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Volumn 60, Issue 20, 2004, Pages 4431-4441

Configurationally defined sexi- and octinaphthalene derivatives: Synthesis and optical properties

Author keywords

Atropisomerism; CD spectra; Octinaphthalene; Oxidative coupling; Sexinaphthalene

Indexed keywords

2 HYDROXYNAPHTHYL; COPPER; NAPHTHALENE DERIVATIVE; QUATERNAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 1942436908     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.03.055     Document Type: Article
Times cited : (18)

References (36)
  • 1
    • 0001001058 scopus 로고    scopus 로고
    • A preliminary communication of part of this work has been published:
    • A preliminary communication of part of this work has been published: Fuji K., Furuta T., Tanaka K. Org. Lett. 3:2001;169-171
    • (2001) Org. Lett. , vol.3 , pp. 169-171
    • Fuji, K.1    Furuta, T.2    Tanaka, K.3
  • 2
    • 0000718373 scopus 로고    scopus 로고
    • For an extensive review, see: (a)
    • For an extensive review, see: (a) Pu L. Chem. Rev. 98:1998;2405-2494
    • (1998) Chem. Rev. , vol.98 , pp. 2405-2494
    • Pu, L.1
  • 19
    • 0037177321 scopus 로고    scopus 로고
    • Optically active polynaphthalenes connected at 1.4-positions were reported. See: (a)
    • Optically active polynaphthalenes connected at 1.4-positions were reported. See: (a) Habaue S., Seko T., Okamoto Y. Macromolecules. 35:2002;2437-2439
    • (2002) Macromolecules , vol.35 , pp. 2437-2439
    • Habaue, S.1    Seko, T.2    Okamoto, Y.3
  • 21
    • 0001504683 scopus 로고
    • A 9-mer of naphthalene connected at 1.5-positions was also reported. See: (c)
    • A 9-mer of naphthalene connected at 1.5-positions was also reported. See: (c) Marin G.H., Horak V. J. Org. Chem. 59:1994;4267-4271
    • (1994) J. Org. Chem. , vol.59 , pp. 4267-4271
    • Marin, G.H.1    Horak, V.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.