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Volumn 2, Issue 3, 2000, Pages 327-330

Application of olefin cross-metathesis to organometallics. Synthesis of unsaturated ferrocenyl alcohols and ketones

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EID: 0000904154     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol991282e     Document Type: Article
Times cited : (22)

References (42)
  • 12
  • 22
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    • See ref le for a review of cross-metathesis. See also: (a) Crowe, W. E.; Zhang, Z. J. J. Am. Chem. Soc. 1993, 115, 10998.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 10998
    • Crowe, W.E.1    Zhang, Z.J.2
  • 30
    • 0031031663 scopus 로고    scopus 로고
    • 2Ru=CHFc in low (36%) yield; see: Wu, Z.; Nguyen, S. T.; Gubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1995, 117, 550. See also: Buretea, M.; Tilley, T. D. Organometallics 1997, 16, 1507. Martín-Alvarez, J. M.; Hampel, F.; Arif, A. M.; Gladysz, J. A. Organometallics 1999, 18, 955.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 677
    • Rutjes, F.P.J.T.1    Schoemaker, H.E.2
  • 31
    • 0001698392 scopus 로고
    • 2Ru=CHFc in low (36%) yield; see: Wu, Z.; Nguyen, S. T.; Gubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1995, 117, 550. See also: Buretea, M.; Tilley, T. D. Organometallics 1997, 16, 1507. Martín-Alvarez, J. M.; Hampel, F.; Arif, A. M.; Gladysz, J. A. Organometallics 1999, 18, 955.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 550
    • Wu, Z.1    Nguyen, S.T.2    Gubbs, R.H.3    Ziller, J.W.4
  • 32
    • 0000583378 scopus 로고    scopus 로고
    • 2Ru=CHFc in low (36%) yield; see: Wu, Z.; Nguyen, S. T.; Gubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1995, 117, 550. See also: Buretea, M.; Tilley, T. D. Organometallics 1997, 16, 1507. Martín-Alvarez, J. M.; Hampel, F.; Arif, A. M.; Gladysz, J. A. Organometallics 1999, 18, 955.
    • (1997) Organometallics , vol.16 , pp. 1507
    • Buretea, M.1    Tilley, T.D.2
  • 33
    • 0000576304 scopus 로고    scopus 로고
    • 2Ru=CHFc in low (36%) yield; see: Wu, Z.; Nguyen, S. T.; Gubbs, R. H.; Ziller, J. W. J. Am. Chem. Soc. 1995, 117, 550. See also: Buretea, M.; Tilley, T. D. Organometallics 1997, 16, 1507. Martín-Alvarez, J. M.; Hampel, F.; Arif, A. M.; Gladysz, J. A. Organometallics 1999, 18, 955.
    • (1999) Organometallics , vol.18 , pp. 955
    • Martín-Alvarez, J.M.1    Hampel, F.2    Arif, A.M.3    Gladysz, J.A.4
  • 37
    • 85037507766 scopus 로고    scopus 로고
    • note
    • 11 Interestingly, it was observed that yields tended to be higher when older samples of t-BuLi were employed. We speculate that the presence of lithium hydroxide modulates the reactivity of the generated organolithium.
  • 40
    • 85037492591 scopus 로고    scopus 로고
    • note
    • +, 8), 228 (100).
  • 41
    • 0033533652 scopus 로고    scopus 로고
    • Attempts to engage allyl alcohol in the cross-metathesis reaction were unsuccessful, possibly as a result of competing isomerization reactions. We and others have noted the ability of certain secondary allylic alcohols to undergo isomerization to ketones; see: (a) Hoye, T. R.; Zhao, H. Org. Lett. 1999, 1, 1123.
    • (1999) Org. Lett. , vol.1 , pp. 1123
    • Hoye, T.R.1    Zhao, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.