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Volumn 28, Issue 18, 1998, Pages 3317-3330

Lanthanide catalyzed synthesis of β-hydroxyl amides

Author keywords

[No Author keywords available]

Indexed keywords

AMIDE; ESTER; LANTHANIDE; OXAZOLINE DERIVATIVE;

EID: 0031723481     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919808004440     Document Type: Article
Times cited : (6)

References (29)
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    • For recent examples, see: a) Gant, T. G.; Noe, M. C.; Corey, E. J., Tetrahedron Lett., 1995, 36, 8745. b) Lafargue, P.; Guenot, P.; Lellouche, J.-P., Synlett. 1995, 171. c) Sund, C.; Ylikoski, J. and Kwiatkowski, M., Synthesis, 1987, 853. d) Park, J.; Lee S.; Ahn. K. H. and Cho. C.-W., Tetrahedron Lett., 1995, 36, 7263. e) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J. and Orvig, C., Inorg. Chem. 1992, 31, 5408.
    • (1995) Synlett. , pp. 171
    • Lafargue, P.1    Guenot, P.2    Lellouche, J.-P.3
  • 3
    • 84987205225 scopus 로고
    • For recent examples, see: a) Gant, T. G.; Noe, M. C.; Corey, E. J., Tetrahedron Lett., 1995, 36, 8745. b) Lafargue, P.; Guenot, P.; Lellouche, J.-P., Synlett. 1995, 171. c) Sund, C.; Ylikoski, J. and Kwiatkowski, M., Synthesis, 1987, 853. d) Park, J.; Lee S.; Ahn. K. H. and Cho. C.-W., Tetrahedron Lett., 1995, 36, 7263. e) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J. and Orvig, C., Inorg. Chem. 1992, 31, 5408.
    • (1987) Synthesis , pp. 853
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    • For recent examples, see: a) Gant, T. G.; Noe, M. C.; Corey, E. J., Tetrahedron Lett., 1995, 36, 8745. b) Lafargue, P.; Guenot, P.; Lellouche, J.-P., Synlett. 1995, 171. c) Sund, C.; Ylikoski, J. and Kwiatkowski, M., Synthesis, 1987, 853. d) Park, J.; Lee S.; Ahn. K. H. and Cho. C.-W., Tetrahedron Lett., 1995, 36, 7263. e) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J. and Orvig, C., Inorg. Chem. 1992, 31, 5408.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 7263
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  • 5
    • 0001577833 scopus 로고
    • For recent examples, see: a) Gant, T. G.; Noe, M. C.; Corey, E. J., Tetrahedron Lett., 1995, 36, 8745. b) Lafargue, P.; Guenot, P.; Lellouche, J.-P., Synlett. 1995, 171. c) Sund, C.; Ylikoski, J. and Kwiatkowski, M., Synthesis, 1987, 853. d) Park, J.; Lee S.; Ahn. K. H. and Cho. C.-W., Tetrahedron Lett., 1995, 36, 7263. e) Hoveyda, H. R.; Karunaratne, V.; Rettig, S. J. and Orvig, C., Inorg. Chem. 1992, 31, 5408.
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    • note
    • We have attempted several different methods to hydrolyze ethyl 4-acetyl-5-methyl-isoxazole-3-carboxylate to the corresponding acid, but in our hands all failed, the only product is 2-acetyl-3-oxobutanenitrile: (matrix presented) When ethyl 4-[1-(1,3-dioxolanyl)-ethyl]-5-methyl-isoxazole-3-carbonate was subjected to hydrolysis, the mixture slowly transformed to 2-acetyl-3-oxobutanenitrile at room temperature.


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