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Volumn , Issue 8, 2008, Pages 1426-1430

Approach to a new dihydrofuran-fused cyclic system by a remarkable switching of endo/exo selectivity of a [4+2] cycloaddition reaction

Author keywords

Anti influenza agent; Cycloaddition; Diastereoselectivity; Pericyclic reaction; Quinodimethanes

Indexed keywords


EID: 53749096669     PISSN: 1434193X     EISSN: 10990690     Source Type: Journal    
DOI: 10.1002/ejoc.200701050     Document Type: Article
Times cited : (9)

References (24)
  • 5
    • 0035906426 scopus 로고    scopus 로고
    • for the results of recent synthetic studies by other groups, see: c
    • for the results of recent synthetic studies by other groups, see: c) H. S. Sutherland, F. E. S. Souza, R. G. A. Rodrigo, J. Org. Chem. 2001, 66, 3639-3641;
    • (2001) J. Org. Chem , vol.66 , pp. 3639-3641
    • Sutherland, H.S.1    Souza, F.E.S.2    Rodrigo, R.G.A.3
  • 11
    • 33748925911 scopus 로고    scopus 로고
    • For recent studies on the synthesis of viridine itself or model compounds, see: a
    • For recent studies on the synthesis of viridine itself or model compounds, see: a) E. H. Sessions, P. A. Jacobi, Org. Lett. 2006, 8, 4125-4128;
    • (2006) Org. Lett , vol.8 , pp. 4125-4128
    • Sessions, E.H.1    Jacobi, P.A.2
  • 14
    • 0037121440 scopus 로고    scopus 로고
    • For synthetic studies of wortmannin and related compounds, see: a
    • For synthetic studies of wortmannin and related compounds, see: a) T. Mizutani, S. Honzawa, S. Tosaki, M. Shibasaki, Angew. Chem. Int. Ed. 2002, 41, 4680-4681;
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 4680-4681
    • Mizutani, T.1    Honzawa, S.2    Tosaki, S.3    Shibasaki, M.4
  • 18
    • 53749095556 scopus 로고    scopus 로고
    • This compound was prepared from methoxyacetyl chloride and N,O-dimethylhydroxylamine in the presence of triethylamine
    • This compound was prepared from methoxyacetyl chloride and N,O-dimethylhydroxylamine in the presence of triethylamine.
  • 23
    • 53749085042 scopus 로고    scopus 로고
    • We suppose that the o-quinodimethane intermediate, having an outward-oriented cyano group, would be largely transformed into compound 16 by the [1,5]-sigmatropic rearrangement pathway.
    • We suppose that the o-quinodimethane intermediate, having an outward-oriented cyano group, would be largely transformed into compound 16 by the [1,5]-sigmatropic rearrangement pathway.
  • 24
    • 53749091369 scopus 로고    scopus 로고
    • [3b]
    • [3b]


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.