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Volumn 47, Issue 49, 2008, Pages 9547-9550

Oxidative homocoupling of aryl, alkenyl, and alkynyl Grignard reagents with TEMPO and dioxygen

Author keywords

Biaryls; C C coupling; Dienes; Diynes; Nitroxides

Indexed keywords

MAGNESIUM COMPOUNDS; NITROGEN OXIDES; OXYGEN; TRANSITION METALS;

EID: 56749122100     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200804197     Document Type: Article
Times cited : (138)

References (26)
  • 4
    • 56749129716 scopus 로고    scopus 로고
    • For reviews on the use of TEMPO in synthesis, see: a
    • For reviews on the use of TEMPO in synthesis, see: a) T. Vogler, A. Studer, Synthesis 2008, 2163;
    • (2008) Synthesis , pp. 2163
    • Vogler, T.1    Studer, A.2
  • 8
    • 38349133722 scopus 로고    scopus 로고
    • for the use of TEMPO as an oxidant in rhodium-catalyzed C-H arylation reactions, see: e T. Vogler, A. Studer, Org. Lett. 2008, 10, 129.
    • for the use of TEMPO as an oxidant in rhodium-catalyzed C-H arylation reactions, see: e) T. Vogler, A. Studer, Org. Lett. 2008, 10, 129.
  • 10
    • 0035498332 scopus 로고    scopus 로고
    • for a review, see
    • for a review, see: C. Ollivier, P. Renaud, Chem. Rev. 2001, 101, 3415.
    • (2001) Chem. Rev , vol.101 , pp. 3415
    • Ollivier, C.1    Renaud, P.2
  • 14
    • 15044349486 scopus 로고    scopus 로고
    • For the coupling of alkynyl metal compounds with dinitrogen tetroxide, see
    • For the coupling of alkynyl metal compounds with dinitrogen tetroxide, see: C. J. Woltermann, H. Shechter, Helv. Chim. Acta 2005, 88, 354.
    • (2005) Helv. Chim. Acta , vol.88 , pp. 354
    • Woltermann, C.J.1    Shechter, H.2
  • 19
    • 56749142420 scopus 로고    scopus 로고
    • 2) prior to the renewed addition of PhMgBr. (The product was obtained in the same yield with or without this extra step.)
    • 2) prior to the renewed addition of PhMgBr. (The product was obtained in the same yield with or without this extra step.)
  • 20
    • 56749092634 scopus 로고    scopus 로고
    • The following amounts of PhMgBr were added: 13 mol% in the third and fourth cycles, 12 mol% in the fifth and sixth cycles, and 11 mol% in the seventh and eighth cycles.
    • The following amounts of PhMgBr were added: 13 mol% in the third and fourth cycles, 12 mol% in the fifth and sixth cycles, and 11 mol% in the seventh and eighth cycles.
  • 21
    • 54749090939 scopus 로고    scopus 로고
    • For transition-metal-catalyzed aerobic oxidations, see
    • For transition-metal-catalyzed aerobic oxidations, see: J. Piera, J.-E. Bäckvall, Angew. Chem. 2008, 120, 3558;
    • (2008) Angew. Chem , vol.120 , pp. 3558
    • Piera, J.1    Bäckvall, J.-E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.