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For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
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Bloch, R.1
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For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
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Calmes, M.1
Daunis, J.2
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For reviews, see: (1) Duthaler, R. O. Tetrahedron 1994, 50, 1539. (m) Hegedus, L. Acc. Chem. Res. 1995, 28, 299. (n) Bloch, R. Chem. Rev. 1998, 98, 1407. (o) Calmes, M.; Daunis, J. Amino Acids 1999, 16, 215. (p) Ma, J.-A. Angew. Chem., Int. Ed. 2003, 42, 4290.
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28
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0345098567
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For an example of the tandem hydroformylation-enamine formation sequence, see: Ahmed, M.; Seayad, A. M.; Jackstell, R.; Beller, M., Angew. Chem., Int. Ed. 2003, 42, 5615.
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Ahmed, M.1
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Oare D. A.; Henderson, M. A.; Sanner, M. A.; Heathcock C. H. J. Org. Chem. 1990, 55, 132
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Oare, D.A.1
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Heathcock, C.H.4
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10044228995
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note
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3).
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32
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0037844251
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For related examples using other N-carbamate-protected α-amino amides, see: (a) Nájera, C.; Abellán, T.; Sansano, J. M. Eur. J. Org. Chem. 2000, 2809. (b) Sengupta, S.; Mondal, S.; Das, D. Tetrahedron Lett. 1999, 40, 4107.
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Eur. J. Org. Chem.
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Nájera, C.1
Abellán, T.2
Sansano, J.M.3
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0033591193
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For related examples using other N-carbamate-protected α-amino amides, see: (a) Nájera, C.; Abellán, T.; Sansano, J. M. Eur. J. Org. Chem. 2000, 2809. (b) Sengupta, S.; Mondal, S.; Das, D. Tetrahedron Lett. 1999, 40, 4107.
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Tetrahedron Lett.
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Sengupta, S.1
Mondal, S.2
Das, D.3
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34
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10044244274
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note
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Compound 22 was available in one step from commercial N-Cbz-L-phenylalanine.
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