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Volumn 71, Issue 2, 2006, Pages 763-767

Synthesis and ring size effect of macrocyclic ethynylhelicene oligomers

Author keywords

[No Author keywords available]

Indexed keywords

ABSORPTION; BENZENE; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE; SPECTROSCOPIC ANALYSIS; TEMPERATURE DISTRIBUTION; VAPOR PRESSURE;

EID: 30744463301     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo0521549     Document Type: Article
Times cited : (22)

References (23)
  • 6
    • 0002670428 scopus 로고    scopus 로고
    • Synthesis of enantiomerically pure conjugated ethynylarene macrocycles: (a) Neidlein, U.; Diederich, F. Chem. Commun. 1996, 1493-1494.
    • (1996) Chem. Commun. , pp. 1493-1494
    • Neidlein, U.1    Diederich, F.2
  • 9
    • 0000538245 scopus 로고    scopus 로고
    • In 1998, Fox synthesized an acetylene-bridged cyclic dimer derived from an optically active helicene: Fox, J. M.; Lin, D.; Itagaki, Y.; Fujita, T. J. Org. Chem. 1998, 63, 2031-2038.
    • (1998) J. Org. Chem. , vol.63 , pp. 2031-2038
    • Fox, J.M.1    Lin, D.2    Itagaki, Y.3    Fujita, T.4
  • 20
    • 30744432829 scopus 로고    scopus 로고
    • note
    • The unfolding of the helical heptamer was rapid in THF, and the CD (5 μM, 25°C) spectrum observed 10 min after dissolution exhibited the formation of a monomeric random coil structure.
  • 21
    • 30744454769 scopus 로고    scopus 로고
    • note
    • See the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.