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Volumn 355, Issue 2-3, 2013, Pages 294-296

Asymmetric α-amination of aldehydes by a recyclable resin-supported peptide catalyst

Author keywords

Enantioselective amination; Peptide catalysts; Recyclable catalysts; Resin supported catalysts

Indexed keywords


EID: 84875736247     PISSN: 16154150     EISSN: 16154169     Source Type: Journal    
DOI: 10.1002/adsc.201200611     Document Type: Article
Times cited : (14)

References (31)
  • 12
    • 4143049101 scopus 로고    scopus 로고
    • a values of proline and N-methylacetoamide in DMSO are ~12 and ~26, respectively
    • a values of proline and N-methylacetoamide in DMSO are ~12 and ~26, respectively, see: a) S. Saito, H. Yamamoto, Acc. Chem. Res. 2004, 37, 570
    • (2004) Acc. Chem. Res. , vol.37 , pp. 570
    • Saito, S.1    Yamamoto, H.2
  • 14
    • 18244393987 scopus 로고    scopus 로고
    • Wennemers et al. have successfully designed peptide catalysts including a carboxyl group at the side chain of a peptide residue
    • Wennemers et al. have successfully designed peptide catalysts including a carboxyl group at the side chain of a peptide residue; see: a) P. Krattiger, R. Kovasy, J. D. Revell, S. Ivan, H. Wennemers, Org. Lett. 2005, 7, 1101
    • (2005) Org. Lett. , vol.7 , pp. 1101
    • Krattiger, P.1    Kovasy, R.2    Revell, J.D.3    Ivan, S.4    Wennemers, H.5
  • 19
    • 23044482261 scopus 로고    scopus 로고
    • It is reported that the peptide catalyst with a hydroxy group next to an N-terminal prolyl residue is effective for an enantioselective aldol reaction
    • It is reported that the peptide catalyst with a hydroxy group next to an N-terminal prolyl residue is effective for an enantioselective aldol reaction, see: M. R. M. Andreae, A. P. Davis, Tetrahedron: Asymmetry 2005, 16, 2487.
    • (2005) Tetrahedron: Asymmetry , vol.16 , pp. 2487
    • Andreae, M.R.M.1    Davis, A.P.2
  • 27
    • 47749137879 scopus 로고    scopus 로고
    • For a review of supported proline and proline derivatives, see
    • For a review of supported proline and proline derivatives, see: M. Gruttadauria, F. Giacalone, R. Noto, Chem. Soc. Rev. 2008, 37, 1666.
    • (2008) Chem. Soc. Rev. , vol.37 , pp. 1666
    • Gruttadauria, M.1    Giacalone, F.2    Noto, R.3
  • 28
    • 0032564916 scopus 로고    scopus 로고
    • Miller et al. developed the peptide catalysts containing a D-Pro-Aib sequence. For examples
    • Miller et al. developed the peptide catalysts containing a D-Pro-Aib sequence. For examples, see: a) S. J. Miller, G. T. Copeland, N. Papaioannou, T. E. Horstmann, E. M. Ruel, J. Am. Chem. Soc. 1998, 120, 1629
    • (1998) J. Am. Chem. Soc. , vol.120 , pp. 1629
    • Miller, S.J.1    Copeland, G.T.2    Papaioannou, N.3    Horstmann, T.E.4    Ruel, E.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.