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Volumn 61, Issue 16, 1996, Pages 5384-5390

Reactions of tin(IV) enolates obtained from O-stannyl ketyls under neutral free radical conditions

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EID: 0001016229     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo960639e     Document Type: Article
Times cited : (19)

References (54)
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    • (d) Hart, D. J. Science 1984, 223, 883.
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    • Hart, D.J.1
  • 6
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    • Kasiser, E. T., Kevan, L. Eds., Wiley Interscience: New York
    • For reveiws of ketyl radical anions, see: (a) Hirota, N. Radical Ions; Kasiser, E. T., Kevan, L. Eds., Wiley Interscience: New York, 1968; pp 35-85. (b) Russell, G. A. Radical Ions; Kasiser, E. T., Kevan, L., Eds., Wiley Interscience: New York, 1968; pp 87-150. (c) Forrester, A. R.; Hay, J. M.; Thompson, R. H. Organic Chemistry of Stable Free Radicals; Academic Press: New York, 1968; pp 82-90.
    • (1968) Radical Ions , pp. 35-85
    • Hirota, N.1
  • 7
    • 0001884928 scopus 로고
    • Kasiser, E. T., Kevan, L., Eds., Wiley Interscience: New York
    • For reveiws of ketyl radical anions, see: (a) Hirota, N. Radical Ions; Kasiser, E. T., Kevan, L. Eds., Wiley Interscience: New York, 1968; pp 35-85. (b) Russell, G. A. Radical Ions; Kasiser, E. T., Kevan, L., Eds., Wiley Interscience: New York, 1968; pp 87-150. (c) Forrester, A. R.; Hay, J. M.; Thompson, R. H. Organic Chemistry of Stable Free Radicals; Academic Press: New York, 1968; pp 82-90.
    • (1968) Radical Ions , pp. 87-150
    • Russell, G.A.1
  • 8
    • 0003695891 scopus 로고
    • Academic Press: New York
    • For reveiws of ketyl radical anions, see: (a) Hirota, N. Radical Ions; Kasiser, E. T., Kevan, L. Eds., Wiley Interscience: New York, 1968; pp 35-85. (b) Russell, G. A. Radical Ions; Kasiser, E. T., Kevan, L., Eds., Wiley Interscience: New York, 1968; pp 87-150. (c) Forrester, A. R.; Hay, J. M.; Thompson, R. H. Organic Chemistry of Stable Free Radicals; Academic Press: New York, 1968; pp 82-90.
    • (1968) Organic Chemistry of Stable Free Radicals , pp. 82-90
    • Forrester, A.R.1    Hay, J.M.2    Thompson, R.H.3
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    • Hartley, F. R., Ed.; J. Wiley & Sons: New York, Chapter 8
    • (g) Molander, G. A. The Chemistry of the Metal-Carbon Bond; Hartley, F. R., Ed.; J. Wiley & Sons: New York, 1989; Vol. 5, Chapter 8, pp 319-396.
    • (1989) The Chemistry of the Metal-Carbon Bond , vol.5 , pp. 319-396
    • Molander, G.A.1
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    • 85022544314 scopus 로고    scopus 로고
    • in press
    • Alcohol 38 was converted into its p-bromobenzoate ester prior to X-ray diffraction. For single crystal X-ray analyses of 38 and 40, see: Abboud, K. A.; Xie, Y.; Enholm, E. J. Acta Crystallogr. C, in press.
    • Acta Crystallogr. C
    • Abboud, K.A.1    Xie, Y.2    Enholm, E.J.3
  • 34
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    • note
    • 4 The reaction was diluted (0.10 M) to separate reactive partners and prevent a bimolecular aldol and allow the tin enolate to remain predominantly unreacted until workup.


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