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Volumn 130, Issue 37, 2008, Pages 12214-12215

Rhodium-catalyzed substitution reaction of aryl fluorides with disulfides: P-orientation in the polyarylthiolation of polyfluorobenzenes

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE DERIVATIVE; DISULFIDE; FLUORIDE; RHODIUM;

EID: 51949103726     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja8049996     Document Type: Article
Times cited : (200)

References (37)
  • 1
    • 84906432727 scopus 로고    scopus 로고
    • Review: Perutz, R. N.; Braun, T. In Transition Metal-mediated C-F Bond Activation; Mingos, D. M. P., Crabtree, R. H., Eds.; Comprehensive Organometallic Chemistry; Elsevier: 2007; 1, p 725.
    • Review: Perutz, R. N.; Braun, T. In Transition Metal-mediated C-F Bond Activation; Mingos, D. M. P., Crabtree, R. H., Eds.; Comprehensive Organometallic Chemistry; Elsevier: 2007; Vol. 1, p 725.
  • 2
    • 0035903607 scopus 로고    scopus 로고
    • Recent examples:(a) Böhm, V. P. W.; Gstöttmayr, C. W. K.; Weskamp, T.; Herrmann, W. A. Angew Chem., Int. Ed. 2001, 40, 3387.
    • Recent examples:(a) Böhm, V. P. W.; Gstöttmayr, C. W. K.; Weskamp, T.; Herrmann, W. A. Angew Chem., Int. Ed. 2001, 40, 3387.
  • 23
    • 24644438084 scopus 로고    scopus 로고
    • CH and CS bond: Arisawa, M.; Fujimoto, K.; Morinaka, S.; Yamaguchi, M. J. Am. Chem. Soc. 2005, 127, 12226.
    • (d) CH and CS bond: Arisawa, M.; Fujimoto, K.; Morinaka, S.; Yamaguchi, M. J. Am. Chem. Soc. 2005, 127, 12226.
  • 25
    • 22544478748 scopus 로고    scopus 로고
    • PP and PS bonds: Arisawa, M.; Ono, T.; Yamaguchi, M. Tetrahedron Lett. 2005, 46, 5669.
    • (f) PP and PS bonds: Arisawa, M.; Ono, T.; Yamaguchi, M. Tetrahedron Lett. 2005, 46, 5669.
  • 33
    • 51949111935 scopus 로고    scopus 로고
    • 4 (0.25 mol%) and dppBz (0.5 mol%) in refluxing chlorobenzene for 3 h, the corresponding sulfide was obtained only in 7% with the recovery of the starting materials in more than 90% yields. In the absence of Rh complex, the yield was less than 1%. The results do not coincide with the simple nucleophilic aromatic substitution mechanism.
    • 4 (0.25 mol%) and dppBz (0.5 mol%) in refluxing chlorobenzene for 3 h, the corresponding sulfide was obtained only in 7% with the recovery of the starting materials in more than 90% yields. In the absence of Rh complex, the yield was less than 1%. The results do not coincide with the simple nucleophilic aromatic substitution mechanism.
  • 34
    • 51949105868 scopus 로고    scopus 로고
    • A related p-tendency in the reaction of hexafluorobenzene: Malichenko, B. F.; Robota, L. P. J. Org Chem. USSR 1975, 11, 772.
    • (a) A related p-tendency in the reaction of hexafluorobenzene: Malichenko, B. F.; Robota, L. P. J. Org Chem. USSR 1975, 11, 772.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.