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Volumn 45, Issue 40, 2004, Pages 7519-7523

Synthesis of 'difficult' peptide sequences: Application of a depsipeptide technique to the Jung-Redemann 10- and 26-mers and the amyloid peptide Aβ(1-42)

Author keywords

Amyloid peptide; Bsmoc group; Depsipeptides; Difficult sequences; O N shift; Protecting groups

Indexed keywords

AMYLOID BETA PROTEIN[1-42]; PEPTIDE; SERINE; THREONINE;

EID: 4444382945     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2004.07.162     Document Type: Article
Times cited : (174)

References (19)
  • 6
    • 4444357327 scopus 로고    scopus 로고
    • note
    • If deblocking is difficult the instrument is programmed to add additional deblocking and coupling steps
  • 13
    • 0028847274 scopus 로고
    • For related work on the use of the O→N rearrangement in the development of water-soluble prodrugs see: R. Oliyai, and V.J. Stella Bioorg. Med. Chem. Lett. 5 1995 2735
    • (1995) Bioorg. Med. Chem. Lett. , vol.5 , pp. 2735
    • Oliyai, R.1    Stella, V.J.2
  • 16
    • 0001502832 scopus 로고    scopus 로고
    • the very first example of the use of related methodology for the synthesis of a difficult peptide was described by Horikawa and Ohfune and co-workers (M. Horikawa, T. Nakajima, and Y. Ohfune Synlett 1998 609
    • (1998) Synlett , pp. 609
    • Horikawa, M.1    Nakajima, T.2    Ohfune, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.