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Volumn , Issue 12, 2005, Pages 1869-1872

A novel rearrangement of arylvinylidenecyclopropanes to naphthalene derivatives catalyzed by Lewis acids or Brønsted acids

Author keywords

Arylvinylidenecyclopropanes; Br nsted acids; Lewis acids; Naphthalene derivatives; Rearrangement

Indexed keywords

2 METHYL 1,4 DIPHENYLNAPHTHALENE; ARYLVINYLIDENECYCLOPROPANE; CYCLOPROPANE DERIVATIVE; DIPHENYLVINYLIDENECYCLOPROPANE; LEWIS ACID; NAPHTHALENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 23644457608     PISSN: 09365214     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2005-871565     Document Type: Article
Times cited : (43)

References (64)
  • 53
    • 0034603541 scopus 로고    scopus 로고
    • On the other hand, Kilburn reported Lewis acid mediated cascade reactions of silyl-substituted methylenecyclopropane with ketones and aldehydes: (c) Peron, G. L. N.; Kitteringham, J.; Kilburn, J. D. Tetrahedron Lett. 2000, 41, 1615.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 1615
    • Peron, G.L.N.1    Kitteringham, J.2    Kilburn, J.D.3
  • 59
    • 84982381526 scopus 로고
    • For isomerization of alkenylidenecyclopropanes catalyzed by Lewis acids: Fitjer, L. Angew. Chem., Int. Ed. Engl. 1975, 14, 360.
    • (1975) Angew. Chem., Int. Ed. Engl. , vol.14 , pp. 360
    • Fitjer, L.1
  • 60
    • 33645184449 scopus 로고    scopus 로고
    • note
    • 13C NMR spectral data and analytic data of the compounds shown in Tables 1 and 2 and Scheme 2, and detailed experimental procedures for their preparation, are available upon request from the author.
  • 61
    • 0004210270 scopus 로고    scopus 로고
    • Rappoport, Z.; Stang, P. J., Eds.; John Wiley & Sons: New York
    • -1, respectively; thus, initial protonation might take place to give the most thermodynamically stable cationic intermediate A-1 (Figure 1): (a) Siehl, H.-U.; Aue, D. H. Dicoordinated Carbocations; Rappoport, Z.; Stang, P. J., Eds.; John Wiley & Sons: New York, 1997, 137-138.
    • (1997) Dicoordinated Carbocations , pp. 137-138
    • Siehl, H.-U.1    Aue, D.H.2
  • 62
    • 0002846538 scopus 로고
    • (b) The stabilizing effect of cyclopropyl substituents on carbocations is well documented: Olah, G. A.; Reddy, V. P.; Prakash, G. K. S. Chem. Rev. 1992, 92, 69.
    • (1992) Chem. Rev. , vol.92 , pp. 69
    • Olah, G.A.1    Reddy, V.P.2    Prakash, G.K.S.3
  • 64
    • 33645178281 scopus 로고    scopus 로고
    • note
    • + + 1), 323.1794; found, 323.1786.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.