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Volumn 7, Issue 8, 1996, Pages 2251-2262

Synthesis, chiroptical and redox properties of axially chiral binapthol-based oligomers

Author keywords

[No Author keywords available]

Indexed keywords

1,1' BINAPHTHYL DERIVATIVE;

EID: 0030221422     PISSN: 09574166     EISSN: None     Source Type: Journal    
DOI: 10.1016/0957-4166(96)00280-7     Document Type: Article
Times cited : (52)

References (29)
  • 22
    • 85030274283 scopus 로고    scopus 로고
    • 11. Monomer 4 could be considered as having of two 'independent' naphthol-monoacetylene chromophores due to the orthogonal disposition of the two naphthol rings. However, a new type of naphthol-diacetylene-naphthol chromophore unit was inserted between the two terminal naphthol-monoacetylene chromophores for oligomers 1-3
    • 11. Monomer 4 could be considered as having of two 'independent' naphthol-monoacetylene chromophores due to the orthogonal disposition of the two naphthol rings. However, a new type of naphthol-diacetylene-naphthol chromophore unit was inserted between the two terminal naphthol-monoacetylene chromophores for oligomers 1-3.
  • 25
    • 84987357770 scopus 로고
    • and references cited therein
    • 13. Alzeer, J.; Vasella, A. Helv. Chim. Acta 1995, 78, 1219 and references cited therein.
    • (1995) Helv. Chim. Acta , vol.78 , pp. 1219
    • Alzeer, J.1    Vasella, A.2
  • 26
    • 0342553400 scopus 로고
    • 14. In one of the cyclic binaphthol-containing oligomer series, the molar rotation was proportional to the number of chiral binaphthol groups inside the molecule. However, in another related series, no relationship could be established, see Anderson, S.; Neidlein, U.; Gramlich, V.; Diederich, F. Angew. Chem. Int. Ed. Engl. 1995, 34, 1596.
    • (1995) Angew. Chem. Int. Ed. Engl. , vol.34 , pp. 1596
    • Anderson, S.1    Neidlein, U.2    Gramlich, V.3    Diederich, F.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.