15
, pp. 3351
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Sheng, Y.-F.1
Li, G.-Q.2
Kang, Q.3
Zhang, A.-J.4
You, S.-L.5
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28
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77949270565
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For selected examples
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For selected examples:
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30
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24044465512
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Rueping M., Sugiono E., Azap C., Theissmann T., and Bolte M. Org. Lett. 7 (2005) 3781
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(2005)
Org. Lett.
, vol.7
, pp. 3781
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Rueping, M.1
Sugiono, E.2
Azap, C.3
Theissmann, T.4
Bolte, M.5
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39
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77949262623
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For selected examples
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For selected examples:
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42
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33846157409
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Liu H., Cun L.-F., Mi A.-Q., Jiang Y.-Z., and Gong L.-Z. Org. Lett. 8 (2006) 6023
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(2006)
Org. Lett.
, vol.8
, pp. 6023
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Liu, H.1
Cun, L.-F.2
Mi, A.-Q.3
Jiang, Y.-Z.4
Gong, L.-Z.5
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43
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30544453001
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Akiyama T., Tamura Y., Itoh J., Morita H., and Fuchibe K. Synlett (2006) 141
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(2006)
Synlett
, pp. 141
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Akiyama, T.1
Tamura, Y.2
Itoh, J.3
Morita, H.4
Fuchibe, K.5
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44
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56449130065
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Gioia C., Hauville A., Bernardi L., Fini F., and Ricci A. Angew. Chem., Int. Ed. 47 (2008) 9236
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(2008)
Angew. Chem., Int. Ed.
, vol.47
, pp. 9236
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Gioia, C.1
Hauville, A.2
Bernardi, L.3
Fini, F.4
Ricci, A.5
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45
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77949271803
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For selected examples
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For selected examples:
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46
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33845205051
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Chen X.-H., Xu X.-Y., Liu H., Cun L.-F., and Gong L.-Z. J. Am. Chem. Soc. 128 (2006) 14082
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(2006)
J. Am. Chem. Soc.
, vol.128
, pp. 14082
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Chen, X.-H.1
Xu, X.-Y.2
Liu, H.3
Cun, L.-F.4
Gong, L.-Z.5
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47
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70350307205
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Li N., Chen X.-H., Song J., Luo S.-W., Fan W., and Gong L.-Z. J. Am. Chem. Soc. 131 (2009) 15301
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(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 15301
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Li, N.1
Chen, X.-H.2
Song, J.3
Luo, S.-W.4
Fan, W.5
Gong, L.-Z.6
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49
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77949273611
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For selected examples
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For selected examples:
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54
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45749136440
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Hu W.-H., Xu X.-F., Zhou J., Liu W.-J., Huang H.-X., Hu J., Yang L.-P., and Gong L.-Z. J. Am. Chem. Soc. 130 (2008) 7782
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(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7782
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Hu, W.-H.1
Xu, X.-F.2
Zhou, J.3
Liu, W.-J.4
Huang, H.-X.5
Hu, J.6
Yang, L.-P.7
Gong, L.-Z.8
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59
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68249145925
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Muratore M.E., Holloway C.A., Pilling A.W., Storer R.I., Trevitt G., and Dixon D.J. J. Am. Chem. Soc. 131 (2009) 10796
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(2009)
J. Am. Chem. Soc.
, vol.131
, pp. 10796
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Muratore, M.E.1
Holloway, C.A.2
Pilling, A.W.3
Storer, R.I.4
Trevitt, G.5
Dixon, D.J.6
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61
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70350346454
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Zhang Q.-W., Fan C.-A., Zhang H.-J., Tu Y.-Q., Zhao Y.-M., Gu P., and Chen Z.-M. Angew. Chem., Int. Ed. 48 (2009) 8572
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(2009)
Angew. Chem., Int. Ed.
, vol.48
, pp. 8572
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Zhang, Q.-W.1
Fan, C.-A.2
Zhang, H.-J.3
Tu, Y.-Q.4
Zhao, Y.-M.5
Gu, P.6
Chen, Z.-M.7
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70
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in press. doi:10.1002/chem.200902698
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Xu, S.; Wang, Z.; Li, Y.; Zhang, X.; Wang, H.; Ding, K. Chem.-Eur. J., in press. doi:10.1002/chem.200902698
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Chem.-Eur. J
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Xu, S.1
Wang, Z.2
Li, Y.3
Zhang, X.4
Wang, H.5
Ding, K.6
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71
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77949262621
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For reviews on asymmetric Friedel-Crafts reactions
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For reviews on asymmetric Friedel-Crafts reactions:
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75
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69249092514
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After the acceptance of this manuscript, Goodman et al. reported an excellent theoretical investigation into chiral phosphoric acid-catalyzed Friedel-Crafts reactions of various imines
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You S.-L., Cai Q., and Zeng M. Chem. Soc. Rev. 38 (2009) 2190 After the acceptance of this manuscript, Goodman et al. reported an excellent theoretical investigation into chiral phosphoric acid-catalyzed Friedel-Crafts reactions of various imines
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(2009)
Chem. Soc. Rev.
, vol.38
, pp. 2190
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You, S.-L.1
Cai, Q.2
Zeng, M.3
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77
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77949270561
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For other literature reports in which the configuration of the final products could be switched in chiral phosphoric-acid catalysis caused only by changes of 3,3′-substitution group on the catalyst, please see: Ref. 2b,3e,4e,j,6a,b and
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For other literature reports in which the configuration of the final products could be switched in chiral phosphoric-acid catalysis caused only by changes of 3,3′-substitution group on the catalyst, please see: Ref. 2b,3e,4e,j,6a,b and
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78
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35048880194
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Wanner M.J., van der Haas R.N.S., de Cuba K.R., van Maarseveen J.H., and Hiemstra H. Angew. Chem., Int. Ed. 46 (2007) 7485
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(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 7485
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Wanner, M.J.1
van der Haas, R.N.S.2
de Cuba, K.R.3
van Maarseveen, J.H.4
Hiemstra, H.5
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79
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11244282931
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Gaussian, Wallingford, CT
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Frisch M.J., Trucks G.W., Schlegel H.B., Scuseria G.E., Robb M.A., Cheeseman J.R., Montgomery J.J.A., Vreven T., Kudin K.N., Burant J.C., Millam J.M., Iyengar S.S., Tomasi J., Barone V., Mennucci B., Cossi M., Scalmani G., Rega N., Petersson G.A., Nakatsuji H., Hada M., Ehara M., Toyota K., Fukuda R., Hasegawa J., Ishida M., Nakajima T., Honda Y., Kitao O., Nakai H., Klene M., Li X., Knox J.E., Hratchian H.P., Cross J.B., Bakken V., Adamo C., Jaramillo J., Gomperts R., Stratmann R.E., Yazyev O., Austin A.J., Cammi R., Pomelli C., Ochterski J.W., Ayala P.Y., Morokuma K., Voth G.A., Salvador P., Dannenberg J.J., Zakrzewski V.G., Dapprich S., Daniels A.D., Strain M.C., Farkas O., Malick D.K., Rabuck A.D., Raghavachari K., Foresman J.B., Ortiz J.V., Cui Q., Baboul A.G., Clifford S., Cioslowski J., Stefanov B.B., Liu G., Liashenko A., Piskorz P., Komaromi I., Martin R.L., Fox D.J., Keith T., Al-Laham M.A., Peng C.Y., Nanayakkara A., Challacombe M., Gill P.M.W., Johnson B., Chen W., Wong M.W., Gonzalez C., and Pople J.A. Gaussian 03 (Revision D.01) (2004), Gaussian, Wallingford, CT
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(2004)
Gaussian 03 (Revision D.01)
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Frisch, M.J.1
Trucks, G.W.2
Schlegel, H.B.3
Scuseria, G.E.4
Robb, M.A.5
Cheeseman, J.R.6
Montgomery, J.J.A.7
Vreven, T.8
Kudin, K.N.9
Burant, J.C.10
Millam, J.M.11
Iyengar, S.S.12
Tomasi, J.13
Barone, V.14
Mennucci, B.15
Cossi, M.16
Scalmani, G.17
Rega, N.18
Petersson, G.A.19
Nakatsuji, H.20
Hada, M.21
Ehara, M.22
Toyota, K.23
Fukuda, R.24
Hasegawa, J.25
Ishida, M.26
Nakajima, T.27
Honda, Y.28
Kitao, O.29
Nakai, H.30
Klene, M.31
Li, X.32
Knox, J.E.33
Hratchian, H.P.34
Cross, J.B.35
Bakken, V.36
Adamo, C.37
Jaramillo, J.38
Gomperts, R.39
Stratmann, R.E.40
Yazyev, O.41
Austin, A.J.42
Cammi, R.43
Pomelli, C.44
Ochterski, J.W.45
Ayala, P.Y.46
Morokuma, K.47
Voth, G.A.48
Salvador, P.49
Dannenberg, J.J.50
Zakrzewski, V.G.51
Dapprich, S.52
Daniels, A.D.53
Strain, M.C.54
Farkas, O.55
Malick, D.K.56
Rabuck, A.D.57
Raghavachari, K.58
Foresman, J.B.59
Ortiz, J.V.60
Cui, Q.61
Baboul, A.G.62
Clifford, S.63
Cioslowski, J.64
Stefanov, B.B.65
Liu, G.66
Liashenko, A.67
Piskorz, P.68
Komaromi, I.69
Martin, R.L.70
Fox, D.J.71
Keith, T.72
Al-Laham, M.A.73
Peng, C.Y.74
Nanayakkara, A.75
Challacombe, M.76
Gill, P.M.W.77
Johnson, B.78
Chen, W.79
Wong, M.W.80
Gonzalez, C.81
Pople, J.A.82
more..
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90
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77949271797
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Chiral phosphoric acids used in the activation of carbonyl compounds, see: Ref. 6c and
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Chiral phosphoric acids used in the activation of carbonyl compounds, see: Ref. 6c and
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91
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34250725648
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Rueping M., Ieawsuwan W., Antonchick A.P., and Nachtsheim B.J. Angew. Chem., Int. Ed. 46 (2007) 2097
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(2007)
Angew. Chem., Int. Ed.
, vol.46
, pp. 2097
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Rueping, M.1
Ieawsuwan, W.2
Antonchick, A.P.3
Nachtsheim, B.J.4
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102
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77949270560
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note
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It has been reported that the configuration of the major product can be reversed simply by using different solvents in chiral phosphoric acid-catalyzed aza-Diels-Alder reaction, see Ref. 5d.
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