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Volumn 131, Issue 24, 2009, Pages 8642-8648

Nanosized hybrid oligoamide foldamers: Aromatic templates for the folding of multiple aliphatic units

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC COMPOUNDS; CONFORMATIONS; MONOMERS; OLIGOMERS; STABILITY;

EID: 67650545651     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9019758     Document Type: Article
Times cited : (64)

References (81)
  • 1
    • 57149145479 scopus 로고    scopus 로고
    • For recent reviews, see
    • For recent reviews, see: (a) Li, Z.-T.; Hou, J.-L.; Li, C. Acc. Chem. Res. 2008, 41, 1343-1353.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1343-1353
    • Li, Z.-T.1    Hou, J.-L.2    Li, C.3
  • 4
  • 34
    • 34447560486 scopus 로고    scopus 로고
    • Neidle, S., Balasubramanian, S., Eds.; RSC Publishing, U.K.
    • (b) Quadruplex Nucleic Acids; Neidle, S., Balasubramanian, S., Eds.; RSC Publishing, U.K., 2006.
    • (2006) Quadruplex Nucleic Acids
  • 37
    • 57349134690 scopus 로고    scopus 로고
    • and references therein
    • (a) Horne, W. S.; Gellman, S. H. Acc. Chem. Res. 2008, 41, 1399-1408, and references therein.
    • (2008) Acc. Chem. Res. , vol.41 , pp. 1399-1408
    • Horne, W.S.1    Gellman, S.H.2
  • 68
    • 67650542283 scopus 로고    scopus 로고
    • note
    • A dimer is flat; longer oligomers have a helical shape that imposes ca. 10° twists at the aryl-amide linkages. See ref 15.
  • 70
    • 67650536425 scopus 로고    scopus 로고
    • note
    • The synthesis of P is reported in the supporting information. Note that this P unit differs from the monomer described in ref 14 in that it does not have an isobutoxy substituent in position 4.
  • 71
    • 33344465856 scopus 로고    scopus 로고
    • For an account on the chain-length dependence test, see
    • For an account on the chain-length dependence test, see: (a) Stone, M. T.; Heemstra, J. M.; Moore, J. S. Acc. Chem. Res. 2006, 39, 11-20.
    • (2006) Acc. Chem. Res. , vol.39 , pp. 11-20
    • Stone, M.T.1    Heemstra, J.M.2    Moore, J.S.3
  • 73
    • 67650545421 scopus 로고    scopus 로고
    • note
    • Though unlikely, the possibility that diastereomeric conformers would have rigorously identical NMR spectra cannot be ruled out on the basis of NMR measurements but was excluded based on chiral HPLC data.
  • 74
    • 60149094817 scopus 로고    scopus 로고
    • For a recent description of long ethylene glycol oligomers prepared stepwise, see
    • For a recent description of long ethylene glycol oligomers prepared stepwise, see: French, A. C.; Thomson, A. L.; Davis, B. G. Angew. Chem., Int. Ed. 2009, 48, 1248-1252.
    • (2009) Angew. Chem., Int. Ed. , vol.48 , pp. 1248-1252
    • French, A.C.1    Thomson, A.L.2    Davis, B.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.