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Volumn 693, Issue 21-22, 2008, Pages 3337-3345

Coupling of Fischer carbene complexes with conjugated enediynes featuring radical traps: Novel structure and reactivity features of chromium complexed arene diradical species

Author keywords

Conjugated enediyne; Diradicals; Fischer carbene; Radical cyclization

Indexed keywords

ACETYLENE; CHLORINE COMPOUNDS; CHROMIUM; CYCLIZATION; NONMETALS; OLEFINS; OXYGEN;

EID: 52049101348     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2008.08.003     Document Type: Article
Times cited : (13)

References (39)
  • 11
    • 33847032530 scopus 로고    scopus 로고
    • For a recurring annual series on the reactivity of carbene complexes, see; earlier editions of the series
    • For a recurring annual series on the reactivity of carbene complexes, see;. Herndon J.W. Coord. Chem. Rev. 251 (2007) 1158-1258 earlier editions of the series
    • (2007) Coord. Chem. Rev. , vol.251 , pp. 1158-1258
    • Herndon, J.W.1
  • 12
    • 0000996219 scopus 로고    scopus 로고
    • For a preliminary account of this work, see;
    • For a preliminary account of this work, see;. Herndon J.W., and Wang H. J. Org. Chem. 63 (1998) 4562-4563
    • (1998) J. Org. Chem. , vol.63 , pp. 4562-4563
    • Herndon, J.W.1    Wang, H.2
  • 15
    • 85064667006 scopus 로고    scopus 로고
    • The incorrect assignment was based on accidental isochrony attributed to the two alkene protons of 13a, coupled with a preponderance of evidence that suggests radical cyclizations favor 5-exo processes over 6-endo processes. See: Curran, D.P. Synthesis 1988, 417-439 and Synthesis 1988, 489-513.
    • The incorrect assignment was based on accidental isochrony attributed to the two alkene protons of 13a, coupled with a preponderance of evidence that suggests radical cyclizations favor 5-exo processes over 6-endo processes. See: Curran, D.P. Synthesis 1988, 417-439 and Synthesis 1988, 489-513.
  • 16
    • 85022802126 scopus 로고
    • For oxidative dehydrogenation by chromium(0) species, see;
    • For oxidative dehydrogenation by chromium(0) species, see;. Tumer S.U., Herndon J.W., and McMullen L.A. J. Am. Chem. Soc. 114 (1992) 8394-8404
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 8394-8404
    • Tumer, S.U.1    Herndon, J.W.2    McMullen, L.A.3
  • 18
  • 26
    • 34247624723 scopus 로고    scopus 로고
    • 3 complexes see;
    • 3 complexes see;. Uemura M. Org. React. 67 (2006) 217-657
    • (2006) Org. React. , vol.67 , pp. 217-657
    • Uemura, M.1
  • 28
    • 52049126893 scopus 로고    scopus 로고
    • Frisch, M.J. et al, Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
    • Frisch, M.J. et al, Gaussian 03, revision C.02; Gaussian, Inc.: Wallingford, CT, 2004.
  • 33
    • 33846405747 scopus 로고
    • The value for the C-O bond in the simple ketone benzophenone is 1.23 Å;
    • The value for the C-O bond in the simple ketone benzophenone is 1.23 Å;. Fleischer E.B., Sung N., and Hawkinson S. J. Phys. Chem. 72 (1968) 4311-4312
    • (1968) J. Phys. Chem. , vol.72 , pp. 4311-4312
    • Fleischer, E.B.1    Sung, N.2    Hawkinson, S.3
  • 39
    • 52049083291 scopus 로고    scopus 로고
    • For a General Experimental, see the Supplementary Material.
    • For a General Experimental, see the Supplementary Material.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.