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Volumn 72, Issue 23, 2007, Pages 8737-8740

Alkenylzirconocene-mediated preparation of alkenylphosphines

Author keywords

[No Author keywords available]

Indexed keywords

ALKENYLPHOSPHINES; CHLOROPHOSPHINE;

EID: 35948969743     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo071089v     Document Type: Article
Times cited : (22)

References (62)
  • 15
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    • (e) Bauer, E. B.; Gladysz J. A. In Handbook of Metathesis; Grubbs, R. H., Ed.; Wiley-VCH: Weinheim, 2003; Vol. 2, Chapter 2.11, p 403.
    • (2003) Handbook of Metathesis , vol.2 , pp. 403
    • Bauer, E.B.1    Gladysz, J.A.2
  • 23
    • 84948269443 scopus 로고
    • Kosolapoff, G. M, Maier, L, Eds, Wiley-Interscience: New York, Chapter 1 p
    • Maier, L. In Organic Phosphorus Compounds; Kosolapoff, G. M., Maier, L., Eds.; Wiley-Interscience: New York, 1972; Vol. 1, Chapter 1 p 32.
    • (1972) Organic Phosphorus Compounds , vol.1 , pp. 32
    • Maier, L.1
  • 29
    • 0012730763 scopus 로고    scopus 로고
    • Togni, A, Grutzmacher, H, Eds, Wiley-VCH: Weinheim, Chapter 5, p
    • (f) Wicht, D. K.; Glueck, D. S. In Catalytic Heterofunctionalization; Togni, A., Grutzmacher, H., Eds.; Wiley-VCH: Weinheim, 2001; Chapter 5, p 143.
    • (2001) Catalytic Heterofunctionalization , pp. 143
    • Wicht, D.K.1    Glueck, D.S.2
  • 30
    • 0000526513 scopus 로고
    • For other methods of preparing alkenylphosphines, see: a
    • For other methods of preparing alkenylphosphines, see: (a) Walsh, E. N.; Beck, T. M.; Woodstock, W. H. J. Am. Chem. Soc. 1955, 77, 929.
    • (1955) J. Am. Chem. Soc , vol.77 , pp. 929
    • Walsh, E.N.1    Beck, T.M.2    Woodstock, W.H.3
  • 46
    • 0034817177 scopus 로고    scopus 로고
    • Reactions of zirconacyclopentadienes with chlorodiphenylphosphine in the presence of CuCl were reported, see: (a) Doherty, S, Knight, J. G, Robins, E. G, Scanlan, T. H, Champkin, P. A, Clegg, W. J. Am. Chem. Soc. 2001, 123, 5110
    • Reactions of zirconacyclopentadienes with chlorodiphenylphosphine in the presence of CuCl were reported, see: (a) Doherty, S.; Knight, J. G.; Robins, E. G.; Scanlan, T. H.; Champkin, P. A.; Clegg, W. J. Am. Chem. Soc. 2001, 123, 5110.
  • 48
    • 0033001928 scopus 로고    scopus 로고
    • For preparation of (E)-2-arylvinylphosphonate from me reaction of (E)-2-arylvinylzirconocene and chlorophosphonate using CuBr as a catalyst, see: Zhong, P.; Huang, X.; Xiong, Z.-X. Synlett 1999, 721.
    • For preparation of (E)-2-arylvinylphosphonate from me reaction of (E)-2-arylvinylzirconocene and chlorophosphonate using CuBr as a catalyst, see: Zhong, P.; Huang, X.; Xiong, Z.-X. Synlett 1999, 721.
  • 52
    • 35948969884 scopus 로고    scopus 로고
    • Togni, A, Grutzmacher, H, Eds, Wiley-VCH: Weinheim, Chapter 8, p
    • (c) Igau, A. In Catalytic Heterofunctionalization; Togni, A., Grutzmacher, H., Eds.; Wiley-VCH: Weinheim, 2001; Chapter 8, p 253.
    • (2001) Catalytic Heterofunctionalization , pp. 253
    • Igau, A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.