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For examples, see; a) Fart, D. J. Science, 1984, 223, 883.
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Fart, D.J.1
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f) Curran, D. P.; Porter, N. A.; Giese, B. In Stereochemistry of Radical Reactions, VCH, New York, 1996.
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Stereochemistry of Radical Reactions
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Curran, D.P.1
Porter, N.A.2
Giese, B.3
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4944230527
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For reviews of the chemistry of organotin compounds, see: a) Neumann, W. P. Synthesis, 1987, 665.
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Synthesis
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Neumann, W.P.1
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8
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0003579939
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Paquette, T. A. Ed., Wiley, New York
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b) RajanBabu, T. V. In Encyclopedia of Reagents for Organic Synthesis, Paquette, T. A. Ed., Wiley, New York, 1985.
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Encyclopedia of Reagents for Organic Synthesis
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RajanBabu, T.V.1
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10
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0000315424
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Trost, B, M.; Fleming, I. Eds. Pergamon, Oxford
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d) Curran, D. P. In Comprehensive Organic Synthesis, Trost, B, M.; Fleming, I. Eds. Pergamon, Oxford, 1991, Vol. 4, p. 779.
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Comprehensive Organic Synthesis
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Curran, D.P.1
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e) Ryu, I.; Sonoda, N.; Curran, D. P. Chem. Rev. 1996, 96, 177.
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Chem. Rev.
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Ryu, I.1
Sonoda, N.2
Curran, D.P.3
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f) Ryu, I.; Sonoda, N. Angew. Chem., Int. Ed. Engl. 1996, 35, 1050.
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Ryu, I.1
Sonada, N.2
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14
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0026059062
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As another example of catalytic use of tributyltin hydride, intermolecular cyclization of organotin compounds has been shown. See; Kim, S.; Lee, S. Tetrahedron Lett. 1991, 32, 6575.
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Tetrahedron Lett.
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Kim, S.1
Lee, S.2
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18
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0001639833
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Hays, D. S.; Scholl, M.; Fu, G. C. J. Org. Chem. 1996, 61, 6751.
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Scholl, M.2
Fu, G.C.3
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19
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0030800209
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Lopez, R. M.; Hays, D. S.; Fu, G. C. J. Am. Chem. Soc. 1997, 119, 6949.
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Lopez, R.M.1
Hays, D.S.2
Fu, G.C.3
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Tormo, J.; Hays, D. S.; Fu, G. C. J. Org. Chem. 1998, 63, 5296.
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Tormo, J.1
Hays, D.S.2
Fu, G.C.3
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22
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0033593393
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More recently, R. E. Maleczka, Jr. showed a new approach for the catalytic use of organotin compounds. See: Terstiege, I.; Maleczka, Jr. R. E. J. Org. Chem. 1999, 64, 342.
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Terstiege, I.1
Maleczka R.E., Jr.2
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23
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0009577441
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and references cited therein
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For reviews of the chemistry of hindered ,2,3-selenadiazoles, see: Ando, W.; Tokitoh, N. Heteroatom Chem. 1989, 2, 1 and references cited therein.
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Heteroatom Chem.
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Ando, W.1
Tokitoh, N.2
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24
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0009577309
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In the absence of benzene, the yield of 5a was slightly decreased (55 %)
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In the absence of benzene, the yield of 5a was slightly decreased (55 %).
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-
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25
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0009577737
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note
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3Sn radical to 1,2,3-selenadiazole, the addition of the vinyl radical to the carbon-carbon double bond and the intramolecular cyclization were faster than that of the reaction of the tributylstannyl radical with hydroquinone.
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