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RSC Advances
Journal Name ARTICLE
(228 mg, 1.50 mmol), and DMF (6 mL) were added to a 22 Y. Ji, T. Brueckl, R. D. Baxter, Y. Fujiwara, I. B. Seiple, S. Su, D.
DOI: 10.1039/C6RA15547B
reaction tube with Teflon screw cap equipped with a stir bar.
The tube was sealed and the solution was placed into a
G. Blackmond and P. S. Baran, Proc. Natl. Acad. Sci., 2011,
108, 14411-14415.
preheated 75
the oil bath and cooled to room temperature, and then
(trifluoromethoxy)benzene (65 µL, 0.50 mmol) was added as 24 K. A. McReynolds, R. S. Lewis, L. K. G. Ackerman, G. G.
C oil bath for 3 h. The tube was removed from 23 T. Schareina, X.-F. Wu, A. Zapf, A. Cotté, M. Gotta and M.
Beller, Top. Catal., 2012, 55, 426-431.
an internal standard. The reaction mixture was then filtered
through a layer of celite. The filtrate was analyzed by 19F NMR
and GC-MS.
Dubinina, W. W. Brennessel and D. A. Vicic, J. Fluorine Chem.,
2010, 131, 1108-1112.
25 G. Shi, C. Shao, S. Pan, J. Yu and Y. Zhang, Org. Lett., 2015, 17
,
,
,
38-41.
26 D. J. Burton and D. M. Wiemers, J. Am. Chem. Soc., 1985, 107
5014-5015.
27 D. M. Wiemers and D. J. Burton, J. Am. Chem. Soc., 1986, 108
832-834.
Acknowledgements
Financial support from National Natural Science Foundation of
China (21372044), and Fuzhou University (022494) is gratefully
acknowledged.
28 M. Huiban, M. Tredwell, S. Mizuta, Z. Wan, X. Zhang, T. L.
Collier, V. Gouverneur and J. Passchier, Nat Chem, 2013, 5,
941-944.
29 Q.-Y. Chen and S.-W. Wu, J. Chem. Soc. Chem. Commun.,
References
1989, 705-706.
30 J.-X. Duan, D.-B. Su and Q.-Y. Chen, J. Fluorine Chem., 1993,
61, 279-284.
1
2
M. Schlosser, Angew. Chem. Int. Ed., 2006, 45, 5432-5446.
R. P. Singh and J. n. M. Shreeve, Tetrahedron, 2000, 56
7613-7632.
31 J. G. MacNeil Jr and D. J. Burton, J. Fluorine Chem., 1991, 55
,
,
225-227.
32 J. Zheng, J.-H. Lin, X.-Y. Deng and J.-C. Xiao, Org. Lett., 2015,
17, 532-535.
33 X. Zhang, J. Wang and Z. Wan, Org. Lett., 2015, 17, 2086-
2089.
34 J. Wang, X. Zhang, Z. Wan and F. Ren, Org. Process Res. Dev.,
2016, 20, 836-839.
35 J.-Y. Yang, X.-H. Xu and F.-L. Qing, J. Fluorine Chem., 2016,
186, 45-51.
3
4
5
6
7
S. Roy, B. T. Gregg, G. W. Gribble, V.-D. Le and S. Roy,
Tetrahedron, 2011, 67, 2161-2195.
P. Kirsch, Modern fluoroorganic chemistry
: synthesis,
reactivity, applications, Wiley-VCH, Weinheim, 2004.
K. Uneyama and Editor, Organofluorine Chemistry, Blackwell
Publishing Ltd., 2006.
R. J. Lundgren and M. Stradiotto, Angew. Chem. Int. Ed.,
2010, 49, 9322-9324.
36 G. Zhao, H. Wu, Z. Xiao, Q.-Y. Chen and C. Liu, RSC Advances,
T. Besset, C. Schneider and D. Cahard, Angew. Chem. Int. Ed.,
2012, 51, 5048-5050.
2016, 6, 50250-50254.
37 X. Linꢀ, C. Houꢀ, H. Li and Z. Weng, Chem.-Eur. J., 2016, 22
,
8
9
A. Studer, Angew. Chem. Int. Ed., 2012, 51, 8950-8958.
T. Furuya, A. S. Kamlet and T. Ritter, Nature, 2011, 473, 470-
477.
2075-2084.
38 Z. Weng, R. Lee, W. Jia, Y. Yuan, W. Wang, X. Feng and K.-W.
Huang, Organometallics, 2011, 30, 3229-3232.
39 M. Oishi, H. Kondo and H. Amii, Chem. Commun., 2009,
1909-1911.
10 T. Liu and Q. Shen, Eur. J. Org. Chem., 2012, 2012, 6679-6687.
11 Z. Jin, G. B. Hammond and B. Xu, Aldrichim. Acta, 2012, 45
67-83.
,
40 Z. Gonda, S. Kovács, C. Wéber, T. Gáti, A. Mészáros, A.
Kotschy and Z. Novák, Org. Lett., 2014, 16, 4268-4271.
41 H. Morimoto, T. Tsubogo, N. D. Litvinas and J. F. Hartwig,
Angew. Chem. Int. Ed., 2011, 50, 3793-3798.
42 M. G. Mormino, P. S. Fier and J. F. Hartwig, Org. Lett., 2014,
16, 1744-1747.
12 Y. Ye and M. S. Sanford, Synlett, 2012, 23, 2005-2013.
13 P. Chen and G. Liu, Synthesis, 2013, 45, 2919-2939.
14 J. Xu, X. Liu and Y. Fu, Tetrahedron Lett., 2014, 55, 585-594.
15 X. Liu, C. Xu, M. Wang and Q. Liu, Chem. Rev., 2015, 115
683-730.
,
,
16 J. Charpentier, N. Früh and A. Togni, Chem. Rev., 2015, 115
650-682.
43 G. Hu, L. Tao, CN101235030, 2008.
44 K. Kossen, S. D. Seiwert, V. Serebryany, D. Ruhrmund, L.
Beigelman, L. F. M. Raveglia, S. Vallese, I. Bianchi, T. Hu,
WO2009149188A1, 2009.
45 T. Kawasaki-Takasuka and T. Yamazaki, Tetrahedron, 2015,
71, 6824-6831.
46 G. K. S. Prakash, F. Wang, Z. Zhang, R. Haiges, M. Rahm, K. O.
Christe, T. Mathew and G. A. Olah, Angew. Chem. Int. Ed.,
2014, 53, 11575-11578.
17 U. Teruo and I. Sumi, Tetrahedron Lett., 1990, 31, 3579-3582.
18 T. Umemoto, Chem. Rev., 1996, 96, 1757-1778.
19 A. Sato, J. Han, T. Ono, A. Wzorek, J. L. Acena and V. A.
Soloshonok, Chem. Commun., 2015, 51, 5967-5970.
20 A. Zanardi, M. A. Novikov, E. Martin, J. Benet-Buchholz and V.
V. Grushin, J. Am. Chem. Soc., 2011, 133, 20901-20913.
21 A. Lishchynskyi, M. A. Novikov, E. Martin, E. C. Escudero-
Adán, P. Novák and V. V. Grushin, J. Org. Chem., 2013, 78
,
47 H. Serizawa, K. Aikawa and K. Mikami, Chem.-Eur. J., 2013, 19
17692-17697.
,
11126-11146.
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