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Volumn 71, Issue 4, 1998, Pages 927-932

Stereoelectronic Effects on the One-Electron Donor Reactivity of Trivalent Phosphorus Compounds. Experimental and Theoretical Investigations

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Indexed keywords


EID: 0000604641     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.71.927     Document Type: Article
Times cited : (5)

References (33)
  • 14
    • 85034480408 scopus 로고    scopus 로고
    • note
    • ·+ have been described in Refs. 1c and 1e.
  • 16
    • 85034468984 scopus 로고    scopus 로고
    • note
    • The size of the ligand Z (OMe or Ph) in 4a and 4b is not significant with respect to t-butyl. Therefore, for these compounds, the conformer with 5-t-butyl being axial contributes very little, if any.
  • 22
    • 85034477236 scopus 로고    scopus 로고
    • note
    • n)= 1.55 from Ref. 14 were used. For cyclic compounds 2 - 4, inductive effects from the ring were assumed to be equivalent to the sum of the effects from two ethoxy groups.
  • 28
    • 85034471368 scopus 로고    scopus 로고
    • Highly likely, this order is predictable also for phenylphosphonates 2b and 3b
    • Highly likely, this order is predictable also for phenylphosphonates 2b and 3b.
  • 33
    • 84893169025 scopus 로고    scopus 로고
    • Brett Bode, Iowa State University
    • M. W. Schmidt, K. K. Baldridge, J. A. Boatz, S. T. Elbert, M. S. Gordon, J. J. Jensen, S. Koseki, N. Matsunaga, K. A. Nguyen, S. Su, T. L. Windus, M. Dupuis, and J. A. Montgomery, J. Comput. Chem., 14, 1347 (1993); MacGAMESS 92.0 for the PowerMacintosh, Brett Bode, Iowa State University (1997).
    • (1997) MacGAMESS 92.0 for the PowerMacintosh


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.