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Volumn 73, Issue 7, 2008, Pages 2687-2694

Expanding the registry of aromatic amide foldamers: Folding, photochemistry and assembly using diaza-anthracene units

Author keywords

[No Author keywords available]

Indexed keywords

ADDITION REACTIONS; ANTHRACENE; CONFORMATIONS; SOLID STATE REACTIONS; SYNTHESIS (CHEMICAL); THERMODYNAMIC STABILITY;

EID: 41649110297     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo702602w     Document Type: Article
Times cited : (58)

References (73)
  • 1
    • 37249043079 scopus 로고    scopus 로고
    • Foldamers Based on Local Conformational Preferences
    • For reviews, see:, Hecht, S, Huc, I, Eds, Wiley-VCH: Weinheim
    • For reviews, see: Cuccia, L.; Huc, I. Foldamers Based on Local Conformational Preferences. In Foldamers: Structure, Properties and Applications; Hecht, S., Huc, I., Eds.; Wiley-VCH: Weinheim, 2007; pp 3-33.
    • (2007) Foldamers: Structure, Properties and Applications , pp. 3-33
    • Cuccia, L.1    Huc, I.2
  • 11
    • 34248391448 scopus 로고    scopus 로고
    • Li, C.; Wang, G. T.; Y, H. P.; Jiang, X. K.; Li, Z. T.; Wang, R. X. Org. Lett. 2007, 9, 1797.
    • (a) Li, C.; Wang, G. T.; Y, H. P.; Jiang, X. K.; Li, Z. T.; Wang, R. X. Org. Lett. 2007, 9, 1797.
  • 34
    • 41649103142 scopus 로고    scopus 로고
    • Foldamers Based on Remote Intrastrans Interactions
    • For a review, see:, Hecht, S, Huc, I, Eds, Wiley-VCH: Weinheim
    • For a review, see: Le Grel, P.; Guichard G. Foldamers Based on Remote Intrastrans Interactions. In Foldamers: Structure, Properties and Applications; Hecht, S., Huc, I., Eds.; Wiley-VCH: Weinheim, 2007; pp 35-75.
    • (2007) Foldamers: Structure, Properties and Applications , pp. 35-75
    • Le Grel, P.1    Guichard, G.2
  • 57
    • 41649101695 scopus 로고    scopus 로고
    • 1,8-Diaza-anthracenes are formally pyrido-quinolines, but their photochemical and photophysical behaviors relate to that of anthracene. These units were thus named diaza-anthracenes in this manuscript.
    • 1,8-Diaza-anthracenes are formally pyrido-quinolines, but their photochemical and photophysical behaviors relate to that of anthracene. These units were thus named diaza-anthracenes in this manuscript.
  • 68
    • 17644381893 scopus 로고    scopus 로고
    • For recent examples, see: a
    • For recent examples, see: (a) Nakamura, A. ; Inoue, Y. J. Am. Chem. Soc. 2005, 127, 5338.
    • (2005) J. Am. Chem. Soc , vol.127 , pp. 5338
    • Nakamura, A.1    Inoue, Y.2
  • 73
    • 41649083631 scopus 로고    scopus 로고
    • 2 values and the residual distribution.
    • 2 values and the residual distribution.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.