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and references therein
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Hewawasam, P.; Gribkoff, V. K.; Pendri, Y.; Dworetzky, S. I.; Meanwell, N. A.; Martinez, E.; Boissard, C. G.; Post-Munson, D. J.; Trojnacki, J. T.; Yeleswaram, K.; Pajor, L. M.; Knipe, J.; Gao, Q.; Perrone, R.; Starrett, J. E., Jr. Bioorg. Med. Chem. Lett. 2002, 12, 1023-1026 and references therein.
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For the synthesis of fluorous analogues of indole alkaloids, see: Shibata, N.; Tarui, T.; Doi, Y.; Kirk, K. L. Angew. Chem., Int. Ed. 2001, 40, 4461-4463.
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For a stoichiometric enantioselective fluorination of oxindoles, see: Shibata, N.; Suzuki, E.; Asahi, T.; Shiro, M. J. Am. Chem. Soc. 2001, 123, 7001-7009.
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33444465159
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note
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For details, see Supporting Information.
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17
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33444478095
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note
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In the case of 5i, the enantiomeric excess was also improved. See Supporting Information.
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18
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0037459672
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For stoichiometric reactions, see: (a) Shibata, N.; Ishimaru, T.; Suzuki, E.; Kirk, K. L. J. Org. Chem. 2003, 68, 2494-2497.
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20
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0037174368
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and references therein
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For discussion on the Pd enolates, see: Hamashima, Y.; Hotta, D.; Sodeoka, M. J. Am. Chem. Soc. 2002, 124, 11240-11241 and references therein.
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(c) Greedy, B.; Paris, J.-M.; Vidal, T.; Gouverneur, V. Angew. Chem., Int. Ed. 2003, 42, 3291 -3294.
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During the reviewing process of this manuscript, the following papers appeared: (a) Enders, D.; Hüttl, M. R. M. Synlett 2005, 6, 991-993.
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(b) Marigo, M.; Fielenbach, D.; Braunton, A.; Kjærsgaard, A.; Jørgensen, K. A. Angew. Chem., Int. Ed. 2005, 44, 3703-3706.
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