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Volumn 79, Issue 15, 2014, Pages 7132-7140

N-heterocyclic carbene-assisted, Bis(phosphine)nickel-catalyzed cross-couplings of diarylborinic acids with aryl chlorides, tosylates, and sulfamates

Author keywords

[No Author keywords available]

Indexed keywords

CATALYSIS; CATALYST ACTIVITY; CHLORINE COMPOUNDS; NICKEL; NICKEL COMPOUNDS; ORGANIC COMPOUNDS; PHOSPHORUS COMPOUNDS; SULFUR COMPOUNDS;

EID: 84905370051     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo501291y     Document Type: Article
Times cited : (41)

References (108)
  • 64
    • 0034721714 scopus 로고    scopus 로고
    • Besides steric hindrance, a coordinative stabilization between carbonyl and nickel ion in the intermediates of ArNi(II)Cl or ArNi(II)Ar′ was proposed to be the other factor hampering the coupling. - 8660
    • Besides steric hindrance, a coordinative stabilization between carbonyl and nickel ion in the intermediates of ArNi(II)Cl or ArNi(II)Ar′ was proposed to be the other factor hampering the coupling. Inada, K.; Miyaura, N. Tetrahedron 2000, 56, 8657-8660
    • (2000) Tetrahedron , vol.56 , pp. 8657
    • Inada, K.1    Miyaura, N.2
  • 78
    • 84905364152 scopus 로고    scopus 로고
    • A patent is pending on the process, CN Pat. Appl. 201410201297.8
    • A patent is pending on the process, Zou, G.; Ke, H.; Duan, G.; Shi, W.; Zhai, J. CN Pat. Appl. 201410201297.8, 2014.
    • (2014)
    • Zou, G.1    Ke, H.2    Duan, G.3    Shi, W.4    Zhai, J.5
  • 79
    • 84905387574 scopus 로고
    • (CIRD Galderma, France) U.S. Pat. Appl. US4717720 A 19880105
    • Shroot, B.; Eustache, J.; Bernardon, J.-M. (CIRD Galderma, France) U.S. Pat. Appl. US4717720 A 19880105, 1988.
    • (1988)
    • Shroot, B.1    Eustache, J.2    Bernardon, J.-M.3
  • 81
    • 84905395991 scopus 로고    scopus 로고
    • (Medichem, S.A. Spain) U.S. Pat. Appl. US8119834 B2 20120221
    • Serrano, J. P. (Medichem, S.A., Spain) U.S. Pat. Appl. US8119834 B2 20120221, 2012.
    • (2012)
    • Serrano, J.P.1
  • 82
    • 84905370840 scopus 로고
    • (CIRD Galderma, France) E.P. Pat. Appl. EP0199636 A1 19861029
    • Shroot, B.; Eustache, J.; Bernardon, J.-M. (CIRD Galderma, France) E.P. Pat. Appl. EP0199636 A1 19861029, 1986.
    • (1986)
    • Shroot, B.1    Eustache, J.2    Bernardon, J.-M.3
  • 84
    • 84905373566 scopus 로고    scopus 로고
    • (Dipharma SpA, Italy) U.S. Pat. Appl. US7345189 B2 20080318
    • Castaldi, G.; Allegrini, P.; Razzetti, G.; Ercoli, M. (Dipharma SpA, Italy) U.S. Pat. Appl. US7345189 B2 20080318, 2008.
    • (2008)
    • Castaldi, G.1    Allegrini, P.2    Razzetti, G.3    Ercoli, M.4
  • 85
    • 84905388808 scopus 로고    scopus 로고
    • (CIRD Galderma, France) U.S. Pat. Appl. US7498461 B2 20090303
    • Terranova, E.; Pascal, J.-C. (CIRD Galderma, France) U.S. Pat. Appl. US7498461 B2 20090303, 2009.
    • (2009)
    • Terranova, E.1    Pascal, J.-C.2
  • 94
    • 0002634691 scopus 로고
    • 1-(6-Methoxynaphthalen-2-yl)ethanone could also be readily prepared in large scales - 8
    • 1-(6-Methoxynaphthalen-2-yl)ethanone could also be readily prepared in large scales: Arsenijevic, L.; Arsenijevic, V.; Horeau, A.; Jacques, J. Org. Synth. 1973, 53, 5-8
    • (1973) Org. Synth. , vol.53 , pp. 5
    • Arsenijevic, L.1    Arsenijevic, V.2    Horeau, A.3    Jacques, J.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.