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Volumn 19, Issue 11, 2000, Pages 2058-2060

Synthesis of biaryl P,N ligands by novel palladium-catalyzed phosphination using triarylphosphines: Catalytic application of C-P activation

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[No Author keywords available]

Indexed keywords


EID: 0000057083     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9909338     Document Type: Article
Times cited : (87)

References (32)
  • 2
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    • The Royal Chemical Society: London
    • (b) Organophosphorous Chemistry; The Royal Chemical Society: London, 1969-1983; Vols. 1-15.
    • (1969) Organophosphorous Chemistry , vol.1-15
  • 3
    • 0032976808 scopus 로고    scopus 로고
    • For leading references, see: (a) Ding, K.; Wang, Y.; Yun, H.; Liu, J.; Wu, Y.; Terada, M.; Okubo, Y.; Mikami, K. Chem. Eur. J. 1999, 5, 1734-1737. (b) Martorell, G.; Garcias, X.; Janura, M.; Saá, J. M. J. Org. Chem. 1998, 63, 3463-3467. (c) Bringmann, G.; Wuzik, A.; Vedder, C.; Pfeiffer, M.; Stalke, D. Chem. Commun. 1998, 1211-1212.
    • (1999) Chem. Eur. J. , vol.5 , pp. 1734-1737
    • Ding, K.1    Wang, Y.2    Yun, H.3    Liu, J.4    Wu, Y.5    Terada, M.6    Okubo, Y.7    Mikami, K.8
  • 4
    • 0001281090 scopus 로고    scopus 로고
    • For leading references, see: (a) Ding, K.; Wang, Y.; Yun, H.; Liu, J.; Wu, Y.; Terada, M.; Okubo, Y.; Mikami, K. Chem. Eur. J. 1999, 5, 1734-1737. (b) Martorell, G.; Garcias, X.; Janura, M.; Saá, J. M. J. Org. Chem. 1998, 63, 3463-3467. (c) Bringmann, G.; Wuzik, A.; Vedder, C.; Pfeiffer, M.; Stalke, D. Chem. Commun. 1998, 1211-1212.
    • (1998) J. Org. Chem. , vol.63 , pp. 3463-3467
    • Martorell, G.1    Garcias, X.2    Janura, M.3    Saá, J.M.4
  • 5
    • 0001834957 scopus 로고    scopus 로고
    • For leading references, see: (a) Ding, K.; Wang, Y.; Yun, H.; Liu, J.; Wu, Y.; Terada, M.; Okubo, Y.; Mikami, K. Chem. Eur. J. 1999, 5, 1734-1737. (b) Martorell, G.; Garcias, X.; Janura, M.; Saá, J. M. J. Org. Chem. 1998, 63, 3463-3467. (c) Bringmann, G.; Wuzik, A.; Vedder, C.; Pfeiffer, M.; Stalke, D. Chem. Commun. 1998, 1211-1212.
    • (1998) Chem. Commun. , pp. 1211-1212
    • Bringmann, G.1    Wuzik, A.2    Vedder, C.3    Pfeiffer, M.4    Stalke, D.5
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    • 85086353090 scopus 로고    scopus 로고
    • note
    • 3 gave 64% and 61% yields of pyphos 2, respectively.
  • 19
    • 85086351636 scopus 로고    scopus 로고
    • note
    • 1H NMR integration from the crude reaction mixture.
  • 23
    • 0011404010 scopus 로고
    • For substitutents on the phenyl ring of BINAP, see: (a) Takaya, H.; Mashima, K.; Koyano, K.; Yagi, M.; Kumobayashi, H.; Taketomi, T.; Akutagawa, S.; Noyori, R. J. Org. Chem. 1986, 51, 629-635. (b) Mashima, K.; Matsumura, Y.-I.; Kusano, K.; Kumobayashi, H.; Sayo, N.; Hori, Y.; Ishizaki, T.; Akutagawa, S.; Takaya, H. J. Chem. Soc., Chem. Commun. 1991, 609-610.
    • (1986) J. Org. Chem. , vol.51 , pp. 629-635
    • Takaya, H.1    Mashima, K.2    Koyano, K.3    Yagi, M.4    Kumobayashi, H.5    Taketomi, T.6    Akutagawa, S.7    Noyori, R.8
  • 31
    • 85086351620 scopus 로고    scopus 로고
    • note
    • 31P NMR, with a chemical shift of 24.1 ppm.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.