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1
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32844457119
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For selected reviews on asymmetric organocatalysis, see:
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For selected reviews on asymmetric organocatalysis, see:. List B. Chem. Commun. (2006) 819-824
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(2006)
Chem. Commun.
, pp. 819-824
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List, B.1
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12
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0037955602
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Tang Z., Jiang F., Yu L.-T., Cui S., Gong L.-Z., Mi A.-Q., Jiang Y.-Z., and Wu Y.-D. J. Am. Chem. Soc. 125 (2003) 5262-5263
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(2003)
J. Am. Chem. Soc.
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Tang, Z.1
Jiang, F.2
Yu, L.-T.3
Cui, S.4
Gong, L.-Z.5
Mi, A.-Q.6
Jiang, Y.-Z.7
Wu, Y.-D.8
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13
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16444382686
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Guo H.-M., Cun L.-F., Gong L.-Z., Mi A.-Q., and Jiang Y.-Z. Chem. Commun. (2005) 1450-1452
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(2005)
Chem. Commun.
, pp. 1450-1452
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Guo, H.-M.1
Cun, L.-F.2
Gong, L.-Z.3
Mi, A.-Q.4
Jiang, Y.-Z.5
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14
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21244479264
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Tang Z., Yang Z.-H., Chen X.-H., Cun L.-F., Mi A.-Q., Jiang Y.-Z., and Gong L.-Z. J. Am. Chem. Soc. 127 (2005) 9285-9289
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(2005)
J. Am. Chem. Soc.
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Tang, Z.1
Yang, Z.-H.2
Chen, X.-H.3
Cun, L.-F.4
Mi, A.-Q.5
Jiang, Y.-Z.6
Gong, L.-Z.7
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15
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33846318551
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Chen X.-H., Luo S.-W., Tang Z., Cun L.-F., Mi A.-Q., Jiang Y.-Z., and Gong L.-Z. Chem. Eur. J. 13 (2007) 689-701
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(2007)
Chem. Eur. J.
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Chen, X.-H.1
Luo, S.-W.2
Tang, Z.3
Cun, L.-F.4
Mi, A.-Q.5
Jiang, Y.-Z.6
Gong, L.-Z.7
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16
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38549151128
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Xiong Y., Wang F., Dong S.X., Liu X.H., and Feng X.M. Synlett (2008) 73-76
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(2008)
Synlett
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Xiong, Y.1
Wang, F.2
Dong, S.X.3
Liu, X.H.4
Feng, X.M.5
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19
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5644270179
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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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(2004)
Synlett
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Shi, L.-X.1
Sun, Q.2
Ge, Z.-M.3
Zhu, Y.-Q.4
Cheng, T.-M.5
Li, R.-T.6
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26
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33846226531
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For a very interesting paper on the asymmetric Rauhut-Currier reaction catalyzed by protected cysteine, see:
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For a very interesting paper on the asymmetric Rauhut-Currier reaction catalyzed by protected cysteine, see:. Aroyan C.E., and Miller S.J. J. Am. Chem. Soc. 129 (2007) 256-267
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(2007)
J. Am. Chem. Soc.
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Aroyan, C.E.1
Miller, S.J.2
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0035825097
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Notz W., Sakthivel K., Bui T., Zhong G., and Barbas III C.F. Tetrahedron Lett. 42 (2001) 199-201
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(2001)
Tetrahedron Lett.
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Notz, W.1
Sakthivel, K.2
Bui, T.3
Zhong, G.4
Barbas III, C.F.5
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33
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28044432333
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Intramolecular Michael addition:
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Intramolecular Michael addition:. Hayashi Y., Gotoh H., Tamura T., Yamaguchi H., Masui R., and Shoje M. J. Am. Chem. Soc. 127 (2005) 16028-16029
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(2005)
J. Am. Chem. Soc.
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Hayashi, Y.1
Gotoh, H.2
Tamura, T.3
Yamaguchi, H.4
Masui, R.5
Shoje, M.6
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34
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33745726080
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For review on the application of chiral organoselenium compounds in asymmetric catalysis, see:
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For review on the application of chiral organoselenium compounds in asymmetric catalysis, see:. Braga A.L., Lüdtke D.S., Vargas F., and Braga R.C. Synlett (2006) 1453-1466
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(2006)
Synlett
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Braga, A.L.1
Lüdtke, D.S.2
Vargas, F.3
Braga, R.C.4
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37
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46749089277
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note
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2S + H+: 447.2098.
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38
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36148949747
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Braga A.L., Vargas F., Galetto F.Z., Paixão M.W., Schwab R.S., and Taube P.S. Eur. J. Org. Chem. (2007) 5327-5331
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Eur. J. Org. Chem.
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Braga, A.L.1
Vargas, F.2
Galetto, F.Z.3
Paixão, M.W.4
Schwab, R.S.5
Taube, P.S.6
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39
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33646900442
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Braga A.L., Schneider P.H., Paixão M.W., Deobald A.M., Peppe C., and Bottega D.P. J. Org. Chem. 71 (2006) 4305-4307
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(2006)
J. Org. Chem.
, vol.71
, pp. 4305-4307
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Braga, A.L.1
Schneider, P.H.2
Paixão, M.W.3
Deobald, A.M.4
Peppe, C.5
Bottega, D.P.6
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40
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30344479954
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Schneider A., Rodrigues O.E.D., Paixão M.W., Braga A.L., and Wessjohann L.A. Tetrahedron Lett. 47 (2006) 1019-1102
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(2006)
Tetrahedron Lett.
, vol.47
, pp. 1019-1102
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Schneider, A.1
Rodrigues, O.E.D.2
Paixão, M.W.3
Braga, A.L.4
Wessjohann, L.A.5
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41
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46749095629
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note
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4, and the solvent was removed under vacuum. The crude mixture was purified by column chromatography on silica gel eluting with hexane-ethyl acetate (8:2) and the ee's were determined by HPLC analysis using Chiralcel OD-H or Chiralpak AD-H columns.
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