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Volumn 14, Issue 2, 2012, Pages 503-508

High pressure promoted aza-Michael addition of primary and secondary amines to α-substituted acrylates

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EID: 84857177544     PISSN: 14639262     EISSN: 14639270     Source Type: Journal    
DOI: 10.1039/c2gc16220b     Document Type: Article
Times cited : (22)

References (54)
  • 3
    • 0003781112 scopus 로고
    • K. Matsumoto and R. Morrin Acheson, J. Wiley & Sons, New York
    • Organic Synthesis at High Pressures, ed. K. Matsumoto and R. Morrin Acheson, J. Wiley & Sons, New York, 1991.
    • (1991) Organic Synthesis at High Pressures
  • 8
    • 0003988003 scopus 로고    scopus 로고
    • R. Winter and J. Jonas, Kluwer Verlag, Amsterdam
    • G. Jenner, in High Pressure Molecular Science, ed. R. Winter and J. Jonas, Kluwer Verlag, Amsterdam, 1999, pp. 291.
    • (1999) High Pressure Molecular Science , pp. 291
    • Jenner, G.1
  • 11
    • 84857150773 scopus 로고    scopus 로고
    • Recent review:, Very recent results
    • Recent review: A. Yu. Rulev Russ. Chem. Rev. 2011 80 211. Very recent results:.
    • (2011) Russ. Chem. Rev. , vol.80 , pp. 211
    • Rulev, A.Y.1
  • 25
    • 0003693460 scopus 로고    scopus 로고
    • For a discussion of the synthesis and biology of β-amino acids see:, E. Juaristi, Wiley–VCH, New York
    • For a discussion of the synthesis and biology of β-amino acids see: Enantioselective Synthesis of β-Amino Acids, ed. E. Juaristi, Wiley–VCH, New York, 1997.
    • (1997) Enantioselective Synthesis of β-Amino Acids
  • 41
    • 0035898796 scopus 로고    scopus 로고
    • See for instance
    • See for instance: G. Jenner Tetrahedron Lett. 2001 42 4807.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 4807
    • Jenner, G.1
  • 46
    • 0033603443 scopus 로고    scopus 로고
    • this paper, the importance of the role played by the hydrogen bonding due to the protic solvent (MeOH) is also highlighted. One can expect that the CO protonation facilitates in turn the keto–enol tatomerism, the two steps being favoured under pressure
    • F. Dumas C. Fressigné J. Langlet C. Giessner-Prettre J. Org. Chem. 1999 64 4725. In this paper, the importance of the role played by the hydrogen bonding due to the protic solvent (MeOH) is also highlighted. One can expect that the CO protonation facilitates in turn the keto–enol tatomerism, the two steps being favoured under pressure:.
    • (1999) J. Org. Chem. , vol.64 , pp. 4725
    • Dumas, F.1    Fressigné, C.2    Langlet, J.3    Giessner-Prettre, C.4
  • 52
    • 84862216257 scopus 로고    scopus 로고
    • If the effect of pressure on H-bonds in solution has been extensively studied in water [see for instance
    • If the effect of pressure on H-bonds in solution has been extensively studied in water [see for instance: L. Kangur K. Leiger A. Freiberg J. Phys.: Conf. Ser. 2008 121 1.
    • (2008) J. Phys.: Conf. Ser. , vol.121 , pp. 1
    • Kangur, L.1    Leiger, K.2    Freiberg, A.3
  • 53
    • 0042511922 scopus 로고    scopus 로고
    • ], it has been less considered in organic mediaSee however ref. 8 above and
    • M. P. Williamson K. Akasaka M. Refaee Protein Sci. 2003 12 1971.], it has been less considered in organic media. See however ref. 8 above and.
    • (2003) Protein Sci. , vol.12 , pp. 1971
    • Williamson, M.P.1    Akasaka, K.2    Refaee, M.3


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