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For reagent-controlled, enantioselective α-fluorination of carbonyl compounds, see: a) E. Differding, R. W. Lang, Tetrahedron Lett. 1988, 29, 6087-6090; b) F. A. Davis, P. Zhou, C. K. Murphy, G. Sundarababu, H. Qi, W. Han, R. M. Przeslawski, B.-C. Chen, P. J. Carroll, J. Org. Chem. 1998, 63, 2273-2280; c) Z. Liu, N. Shibata, Y. Takeuchi, J. Org. Chem. 2000, 65, 7583-7587; d) N. Shibata, E. Suzuki, T. Asahi, M. Shiro, J. Am. Chem. Soc. 2001, 123, 7001-7009; e) P. Mohar, J. Baudoux, J.-C. Plaquevent, D. Cahard, Angew. Chem. 2001, 113, 4339-4341; Angew. Chem. Int. Ed. 2001, 40, 4214-4216.
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For reagent-controlled, enantioselective α-fluorination of carbonyl compounds, see: a) E. Differding, R. W. Lang, Tetrahedron Lett. 1988, 29, 6087-6090; b) F. A. Davis, P. Zhou, C. K. Murphy, G. Sundarababu, H. Qi, W. Han, R. M. Przeslawski, B.-C. Chen, P. J. Carroll, J. Org. Chem. 1998, 63, 2273-2280; c) Z. Liu, N. Shibata, Y. Takeuchi, J. Org. Chem. 2000, 65, 7583-7587; d) N. Shibata, E. Suzuki, T. Asahi, M. Shiro, J. Am. Chem. Soc. 2001, 123, 7001-7009; e) P. Mohar, J. Baudoux, J.-C. Plaquevent, D. Cahard, Angew. Chem. 2001, 113, 4339-4341; Angew. Chem. Int. Ed. 2001, 40, 4214-4216.
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