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5
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0000221805
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Solid-supported oxidants
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Trost, B.M., Ed.; Pergamon Press: Oxford
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Lazlo, P.1
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d) Singh, R. P.; Subbarao, H. N.; Dev, S. Tetrahedron 1979, 35, 1789-1793;
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Singh, R.P.1
Subbarao, H.N.2
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33845320453
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e) Brunelet, T.; Jouitteau, C.; Gelbard, G. J.org.chem. 1986, 51, 4016-4022;
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Brunelet, T.1
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0031010928
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and ref. cited therein
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i) Kabalka, G. W.; Pagni, R. M. Tetrahedron 1997, 53, 7999-8065 and ref. cited therein.
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Kabalka, G.W.1
Pagni, R.M.2
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15
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0343897065
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Exchange property of Ti(IV) and Zr(IV) oxides grafted on silica gel surface. Sorption of Cr(VI) from an acid solution
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Abe, M.; Kataoka, T., Suzuki, T., Eds.; Elsevier-Kodansha: Tokyo
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Gushikem, Y.; Peixoto, C R. M.; Kubota, L. K. Exchange property of Ti(IV) and Zr(IV) oxides grafted on silica gel surface. Sorption of Cr(VI) from an acid solution. In New Developments in Ion Exchange. Fundamentals and Applications; Abe, M.; Kataoka, T., Suzuki, T., Eds.; Elsevier-Kodansha: Tokyo, 1991; pp. 607-612.
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Gushikem, Y.1
Peixoto, C.R.M.2
Kubota, L.K.3
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16
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0000874372
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Peixoto, C. R. M.; Gushikem, Y.; Baccan, N. Analyst 1992, 117, 1029-1032.
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Peixoto, C.R.M.1
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Baccan, N.3
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18
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0000482698
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For some examples of catalytic chromium(VI) oxidations using t-butyl hydroperoxide as cooxidant, see: a) Pearson, A .J.; Chen, Y. S.; Hsu, S. Y.; Ray, T. Tetrahedron Lett. 1984, 25, 1235-1238;
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Pearson, A.J.1
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Hsu, S.Y.3
Ray, T.4
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19
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37049098258
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b) Pearson, A. J.; Chen, Y. S.; Han, G. R., Hsu, S. Y.; Ray, T. J.Chem.Soc Perkin Trans. I 1985, 267-273;
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Hsu, S.Y.4
Ray, T.5
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22
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33847089541
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For a general use of t-butyl hydroperoxide on allylic oxidations, see: e) Umbreit, M. A.; Sharpless, K. B. J.Am.Chem.Soc. 1977. 99, 5526-5528;
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Umbreit, M.A.1
Sharpless, K.B.2
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24
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0002812520
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Oxidation adjacent to C=C bonds
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Trost, B.M., Ed.; Pergamon Press: Oxford
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g) Page, P. C. B.; McCarthy, T. J. Oxidation adjacent to C=C bonds. In Comprehensive Organic Synthesis; Trost, B.M., Ed.; Pergamon Press: Oxford; vol. 7, 1991; pp. 83-117;
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Page, P.C.B.1
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0342276132
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i) Salvador, J. A. R.; Melo, M. L. S.; Neves, A. S. C. Tetrahedron Lett. 1997, 38, 119-122.
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Salvador, J.A.R.1
Melo, M.L.S.2
Neves, A.S.C.3
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27
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0013615488
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note
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The t-butyl hydroperoxide used was commercial grade, 70% aqueous solution.
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-
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28
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37049084166
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Actually, reports on the literature concerning allylic oxidations on limonene 1 show either a slight selectivity toward the carbon C6 (references 8b, 8g and 11) or a great selectivity toward carbon 3 reference 8h. It is noteworthy that this selectivity was contested by
-
Actually, reports on the literature concerning allylic oxidations on limonene 1 show either a slight selectivity toward the carbon C6 (references 8b, 8g and 11) or a great selectivity toward carbon 3 (reference 8h. It is noteworthy that this selectivity was contested by A. F. Thomas And Y. Bessière In Nat.Prod.Rep. 1989, 6, 291-309)
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Nat.Prod.Rep.
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Thomas, A.F.1
Bessière, Y.2
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29
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0001625286
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a) Dauben, W. G.; Lorber, M.; Fullerton, D. S. J.Org.Chem. 1969, 34, 3587-3592;
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Dauben, W.G.1
Lorber, M.2
Fullerton, D.S.3
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33
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0000211760
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Compound 15 presented spectral and physical data in agreement with those reported in the literature for the (6R, 1 'S)-epi-hernandulcin
-
Compound 15 presented spectral and physical data in agreement with those reported in the literature for the (6R, 1 'S)-epi-hernandulcin. See Mori, K.; Kato, M. Tetrahedron 1986, 42, 5895-5900.
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(1986)
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Mori, K.1
Kato, M.2
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