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Volumn 131, Issue 10, 2009, Pages 3466-3467

Palladium-catalyzed C-H Bond functionalization with arylsulfonyl chlorides

Author keywords

[No Author keywords available]

Indexed keywords

C-C BOND FORMATION; C-H BOND; CATALYZED SYNTHESIS; FUNCTIONALIZATIONS; ORGANIC SYNTHESIS; REACTION PARAMETERS;

EID: 68049140862     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja900200g     Document Type: Article
Times cited : (434)

References (35)
  • 1
  • 18
    • 70249101912 scopus 로고    scopus 로고
    • Simpkins, N. S. Sulfones in Organic Synthesis; Pergamon Press: Oxford, U.K., 1993. and references therein.
    • (a) Simpkins, N. S. Sulfones in Organic Synthesis; Pergamon Press: Oxford, U.K., 1993. and references therein.
  • 28
    • 33947087900 scopus 로고    scopus 로고
    • Sulfonylation without regioselectivity by the Friedel-Crafts method: Olah, G. A.; Kobayashi, S.; Nishimura, J. J. Am. Chem. Soc. 1973, 95, 564.
    • Sulfonylation without regioselectivity by the Friedel-Crafts method: Olah, G. A.; Kobayashi, S.; Nishimura, J. J. Am. Chem. Soc. 1973, 95, 564.
  • 30
    • 70249095748 scopus 로고    scopus 로고
    • In contrast to Cu-catalyzed chlorinations,3c we observed trace chlorination in our system in the absence of a palladium cocatalyst.
    • (a) In contrast to Cu-catalyzed chlorinations,3c we observed trace chlorination in our system in the absence of a palladium cocatalyst.
  • 31
    • 0013487064 scopus 로고
    • Arylsulfonyl chlorides react with DMF to form amidinium arenesulfonate salts, which we believe may play a role in enabling chlorination. See
    • (b) Arylsulfonyl chlorides react with DMF to form amidinium arenesulfonate salts, which we believe may play a role in enabling chlorination. See: Ulery, H. E. J. Org. Chem. 1965, 30, 2464.
    • (1965) J. Org. Chem , vol.30 , pp. 2464
    • Ulery, H.E.1
  • 32
    • 57349117057 scopus 로고    scopus 로고
    • For a previous report of sulfonyl chlorides as chlorinating agents for alkenes, see
    • (a) For a previous report of sulfonyl chlorides as chlorinating agents for alkenes, see: Gaspar, B.; Carreira, E. M. Angew. Chem., Int. Ed. 2008, 120, 5842.
    • (2008) Angew. Chem., Int. Ed , vol.120 , pp. 5842
    • Gaspar, B.1    Carreira, E.M.2
  • 33
    • 70249093075 scopus 로고    scopus 로고
    • Sulfonyl chlorides are competitive in price to reported chlorinating agents (NCS3a and 1,1,2,2-tetrachloroethane3c).
    • (b) Sulfonyl chlorides are competitive in price to reported chlorinating agents (NCS3a and 1,1,2,2-tetrachloroethane3c).
  • 34
    • 28744458623 scopus 로고    scopus 로고
    • For relevant studies on desulfitative cross-couplings, see: a
    • For relevant studies on desulfitative cross-couplings, see: (a) Dubbaka, S. R.; Vogel, P. Angew. Chem., Int. Ed. 2005, 44, 7674.
    • (2005) Angew. Chem., Int. Ed , vol.44 , pp. 7674
    • Dubbaka, S.R.1    Vogel, P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.