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0642382532
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Bardolino
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There has been a recent report about the diastereoselective radical-radical reaction of a chiral nitroxyl radical with a prochiral carbon radical: R. Braslau, L. Burrill, L. Mahal, T. Wedeking, Abstr. Pap. 7th Int. Symp. Org. Free Radicals, Bardolino, 1996, p.45.
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Braslau, R.1
Burrill, L.2
Mahal, L.3
Wedeking, T.4
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8
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48749136090
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Tin hydrides in which tin is the only chiral center undergo racemization when exposed to radical chain reaction conditions: a) M. Gielen, Y. Tondeur, J. Organomet. Chem. 1979, 169, 265-281; b) M. Gielen, Pure Appl. Chem. 1980, 52, 657-667.
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Gielen, M.1
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0642382533
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Tin hydrides in which tin is the only chiral center undergo racemization when exposed to radical chain reaction conditions: a) M. Gielen, Y. Tondeur, J. Organomet. Chem. 1979, 169, 265-281; b) M. Gielen, Pure Appl. Chem. 1980, 52, 657-667.
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J. O. Metzger, K. Schwarzkopf, M. Blumenstein, 25. Hauptversammlung der Gesellschaft Deutscher Chemiker, Münster, short presentation, p. 403; J. O. Metzger, M. Blumenstein, A. Hayen, K. Schwarzkopf, Abstr. Pap. 7th Int. Symp. Org. Free Radicals, Bardolino, 1996, p. 124.
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25. Hauptversammlung der Gesellschaft Deutscher Chemiker
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0642382534
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Bardolino
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J. O. Metzger, K. Schwarzkopf, M. Blumenstein, 25. Hauptversammlung der Gesellschaft Deutscher Chemiker, Münster, short presentation, p. 403; J. O. Metzger, M. Blumenstein, A. Hayen, K. Schwarzkopf, Abstr. Pap. 7th Int. Symp. Org. Free Radicals, Bardolino, 1996, p. 124.
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37049072213
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and references therein
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Enantioselective abstractions of hydrogen atoms from chiral, racemic substrates by chiral radicals have been reported: H.-S. Dang, V. Diart, B. P. Roberts, D. A. Tocher, J. Chem. Soc. Perkin Trans. 2 1994, 1039-1045, and references therein.
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MOPAC61C
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0642382526
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Bardolino
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2-symmetric binaphthyl substituent synthesized by a different route, and its use in the enantioselective reduction of an α-bromoketone (10-41%ee), was recently presented: D. P. Curran, D. Nanni, Abstr. Pap. 7th Int. Symp. Org. Free Radicals, Bardolino, 1996, p. 66.
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