메뉴 건너뛰기




Volumn , Issue 5, 2001, Pages 487-496

Diastereoselective SmI2 mediated cascade radical cyclisations of methylenecyclopropane derivatives - Syntheses of paeonilactone B and 6-epi-paeonilactone A

Author keywords

[No Author keywords available]

Indexed keywords

ALCOHOLS; ALKYLATION; AROMATIC HYDROCARBONS; CHELATION; CHEMICAL BONDS; DIMERIZATION; ETHERS; FREE RADICAL REACTIONS; STEREOCHEMISTRY; SYNTHESIS (CHEMICAL);

EID: 0035820173     PISSN: 14727781     EISSN: None     Source Type: Journal    
DOI: 10.1039/b009513n     Document Type: Article
Times cited : (46)

References (55)
  • 1
    • 0000721036 scopus 로고    scopus 로고
    • For a review, see: (a) M. Malacria, Chem. Rev., 1996, 96, 289.
    • (1996) Chem. Rev. , vol.96 , pp. 289
    • Malacria, M.1
  • 6
    • 0034616110 scopus 로고    scopus 로고
    • and references therein
    • (f) B.P. Haney and D.P. Curran, J. Org. Chem., 2000, 65, 2007 and references therein.
    • (2000) J. Org. Chem. , vol.65 , pp. 2007
    • Haney, B.P.1    Curran, D.P.2
  • 13
    • 33845280002 scopus 로고
    • Surprisingly few cascade radical processes initiated by samarium diiodide have been reported. Two notable examples are: (a) T.L. Fevig, R.L. Elliott and D.P. Curran, J. Am. Chem. Soc., 1988, 110, 5064.
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 5064
    • Fevig, T.L.1    Elliott, R.L.2    Curran, D.P.3
  • 35
    • 0002468923 scopus 로고
    • S. Wolff and W.C. Agosta, J. Chem. Res., Synop., 1981, 78; A.L.J. Beckwith, G. Phillipou and A.K. Serelis, Tetrahedron Lett., 1981, 22, 2811. See also refs. 20 and 21.
    • (1981) J. Chem. Res., Synop. , pp. 78
    • Wolff, S.1    Agosta, W.C.2
  • 37
    • 33751392448 scopus 로고
    • See also ref. 4a
    • 2 mediated cyclisations of unactivated olefinic ketones, see: G.A. Molander and J.A. McKie, J. Org. Chem., 1992, 57, 3132. See also ref. 4a.
    • (1992) J. Org. Chem. , vol.57 , pp. 3132
    • Molander, G.A.1    McKie, J.A.2
  • 38
    • 33748366516 scopus 로고
    • 2 mediated cyclisations of unactivated olefinic ketones: see ref. 14 and A.L.J. Beckwith, Tetrahedron, 1981, 37, 3073.
    • (1981) Tetrahedron , vol.37 , pp. 3073
    • Beckwith, A.L.J.1
  • 43
    • 0010720585 scopus 로고
    • and references cited therein
    • T.V. RajanBabu, Acc. Chem. Res., 1991, 24, 139 and references cited therein.
    • (1991) Acc. Chem. Res. , vol.24 , pp. 139
    • RajanBabu, T.V.1
  • 44
    • 0000607817 scopus 로고    scopus 로고
    • and references cited therein
    • A.L.J. Beckwith and D.M. Page, Tetrahedron, 1999, 55, 3246 and references cited therein.
    • (1999) Tetrahedron , vol.55 , pp. 3246
    • Beckwith, A.L.J.1    Page, D.M.2
  • 45
    • 0011242843 scopus 로고    scopus 로고
    • The stereochemistry of 35 and 36 was determined by NOE studies
    • The stereochemistry of 35 and 36 was determined by NOE studies.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.