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0000337052
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(b) Clarembeau, M.; Cravador, A.; Dumont, W.; Hevesi, L.; Krief, A.; Lucchetti, J.; Van Ende, D. Tetrahedron 1985, 41, 4793.
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27
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0025032226
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Oxidation of organic selenols or selenolates using perborate: McKillop, A.; Koyuncu, D.; Krief, A.; Dumont, W.; Renier, P.; Trabelsi, M. Tetrahedron Lett. 1990, 31, 5007.
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28
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17144402655
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(b) Krief, A.; De Mahieu, A. F.; Dumont, W.; Trabelsi, M. Synthesis 1988, 131.
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31
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0035137726
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Oxidation of organic selenols or selenolates using iodine: (a) Block, E.; Birringer, M.; Jiang, W.; Nakahodo, T.; Thompson, H. J.; Toscano, U. P. J.; Zhang, H.; Zhu, X. J. Agric. Food Chem. 2001, 49, 458.
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32
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0001312398
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(b) Meinke, P. T.; Krafft, G. A.; Guram, A. J. J. Org. Chem. 1988, 53, 3632.
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Meinke, P.T.1
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33
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4143091491
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(a) Krief, A.; Trabelsi, M.; Dumont, W.; Derock, M. Synlett 2004, 1751.
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Synlett
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34
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17144432386
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note
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13a
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35
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17144378654
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note
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4 and EtOH (1:1:3 molar equiv each) leads to the evolvement of dihydrogen (2.58 molar equiv, 86% of the expected amount), sequential addition of DMF and decyl bromide produces an additional formation of hydrogen (0.42 molar equiv, 14% of the expected amount).
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36
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0000535303
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77Se NMR. For a related work see: Cusik, J.; Dance, I. Polyhedron 1991, 10, 2629.
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(1991)
Polyhedron
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Cusik, J.1
Dance, I.2
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37
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17144416221
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note
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4 and EtOH (1:2:6 mol equiv).
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38
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17144399639
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note
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(b) Another 0.81 molar equiv of dihydrogen is evolved if aq EtOH (4 molar equiv each), is added before that of the second crop of elemental selenium.
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39
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0000821865
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(a) Liotta, D.; Sunay, U.; Santiesteban, H.; Markiewick, W. J. Org. Chem. 1981, 46, 2605.
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Liotta, D.1
Sunay, U.2
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Markiewick, W.4
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44
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0000037070
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Miyashita, M.; Hosshino, M.; Yoshikoshi, A. Tetrahedron Lett. 1988, 29, 347.
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(1988)
Tetrahedron Lett.
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Miyashita, M.1
Hosshino, M.2
Yoshikoshi, A.3
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