Chin. J. Org. Chem. ›› 2014, Vol. 34 ›› Issue (5): 837-851.DOI: 10.6023/cjoc201311012 Previous Articles Next Articles
Reviews
王光祖a, 赫侠平a, 戴建军a, 许华建a,b
收稿日期:2013-11-09
修回日期:2013-12-23
发布日期:2014-01-02
通讯作者:
许华建，戴建军
E-mail:hjxu@hfut.edu.cn;daijj@hfut.edu.cn
基金资助:国家自然科学基金（Nos. 21272050，21072040）资助项目.
Wang Guangzua, He Xiapinga, Dai Jianjuna, Xu Huajiana,b
Received:2013-11-09
Revised:2013-12-23
Published:2014-01-02
Supported by:Project supported by the National Natural Science Foundation of China (Nos. 21272050, 21072040).
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Wang Guangzu, He Xiaping, Dai Jianjun, Xu Huajian. Recent Advances in Copper-Promoted Trifluoromethylation Reactions[J]. Chin. J. Org. Chem., 2014, 34(5): 837-851.
| [1] (a) Uneyama, K. Organofluorine Chemistry, Blackwell, Oxford, U. K., 2006. (b) Hird, M. Chem. Soc. Rev. 2007, 36, 2070. (c) Kirk, K. L. Org. Process Res. Dev. 2008, 12, 305. (d) O'Hagan, D. Chem. Soc. Rev. 2008, 37, 308. (e) Ojima, I. Fluorine in Medicinal Chemistry and Chemical Biology, Wiley-Blackwell, Chichester, U.K., 2009. (f) Filler, R.; Saha, R. Future Med. Chem. 2009, 1, 777.(g) Daniels, S.; Tohid, S. F. M.; Velanguparackel, W.; Westwell, A. D. Expert Opin. Drug Discovery 2010, 5, 291. (h) Acena, J. L.; Simon-Fuentes, A.; Fustero, S. Curr. Org. Chem. 2010, 14, 928. (i) Wang, X.; Zhang, Y.; Wang, J. Sci. Sin. Chim. 2012, 42, 1417. (j) Yu, H. Z; Su. S. Q, Zhang , C; Dang, Z. M. Chin. J. Org. Chem. 2013, 33, 1628 (in Chinese). (于海珠, 苏圣钦, 张弛, 党智敏, 有机化学, 2013, 33, 1628.) (k) Liu, T. F; Shen, Q, L. Eur. J. Org. Chem.2012, 6679.[2] (a) Welch, J. T. Tetrahedron 1987, 43, 3123. (b) Kirsch, P. Modern Fluoroorganic Chemistry: Synthesis, Reactivity, Applications, Wiley-VCH, Weinheim, 2004. (c) Shimizu, M.; Hiyama, T. Angew. Chem., Int. Ed. 2005, 44, 214. (d) Schlosser, M. Angew. Chem., Int. Ed. 2006, 45, 5432. (e) Muller, K.; Faeh, C.; Diederich, F. Science 2007, 317, 1881. (f) Bonnet-Delpon, D. Bioorganic and Medicinal Chemistry of Fluorine, Wiley-VCH, Hoboken, NJ, 2008. (g) Purser, S.; Moore, P. R.; Swallow, S.; Gouverneur, V. Chem. Soc. Rev. 2008, 37, 320. (h) Hagmann, W. K. J. Med. Chem. 2008, 51, 4359. (i) Pursor, S.; Moore, P. R.; Swallow, S.; Gouverneur, V. Chem. Soc. Rev. 2008, 37, 320. (j) Ojima, I. Fluorine in Medicinal Chemistry and Chemical Biology, Wiley-Blackwell, Chichester, 2009. (k) Lin, G.-Q.; You, Q.-D.; Cheng, J.-F. Chiral Drugs: Chemistry and Biological Action, Wiley-VCH, Hoboken, 2011.[3] (a) Swarts, F. Bull. Acad. R. Belg. 1892, 24, 309. (b) Boswell, G. A., Jr.; Ripka, W. C.; Scribner, R. M.; Tullock, C. W. Org. React. 1974, 21, 1.[4] Kazuyuki, S.; Masaaki, O.; Akira, A.; Itsumaro, K. Org. Lett. 2013, 23, 4359. [5] (a) Mizuta, S.; Verhoog, S.; Engle, K. M.; Khotavivattana, T.; O'Duill, M.; Wheelhouse, K.; Rassias, G.; Medebielle, M.; Gouverneur, V. J. Am. Chem. Soc. 2013, 135, 2505. (b) Yasu, Y.; Koike, T.; Akita, M. Org. Lett. 2013, 15, 2137. (c) Herrmann, A. T.; Smith, L. L.; Zakarian, A. J. Am. Chem. Soc. 2012, 134, 6976. (d) Iqbal, N.; Choi, S.; Kim, E.; Cho, E. J. J. Org. Chem. 2012, 77, 11383. (e) Mizuta, S.; Engle, K. M.; Verhoog, S.; Galicia-López, O.; O'Duill, M.; Médebielle, M.; Wheelhouse, K.; Rassias, G.; Thompson, A. L.; Gouverneur, V. Org. Lett. 2013, 15, 1250. [6] (a) Wang, X.; Truesdale, L.; Yu, J.-Q. J. Am. Chem. Soc. 2010, 132, 3648. (b) Ye, Y.; Ball, N. D.; Kampf, J. W.; Sanford, M. S. J. Am. Chem. Soc. 2010, 132, 14682. (c) Ball, N. D.; Gary, J. B.; Ye, Y.; Sanford, M. S. J. Am. Chem. Soc. 2011, 133, 7577. (d) Cho, E. J.; Buchwald, S. L. Org. Lett. 2011, 13, 6552. (e) Hafner, A.; Brase, S. Angew. Chem., Int. Ed. 2012, 51, 3713. (f) Zhang, X. G.; Dai, H. X.; Wasa, M.; Yu, J. Q. J. Am. Chem. Soc. 2012, 134, 11948.[7] (a) Hafner, A.; Bihlmeier, A.; Nieger, M.; Klopper, W.; Brase, S. J. Org. Chem. 2013, 78, 7938. (b) Hafner, A.; Feuerstein, T. J.; Bräse, S. Org. Lett. 2013, 15, 3468. (c) Ye, Y.; Lee, S. H.; Sanford, M. S. Org. Lett. 2011, 13, 5464. (d) Wang, X.; Xu, Y.; Mo, F.; Ji, G.; Qiu, D.; Feng, J.; Ye, Y.; Zhang, S.; Zhang, Y.; Wang, J. J. Am. Chem. Soc. 2013, 135, 10330. (e) Zeng, Y.; Zhang, L.; Zhao, Y.; Ni, C.; Zhao, J.; Hu, J. J. Am. Chem. Soc. 2013, 135, 2955.[8] (a) Dubinina, G. G.; Brennessel, W. W.; Miller, J. L.; Vicic, D. A. Organometallics 2008, 27, 3933. (b) Hao, F.; Jiang, H. W.; Zong, G.; Zhou, Z.; Du, R. B.; Chen, Q. Y.; Xiao, J. C. J. Org. Chem. 2012, 77, 3604. (c) Gao, J. R.; Wu, H.; Xiang, B.; Yu, W. B.; Han, L.; Jia, Y. X. J. Am. Chem. Soc. 2013, 135, 2983.[9] (a) Parsons, A. T.; Senecal, T. D.; Buchwald, S. L. Angew. Chem., Int. Ed. 2012, 51, 2947. (b) Patra, T.; Deb, A.; Manna, S.; Sharma, U.; Maiti, D. Eur. J. Org. Chem. 2013, 2013, 5247.[10] (a) Kobayashi, Y.; Kumadaki, I. Tetrahedron Lett. 1969, 10, 4095. (b) Kobayashi, Y.; Yamamoto, K.; Kumadaki, I. Tetrahedron Lett. 1979, 20, 4071.[11] (a) Kondratenko, N. V.; Vechirko, E. P.; Yagupolskii, L. M. Synthesis 1980, 932. (b) Kremlev, M. M.; Tyrra, W.; Mushta, A. I.; Naumann, D.; Yagupolskii, Y. L. J. Fluorine Chem. 2010, 131, 212. (c) Nowak, I. Robins, M. J. J. Org. Chem. 2007, 72, 2678.[12] (a) Burton, D. J.; Wiemers, D. M. J. Am. Chem. Soc. 1985, 107, 5014. (b) Burton, D. J.; Wiemers, D. M. J. Am. Chem. Soc. 1986, 108, 832. (c) Clark, J. H.; McClinton, M. A.; Blade, R. J. J. Chem. Soc., Chem. Commun. 1988, 638.[13] Carr, G. E.; Chambers, R. D.; Holmes, T. F.; Parker, D. G. J. Chem. Soc., Perkin Trans. 1 1988, 921[14] Su, D. B.; Duan, J. X.; Chen, Q. Y. Tetrahedron Lett. 1991, 32, 7689.[15] Chen, Q. Y.; Duan, J. X. J. Chem. Soc., Chem. Commun. 1993, 1389.[16] (a) McLoughlin, V. C. R.; Thrower, J. Tetrahedron 1969, 25, 5921.(b) Lin, T. S.; Gao, Y. S. J. Med. Chem. 1983, 26, 598. (c) Duan, J. X.; Su, D. B.; Wu, J. P.; Chen, Q. Y. J. Fluorine Chem. 1994, 66, 167. (d) Su, D. B.; Duan, J. X.; Chen, Q. Y. Tetrahedron Lett. 1991, 32, 7689. (e) Su, D. B.; Duan, J. X.; Yu, A.; Chen, Q. Y. J. Fluorine Chem. 1993, 65, 11. (f) Langlois, B. R.; Roques, N. J. Fluorine Chem. 2007, 128, 1318. (g) Qing, F. Chin. J. Org. Chem. 2012, 32, 815 (in Chinese). (卿凤翎, 有机化学, 2012, 32, 815.)[17] (a) Yang, C.-T.; Zhang, Z.-Q.; Liu, Y.-C.; Liu, L. Angew. Chem., Int. Ed. 2011, 50, 3904. (b) Yang, C.-T.; Zhang, Z.-Q.; Liang, J.; Liu, J.-H.; Lu, X.-Y.; Chen, H.-H.; Liu, L. J. Am. Chem. Soc. 2012, 134, 11124.(c) Yang, C.-T.; Zhang, Z.-Q.; Tajuddin, H.; Wu, C.-C.; Liang, J.; Liu, J.-H.; Fu, Y.; Czyzewska, M.; Steel, P. G.; Marder, T. B.; Liu, L. Angew. Chem., Int. Ed. 2012, 51, 528. (d) Ren, P.; Stern, L.-A.; Hu, X. Angew. Chem., Int. Ed. 2012, 51, 9110. (e) Nishino, M.; Hirano, K.; Satoh, T.; Miura, M. Angew. Chem., Int. Ed. 2012, 51, 6993. (f) Wu, J.-C.; Song, R.-J.; Wang, Z.-Q.; Huang, X.-C.; Xie, Y.-X.; Li, J.-H. Angew. Chem., Int. Ed. 2012, 51, 6993. (g) Kitching, M. O.; Hurst, T. E.; Snieckus, V. Angew. Chem., Int. Ed. 2012, 51, 2925. (h) Wang, L.; Huang, H.; Priebbenow, D. L.; Pan, F.-F.; Bolm, C. Angew. Chem., Int. Ed. 2013, 52, 3478. (i) Uyeda, C.; Tan, Y.; Fu, G. C.; Peters, J. C. J. Am. Chem. Soc. 2013, 135, 9548. (j) Deng, W.; Liu, L.; Guo, Q.-X. Chin. J. Org. Chem. 2004, 24, 150 (in Chinese). (邓维, 刘磊, 郭庆祥, 有机化学, 2004, 24, 150.) (k) Xu, H.-J.; Man, Q.-S.; Lin, Y.-C.; Li, Y.-Y.; Feng, Y.-S. Chin. J. Org. Chem. 2010, 30, 9 (in Chinese). (许华建, 蔄秋石, 林义成, 李源源, 冯乙巳, 有机化学, 2010, 30, 9.)[18] Dubinina, G. G.; Furutachi, H.; Vicic, D. A. J. Am. Chem. Soc. 2008, 130, 8600.[19] Oishi, M.; Kondo, H.; Amii, H. Chem. Commun. 2009, 1909.[20] Zhang, S.-L.; Liu, L.; Fu, Y.; Guo, Q.-X. Organometallics 2007, 26, 4546.[21] Morimoto, H.; Tsubogo, T.; Litvinas, N. D.; Hartwig, J. F. Angew. Chem., Int. Ed. 2011, 50, 3793. [22] (a) Zanardi, A.; Novikov, M. A.; Martin, E.; Benet-Buchholz, J.; Grushin, V. V. J. Am. Chem. Soc. 2011, 133, 20901. (b) Tomashenko, O. A.; Escudero-Adan, E. C.; Belmonte, M. M.; Grushin, V. V. Angew. Chem., Int. Ed. 2011, 50, 7655.[23] Zhang, C. P.; Wang, Z. L.; Chen, Q. Y.; Zhang, C. T.; Gu, Y. C.; Xiao, J. C. Angew. Chem., Int. Ed. 2011, 50, 1896.[24] Weng, Z.; Lee, R.; Jia, W.; Yuan, Y.; Wang, W.; Feng, X.; Huang, K. W. Organometallics 2011, 30, 3229.[25] Kondo, H.; Oishi, M.; Fujikawa, K.; Amii, H. Adv. Synth. Catal. 2011, 353, 1247.[26] Knauber, T.; Arikan, F.; Roschenthaler, G.-V.; Goossen, L. J. Chem. Eur. J. 2011, 17, 2689.[27] Schareina, T.; Wu, X.-F.; Zapf, A.; Cotté, A.; Gotta, M.; Beller, M. Top. Catal. 2012, 55, 426.[28] Duan, C.; Li, Y.; Chen, T.; Wang, H.; Zhang, R.; Jin, K.; Wang, X. Synlett 2011, 1713.[29] Chen, M.; Buchwald, S. L. Angew. Chem., Int. Ed. 2013, 52, 11628.[30] Hafner, A.; Braese, S. Adv. Synth. Catal. 2011, 353, 3044.[31] Kawai, H.; Furukawa, T.; Nomura, Y.; Tokunaga, E.; Shibata, N. Org. Lett. 2011, 13, 3596.[32] Miyake, Y.; Ota, S.; Nishibayashi, Y. Chem.-Eur. J. 2012, 18, 13255.[33] Miyake, Y.; Ota, S.; Shibata, M.; Nakajima, K.; Nishibayashi, Y. Chem. Commum. 2013, 49, 7809.[34] Larsson, J. M.; Pathipati, S. R.; Szabo, K. J. J. Org. Chem. 2013, 78, 7330.[35] Zhao, T. S.; Szabo, K. J. Org. Lett. 2012, 14, 3966.[36] Novak, P.; Lishchynskyi, A.; Grushin, V. V. J. Am. Chem. Soc. 2012, 134, 16167.[37] Ambler, B. R.; Altman, R. A. Org. Lett. 2013.[38] Chu, L.; Qing, F.-L. Org. Lett. 2010, 12, 5060.[39] Senecal, T. D.; Parsons, A. T.; Buchwald, S. L. J. Org. Chem. 2011, 76, 1174.[40] Xu, J.; Luo, D. F.; Xiao, B.; Liu, Z. J.; Gong, T. J.; Fu, Y.; Liu, L. Chem. Commun. 2011, 47, 4300.[41] Zhang, C. P.; Cai, J.; Zhou, C. B.; Wang, X. P.; Zheng, X.; Gu, Y. C.; Xiao, J. C. Chem. Commun. 2011, 47, 9516.[42] Liu, T.; Shen, Q. Org. Lett. 2011, 13, 2342.[43] Huang, Y.; Fang, X.; Lin, X.; Li, H.; He, W.; Huang, K.-W.; Yuan, Y.; Weng, Z. Tetrahedron 2012, 68, 9949.[44] Ji, Y.; Brueckl, T.; Baxter, R. D.; Fujiwara, Y.; Seiple, I. B.; Su, S.; Blackmond, D. G.; Baran, P. S. Proc. Natl. Acad. Sci. U. S. A. 2011, 108, 14411.[45] Ye, Y.; Kunzi, S. A.; Sanford, M. S. Org. Lett. 2012, 14, 4979.[46] Li, Y.; Wu, L.; Neumann, H.; Beller, M. Chem. Commun. 2013, 49, 2628.[47] Litvinas, N. D.; Fier, P. S.; Hartwig, J. F. Angew. Chem., Int. Ed. 2012, 51, 536.[48] Liu, T.; Shao, X.; Wu, Y.; Shen, Q. Angew. Chem., Int. Ed. 2012, 51, 555.[49] Novák, P.; Lishchynskyi, A.; Grushin, V. V. Angew. Chem., Int. Ed. 2012, 51, 7767.[50] Khan, B. A.; Buba, A. E.; Goossen, L. J. Chem.-Eur. J. 2012, 18, 1577.[51] Ye, Y.; Sanford, M. S. J. Am. Chem. Soc. 2012, 134, 9034.[52] Xu, J.; Xiao, B.; Xie, C. Q.; Luo, D. F.; Liu, L.; Fu, Y. Angew. Chem., Int. Ed. 2012, 51, 12551.[53] Zheng, H.; Huang, Y.; Wang, Z.; Li, H.; Huang, K.-W.; Yuan, Y.; Weng, Z. Tetrahedron Lett. 2012, 53, 6646.[54] Chu, L.; Qing, F.-L. J. Am. Chem. Soc. 2010, 132, 7262.[55] Weng, Z.; Li, H.; He, W.; Yao, L.-F.; Tan, J.; Chen, J.; Yuan, Y.; Huang, K.-W. Tetrahedron 2012, 68, 2527.[56] Luo, D.-F.; Xu, J.; Fu, Y.; Guo, Q.-X. Tetrahedron Lett. 2012, 53, 2769.[57] Zhang, K.; Qiu, X.-L.; Huang, Y.; Qing, F.-L. Eur. J. Org. Chem. 2012, 58.[58] Shimizu, R.; Egami, H.; Nagi, T.; Chae, J.; Hamashima, Y.; Sodeoka, M. Tetrahedron Lett. 2010, 51, 5947.[59] Chu, L.; Qing, F. L. J. Am. Chem. Soc. 2012, 134, 1298.[60] Pair, E.; Monteiro, N.; Bouyssi, D.; Baudoin, O. Angew. Chem., Int. Ed. 2013, 52, 5346.[61] Feng, C.; Loh, T.-P. Chem. Sci. 2012, 3, 3458.[62] Ilchenko, N. O.; Janson, P. G.; Szabo, K. J. Chem. Commun. 2013, 49, 6614.[63] Wang, X.; Ye, Y.; Ji, G.; Xu, Y.; Zhang, S.; Feng, J.; Zhang, Y.; Wang, J. Org. Lett. 2013, 15, 3730.[64] Xu, J.; Fu, Y.; Luo, D. F.; Jiang, Y. Y.; Xiao, B.; Liu, Z. J.; Gong, T. J.; Liu, L. J. Am. Chem. Soc. 2011, 133, 15300.[65] Parsons, A. T.; Buchwald, S. L. Angew. Chem., Int. Ed. 2011, 50, 9120.[66] Wang, X.; Ye, Y.; Zhang, S.; Feng, J.; Xu, Y.; Zhang, Y.; Wang, J. J. Am. Chem. Soc. 2011, 133, 16410.[67] Chu, L.; Qing, F.-L. Org. Lett. 2010, 14, 2106. [68] Mitsudera, H.; Li, C.-J. Tetrahedron Lett. 2011, 52, 1898.[69] (a) Chu, L. L.; Qing, F. L. Chem. Commun. 2010, 46, 6285. (b) Xiao, H. Q.; Huang, Y. Z.; Qing, F.-L. Tetrahedron 2010, 21, 2949.[70] Hu, M.; Ni, C.; Hu, J. J. Am. Chem. Soc. 2012, 134, 15257.[71] Dai, J. J.; Fang, C.; Xiao, B.; Yi, J.; Xu, J.; Liu, Z. J.; Lu, X.; Liu, L.; Fu, Y. J. Am. Chem. Soc. 2013, 135, 8436.[72] Danoun, G.; Bayarmagnai, B.; Grunberg, M. F.; Goossen, L. J. Angew. Chem., Int. Ed. 2013, 52, 7972.[73] (a) Shang, R.; Liu, L. Sci. China Chem. 2011, 54, 1670. (b) Shang, R.; Fu, Y.; Li, J.-B.; Zhang, S.-L.; Guo, Q.-X.; Liu, L. J. Am. Chem. Soc. 2009, 131, 5738. (c) Shang, R.; Yang, Z. W.; Wang, Y.; Zhang, S.-L.; Liu, L. J. Am. Chem. Soc. 2010, 132, 14391.(d) Dai, J.-J.; Liu, J.-H.; Luo, D.-F.; Liu, L. Chem. Commun. 2011, 47, 677.[74] Li, Z. J; Cui, Z. L; Liu Z. Q. Org. Lett. 2013, 15, 406.[75] He, Z.; Luo, T.; Hu, M.; Cao, Y.; Hu, J. Angew. Chem., Int. Ed. 2012, 51, 3944.[76] He, Z.; Zhang, R.; Hu, M.; Li, L.; Ni, C.; Hu, J. Chem. Sci. 2012, 4, 3478.[77] Anna E. A. ; David W. C.; MacMillan, D. W. C. J. Am. Chem. Soc. 2012, 132, 4986.[78] (a) Nagib, D. A.; Scott, M. E.; MacMillan, D. W. C. J. Am. Chem. Soc. 2009, 131, 10875. (b) Nagib, D. A.; MacMillan, D. W. C. Nature 2011, 480, 224. (c) Pham, P. V.; Nagib, D. A.; MacMillan, D. W. C. Angew. Chem., Int. Ed. 2011, 50, 6119. (d) Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Chem. Rev. 2013, 113, 5322.[79] Deng, Q. H.; Wadepohl, H.; Gade, L. H. J. Am. Chem. Soc. 2012, 134, 10769. [80] Janson, P. G.; Ghoneim, I.; Ilchenko, N. O.; Szabó, K. J. Org. Lett. 2012, 14, 2882.[81] Zhu, R.; Buchwald, S. L. J. Am. Chem. Soc. 2012, 134, 12462.[82] Ilchenko, N. O.; Janson, P. G.; Szabo, K. J. J. Org. Chem. 2013, 78, 11087.[83] Kong, W.; Casimiro, M.; Merino, E.; Nevado, C. J. Am. Chem. Soc. 2013, 135, 14480.[84] Egami, H.; Shimizu, R.; Sodeoka, M. J. Fluorine Chem. 2013, 152, 51.[85] Zhang, Y. Q.; Liu, J. D.; Xu, H. Org. Biomol. Chem. 2013, 11, 6242.[86] Liu, X.; Xiong, F.; Huang, X.; Xu, L.; Li, P.; Wu, X. Angew. Chem., Int. Ed. 2013, 52, 6962. [87] Chen, Z. M.; Bai, W.; Wang, S. H.; Yang, B. M.; Tu, Y. Q.; Zhang, F. M. Angew. Chem., Int. Ed. 2013, 52, 9781.[88] Qing, F.-L.; Chu, L. Synthesis 2012, 44, 1521.Lin, X.; Wang, G.; Li, H.; Huang, Y.; He, W.; Ye, D.; Huang, K.-W.; Yuan, Y.; Weng, Z. Tetrahedron 2013, 69, 2628. |
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