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Volumn 74, Issue 10, 2009, Pages 4013-4016

Biphenylene-substituted ruthenocenylphosphine for Suzuki-Miyaura coupling of sterically hindered aryl bromides

Author keywords

[No Author keywords available]

Indexed keywords

ARYL BROMIDES; ARYLBORONIC ACIDS; BIPHENYLENE; CATALYTIC SYSTEM; CHEMICAL EQUATIONS; SUZUKI-MIYAURA COUPLING; SUZUKI-MIYAURA REACTION;

EID: 65949115293     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo900550g     Document Type: Article
Times cited : (32)

References (51)
  • 22
    • 0002812967 scopus 로고    scopus 로고
    • For recent reviews on Suzuki-Miyaura reaction, see:
    • For recent reviews on Suzuki-Miyaura reaction, see: (a) Miyaura, N. Top. Curr. Chem. 2002, 219, 11.
    • (2002) Top. Curr. Chem. , vol.219 , pp. 11
    • Miyaura, N.1
  • 27
    • 65949119303 scopus 로고    scopus 로고
    • See also ref 1e.
    • (f) See also ref 1e.
  • 32
    • 0036420063 scopus 로고    scopus 로고
    • For Suzuki-Miyaura reactions of 1b or its mesityl analogue with 2b in the presence of less than 0.1 mol % of Pd catalyst, see:
    • For Suzuki-Miyaura reactions of 1b or its mesityl analogue with 2b in the presence of less than 0.1 mol % of Pd catalyst, see: (a) Feuersten, M.; Berthiol, F.; Doucet, H.; Santelli, M. Synlett 2002, 1807.
    • (2002) Synlett , pp. 1807
    • Feuersten, M.1    Berthiol, F.2    Doucet, H.3    Santelli, M.4
  • 33
    • 65949099499 scopus 로고    scopus 로고
    • See also ref 5d.
    • (b) See also ref 5d.
  • 34
    • 0032747809 scopus 로고    scopus 로고
    • For some examples of the beneficial effect of increasing the L/Pd ratio on catalytic activity, see:
    • For some examples of the beneficial effect of increasing the L/Pd ratio on catalytic activity, see: (a) Wolfe, J. P.; Singer, R. A.; Yang, B. H.; Buchwald, S. L. J. Am. Chem. Soc. 1999, 121, 9550.
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 9550
    • Wolfe, J.P.1    Singer, R.A.2    Yang, B.H.3    Buchwald, S.L.4
  • 36
    • 0035903968 scopus 로고    scopus 로고
    • For Suzuki-Miyaura reactions of 1a with ortho-unsubstituted arylboronic acid, see:
    • For Suzuki-Miyaura reactions of 1a with ortho-unsubstituted arylboronic acid, see: (a) Feuerstein, M.; Doucet, H.; Santelli, M. Tetrahedron Lett. 2002, 42, 6667.
    • (2002) Tetrahedron Lett. , vol.42 , pp. 6667
    • Feuerstein, M.1    Doucet, H.2    Santelli, M.3
  • 39
    • 65949119966 scopus 로고    scopus 로고
    • See also refs 5b and 5c.
    • (d) See also refs 5b and 5c.
  • 40
    • 0035211775 scopus 로고    scopus 로고
    • For Mizoroki-Heck reactions of 1a, see:
    • For Mizoroki-Heck reactions of 1a, see: (a) Feuerstein, M.; Doucet, H.; Santelli, M. Synlett 2001, 1980.
    • (2001) Synlett , pp. 1980
    • Feuerstein, M.1    Doucet, H.2    Santelli, M.3
  • 51
    • 65949083977 scopus 로고    scopus 로고
    • See also refs 5b and 5c.
    • (d) See also refs 5b and 5c.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.