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Volumn , Issue 24, 1999, Pages 2535-2536

Oxy-Cope rearrangements of fluorinated divinylcyclohexanols: A modular method for the construction of selectively fluorinated cyclic ketones

Author keywords

[No Author keywords available]

Indexed keywords

CYCLOHEXANOL DERIVATIVE; KETONE DERIVATIVE;

EID: 0033592965     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/a908450i     Document Type: Conference Paper
Times cited : (16)

References (22)
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    • For reviews of [3,3]-rearrangements of fluorinated substrates, see: S. T. Purrington and S. C. Weeks, J. Fluorine Chem., 1992, 56, 165; V. G. Andreev and A. F. Kolomiets, A. F. Usp. Khim., 1993, 62, 594. Rearrangements in the context of fluorinated building block chemistry are discussed in: J. M. Percy, Top. Curr. Chem., 1997, 193, 131; J. M. Percy and M. E. Prime, J. Fluorine Chem., 1999, in the press.
    • (1992) J. Fluorine Chem. , vol.56 , pp. 165
    • Purrington, S.T.1    Weeks, S.C.2
  • 4
    • 0039862822 scopus 로고
    • A. F.
    • For reviews of [3,3]-rearrangements of fluorinated substrates, see: S. T. Purrington and S. C. Weeks, J. Fluorine Chem., 1992, 56, 165; V. G. Andreev and A. F. Kolomiets, A. F. Usp. Khim., 1993, 62, 594. Rearrangements in the context of fluorinated building block chemistry are discussed in: J. M. Percy, Top. Curr. Chem., 1997, 193, 131; J. M. Percy and M. E. Prime, J. Fluorine Chem., 1999, in the press.
    • (1993) Usp. Khim. , vol.62 , pp. 594
    • Andreev, V.G.1    Kolomiets, A.F.2
  • 5
    • 0002551083 scopus 로고    scopus 로고
    • For reviews of [3,3]-rearrangements of fluorinated substrates, see: S. T. Purrington and S. C. Weeks, J. Fluorine Chem., 1992, 56, 165; V. G. Andreev and A. F. Kolomiets, A. F. Usp. Khim., 1993, 62, 594. Rearrangements in the context of fluorinated building block chemistry are discussed in: J. M. Percy, Top. Curr. Chem., 1997, 193, 131; J. M. Percy and M. E. Prime, J. Fluorine Chem., 1999, in the press.
    • (1997) Top. Curr. Chem. , vol.193 , pp. 131
    • Percy, J.M.1
  • 6
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    • in the press
    • For reviews of [3,3]-rearrangements of fluorinated substrates, see: S. T. Purrington and S. C. Weeks, J. Fluorine Chem., 1992, 56, 165; V. G. Andreev and A. F. Kolomiets, A. F. Usp. Khim., 1993, 62, 594. Rearrangements in the context of fluorinated building block chemistry are discussed in: J. M. Percy, Top. Curr. Chem., 1997, 193, 131; J. M. Percy and M. E. Prime, J. Fluorine Chem., 1999, in the press.
    • (1999) J. Fluorine Chem.
    • Percy, J.M.1    Prime, M.E.2
  • 8
    • 0001763046 scopus 로고    scopus 로고
    • P. E. Lindner and D. M. Lemal, J. Org. Chem., 1996, 61, 5109; P. E. Lindner, R. A. Correa, J. Gino and D. M. Lemal, J. Am. Chem. Soc., 1996, 118, 2556.
    • (1996) J. Org. Chem. , vol.61 , pp. 5109
    • Lindner, P.E.1    Lemal, D.M.2
  • 12
    • 1842421239 scopus 로고    scopus 로고
    • D. Schirlin, J. M. Rondeau, B. Podlogar, C. Tardif, C. Tarnus, V. Vandorsselaer and R. Farr, ACS Symp. Ser., 1996, 639, 169; H. L. Sham, ACS Symp. Ser., 1996, 639, 184.
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    • Sham, H.L.1
  • 19
    • 0012252274 scopus 로고
    • N. Y. Jing and D. M. Lemal, J. Am. Chem. Soc., 1993, 115, 8481. In a study of a Cope rearrangement of a perfluorinated hexadiene, the substitution of a chlorine atom for a fluorine atom was reported to exert only a minimal effect upon rearrangement rate and outcome. Products of biradical pathways reported by these authors were not detected in our study.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 8481
    • Jing, N.Y.1    Lemal, D.M.2
  • 20
    • 0343549572 scopus 로고    scopus 로고
    • note
    • +).
  • 22
    • 0343985583 scopus 로고    scopus 로고
    • note
    • 2) was 0.0718 (all data). CCDC 182/1482. See http://www.rsc.org/suppdata/cc/1999/2535/ for crystallographic data in .cif format.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.