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Volumn 47, Issue 37, 2008, Pages 7099-7102

A nonpeptidic reverse turn that promotes parallel sheet structure stabilized by C-H⋯O hydrogen bonds in a cyclopropane γ-peptide

Author keywords

Foldamers; Hydrogen bonds; Parallel turns; Peptidomimetics

Indexed keywords


EID: 54749116520     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200802648     Document Type: Article
Times cited : (45)

References (56)
  • 31
    • 54749128661 scopus 로고    scopus 로고
    • For full details of the FTIR, DMSO titration, and temperature coefficient data see the Supporting Information
    • For full details of the FTIR, DMSO titration, and temperature coefficient data see the Supporting Information.
  • 33
    • 2342507250 scopus 로고    scopus 로고
    • For a cyclopropyl β-amino acid that populates a helical conformation see
    • For a cyclopropyl β-amino acid that populates a helical conformation see: S. De Pol, C. Zorn, C. D. Klein, O. Zerbe, O. Reiser, Angew. Chem. 2004, 116, 517;
    • (2004) Angew. Chem , vol.116 , pp. 517
    • De Pol, S.1    Zorn, C.2    Klein, C.D.3    Zerbe, O.4    Reiser, O.5
  • 44
    • 54749154139 scopus 로고    scopus 로고
    • CCDC 674635 (6), 674637 (7), 690077 (9)and 674636 (12) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
    • CCDC 674635 (6), 674637 (7), 690077 (9)and 674636 (12) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data_request/cif.
  • 51
    • 0036943504 scopus 로고    scopus 로고
    • It has been commented that contact atom pairs that occur in molecular crystals should not necessarily be considered as prime promoters of the (intermolecular) interaction but rather as a result of long range effects. J. D. Dunitz, A. Gavezzotti, Helv. Chim. Acta 2002, 85, 3949
    • It has been commented that "contact atom pairs that occur in molecular crystals should not necessarily be considered as prime promoters of the (intermolecular) interaction but rather as a result of long range effects". J. D. Dunitz, A. Gavezzotti, Helv. Chim. Acta 2002, 85, 3949.
  • 54
    • 54749119770 scopus 로고    scopus 로고
    • αH protons that function as hydrogen-bond donors possess significantly higher temperature coefficients than those that do not. Full details of the temperature coefficient data can be found in the Supporting Information.
    • αH protons that function as hydrogen-bond donors possess significantly higher temperature coefficients than those that do not. Full details of the temperature coefficient data can be found in the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.