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(10) For recent examples on selective oxidative arylations, see: (a) Lou,
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2016, 6, 3890. (b) Sun, D.; Li, B.; Lan, J.; Huang, Q.; You, J. Chem.
Commun. 2016, 52, 3635. (c) Yang, Z.; Qiu, F.-C.; Gao, J.; Li, Z.-W.;
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(11) For an elegant example on selective oxidative arylation controlled
by both ligand and directing group of arylating reagent, see: Xu, H.;
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(12) For reported examples on arylations of multisubstituted arenes
with arylboronic acids, see: (a) Yang, S.-D.; Sun, C.-L.; Fang, Z.; Li, B.-
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an example on non-selective iron-catalyzed arylation of arenes with aryl-
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Angew. Chem., Int. Ed. 2008, 47, 8897.
(13) For reported examples on transition-metal-catalyzed arylations of
monosubstituted arenes with aryl halides in low selectivities, see: (a)
Yanagisawa, S.; Sudo, T.; Noyori, R.; Itami, K. J. Am. Chem. Soc. 2006,
128, 11748. (b) Lafrance, M.; Fagnou, K. J. Am. Chem. Soc. 2006, 128,
16496. (c) Qin, C.; Lu, W. J. Org. Chem. 2008, 73, 7424. (d) Mousseau, J.
J.; Vallée, F.; Lorion, M. M.; Charette, A. B. J. Am. Chem. Soc. 2010, 132,
14412. (e) Liu, W.; Cao, H.; Lei, A. Angew. Chem., Int. Ed. 2010, 49,
2004. (f) Li, H.; Sun, C.-L.; Yu, M.; Yu, D.-G.; Li, B.-J.; Shi, Z.-J. Chem.
Eur. J. 2011, 17, 3593. (g) Hong, W.; Qiu, Y.; Yao, Z.; Wang, Z.; Jiang, S.
Tetrahedron Lett. 2011, 52, 4916. (h) Wang, Y.-N.; Guo, X.-Q.; Zhu, X.-
H.; Zhong, R.; Cai, L.-H.; Hou, X.-F. Chem. Commun. 2012, 48, 10437. (i)
Durak, L. J.; Lewis, J. C. Organometallics 2014, 33, 620. (j) Zhou, Q.;
Wang, Y.-N.; Guo, X.-Q.; Zhu, X.-H.; Li, Z.-M.; Hou, X.-F. Organome-
tallics 2015, 34, 1021.
AUTHOR INFORMATION
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Corresponding Author
Notes
The authors declare no competing financial interests.
ACKNOWLEDGMENT
We thank the National Natural Science Foundation of China
(21402096, 21421062), Tianjin Applied Basic Research Project
and Cutting-edge Technology Research Plan (14JCYBJC41400)
and the “1000-Youth Talents Plan” for financial support.
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