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Volumn 55, Issue 22, 1999, Pages 6739-6748

Synthesis and thermolysis of 3-substituted 3- trimethylsilylcyclopropenes

Author keywords

Cyclopropenes; Kinetics; Rearrangements; X Ray crystallography

Indexed keywords

CYCLOPROPANE DERIVATIVE; FURAN DERIVATIVE; TEREPHTHALIC ACID; TRIMETHYLSILYL DERIVATIVE;

EID: 0033612104     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(99)00276-8     Document Type: Article
Times cited : (14)

References (21)
  • 3
    • 0013560814 scopus 로고
    • Ph.D. Thesis. Harvard University
    • Clauberg, H. Ph.D. Thesis. Harvard University, 1993.
    • (1993)
    • Clauberg, H.1
  • 5
    • 0013549766 scopus 로고
    • Thermal dimerization: Flowers, M. C., Frey, H. M., Höpf, H. J. C. S. Chem. Comm. 1972, 1284-1285. Lewis acid dimerization: Tetrahedron Lett. 1975, 52, 4673-4676.
    • (1975) Tetrahedron Lett. , vol.52 , pp. 4673-4676
  • 7
    • 0013551092 scopus 로고    scopus 로고
    • submitted for publication
    • Han, S.; Kass, S. submitted for publication.
    • Han, S.1    Kass, S.2
  • 9
    • 0013532656 scopus 로고    scopus 로고
    • note
    • Crytallographic data along with the refined coordinates and bond distances can be found in the supplemental material.
  • 14
    • 0013560815 scopus 로고    scopus 로고
    • note
    • 3 we found that it was necessary to filter the solvent through neutral alumina so as to neutralize it.
  • 15
    • 0013517724 scopus 로고    scopus 로고
    • note
    • The cited errors represent the standard errors in the slope and intercept of the Erying plot.
  • 18
    • 0013556318 scopus 로고    scopus 로고
    • note
    • Other intermediates such as the biradical formed by making a σ bond between the two ends of the allylic radical in 9 (the radical equivalent of the possible intermediate suggested in the acid-catalyzed pathway) or the tricyclic compound formed by combining the two radical centers were explored. In each case either a higher energy species was obtained or the compound reverted without a barrier to one of the substrates we had already examined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.