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Volumn 2, Issue 10, 2011, Pages 1976-1979

Synthesis of human GLP-1 (7-36) by chemoselective α-ketoacid- hydroxylamine peptide ligation of unprotected fragments

Author keywords

[No Author keywords available]

Indexed keywords

C-TERMINAL PEPTIDES; CHEMOSELECTIVE; CHEMOSELECTIVE LIGATION; GLUTAMIC ACID; N-TERMINALS; SIDE PRODUCTS; SIDE-CHAINS; TYROSINE RESIDUES;

EID: 81355133818     PISSN: 20416520     EISSN: 20416539     Source Type: Journal    
DOI: 10.1039/c1sc00398d     Document Type: Article
Times cited : (34)

References (48)
  • 41
    • 80051716204 scopus 로고    scopus 로고
    • A. M. Thayer C&EN 2011 89 21 25
    • (2011) C&EN , vol.89 , pp. 21-25
    • Thayer, A.M.1
  • 42
    • 0023774844 scopus 로고
    • These peptide fragments also have appreciable solubility in the buffered system typically used in native chemical ligation (6 M guanidinium·HCl, 0.1 M phosphate buffer). Unfortunately the KAHA ligation did not proceed under these conditions
    • K. Mori K. Koseki Tetrahedron 1988 44 6013 6020
    • (1988) Tetrahedron , vol.44 , pp. 6013-6020
    • Mori, K.1    Koseki, K.2
  • 43
    • 77951856368 scopus 로고    scopus 로고
    • Higher reactant concentrations are not detrimental to the ligation but are rarely possible with medium-sized peptide fragments. This concentration range is comparable to the preferred conditions for native chemical ligation For new procedures for the synthesis of peptide hydroxylamines, see
    • M. A. Flores J. W. Bode Org. Lett. 2010 12 1924 1927
    • (2010) Org. Lett. , vol.12 , pp. 1924-1927
    • Flores, M.A.1    Bode, J.W.2
  • 45


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.