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Volumn , Issue 1, 1999, Pages 13-14

Novel phosphinite capped cyclodextrin-rhodium catalysts in substrate selective hydroformylation

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EID: 0033238884     PISSN: 03667022     EISSN: None     Source Type: Journal    
DOI: 10.1246/cl.1999.13     Document Type: Article
Times cited : (31)

References (21)
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    • (1993) Tetrahedron:Asymmetry , vol.4 , pp. 1829
    • Sawamura, M.1    Kitayama, K.2    Ito, Y.3
  • 4
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    • M. Sawamura, K. Kitayama, and Y. Ito, Tetrahedron:Asymmetry, 4, 1829 (1993); M. T. Reetz and J. Rudolph, Tetrahedron: Asymmetry, 4, 2405 (1993); M. T. Reetz and S. R. Waldvogel, Angew. Chem., Int. Ed. Engl., 36, 865 (1997).
    • (1993) Tetrahedron: Asymmetry , vol.4 , pp. 2405
    • Reetz, M.T.1    Rudolph, J.2
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    • M. Sawamura, K. Kitayama, and Y. Ito, Tetrahedron:Asymmetry, 4, 1829 (1993); M. T. Reetz and J. Rudolph, Tetrahedron: Asymmetry, 4, 2405 (1993); M. T. Reetz and S. R. Waldvogel, Angew. Chem., Int. Ed. Engl., 36, 865 (1997).
    • (1997) Angew. Chem., Int. Ed. Engl. , vol.36 , pp. 865
    • Reetz, M.T.1    Waldvogel, S.R.2
  • 7
    • 0002911645 scopus 로고
    • J. R. Anderson, E. M. Campi, and W. R. Jackson, Catal. Lett., 9, 55 (1991); E. Monflier, G. Frermy, Y. Castanet, and A. Mortreux, Angew. Chem., Int. Ed. Engl., 34, 2269 (1995); E. Monflier, S. Tilloy, G. Fremy, Y. Castanet, and A. Mortreux, Tetrahedron Lett., 52, 9481 (1995).
    • (1991) Catal. Lett. , vol.9 , pp. 55
    • Anderson, J.R.1    Campi, E.M.2    Jackson, W.R.3
  • 8
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    • J. R. Anderson, E. M. Campi, and W. R. Jackson, Catal. Lett., 9, 55 (1991); E. Monflier, G. Frermy, Y. Castanet, and A. Mortreux, Angew. Chem., Int. Ed. Engl., 34, 2269 (1995); E. Monflier, S. Tilloy, G. Fremy, Y. Castanet, and A. Mortreux, Tetrahedron Lett., 52, 9481 (1995).
    • (1995) Angew. Chem., Int. Ed. Engl. , vol.34 , pp. 2269
    • Monflier, E.1    Frermy, G.2    Castanet, Y.3    Mortreux, A.4
  • 9
    • 0029617263 scopus 로고
    • J. R. Anderson, E. M. Campi, and W. R. Jackson, Catal. Lett., 9, 55 (1991); E. Monflier, G. Frermy, Y. Castanet, and A. Mortreux, Angew. Chem., Int. Ed. Engl., 34, 2269 (1995); E. Monflier, S. Tilloy, G. Fremy, Y. Castanet, and A. Mortreux, Tetrahedron Lett., 52, 9481 (1995).
    • (1995) Tetrahedron Lett. , vol.52 , pp. 9481
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  • 10
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    • "Comprehensive Supramolecular Chemistry," ed by J. L. Atwood, J. E. D. Davies, D. D. McNichol, and F. Vögtle, Pergamon Press, Oxford
    • E. Fenyvesi, L. Szente, N. R. Russell and M. MacNamara in "Comprehensive Supramolecular Chemistry," ed by J. L. Atwood, J. E. D. Davies, D. D. McNichol, and F. Vögtle, Pergamon Press, Oxford (1996), Vol. 3 Cyclodextrins, p. 305.
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  • 14
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    • note
    • 4 unit from the M peak. The observation of these two peaks indicates that the compound is a monophosphinite of β-CD, since the formation of these fragments is impossible otherwise. The TOF-MS in DMF shows a similar m/z pattern as in water but a peak is observed at m/z of 1333.4. This could arise from interactions of β-CD-P with DMF. The appearance of a peak at such a high mass is possible only if the monophosphinite is formed.
  • 15
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    • "Comprehensive Supramolecular Chemistry," ed by J. L. Atwood, J. E. D. Davies, D. D. McNichol, and F. Vögtle, Pergamon Press, Oxford
    • J. Szejtli in "Comprehensive Supramolecular Chemistry," ed by J. L. Atwood, J. E. D. Davies, D. D. McNichol, and F. Vögtle, Pergamon Press, Oxford (1996), Vol. 3 Cyclodextrins, p. 189.
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    • Szejtli, J.1
  • 16
    • 0009050855 scopus 로고    scopus 로고
    • note
    • Although no hydrogenation of olefin took place, isomerization was observed in case of 1-decene and Phb; ca. 30% at conversions over 80%.
  • 17
    • 0009004312 scopus 로고    scopus 로고
    • note
    • 2 as a possible catalytic intermediate. Characterization of the Rh complexes is in progress.
  • 19
    • 0008999029 scopus 로고    scopus 로고
    • note
    • No hydrogenation products were formed in this reaction, but isomerization products were formed to the extent of 25%. However, this does not change the substrate selectivity or TOF since they are defined on the hydroformylation products formed.


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