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Volumn 18, Issue 26, 1999, Pages 5571-5576

Bonding modes in palladium(II) enolates: Consequences for dynamic behavior and reactivity

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EID: 0000258351     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om990613o     Document Type: Article
Times cited : (93)

References (25)
  • 1
    • 0000285862 scopus 로고
    • Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon Press: Oxford
    • Trost, B. M.; Verhoeven, T. R. In Comprehensive Organometallic Chemistry; Wilkinson, G., Stone, F. G. A., Abel, E. W., Eds.; Pergamon Press: Oxford, 1982; Vol. 8, p 838.
    • (1982) Comprehensive Organometallic Chemistry , vol.8 , pp. 838
    • Trost, B.M.1    Verhoeven, T.R.2
  • 17
    • 85034545320 scopus 로고    scopus 로고
    • note
    • 3 is referred to as enolate or C-enolate throughout this work. The alternative name ketonyl (acetonyl when R = Me) is also used in the literature.
  • 20
    • 0010235095 scopus 로고
    • Protonation of the enolate oxygen could take place either in a σ-ketonyl form or in an intermediate π-coordinated enolate to give a vinyl alcohol complex (see: Hillis, J.; Francis, J.; Ori, M.; Tsutsui, M. J. Am. Chem. Soc. 1974, 96, 4800-4804). We have no experimental evidence to favor one pathway or the other.
    • (1974) J. Am. Chem. Soc. , vol.96 , pp. 4800-4804
    • Hillis, J.1    Francis, J.2    Ori, M.3    Tsutsui, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.