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Volumn 69, Issue 6, 2004, Pages 2181-2184

Synthesis and Conformational Studies of Novel Cyclic Peptides Constrained into a 310 Helical Structure by a Heterochiral D-Pro-L-Pro Dipeptide Template

Author keywords

[No Author keywords available]

Indexed keywords

CONFORMATIONS; MOLECULAR DYNAMICS; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL); X RAY CRYSTALLOGRAPHY;

EID: 1642405500     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo030282w     Document Type: Article
Times cited : (16)

References (20)
  • 11
    • 0001399412 scopus 로고    scopus 로고
    • and references cited therein
    • (c) Furstner, A. Angew. Chem., Int. Ed. 2000, 39, 3012-3043 and references cited therein.
    • (2000) Angew. Chem., Int. Ed. , vol.39 , pp. 3012-3043
    • Furstner, A.1
  • 17
    • 0034584873 scopus 로고    scopus 로고
    • For a review on the use of CD in study of protein structure and function, see: Kelly, S. M.; Price, N. C. Curr. Protein Pept. Sci. 2000, 1, 349-384.
    • (2000) Curr. Protein Pept. Sci. , vol.1 , pp. 349-384
    • Kelly, S.M.1    Price, N.C.2
  • 20
    • 1642345833 scopus 로고    scopus 로고
    • note
    • γ atom (C8) of L-proline is disordered in two positions with occupancies of 0.8 and 0.2. Crystallographic data (CIF) can be found in Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.