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Volumn 350, Issue 18, 2008, Pages 2967-2974

Nickel-catalyzed synthesis of phosphonium salts from aryl halides and triphenylphosphine

Author keywords

Coupling; Lipophilicity; Nickel; Phosphorus; Soluble support

Indexed keywords


EID: 57849148540     PISSN: 16154150     EISSN: 15213897     Source Type: Journal    
DOI: 10.1002/adsc.200800542     Document Type: Article
Times cited : (60)

References (76)
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    • Wittig olefination: a T. Rein, T. M. Pederson, Synthesis 2002, 579;
    • Wittig olefination: a) T. Rein, T. M. Pederson, Synthesis 2002, 579;
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    • 2 reagent: f B. R. Castro, Org. React. 1983, 29, 1.
    • 2 reagent: f) B. R. Castro, Org. React. 1983, 29, 1.
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    • Selected reviews on ionic liquids: a X Dupont, R. F. de Souza, P. A. Z. Suarez, Chem. Rev. 2002, 102, 3667;
    • Selected reviews on ionic liquids: a) X Dupont, R. F. de Souza, P. A. Z. Suarez, Chem. Rev. 2002, 102, 3667;
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    • P. Beck, in: Organic Phosphorus Compounds, 2, (Eds. : G. M. Kosolapoff, L. Maier), Wiley-Interscience, Weinheim, 1972, and references cited therein.
    • P. Beck, in: Organic Phosphorus Compounds, Vol. 2, (Eds. : G. M. Kosolapoff, L. Maier), Wiley-Interscience, Weinheim, 1972, and references cited therein.
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    • 0035542414 scopus 로고    scopus 로고
    • For other application of tetraphenylphosphonium salts
    • For other application of tetraphenylphosphonium salts: M. Sefkow, N. Borsuk, M. O. Wolff, Chimica Oggi 2001, 19, 35.
    • (2001) Chimica Oggi , vol.19 , pp. 35
    • Sefkow, M.1    Borsuk, N.2    Wolff, M.O.3
  • 38
    • 41149112464 scopus 로고    scopus 로고
    • Review on the synthesis of tetraarylphosphonium salts: a
    • Review on the synthesis of tetraarylphosphonium salts: a) D. W. Allen, Organophosphorus Chem. 2003, 33, 1;
    • (2003) Organophosphorus Chem , vol.33 , pp. 1
    • Allen, D.W.1
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    • 57849131005 scopus 로고    scopus 로고
    • This Ni(II)-catalyzed reaction has been widely studied, but does not tolerate many functional groups: a) K. Matsumoto, K. Hatano, N. Umezawa, T. Higuchi, Synthesis 2004, 2181;
    • This Ni(II)-catalyzed reaction has been widely studied, but does not tolerate many functional groups: a) K. Matsumoto, K. Hatano, N. Umezawa, T. Higuchi, Synthesis 2004, 2181;
  • 66
    • 57849141003 scopus 로고    scopus 로고
    • 2 was used. This suggests an exchange of counterion.
    • 2 was used. This suggests an exchange of counterion.
  • 67
    • 57849146321 scopus 로고    scopus 로고
    • Deprotection of the acetal was performed during the work-up. See Supporting Information
    • Deprotection of the acetal was performed during the work-up. See Supporting Information.
  • 68
    • 57849092924 scopus 로고    scopus 로고
    • See Supporting Information for further experimental details
    • See Supporting Information for further experimental details.
  • 71
    • 57849089398 scopus 로고    scopus 로고
    • < Only the TAP from the pre-catalyst was quantitatively recovered.
    • < Only the TAP from the pre-catalyst was quantitatively recovered.
  • 73
    • 0002298089 scopus 로고
    • Nickel
    • For general information see:, Ed, G. Wilkinson, Permagon Press, Elsevier Science, Chap. 50, pp
    • For general information see: F. Meyer, H. Kozlowski, Nickel, in: Comprehensive Coordination Chemistry, (Ed.: G. Wilkinson), Permagon Press, Elsevier Science, 1987, Vol 5, Chap. 50, pp 1-350.
    • (1987) Comprehensive Coordination Chemistry , vol.5 , pp. 1-350
    • Meyer, F.1    Kozlowski, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.