메뉴 건너뛰기




Volumn 38, Issue 18, 1997, Pages 3155-3158

Design of a novel secondary structure scaffolding device: Induction of a reverse turn in tetrapeptides by incorporating a β-amino acid and stereocontrolled free radical α-substitution reactions in peptide motifs

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CIRCULAR DICHROISM; MOLECULAR MODEL; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; PEPTIDE SYNTHESIS; PROTEIN SECONDARY STRUCTURE; TECHNIQUE; X RAY CRYSTALLOGRAPHY;

EID: 0030953890     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(97)00612-6     Document Type: Article
Times cited : (29)

References (34)
  • 22
    • 0028130028 scopus 로고
    • For a review on β-amino acids, see Cole, D.C. Tetrahedron 1994, 50, 9517.
    • (1994) Tetrahedron , vol.50 , pp. 9517
    • Cole, D.C.1
  • 23
    • 0342348662 scopus 로고    scopus 로고
    • The stereochemical assignments were corroborated by independent syntheses from enantiopure components
    • The stereochemical assignments were corroborated by independent syntheses from enantiopure components.
  • 24
    • 0002563284 scopus 로고    scopus 로고
    • and references cited therein; see also ref, 8
    • For a recent review on free radical chemistry involing α-amino acids, see: (a) Easton, C. J. Chem. Rev. 1997, 97, 53, and references cited therein; see also réf. 8.
    • (1997) Chem. Rev. , vol.97 , pp. 53
    • Easton, C.J.1
  • 25
    • 85034533375 scopus 로고
    • For recent reviews on stereochemical control in acyclic systems utilizing free radical chemistry, see: (b) Smadja, W. Synlett 1994, 1.
    • (1994) Synlett , pp. 1
    • Smadja, W.1
  • 27
    • 0342783725 scopus 로고    scopus 로고
    • note
    • 3, at 25 °C, with a 600 MHz Bruker AMX-600 spectrometer.
  • 30
    • 0342348660 scopus 로고    scopus 로고
    • The CD spectrum of the natural tetrapeptide showed much diminished absorption at 220 nm
    • The CD spectrum of the natural tetrapeptide showed much diminished absorption at 220 nm.
  • 31
    • 0342348659 scopus 로고    scopus 로고
    • For clarity, the radical is shown as a singly-occupied p-orbital, which could be delocalized into the carbonyl group of the amide
    • For clarity, the radical is shown as a singly-occupied p-orbital, which could be delocalized into the carbonyl group of the amide.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.