메뉴 건너뛰기




Volumn , Issue 1, 2001, Pages 87-93

Broadening of the substrate tolerance of α-chymotrypsin by using the carbamoylmethyl ester as an acyl donor in kinetically controlled peptide synthesis

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACIDS; CHEMICAL BONDS; ESTERS; HYDROPHOBICITY; REACTION KINETICS; SYNTHESIS (CHEMICAL);

EID: 0035819452     PISSN: 14727781     EISSN: None     Source Type: Journal    
DOI: 10.1039/b004180g     Document Type: Article
Times cited : (24)

References (35)
  • 5
    • 0011232561 scopus 로고
    • ed. S. Udenfriend and J. Meienhofer, Academic Press, San Diego, ch. 3
    • (e) H.-D. Jakubke, in The Peptides, ed. S. Udenfriend and J. Meienhofer, Academic Press, San Diego, 1987, vol. 9, ch. 3.
    • (1987) The Peptides , vol.9
    • Jakubke, H.-D.1
  • 7
    • 0000764007 scopus 로고    scopus 로고
    • preliminary communication
    • Preceding paper: T. Miyazawa, S. Nakajo, M. Nishikawa, K. Hamahara, K. Imagawa, E. Ensatsu, R. Yanagihara and T. Yamada, J. Chem. Soc., Perkin Trans. 1, DOI: 10.1039/b0041831; preliminary communication, T. Miyazawa, S. Nakajo, M. Nishikawa, K. Imagawa, R. Yanagihara and T. Yamada, J. Chem. Soc., Perkin Trans. 1, 1996, 1214.
    • (1996) J. Chem. Soc., Perkin Trans. , vol.1 , pp. 1214
    • Miyazawa, T.1    Nakajo, S.2    Nishikawa, M.3    Imagawa, K.4    Yanagihara, R.5    Yamada, T.6
  • 8
    • 0011180693 scopus 로고    scopus 로고
    • Preliminary communications, ed. C. Kitada, Protein Research Foundation, Osaka
    • Preliminary communications, (a) T. Miyazawa, K. Tanaka, R. Yanagihara and T. Yamada, in Peptide Chemistry 1996, ed. C. Kitada, Protein Research Foundation, Osaka, 1997, p. 33.
    • (1997) Peptide Chemistry 1996 , pp. 33
    • Miyazawa, T.1    Tanaka, K.2    Yanagihara, R.3    Yamada, T.4
  • 11
    • 0026214023 scopus 로고
    • The benzyl and p-nitrobenzyl esters were employed as donor esters in the α-chymotrypsin-catalysed coupling of N-maleyl-or N-glutaryl-L-Leu in an aqueous organic medium, see: V. Schellenberger, A. Görner, A. Könnecke and H.-D. Jakubke, Pept. Res., 1991, 4, 265.
    • (1991) Pept. Res. , vol.4 , pp. 265
    • Schellenberger, V.1    Görner, A.2    Könnecke, A.3    Jakubke, H.-D.4
  • 15
    • 0000933266 scopus 로고
    • R.J. Kerr and C. Niemann, J. Org. Chem., 1958, 23, 304. See also: S.G. Cohen, V.M. Vaidya and R.M. Schultz, Proc. Natl. Acad. Sci. USA, 1970, 66, 249. This ester was also recommended as a carboxy-protecting group for peptide synthesis by conventional chemical methods: J. Martinez, J. Laur and B. Castro, Tetrahedron, 1985, 41, 739.
    • (1958) J. Org. Chem. , vol.23 , pp. 304
    • Kerr, R.J.1    Niemann, C.2
  • 16
    • 0000810027 scopus 로고
    • R.J. Kerr and C. Niemann, J. Org. Chem., 1958, 23, 304. See also: S.G. Cohen, V.M. Vaidya and R.M. Schultz, Proc. Natl. Acad. Sci. USA, 1970, 66, 249. This ester was also recommended as a carboxy-protecting group for peptide synthesis by conventional chemical methods: J. Martinez, J. Laur and B. Castro, Tetrahedron, 1985, 41, 739.
    • (1970) Proc. Natl. Acad. Sci. USA , vol.66 , pp. 249
    • Cohen, S.G.1    Vaidya, V.M.2    Schultz, R.M.3
  • 17
    • 0001417530 scopus 로고
    • R.J. Kerr and C. Niemann, J. Org. Chem., 1958, 23, 304. See also: S.G. Cohen, V.M. Vaidya and R.M. Schultz, Proc. Natl. Acad. Sci. USA, 1970, 66, 249. This ester was also recommended as a carboxy-protecting group for peptide synthesis by conventional chemical methods: J. Martinez, J. Laur and B. Castro, Tetrahedron, 1985, 41, 739.
    • (1985) Tetrahedron , vol.41 , pp. 739
    • Martinez, J.1    Laur, J.2    Castro, B.3
  • 24
    • 0001323502 scopus 로고
    • Incorporation of D-amino acids into peptides via subtilisincatalysed condensation using the 2-chloroethyl esters as acyl donors in tert-amyl alcohol has been reported: A.L. Margolin, D.-F. Tai and A.M. Klibanov, J. Am. Chem. Soc., 1987, 109, 7885.
    • (1987) J. Am. Chem. Soc. , vol.109 , pp. 7885
    • Margolin, A.L.1    Tai, D.-F.2    Klibanov, A.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.