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Volumn 6, Issue 17, 2008, Pages 3096-3104

Ring contraction during the 6π-electrocyclisation of naphthopyran valence tautomers

Author keywords

[No Author keywords available]

Indexed keywords

AROMATIC HYDROCARBONS; ISOMERS; OPTICAL PROPERTIES; PHOTOCHROMISM; SHRINKAGE;

EID: 49549123134     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b807744d     Document Type: Article
Times cited : (28)

References (27)
  • 1
    • 77958465845 scopus 로고    scopus 로고
    • Functional Dyes, ed., S.-H. Kim, Elsevier, Amsterdam
    • For recent reviews see: J. D. Hepworth and B. M. Heron, in Functional Dyes, ed., S.-H. Kim, Elsevier, Amsterdam, 2006, pp. 85-135 and
    • (2006) , pp. 85-135
    • Hepworth, J.D.1    Heron In, B.M.2
  • 8
    • 34247889833 scopus 로고    scopus 로고
    • Examples of the Claisen route to naphthopyrans are known, however, in these instances, the electron withdrawing aryl group is partnered with an electron rich aryl unit to improve reactivity e.g. J. Momoda, S. Matsuoka, H. Nagou, PCT WO 2000075238 (2000); J. Momota, T. Hara, Japanese Patent, JP 09124645 (1997)
    • E. A. Shilova V. P. Perevalov A. Samat C. Moustrou Tetrahedron Lett. 2007 48 4127
    • (2007) Tetrahedron Lett. , vol.48 , pp. 4127
    • Shilova, E.A.1    Perevalov, V.P.2    Samat, A.3    Moustrou, C.4
  • 13
    • 49549106495 scopus 로고    scopus 로고
    • note
    • -3
  • 14
    • 49549084882 scopus 로고    scopus 로고
    • note
    • -3
  • 18
    • 49549112539 scopus 로고    scopus 로고
    • note
    • -3
  • 23
    • 49549106946 scopus 로고    scopus 로고
    • note
    • -3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.