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2542477134
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L.J. Teixeira, M. Seabra, E. Reis, M.T. Girão da Cruz, M.C. Pedroso de Lima, E. Pereira, M.A. Miranda, and M.P.M. Marques J. Med. Chem. 47 2004 2917 2925
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33745507572
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A. Krief Tetrahedron 36 1980 2531 2640
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Krief, A.1
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13
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11844259798
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note
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+ or PhSeH and their utility in organic transformations
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14
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0037463793
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C. Aprile, M. Gruttadauria, M.E. Amato, Noto, F. D'Anna, P. Lo Meo, S. Riela, and R. Noto Tetrahedron 59 2003 2241 2251
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Aprile, C.1
Gruttadauria, M.2
Amato, M.E.3
Noto4
D'Anna, F.5
Lo Meo, P.6
Riela, S.7
Noto, R.8
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15
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0035974349
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M. Gruttadauria, C. Aprile, F. D'Anna, P. Lo Meo, S. Riela, and R. Noto Tetrahedron 57 2001 6815 6822
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Gruttadauria, M.1
Aprile, C.2
D'Anna, F.3
Lo Meo, P.4
Riela, S.5
Noto, R.6
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16
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11844251663
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note
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These two articles cover the stereoselective synthesis of oxygenated heterocyclic rings from mixtures of hydroxy selenides
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19
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0342947407
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2OH after distillation. Following this procedure, we observed the formation of both 1 and 9 ; extraction and purification of the product from the resulting mixture proved to be a long and tedious procedure. During distillation of the final product, extensive decomposition was observed and the product, in our hands, was obtained in a yield of 25-32%
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(1977)
Acta Chem. Scand. Ser. B
, vol.31
, pp. 1-6
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Lingren, B.1
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20
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11844282493
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I.K. Sang, and C.P. Spears Synthesis 1988 133 135 this method involves reaction of 2-bromoethanol with potassium selenocyanate in boiling acetone to give 2-hydroxyethylselenocyanate in 80% yield. The selenocyanate was converted in situ in the presence of sodium borohydride to the corresponding selenolate anions which react with electrophilic substrate
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(1988)
Synthesis
, pp. 133-135
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Sang, I.K.1
Spears, C.P.2
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21
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0242270866
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T.G. Back, and Z. Moussa J. Am. Chem. Soc. 125 2003 13455 13460 this article deals with a series of aliphatic diselenides and selenides containing coordinating substituents which were tested for glutathione peroxidase (GPx)-like catalytic activity in a model system in which the reduction of tert-butyl hydroperoxide with benzyl thiol to afford dibenzyl disulfide and tert-butyl alcohol was performed under standard conditions. In particular, allyl 3-hydroxypropyl selenide rapidly generated 1,2-oxaselenolane Se-oxide in situ by a series of oxidation and [2,3]sigmatropic rearrangement steps
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J. Am. Chem. Soc.
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Back, T.G.1
Moussa, Z.2
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26
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11844279439
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Academic Press Limited London N.
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Tellurium in Organic Synthesis; N. Petragnani 1994 Academic Press Limited London John Wiley and Sons, New York, 1973
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(1994)
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Petragnani1
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27
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11844281266
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note
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2)
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28
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11844282496
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note
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13C (75 MHz), δ 44.29 (N-C), 36.27 (C-C), 9.15 (Te-C)
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29
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11844252951
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note
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2).
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