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Volumn , Issue 8, 1997, Pages 1739-1743

Solvent effects in [4 + 2] cycloadditions of polyhalogenated cyclopentadienes with 4-phenyl-1,2,4-triazoline-3,5-dione

Author keywords

4 Phenyl l,2,4 triazoline 3,5 dione; Acceptor numbers; Cycloadditions; Donor numbers; Solvent effects

Indexed keywords


EID: 33748721692     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199719970816     Document Type: Article
Times cited : (6)

References (55)
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    • Commercially available (Merck)
    • 1c: Commercially available (Merck).
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    • Ph. D. Thesis, Universität Regensburg
    • [17a] H. Schuhbauer, Ph. D. Thesis, Universität Regensburg, 1995.
    • (1995)
    • Schuhbauer, H.1
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    • (1994)
    • Höcht, P.1
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    • H. Roßmaier, Diplomarbeit, Universität Regensburg, 1983
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    • unpublished results. AMI and PM3 semiempirical calculations were carried out using Proquantum™ software (V. 133, Oxford Molecular Ltd., Oxford OX4 46A) and Silicon Graphics™ hardware
    • J. Sauer, H. Schuhbauer, unpublished results. AMI and PM3 semiempirical calculations were carried out using Proquantum™ software (V. 133, Oxford Molecular Ltd., Oxford OX4 46A) and Silicon Graphics™ hardware.
    • Sauer, J.1    Schuhbauer, H.2
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    • note
    • 2j + b" give correlation parameters 0.92 ≤ r ≤ 0.99 and slopes m ≈ 1.0 for the groups of dienes 1a, 1d, 1e and 1b, 1c, respectively.
  • 51
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    • Y. Marcus, Chem. Soc. Rev. 1993, 409-416. Marcus also demonstrated in this paper that acceptor numbers and donor numbers are orthogonal to each other, so that they describe independent properties of the solvent.
    • (1993) Chem. Soc. Rev. , pp. 409-416
    • Marcus, Y.1
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    • (1977) Organikum


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.