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Volumn 36, Issue 17, 1997, Pages 3745-3749

Phosphinoalkylsilanes. 4.1 Hydrozirconation as a Non-Photochemical Route to (phosphinopropyl)silanes: Facile Assembly of the Bis(3-(diphenylphosphino)propyl)silyl ("biPSi") Ligand Framework. Access to the Related Poly(3-(dimethylsilyl)propyl)phosphinesRnP (CH2CH2CH2SiMe2H)3-n (n = 1, R = Ph; n = 0)

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EID: 0011417524     PISSN: 00201669     EISSN: None     Source Type: Journal    
DOI: 10.1021/ic970098r     Document Type: Article
Times cited : (6)

References (26)
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    • 0001727827 scopus 로고    scopus 로고
    • Auburn, M. J.; Holmes-Smith, R. D.; Stobart, S. R. J. Am. Chem. Soc. 1984, 106, 1314. Grundy, S. L., Holmes-Smith, R. D.; Srobart, S. R.; Williams, M. A. Inorg. Chem. 1991, 30, 3333. Stobart, S. R.; Grundy, S. L.; Josiin, F. L. U.S. Patent 4,950,798, 1990; Canadian Patent 1,327,365, 1994.
    • (1984) J. Am. Chem. Soc. , vol.106 , pp. 1314
    • Auburn, M.J.1    Holmes-Smith, R.D.2    Stobart, S.R.3
  • 3
    • 0001028604 scopus 로고
    • Auburn, M. J.; Holmes-Smith, R. D.; Stobart, S. R. J. Am. Chem. Soc. 1984, 106, 1314. Grundy, S. L., Holmes-Smith, R. D.; Srobart, S. R.; Williams, M. A. Inorg. Chem. 1991, 30, 3333. Stobart, S. R.; Grundy, S. L.; Josiin, F. L. U.S. Patent 4,950,798, 1990; Canadian Patent 1,327,365, 1994.
    • (1991) Inorg. Chem. , vol.30 , pp. 3333
    • Grundy, S.L.1    Holmes-Smith, R.D.2    Srobart, S.R.3    Williams, M.A.4
  • 4
    • 0001727827 scopus 로고    scopus 로고
    • U.S. Patent 4,950,798, 1990
    • Auburn, M. J.; Holmes-Smith, R. D.; Stobart, S. R. J. Am. Chem. Soc. 1984, 106, 1314. Grundy, S. L., Holmes-Smith, R. D.; Srobart, S. R.; Williams, M. A. Inorg. Chem. 1991, 30, 3333. Stobart, S. R.; Grundy, S. L.; Josiin, F. L. U.S. Patent 4,950,798, 1990; Canadian Patent 1,327,365, 1994.
    • Stobart, S.R.1    Grundy, S.L.2    Josiin, F.L.3
  • 5
    • 0001727827 scopus 로고    scopus 로고
    • Canadian Patent 1,327,365, 1994
    • Auburn, M. J.; Holmes-Smith, R. D.; Stobart, S. R. J. Am. Chem. Soc. 1984, 106, 1314. Grundy, S. L., Holmes-Smith, R. D.; Srobart, S. R.; Williams, M. A. Inorg. Chem. 1991, 30, 3333. Stobart, S. R.; Grundy, S. L.; Josiin, F. L. U.S. Patent 4,950,798, 1990; Canadian Patent 1,327,365, 1994.
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    • 0000280080 scopus 로고
    • Few such compounds appear to have been reported. See: Soderquist, J. A.; Brown, H. C. J. Org. Chem. 1980, 45, 3571. Soderquist, J. A.; Colberg, J. C.; Del Valle, L. J. Am. Chem. Soc. 1989, 111, 4873.
    • (1980) J. Org. Chem. , vol.45 , pp. 3571
    • Soderquist, J.A.1    Brown, H.C.2
  • 12
    • 0001165564 scopus 로고
    • Few such compounds appear to have been reported. See: Soderquist, J. A.; Brown, H. C. J. Org. Chem. 1980, 45, 3571. Soderquist, J. A.; Colberg, J. C.; Del Valle, L. J. Am. Chem. Soc. 1989, 111, 4873.
    • (1989) J. Am. Chem. Soc. , vol.111 , pp. 4873
    • Soderquist, J.A.1    Colberg, J.C.2    Del Valle, L.3
  • 15
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    • Negishi, E.; Takahashi, T. Aldrichchim. Acta 1985, 18, 31. Jordan, R. F. Adv. Organomet. Chem. 1991, 32, 325.
    • (1991) Adv. Organomet. Chem. , vol.32 , pp. 325
    • Jordan, R.F.1
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    • 0642338607 scopus 로고    scopus 로고
    • note
    • 1H NMR) diallylsilane (1.5 g, 0.013 mol, 38%) condensed at -78 °C.
  • 18
    • 0001168974 scopus 로고
    • Deschler, U.; Kleinschmit, P.; Panster, P. Angew. Chem., Int. Ed. Engl. 1986, 25, 236. Blümel. J. Inorg. Chem. 1994, 33, 5050.
    • (1994) Inorg. Chem. , vol.33 , pp. 5050
    • Blümel, J.1
  • 24


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