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Volumn 53, Issue 10, 2014, Pages 2696-2700

A cobalt-catalyzed alkene hydroboration with pinacolborane

Author keywords

alkenes; cobalt; cross coupling; hydroboration; synthetic methods

Indexed keywords

CHEMO-SELECTIVITY; COBALT CATALYST; COBALT COMPLEXES; CROSS-COUPLINGS; HYDROBORATION; SYNTHETIC METHODS; SYSTEM DISPLAYS; TURNOVER NUMBER;

EID: 84897594218     PISSN: 14337851     EISSN: 15213773     Source Type: Journal    
DOI: 10.1002/anie.201310096     Document Type: Article
Times cited : (218)

References (63)
  • 16
    • 0038608640 scopus 로고    scopus 로고
    • (Eds.: A. Togni, H. Grüzmacher), Wiley-VCH, Weinheim, see: Ref. [1b]
    • N. Miyaura, in Catalytic Heterofunctionalization (Eds.:, A. Togni, H. Grüzmacher,), Wiley-VCH, Weinheim, 2001, pp. 1-46. For reviews, see: Ref. [1b]
    • (2001) Catalytic Heterofunctionalization , pp. 1-46
    • Miyaura, N.1
  • 55
    • 0030679756 scopus 로고    scopus 로고
    • Zaidlewicz and Meller reported a Co-catalyzed hyroboration of conjugated dienes with catecholborane. See:, M. Zaidlewicz, J. Meller, Tetrahedron Lett. 1997, 38, 7279
    • (1997) Tetrahedron Lett. , vol.38 , pp. 7279
    • Zaidlewicz, M.1    Meller, J.2
  • 56
    • 84891337963 scopus 로고    scopus 로고
    • During the review of this manuscript, Obligacion and Chirik reported an alkene hydroboration with pinacolborane catalyzed by a bis(imino)pyridine Co complex. See:, J. V. Obligacion, P. J. Chirik, J. Am. Chem. Soc. 2013, 135, 19107.
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 19107
    • Obligacion, J.V.1    Chirik, P.J.2
  • 58
    • 84897660944 scopus 로고    scopus 로고
    • CCDC 972296 (2) and 972297 (3) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via.
    • CCDC 972296 (2) and 972297 (3) contain the supplementary crystallographic data for this paper. These data can be obtained free of charge from The Cambridge Crystallographic Data Centre via www.ccdc.cam.ac.uk/data-request/cif.
  • 61
    • 65949093041 scopus 로고    scopus 로고
    • The Pd/RuPhos catalyst has proved to be effective for cross-couplings between alkylboronic acid derivatives and aryl halides. See Ref. [2c, 5, 19] and, S. D. Dreher, S.-E. Lim, D. L. Sandrock, G. A. Molander, J. Org. Chem. 2009, 74, 3626.
    • (2009) J. Org. Chem. , vol.74 , pp. 3626
    • Dreher, S.D.1    Lim, S.-E.2    Sandrock, D.L.3    Molander, G.A.4
  • 63
    • 0026525838 scopus 로고
    • 1H NMR analysis) and its isomer (≈7 %) arising from the hydroboration of the gem-disubstituted alkene in 7 o and subsequent coupling. Notably, a product (≈5 %) resulting from the hydroboration of both monosubstituted alkene and gem-disubstituted alkene and subsequent coupling with two aryl chlorides was also detected by GC/MS and GC analysis.
    • (1992) Tetrahedron Lett. , vol.33 , pp. 2571
    • Miyaura, N.1    Ishikawa, M.2    Sato, M.3    Suzuki, A.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.