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Volumn 60, Issue 26, 2004, Pages 5635-5645

Application of palladium-catalyzed Pd-aryl/P-aryl exchanges: Preparation of functionalized aryl phosphines by phosphination of aryl bromides using triarylphosphines

Author keywords

Catalysis; Cross coupling; Palladium; Phosphination; Triarylphosphine; Triphenylphosphine

Indexed keywords

ACETOPHENONE DERIVATIVE; ANISOLE DERIVATIVE; BENZALDEHYDE DERIVATIVE; BENZOIC ACID DERIVATIVE; BENZONITRILE; PYRIDINE;

EID: 2942546680     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.04.085     Document Type: Article
Times cited : (46)

References (103)
  • 19
    • 0034721714 scopus 로고    scopus 로고
    • For recent references which avoided the unwanted exchange reactions, see: (a)
    • For recent references which avoided the unwanted exchange reactions, see: (a) Inada K., Miyaura N. Tetrahedron. 56:2000;8657-8660
    • (2000) Tetrahedron , vol.56 , pp. 8657-8660
    • Inada, K.1    Miyaura, N.2
  • 36
    • 0042330514 scopus 로고    scopus 로고
    • After completion of this manuscript, a Ni-catalyzed C-P bond formation of functionalized aryl bromides were reported
    • After completion of this manuscript, a Ni-catalyzed C-P bond formation of functionalized aryl bromides were reported Le Gall E., Troupel M., Nedéléc J.-Y. Tetrahedron. 59:2003;7497-7500
    • (2003) Tetrahedron , vol.59 , pp. 7497-7500
    • Le Gall, E.1    Troupel, M.2    Nedéléc, J.-Y.3
  • 45
    • 0038779254 scopus 로고    scopus 로고
    • 2PH as the phosphinating agent in the presence of CuI catalyst for the preparation of functionalized aromatic phosphines. (a)
    • 2PH as the phosphinating agent in the presence of CuI catalyst for the preparation of functionalized aromatic phosphines. (a) Van Allen D., Venkataraman D. J. Org. Chem. 68:2003;4590-4593
    • (2003) J. Org. Chem. , vol.68 , pp. 4590-4593
    • Van Allen, D.1    Venkataraman, D.2
  • 48
  • 55
    • 0001581042 scopus 로고
    • Previous synthesis of 4-(diphenylphosphino)benzonitirle and methyl 4-(diphenylphosphino)benzoate required a three-steps route and the overall yields were approximately 11 and 21%, respectively. (a)
    • Previous synthesis of 4-(diphenylphosphino)benzonitirle and methyl 4-(diphenylphosphino)benzoate required a three-steps route and the overall yields were approximately 11 and 21%, respectively. (a) Chou W.N., Pomerantz M. J. Org. Chem. 56:1991;2762-2766
    • (1991) J. Org. Chem. , vol.56 , pp. 2762-2766
    • Chou, W.N.1    Pomerantz, M.2
  • 84
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    • and references therein
    • Grushin V.V. Organometallics. 19:2000;1888-1900. and references therein
    • (2000) Organometallics , vol.19 , pp. 1888-1900
    • Grushin, V.V.1
  • 87
    • 33845377107 scopus 로고
    • For review, see: (a)
    • For review, see: (a) Garrou P.E. Chem. Rev. 85:1985;171-185
    • (1985) Chem. Rev. , vol.85 , pp. 171-185
    • Garrou, P.E.1
  • 88
    • 0000094630 scopus 로고
    • For selective aryl-P/aryl-Pd exchange instead of alkyl-P/aryl-Pd exchange, see: (b)
    • For selective aryl-P/aryl-Pd exchange instead of alkyl-P/aryl-Pd exchange, see: (b) Morita D.K., Stille J.K., Norton J.R. J. Am. Chem. Soc. 117:1995;8576-8581
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 8576-8581
    • Morita, D.K.1    Stille, J.K.2    Norton, J.R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.