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Volumn , Issue 9, 1999, Pages 2127-2135

Solid-phase synthesis of oligourea peptidomimetics

Author keywords

Hydantoins; Isocyanates; Oligourea peptidomimetics; Photocleavable linker; Solid phase synthesis

Indexed keywords

CARBAMIC ACID DERIVATIVE; HYDANTOIN DERIVATIVE; ISOCYANIC ACID DERIVATIVE; MONOMER; PEPTIDE; RESIN; UREA DERIVATIVE;

EID: 0032831145     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (72)

References (36)
  • 2
    • 0000517240 scopus 로고
    • [1a] K. Burgess, D. S. Linthicum, H. Shin, Angew. Chem. Int. Ed. Engl. 1995, 34, 907-909; Angew. Chem. 1995, 107, 975-977
    • (1995) Angew. Chem. , vol.107 , pp. 975-977
  • 24
    • 0345404954 scopus 로고    scopus 로고
    • note
    • Although use of a Boc is possible, the Fmoc group has the advantage that the loading of the resin can be determined by monitoring the UV absorption of the dibenzofulvene - piperidine adduct obtained after cleavage of the Fmoc group.
  • 25
    • 0344111029 scopus 로고    scopus 로고
    • note
    • After addition of DiPEA to the monomer solution, the solution turned yellow, indicating formation of the 4-nitrophenolate anion.
  • 28
    • 0344973524 scopus 로고    scopus 로고
    • note
    • [4]
  • 30
    • 0344110430 scopus 로고    scopus 로고
    • note
    • An Fmoc strategy for the solid-phase synthesis of urea peptidomimetics will be reported shortly.
  • 31
    • 0344541979 scopus 로고    scopus 로고
    • note
    • The photocleavable linker is commercially available from Nova-Biochem, Switzerland, but can also be conveniently synthesized:


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.