[1] (a) Filler, R.; Kobayashi, Y.; Yagupolskii, L. M. Organofluorine Compounds in Medicinal Chemistry and Biomedical Applications, Elsevier, Amsterdam, 1993.
(b) Romanenko, V. D.; Kukhar, V. P. Chem. Rev. 2006, 106, 3868.
(c) Muller, K.; Faeh, C.; Diederich, F.; Science 2007, 317, 1881.
(d) Furuya, T.; Kuttruff, C.; Ritter, T.; Curr. Opin. Drug Discovery Dev. 2008, 11, 80.
(e) Ojima, I. Fluorine in Medicinal Chemistry and Chemical Biology, Wiley-Blackwell, 2009.
(f) Liang, T.; Neumann, C. N.; Ritter, T. Angew. Chem., Int. Ed. 2013, 52, 8214.
(g) Ni, C.; Zhu, L.; Hu, J. Acta Chim. Sinica 2015, 73, 90. (倪传法, 朱林桂, 胡金波, 化学学报, 2015, 73, 90.).
(h) Zhang, K.; Xu, X.; Qing, F. Chin. J. Org. Chem. 2015, 35, 556. (张柯, 徐修华, 卿凤翎, 有机化学, 2015, 35, 556.)
[2] For some reviews on fluorination, see:(a) Grushin, V. V. Acc. Chem. Res. 2010, 43, 160.
(b) Cahard, D.; Xu, X.; Couve-Bonnaire, S.; Pannecoucke, X. Chem. Soc. Rev. 2010, 39, 558.
(c) Furuya, T.; Kamlet, A. S.; Ritter, T. Nature 2011, 473, 470.
(d) Lin, A.; Huehls, B.; Yang. J. Org. Chem. Front. 2014, 1, 434. For recent examples, see:
(e) Li, W.; Zhu, Y.; Duan, Y.; Zhang, M.; Zhu, C. Adv. Synth. Catal. 2015, 357, 1277.
(f) Shen, X.; Miao, W.; Ni, C.; Hu, J. Angew. Chem., Int. Ed. 2014, 53, 775.
(g) Shen, X.; Min, Z.; Ni, C.; Zhang, W.; Hu, J. Chem. Sci. 2014, 5, 117.
[3] For some reviews on trifluoromethylation, see:(a) Nie, J.; Guo, H.; Cahard, D.; Ma, J. Chem. Rev. 2011, 111, 455.
(b) Tomashenko, O. A.; Grushin, V. V. Chem. Rev. 2011, 111, 4475.
(c) Studer, A. Angew. Chem., Int. Ed. 2012, 51, 8950.
(d) Furuya, T.;, Kamlet, A. S.; Ritter, T. Nature 2011, 473, 470. For recent examples, see:
(e) Gao, P.; Shen, Y. W.; Fang, R.; Hao, X. H.; Qiu, Z. H.; Yang, F.; Yan, X. B.; Gong, X. J.; Liu, X. Y.; Liang, Y. M. Angew. Chem., Int. Ed. 2014, 53, 7629.
(f) Liu, J. B.; Chen, C.; Chu, L. L.; Qing. F. L. Angew. Chem., Int. Ed. 2015, 54, 11839.
(g) Sahoo, B.; Li, J. L.; Glorius, F. Angew. Chem., Int. Ed. 2015, 54, 11577.
[4] For recent examples, see:(a) Li, L.; Wang, F.; Ni, C.; Hu, J. Angew. Chem., Int. Ed. 2013, 52, 12390.
(b) Min, Q.; Yin, Z.; Feng, Z.; Guo, W.; Zhang, X. J. Am. Chem. Soc. 2014, 136, 1230.
(c) Feng, Z.; Min, Q.; Xiao, Y.; Zhang, B.; Zhang, X. Angew. Chem., Int. Ed. 2014, 53, 1669.
(d) Wang, X.; Liu, G.; Xu, X.; Shibata, N.; Tokunaga, E.; Shibata, N. Angew. Chem., Int. Ed. 2014, 53, 1827.
(e) Chang, D.; Gu, Y.; Shen, Q. Chem. Eur. J. 2015, 21, 6074.
(f) He, Y. T.; Wang, Q.; Li, L. H.; Liu, X. Y.; Xu, P. F.; Liang, Y. M. Org. Lett. 2015, 17, 5188.
(g) Lin, Q. Y.; Xu, X. H.; Zhang, K.; Qing, F. L. Angew. Chem., Int. Ed. 2016, 55, 1479.
(h) Xie, J.; Zhang, T.; Chen, F. Mehrkens, N.; Rominger, F.; Rudolph, M.; Hashmi, A. S. Angew. Chem., Int. Ed. 2016, 55, 2934.
[5] (a) Blackburn, C. M.; England, D. A.; Kolkmann, F. J. Chem. Soc. Chem. Commun. 1981, 930.
(b) Blackburn, G. M.; Kent, D. E.; Kolkmann, F. J. Chem. Soc., Perkin Trans. 1 1984, 1119.
(c) Erickson, J. A.; Mcloughlin, J. I. J. Org. Chem. 1995, 60, 1626.
(d) Kitazume, T.; Kamazaki, T. Experimental Methods in Organic Fluorine Chemistry, Gordon and Breach Science, Tokyo, 1998.
[6] For recent reviews on photoredox catalysis, see:(a) Xuan, J.; Xiao, W. J. Angew. Chem., Int. Ed. 2012, 51, 6828.
(b) Yoon, T. P.; Ischay, M. A.; Du, J. Nat. Chem. 2010, 2, 527.
(c) Narayanam, J. M. R.; Stephenson, C. R. J. Chem. Soc. Rev. 2011, 40, 102.
(d) Tucker, J. W.; Stephenson, C. R. J. J. Org. Chem. 2012, 77, 1617.
(e) Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Chem. Rev. 2013, 113, 5322;
(f) Xi, Y.; Yi, H.; Lei, A. Org. Biomol. Chem. 2013, 11, 2387.
(g) Xie, J.; Jin, H.; Xu, P.; Zhu, C. Tetrahedron Lett. 2014, 55, 36.
[7] (a) Yu, C.; Iqbal, N.; Park, S.; Cho, E. Chem. Commun. 2014, 50, 12884.
(b) Sun, X.; Yu, S. Org. Lett. 2014, 16, 2398.
(c) Su, Y. M.; Hou, Y.; Yin, F.; Xu, Y. M.; Li, Y.; Zheng, X.; Wang, X. S.; Org. Lett. 2014, 16, 2958.
(d) Wang, L.; Wei, X.; Jia, W.; Zhong, J.; Wu. L.; Liu, Q. Org. Lett. 2014, 16, 5842.
(e) Nguyen, J. D.; Tucker, J. W.; Konieczynska, M. D.; Stephenson, C. R. J. J. Am. Chem. Soc. 2011, 133, 4160.
(f) Wallentin, C. J.; Nguyen, J. D.; Finkbeiner. P.; Stephenson, C. R. J. J. Am. Chem. Soc. 2012, 134, 8875.
(g) Jung, J.; Kim, E.; You. Y.; Cho, E. Adv. Synth. Catal. 2014, 356, 2741.
(h) Gu, Z. X.; Zhang, H. L.; Xu, P.; Cheng, Y. X.; Zhu. C. J. Adv. Synth. Catal. 2015, 357, 3057.
(j) Xu, P.; Hu, K. D.; Gu, Z. X.; Cheng, Y. X.; Zhu, C. J. Chem. Commun. 2015, 51, 7222.
[8] (a) Li, W.; Zhu, X.; Mao, H.; Tang, Z.; Cheng, Y.; Zhu, C. Chem. Commun. 2014, 50, 7521.
(b) Qu, C. H.; Xu, P.; Ma, W. J.; Cheng, Y. X.; Zhu, C. J. Chem. Commun. 2015, 51, 13508.
(c) Gu, Z. X.; Zhang, H. L.; Xu, P.; Cheng, Y. X.; Zhu, C. J. Adv. Synth. Catal. 2015, 357, 3057.
(d) Xu, P.; Wang, G. Q.; Zhu, Y. C.; Li, W. P.; Cheng, Y. X.; Li, S. H.; Zhu, C. J. Angew. Chem., Int. Ed. 2016, 55, 2939.
[9] For reviews on aryl migration:(a) Studer, A.; Bossart, M. Tetrahedron 2001, 57, 9649.
(b) Chen, Z. M.; Zhang, X. M.; Tu, Y. Q. Chem. Soc. Rev. 2015, 44, 5220.
[10] For the aryldifluoroacetylation of alkynes reaction, see:Fu, W. J.; Zhu, M.; Zou, G. L.; Xu, C.; Wang, Z. Q.; Ji, B. M. J. Org. Chem. 2015, 80, 4766. |