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Volumn 45, Issue 2, 1980, Pages 315-318

Tests for Free-Radical Intermediates in the Decarbonylation of Aldehydes by Tris(triphenylphosphine)chlororhodium(I)

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EID: 0001532987     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/jo01290a023     Document Type: Article
Times cited : (31)

References (34)
  • 1
    • 85012333999 scopus 로고
    • Taken in part from the Ph.D. Thesis of Stephen H. Harris, University of Rochester,; Sherman Clarke and Elon H. Hooker Fellow, University of Rochester.
    • Taken in part from the Ph.D. Thesis of Stephen H. Harris, University of Rochester, 1979; Sherman Clarke and Elon H. Hooker Fellow, University of Rochester.
    • (1979)
  • 2
    • 37049112093 scopus 로고
    • Dalton Trans., 1576 (1977); J. K. Stille and M. T. Regan, J. Am. Chem. Soc., 96, 1508 and references cited therein.
    • D. L. Egglestone, M. C. Baird, C. J. L. Lock, and G. Turner, J. Chem. Soc., Dalton Trans., 1576 (1977); J. K. Stille and M. T. Regan, J. Am. Chem. Soc., 96, 1508 (1974), and references cited therein.
    • (1974) J. Chem. Soc.
    • Egglestone, D.L.1    Baird, M.C.2    Lock, C.J.L.3    Turner, G.4
  • 3
    • 70350625573 scopus 로고
    • Organotransition Metal Chemistry
    • Y. Ishii and M. Tsutsui, Ed., Plenum Press, New York, p
    • J. A. Osborn, “Organotransition Metal Chemistry”, Y. Ishii and M. Tsutsui, Ed., Plenum Press, New York, 1975, p 65
    • (1975) , pp. 65
    • Osborn, J.A.1
  • 8
    • 0003909732 scopus 로고
    • Isotope Effects in Reaction Rates
    • Ronald Press, New York, pp
    • L. Melander, “Isotope Effects in Reaction Rates”, Ronald Press, New York, 1960, pp 24-32
    • (1960) , pp. 24-32
    • Melander, L.1
  • 12
    • 0001588825 scopus 로고
    • 93, 5465 have previously shown that when 2,2-diphenyl-l-methylcyclopropanecarboxaldehyde-d is decarbonylated with 1 in xylene, 1-deuterio-l-methyl-2,2-diphenylcyclopropane is produced. Thus, processes which would lead to H/D exchange with the solvent were excluded.
    • M. Walborsky and L. E. Allen, J. Am. Chem. Soc., 93, 5465 (1971), have previously shown that when 2,2-diphenyl-l-methylcyclopropanecarboxaldehyde-d is decarbonylated with 1 in xylene, 1-deuterio-l-methyl-2,2-diphenylcyclopropane is produced. Thus, processes which would lead to H/D exchange with the solvent were excluded.
    • (1971) J. Am. Chem. Soc.
    • Walborsky, M.1    Allen, L.E.2
  • 19
    • 0004032955 scopus 로고
    • Free Radicals
    • Wiley, New York, pp
    • J. K. Kochi, “Free Radicals”, Wiley, New York, 1973, pp 466-477.
    • (1973) , pp. 466-477
    • Kochi, J.K.1
  • 24
    • 0004055425 scopus 로고
    • Purification of Laboratory Chemicals
    • Pergamon Press, New York
    • D. P. Perrin, W. L. F. Armarego, and D. F. Perrin, “Purification of Laboratory Chemicals”, Pergamon Press, New York, 1966.
    • (1966)
    • Perrin, D.P.1    Armarego, W.L.F.2    Perrin, D.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.