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Volumn 13, Issue 7, 2011, Pages 1606-1609

Fmoc-based synthesis of peptide thioesters for native chemical ligation employing a tert -butyl thiol linker

Author keywords

[No Author keywords available]

Indexed keywords

2 METHYL 2 PROPANETHIOL; ESTER; PEPTIDE; TERT-BUTYLTHIOL; THIOL DERIVATIVE;

EID: 79953218412     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol1029723     Document Type: Article
Times cited : (34)

References (28)
  • 20
    • 0033621158 scopus 로고    scopus 로고
    • At the C-terminus of a thioester peptide, histidine, cysteine, and glycine are most reactive in NCL
    • At the C-terminus of a thioester peptide, histidine, cysteine, and glycine are most reactive in NCL: Hackeng, T. M.; Griffin, J. H.; Dawson, P. E. Proc. Natl. Acad. Sci. U.S.A. 1999, 96, 10068-10073
    • (1999) Proc. Natl. Acad. Sci. U.S.A. , vol.96 , pp. 10068-10073
    • Hackeng, T.M.1    Griffin, J.H.2    Dawson, P.E.3
  • 26
    • 0030973396 scopus 로고    scopus 로고
    • Essentially, the peptide-phenyl thioester which has been shown to accelerate the NCL reaction is created in situ.
    • Essentially, the peptide-phenyl thioester which has been shown to accelerate the NCL reaction is created in situ. Dawson, P. E.; Churchill, M. J.; Ghadiri, M. R.; Kent, S. B. H. J. Am. Chem. Soc. 1997, 119, 4325-4329
    • (1997) J. Am. Chem. Soc. , vol.119 , pp. 4325-4329
    • Dawson, P.E.1    Churchill, M.J.2    Ghadiri, M.R.3    Kent, S.B.H.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.