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Mechanistic studies: (a) Cheong, P. H.-Y.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 13912.
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Mechanistic studies: (a) Cheong, P. H.-Y.; Houk, K. N. J. Am. Chem. Soc. 2004, 126, 13912.
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For approaches to proline immobilization, see: c
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For approaches to proline immobilization, see: (c) Benaglia, M.; Cinquini, M.; Cozzi, F.; Puglisi, A.; Celentano, G. Adv. Synth. Catal. 2002, 344, 533.
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(d) Benaglia, M.; Cinquini, M.; Cozzi, F.; Puglisi, A.; Celentano, G. J. Mol. Catal. A: Chem. 2003, 204-205, 157.
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Celentano, G.5
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(e) Kondo, K.; Yamano, T.; Takemoto, K. Makromol. Chem. 1985, 186, 1781.
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(f) Sakthivel, K.; Notz, W.; Bui, T.; Barbas, C. F. J. Am. Chem. Soc. 2001, 123, 5260.
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(a) Rostovtsed, V. V.; Green, L. G.; Fokin, V. V.; Sharpless, K. B. Angew. Chem., Int. Ed. 2002, 41, 2596.
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Green, L.G.2
Fokin, V.V.3
Sharpless, K.B.4
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(b) Tornøe, C. W.; Christensen, C.; Meldal, M. J. Org. Chem. 2002, 67, 3057.
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Christensen, C.2
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Font, D.; Jimeno, C.; Pericàs, M. A. Org. Lett. 2006, 8, 4653.
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Org. Lett
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Font, D.1
Jimeno, C.2
Pericàs, M.A.3
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24
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33746690372
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For a different strategy towards catalyst recovery in this reaction, involving the use of ionic liquids, see: a
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For a different strategy towards catalyst recovery in this reaction, involving the use of ionic liquids, see: (a) Guo, H.-M.; Niu, H.-Y.; Xue, M.-X.; Guo, Q.-X.; Cun, L.-F.; Mi, A.-Q.; Jiang, Y.-Z.; Wang, J.-J. Green Chem. 2006, 8, 682.
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Guo, H.-M.1
Niu, H.-Y.2
Xue, M.-X.3
Guo, Q.-X.4
Cun, L.-F.5
Mi, A.-Q.6
Jiang, Y.-Z.7
Wang, J.-J.8
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33750014954
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(b) Huang, K.; Huang, Z.-Z.; Li, X.-L. J. Org. Chem. 2006, 71, 8320.
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J. Org. Chem
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Huang, K.1
Huang, Z.-Z.2
Li, X.-L.3
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26
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4344693780
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For a comment on this discrepancy, see
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For a comment on this discrepancy, see: Hayashi, Y.; Yamaguchi, J.; Sumiya, T.; Hibino, K.; Shoji, M. J. Org. Chem. 2004, 69, 5966.
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(2004)
J. Org. Chem
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Hayashi, Y.1
Yamaguchi, J.2
Sumiya, T.3
Hibino, K.4
Shoji, M.5
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34249286699
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1H NMR spectra of the reaction crudes (in DMF and DMSO) showed small signals due to the formation of the α, α′-bisaminoxylation product which was not observed using chloroform.
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1H NMR spectra of the reaction crudes (in DMF and DMSO) showed small signals due to the formation of the α, α′-bisaminoxylation product which was not observed using chloroform.
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34249334705
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An experiment in DMF with the conditions of entry 1 (Table 2) showed, after 7 h, no progress of the reaction
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An experiment in DMF with the conditions of entry 1 (Table 2) showed, after 7 h, no progress of the reaction.
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0037134880
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For examples of self-aldolization of aldehydes, see: Northrup, A, MacMillan, D. W. C. J. Am. Chem. Soc. 2002, 124, 6798
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For examples of self-aldolization of aldehydes, see: Northrup, A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2002, 124, 6798.
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