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Volumn 18, Issue 12, 1999, Pages 2390-2394

An Effective Route to Cycloruthenated N-Ligands under Mild Conditions

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Indexed keywords


EID: 0001746778     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9901067     Document Type: Article
Times cited : (149)

References (38)
  • 24
    • 85034554734 scopus 로고    scopus 로고
    • note
    • 1H NMR spectroscopy after 65 h reaction. Sixteen percent conversion to this product (with respect to the amount of 2-benzylpyridine used) was observed, but it could never be isolated and thus has not been identified up to now. It is noteworthy that separation of 2g from this latter compound was difficult. This explains the important loss of product observed when comparing the yield obtained and the conversion in solution.
  • 35
    • 85034534022 scopus 로고    scopus 로고
    • The numbering of the aryl protons follows that depicted in Charts 1 and 2
    • The numbering of the aryl protons follows that depicted in Charts 1 and 2.
  • 36
    • 85034564253 scopus 로고    scopus 로고
    • 3CN exchange process
    • 3CN exchange process.
  • 37
    • 85034539677 scopus 로고    scopus 로고
    • n.r. = not resolved due to partial overlap of other protons
    • n.r. = not resolved due to partial overlap of other protons.
  • 38
    • 0000253640 scopus 로고    scopus 로고
    • 3CN to the Ru center, as observed recently by Nelson et al., rather than reflecting the stereoselectivity of the C-H activation process. (See: Attar, S.; Catalane, V. J.; Nelson, J. H. Organometallics 1996, 15, 2932.
    • (1996) Organometallics , vol.15 , pp. 2932
    • Attar, S.1    Catalane, V.J.2    Nelson, J.H.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.