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For recent examples of such pyridines see: H. Paulsen, C. Schmeck, A. Brandes, G. Schmidt, J. Stoltefuss, S. N. Wirtz, N. Lögers, P. Naab, K-D. Bremm, H. Bischoff, D. Schmidt, S. Zaiss, S. Antons, Chimia, 2004, 58, 490.
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For other recent syntheses and uses of mono- and gem-difluorinated propargylic derivatives see: a L. Carroll, Ma. C. Pacheco, L. Garcia, V. Gouverneur, Chem. Commun. 2006, 4113;
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For other recent syntheses and uses of mono- and gem-difluorinated propargylic derivatives see: a) L. Carroll, Ma. C. Pacheco, L. Garcia, V. Gouverneur, Chem. Commun. 2006, 4113;
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For discussions on the stereoselectivity during the dehydroxyfluorination of propargylic alcohols and corresponding cobalt-carbonyl complexes see: a M. Prakesch, E. Kerouredan, D. Grée, R. Grée, J. DeChancie, K. N. Houk, J. Fluorine Chem. 2004, 125, 537;
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For discussions on the stereoselectivity during the dehydroxyfluorination of propargylic alcohols and corresponding cobalt-carbonyl complexes see: a) M. Prakesch, E. Kerouredan, D. Grée, R. Grée, J. DeChancie, K. N. Houk, J. Fluorine Chem. 2004, 125, 537;
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