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Khalafi-Nezhad, A.1
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Selected examples: (a) Yadav, J. S.; Reddy, B. V. S.; Murthy, C. V. S. R.; Kumar, G. M.; Madan, C. Synthesis 2001, 783.
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Synthesis
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Kumar, G.M.4
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(b) Ramesh, C.; Banerjee, J.; Pal, R.; Das, B. Adv. Synth. Catal. 2003, 345, 557.
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(e) Wang, Z.; Sun, X.; Wu, J. Tetrahedron 2008, 64, 5013.
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Wang, Z.1
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(f) Sun, S.; Wang, M.; Deng, H.; Liu, Q. Synthesis 2008, 573.
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Sun, S.1
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14
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40149107277
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and references cited therein
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(g) Liu, C.-R.; Li, M.-B.; Yang, C.-F.; Tian, S.-K. Chem. Commun. 2008, 1249; and references cited therein.
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Liu, C.-R.1
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(b) Esquivias, J.; Gómez-Arrayás, R.; Carretero, J. C. Angew. Chem. Int. Ed. 2006, 45, 629.
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(f) Li, Z.; Duan, Z.; Kang, J.; Wang, H.; Yu, L.; Wu, Y. Tetrahedron 2008, 64, 1924.
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24
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33646468489
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Reviews on chiral phosphoric acid catalysis
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Reviews on chiral phosphoric acid catalysis: (a) Taylor, M. S.; Jacobsen, E. N. Angew. Chem. Int. Ed. 2006, 45, 1520.
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(a) Kang, Q.; Zhao, Z.-A.; You, S.-L. J. Am. Chem. Soc. 2007, 129, 1484.
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(b) Wang, Y.-Q.; Song, J.; Hong, R.; Li, H.; Deng, L. J. Am. Chem. Soc. 2006, 128, 8156.
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34
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(c) Agarwal, S.; Caemmerer, S.; Filali, S.; Froehner, W.; Knoell, J.; Krahl, M. P.; Reddy, K. R.; Knoelker, H.-J. Curr. Org. Chem. 2005, 9, 1601.
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Knoelker, H.-J.8
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36
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38849204313
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For a recent example, see
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(e) For a recent example, see: Pouilhès, A.; Kouklovsky, C.; Langlois, Y.; Baltaze, J.-P.; Vispé, S.; Annereau, J.-P.; Barret, J.-M.; Kruczynski, A.; Bailly, C. Bioorg. Med. Chem. Lett. 2008, 18, 1212.
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Pouilhès, A.1
Kouklovsky, C.2
Langlois, Y.3
Baltaze, J.-P.4
Vispé, S.5
Annereau, J.-P.6
Barret, J.-M.7
Kruczynski, A.8
Bailly, C.9
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38
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67649400854
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note
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4. The solvents were removed under reduced pressure, and the residue was purified by flash chromatography (EtOAc-PE, 1:8 to 1:5) to afford the product.
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-
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39
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67649396032
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note
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2: 336.1626; found: 336.1628.
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