Organofluorine Chemistry. Группа авторов

Matsui, K., Tobita, E., Kondo, K. et al. (1981). Chem. Lett. 10: 1719.

      32 32 Lin, R.W. and Davidson, R.I. (1989). Improved conditions using potassium trifluoroacetate were reported. Trifluoromethylation process. US Patent 4808748, filed 12 December 1985 and issued 28 February 1989.

      33 33 Suzuki, H., Yoshida, Y., and Osuka, A. (1982). Chem. Lett. 11: 135.

      34 34 Carr, G.E., Chambers, R.D., Holmes, T.F. et al. (1988). J. Chem. Soc., Perkin Trans. 1 4: 921.

      35 35 Rijs, N.J. and O'Hair, R.A. (2012). O'Hair discussed the decomposition pathways of metal trifluoroacetates. J. Dalton Trans. 41: 3395.

      36 36 Markovich, K.M., Tantishaiyakul, V., Miller, D.D. et al. (1992). J. Med. Chem. 35: 466.

      37 37 Dong, L.C., Crowe, M., Ammann, J.R. et al. (2004). Tetrahedron Lett. 45: 2731.

      38 38 Chen, M. and Buchwald, S.L. (2013). Angew. Chem. Int. Ed. 52: 11628.

      39 39 McReynolds, K.A., Lewis, R.S., Vicic, D.A. et al. (2010). J. Fluorine Chem. 131: 1108.

      40 40 (a) Lin, X., Hou, C., Weng, Z. et al. (2016). Chem. Eur. J. 22: 2075.(b) Wu, C., Huang, Y., and Weng, Z. (2016). Asian J. Org. Chem. 5: 1406.(c) Lin, X., Han, X., Weng, Z. et al. (2016). RSC Adv. 6: 75465.

      41 41 Zhao, G., Wu, H., Liu, C. et al. (2016). RSC Adv. 6: 50250.

      42 42 Li, Y., Chen, T., Duan, C. et al. (2011). Synlett 12: 1713.

      43 43 (a) Chang, Y. and Cai, C. (2005). Tetrahedron Lett. 46: 3161.(b) Chang, Y. and Cai, C. (2005). J. Fluorine Chem. 126: 937.

      44 44 (a) Boltalina, O.V., Popov, A.A., and Stauss, S.H. (2015). Chem. Rev. 115: 1051.See also, (b) Pimenova, A.S., Kozlov, A.A., Sidorov, L.N. et al. (2007). Dalton Trans.: 5322.

      45 45 Uzkikh, I.S., Dorozhkin, E.I., Boltalina, O.V. et al. (2001). Dokl. Akad. Nauk 379: 344.

      46 46 (a) Goryunkov, A.A., Kuvychko, I.V., Boltalina, O.V. et al. (2003). J. Fluorine Chem. 124: 61.(b) Dorozhkin, E.I., Strauss, S.H., Boltalina, O.V. et al. (2006). Chem. Eur. J. 12: 3876.

      47 47 (a) Darwish, A.D., Avent, A.G., Taylor, R. et al. (2003). Chem. Commun. 3: 1374.(b) Darwish, A.D., Abdul‐Sada, A.K., Taylor, R. et al. (2003). Org. Biomol. Chem. 1: 3102.

      48 48 Dorozhkin, E.I., Goryunkov, A.A., Ioffe, I.N. et al. (2007). Eur. J. Org. Chem. 2007: 5082.

      49 49 Shi, G., Shao, C., Zhang, Y. et al. (2015). Org. Lett. 17: 38.

      50 50 Tung, T.T., Christensen, S.B., and Nielsen, J. (2017). Chem. Eur. J. 23: 18125.

      51 51 Wan, W., Ma, G., Hao, J. et al. (2016). Chem. Commun. 52: 1598.

      52 52 Wang, Y., Hao, J., Wan, W. et al. (2019). Wan and Han also reported a decarboxylative homo‐coupling from potassium difluoroarylacetate by using the combination of AgNO3, (NH4)2S2O8, and KHCO3, affording tetrafluoroethylene‐bridging aromatic products. Synth. Commun. 49: 2961.

      53 53 Wan, W., Li, J., Hao, J. et al. (2017). Org. Biomol. Chem. 15: 5308.

      54 54 Li, Y.‐L., Wang, J.‐B., and Deng, J. (2017). Eur. J. Org. Chem. 2017: 6052.

      55 55 Chen, F. and Hashmi, A.S.K. (2016). Org. Lett. 18: 2880.

      56 56 Lai, C. and Mallouk, T.E. (1993). J. Chem. Soc., Chem. Commun.: 1359.

      57 57 Lin, J., Su, W., Li, Y. et al. (2017). Nat. Commun. 8: 14353.

      58 58 Bazyar, Z. and Hosseini‐Sarvari, M. (2019). Org. Process Res. Dev. 23: 2345.

      59 59 Yang, B., Xu, X.H., and Qing, F.L. (2016). Org. Lett. 18: 5956.

      60 60 Zhou, Y., Xiong, Z., Zhu, G. et al. (2019). Org. Chem. Front. 6: 1022.

      61 61 (a) Meyer, C.F., Hell, S.M., Gouverneur, V. et al. (2019). Angew. Chem. Int. Ed. 58: 8829.(b) Meyer, C.F., Hell, S.M., Gouverneur, V. et al. (2019). Tetrahedron 75: 130679.

      62 62 Bogdanov, V.P., Dmitrieva, V.A., Goryunkov, A.A. et al. (2019). J. Fluorine Chem. 226: 109344.

      63 63 Yang, F., Wu, Y., Wu, Y. et al. (2016). Adv. Synth. Catal. 358: 1699.

      64 64 Hong, G., Yuan, J., Zhang, X. et al. (2019). Org. Chem. Front. 6: 1173.

      65 65 Zhong, S., Hafner, A., Bräse, S. et al. (2015). RSC Adv. 5: 6255.

      66 66 Kawamura, S. and Sodeoka, M. (2019). Bull. Chem. Soc. Jpn. 92: 1245.

      67 67 (a) Kawamura, S. and Sodeoka, M. (2016). Angew. Chem. Int. Ed. 55: 8740.(b) Kawamura, S., Dosei, K., Sodeoka, M. et al. (2017). J. Org. Chem. 82: 12539.(c) Kawamura, S., Henderson, C.J., Sodeoka, M. et al. (2018). Chem. Commun. 54: 11276.(d) Valverde, E., Kawamura, S., Sodeoka, M. et al. (2018). Chem. Sci. 9: 7115.

      68 68 Staveness, D., Bosque, I., and Stephenson, C.R.J. (2016). Acc. Chem. Res. 49: 2295.

      69 69 (a) Beatty, J.W., Douglas, J.J., Stephenson, C.R.J. et al. (2015). Nat. Commun. 6: 7919.(b) Beatty, J.W., Douglas, J.J., Stephenson, C.R.J. et al. (2016). Chem 1: 456.(c) McAtee, R.C., Beatty, J.W., Stephenson, C.R.J. et al. (2018). Org. Lett. 20: 3491.See also, (d) Sun, A., McClain, E.J., Stephenson, C.R.J. et al. (2018). Org. Lett. 20: 3487.

      70 70 Das, S., Hashmi, A.S.K., and Schaub, T. (2019). Adv. Synth. Catal. 361: 720.