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Intramolecular reactions: a) H. Ren, P. Knochel, Angew. Chem. 2006, 118, 3541-3544;
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Angew. Chem. Int. Ed. 2006, 45, 3462-3465;
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Bajracharya, G.B.1
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carbenoid-induced insertion: c H. M. L. Davies, S. J. Hedley, B. R. Bohall, J. Org. Chem. 2005, 70, 10 737-10 742;
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carbenoid-induced insertion: c) H. M. L. Davies, S. J. Hedley, B. R. Bohall, J. Org. Chem. 2005, 70, 10 737-10 742;
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Ir-catalyzed reactions: e Y. Matsuo, A. Iwashita, E. Nakamura, Chem. Lett. 2006, 858-859.
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Ir-catalyzed reactions: e) Y. Matsuo, A. Iwashita, E. Nakamura, Chem. Lett. 2006, 858-859.
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9
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33750895869
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For the cation pool method of electrochemistry, see
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For the "cation pool" method of electrochemistry, see: M. Okajima, K. Soga, T. Nokami, S. Suga, J. Yoshida, Org. Lett. 2006, 8, 5005-5007.
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0040670549
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There is only one report involving photolytic conditions: W. D. Jones, G. P. Foster, J. M. Putinas, J. Am. Chem. Soc. 1987, 109, 5047-5048.
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There is only one report involving photolytic conditions: W. D. Jones, G. P. Foster, J. M. Putinas, J. Am. Chem. Soc. 1987, 109, 5047-5048.
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Iron-catalyzed cross-coupling reactions: a) T. Nagano, T. Hayashi, Org. Lett. 2004, 6, 1297-1299;
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18
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b) A. Fürstner, A. Leitner, M. Mendez, H. Krause, J. Am. Chem. Soc. 2002, 124, 13 856-13 863;
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c) M. Nakamura, K. Matsuo, S. Ito, E. Nakamura, J. Am. Chem. Soc. 2004, 126, 3686-3687;
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d) I. Sapountzis, W. Lin, C. C. Kofink, C. Despotopoulou, P. Knochel, Angew. Chem. 2005, 117, 1682-1685;
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Sapountzis, I.1
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17044409192
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Angew. Chem. Int. Ed. 2005, 44, 1654-1657;
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e) K. Itami, S. Higashi, M. Mineno, J. Yoshida, Org. Lett. 2005, 7, 1219-1222;
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f) L. K. Ottesen, F. Ek, R. Olsson, Org. Lett. 2006, 8, 1771-1773;
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h) J. Kischel, K. Mertins, D. Michalik, A. Zapf, M. Beller, Adv. Synth. Catal. 2007, 349, 865-870.
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Baran and co-workers have recently reported oxidative enolate coupling reactions in the presence of a stoichiometric amount of FeIII or CuII (2 equiv) as the oxidant: a) P. S. Baran, M. P. DeMartino, Angew. Chem. 2006, 118, 7241-7244;
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II (2 equiv) as the oxidant: a) P. S. Baran, M. P. DeMartino, Angew. Chem. 2006, 118, 7241-7244;
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Angew. Chem. Int. Ed. 2006, 45, 7083-7086;
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3 (TMHD = 2,2,6,6-tetramethyl-3,5-heptanedionato, DBM = dibenzoylmethanato) were found to be inactive under the same conditions.
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3 (TMHD = 2,2,6,6-tetramethyl-3,5-heptanedionato, DBM = dibenzoylmethanato) were found to be inactive under the same conditions.
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2O. No product was isolated with the other solvents.
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2O. No product was isolated with the other solvents.
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