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Volumn 121, Issue 43, 1999, Pages 10112-10118

Perturbation of Cope's rearrangement: 1,3,5-triphenylhexa-1,5-diene. Chameleonic or centauric transition region?

Author keywords

[No Author keywords available]

Indexed keywords

ALKADIENE;

EID: 0033520780     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja9908568     Document Type: Article
Times cited : (79)

References (59)
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    • (1963) Molecular Rearrangements , vol.1 , pp. 684-696
    • Rhoads, S.J.1
  • 2
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    • Academic: New York
    • See reviews by (a) Rhoads, S. J. In Molecular Rearrangements; de Mayo, P., Ed.; Wiley: New York, 1963; Vol. 1, pp 684-696; (b) Gajewski, J. J. Hydrocarbon Thermal Rearrangements; Academic: New York, 1981; pp 166-176.
    • (1981) Hydrocarbon Thermal Rearrangements , pp. 166-176
    • Gajewski, J.J.1
  • 3
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    • note
    • 13a).
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    • Baldwin, J. E. J. Comput. Chem. 1998, 19, 222-231; Baldwin, J. E.; Bonacorsi, S. J., Jr.; Burrell, R. C. J. Org. Chem. 1998, 63, 4721- 4725.
    • (1998) J. Comput. Chem. , vol.19 , pp. 222-231
    • Baldwin, J.E.1
  • 21
    • 0030125572 scopus 로고    scopus 로고
    • Kozlowski, P. M.; Dupuis, M.; Davidson, E. R. J. Am. Chem. Soc. 1995, 117, 774-778; Davidson, E. R. J. Phys. Chem. 1996, 100, 6161-6166.
    • (1996) J. Phys. Chem. , vol.100 , pp. 6161-6166
    • Davidson, E.R.1
  • 30
    • 0344556508 scopus 로고    scopus 로고
    • note
    • 24 heats of formation of a few of the relevant phenyl hydrocarbons were based redundantly on a mean of values that included those few experimental values noted and those calculated by the method of group equivalents, which, of course, had been based on the same data but gave somewhat different results. Recalculations that omit the latter values have led to a few quite minor modifications.
  • 32
    • 0344556510 scopus 로고    scopus 로고
    • note
    • 26
  • 36
    • 0344556507 scopus 로고    scopus 로고
    • note
    • -1 (Supporting Information, Figure S5).
  • 37
    • 0344124960 scopus 로고    scopus 로고
    • note
    • -1 for 2,6-diphenylhepta-1,6-diene.
  • 42
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    • Ph.D. Dissertation, (Order-No. 72-18547)
    • (d) Benzon, M. S., Ph.D. Dissertation, Diss. Abstr. Intern. B 1972, Vol. 45, p 1468B (Order-No. 72-18547).
    • (1972) Diss. Abstr. Intern. B , vol.45
    • Benzon, M.S.1
  • 46
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    • R. Wiktor in footnote 129, Scheme 17 and Table 39 of ref 37. See also ref 34
    • R. Wiktor in footnote 129, Scheme 17 and Table 39 of ref 37. See also ref 34.
  • 47
  • 52
    • 0344987468 scopus 로고    scopus 로고
    • Centauric, half man, half horse, is intended as a mnemonically keen sobriquet. A referee suggests a happy alternative: minotauric
    • Centauric, half man, half horse, is intended as a mnemonically keen sobriquet. A referee suggests a happy alternative: minotauric.
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    • Ph.D. Dissertation, Indiana University
    • -1, our calculation from his data).
    • (1985)
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  • 55
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    • note
    • -1. Not only have we stated reservations about the appropriateness of 1,3,4,6-tetraphenylhexa-1,5-diene as model, but the cooperational augmentation indicated by theoretical calculations also argues against its use.
  • 56
    • 0344124959 scopus 로고    scopus 로고
    • note
    • -1 if unconnected enthalpies of activation are considered.
  • 57


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.