Jinzhong Yao et al.
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Acknowledgements
[9] M. Li, C. Wang, H. Ge, Org. Lett. 2011, 13, 2062.
[10] a) L. J. Gooßen, B. Zimmermann, T. Knauber, Angew.
Chem. 2008, 120, 7211; Angew. Chem. Int. Ed. 2008, 47,
7103; b) L. J. Gooßen, C. Linder, N. Rodrꢃguez, P. P.
Lange, Chem. Eur. J. 2009, 15, 9336.
[11] For selected examples, see: a) A. Voutchkova, A.
Coplin, N. E. Leadbeater, R. H. Crabtree, Chem.
Commun. 2008, 6312; b) C. Wang, I. Piel, F. Glorius, J.
Am. Chem. Soc. 2009, 131, 4194; c) W.-Y. Yu, W. N. Sit,
Z. Zhou, A. S. C. Chan, Org. Lett. 2009, 11, 3174; d) K.
Xie, Z. Yang, X. Zhou, X. Li, S. Wang, Z. Tan, X. An,
C.-C. Guo, Org. Lett. 2010, 12, 1564; e) F. Zhang, M. F.
Greaney, Angew. Chem. 2010, 122, 2828; Angew. Chem.
Int. Ed. 2010, 49, 2768.
[12] a) P. Fang, M. Li, H. Ge, J. Am. Chem. Soc. 2010, 132,
11898; b) M. Li, H. Ge, Org. Lett. 2010, 12, 3464.
[13] H. Wang, L. N. Guo, X. H. Duan, Org. Lett. 2012, 14,
4358.
[14] a) M. Kim, J. Park, S. Sharma, A. Kim, E. Park, J. H.
Kwak, Y. H. Jung, I. S. Kim, Chem. Commun. 2013, 49,
925; b) J. Park, M. Kim, S. Sharma, E. Park, A. Kim,
S. H. Lee, J. H. Kwak, Y. H. Jung, I. S. Kim, Chem.
Commun. 2013, 49, 1654.
We gratefully acknowledge the National Basic Research
Program of China (No. 2011CB936003), NSFC (No.
2107216, No. 21272205) and the Program for Zhejiang Lead-
ing Team of S&T Innovation for their financial support.
References
[1] For selected reviews, see: a) O. Baudoin, Angew.
Chem. 2007, 119, 1395; Angew. Chem. Int. Ed. 2007, 46,
1373; b) L. J. Gooßen, N. Rodrꢃguez, K. Gooßen,
Angew. Chem. 2008, 120, 3144; Angew. Chem. Int. Ed.
2008, 47, 3100; c) T. Satoh, M. Miura, Synthesis 2010,
3395; d) N. Rodriguez, L. J. Gooßen, Chem. Soc. Rev.
2011, 40, 5030; e) J. Cornella, I. Larrosa, Synthesis
2012, 44, 653; f) R. Shang, L. Liu, Sci. China Chem.
2011, 54, 1670; g) W. I. Dzik, P. P. Lange, L. J. Gooßen,
Chem. Sci. 2012, 3, 2671.
[2] For selected examples, see: a) L. J. Gooßen, N. Rodrꢃ-
guez, B. Melzer, C. Linder, G. Deng, L. M. Levy, J.
Am. Chem. Soc. 2007, 129, 4824; b) J.-M. Becht, C. L.
Drian, Org. Lett. 2008, 10, 3161; c) Z. Shen, Z. Ni, S.
Mo, J. Wang, Y. Zhu, Chem. Eur. J. 2012, 18, 4859; d) P.
Hu, Y. Shang, W. Su, Angew. Chem. 2012, 124, 6047;
Angew. Chem. Int. Ed. 2012, 51, 5945.
[15] Z. Yang, X. Chen, J. Liu, Q. Gui, K. Xie, M. Li, Z. Tan,
Chem. Commun. 2013, 49, 1560.
[16] L. V. Desai, K. J. Stowers, M. S. Sanford, J. Am. Chem.
Soc. 2008, 130, 13285.
[3] For selected examples of decarboxylative cross-cou-
pling reactions, see: a) P. Forgione, M.-C. Brochu, M.
St-Onge, K. H. Thesen, M. D. Bailey, F. Bilodeau, J.
Am. Chem. Soc. 2006, 128, 11350; b) L. J. Gooßen, G.
Deng, L. M. Levy, Science 2006, 313, 662; c) J.-M.
Becht, C. Catala, C. Le Drian, A. Wagner, Org. Lett.
2007, 9, 1781; d) M. Miyasaka, A. Fukushima, T. Satoh,
K. Hirano, M. Miura, Chem. Eur. J. 2009, 15, 3674;
e) S. Messaoudi, J.-D. Brion, M. Alami, Org. Lett. 2012,
14, 1496. For selected examples of decarboxylative
Heck-type reactions, see: f) A. G. Myers, D. Tanaka,
M. R. Mannion, J. Am. Chem. Soc. 2002, 124, 11250;
g) D. Tanaka, A. G. Myers, Org. Lett. 2004, 6, 433;
h) D. Tanaka, S. P. Romeril, A. G. Myers, J. Am. Chem.
Soc. 2005, 127, 10323.
[4] a) D. K. Rayabarapu, J. A. Tunge, J. Am. Chem. Soc.
2005, 127, 13510; b) H. Kim, P. H. Lee, Adv. Synth.
Catal. 2009, 351, 2827; c) C. Feng, T. P. Loh, Chem.
Commun. 2010, 46, 4779; d) W. Jia, N. Jiao, Org. Lett.
2010, 12, 2000.
[5] a) J. Moon, M. Jeong, H. Nam, J. Ju, J. H. Moon, H. M.
Jung, S. Lee, Org. Lett. 2008, 10, 945; b) H. Feng, D. S.
Ermolat’ev, G. Song, E. V. Van der Eycken, J. Org.
Chem. 2012, 77, 5149.
[17] a) K. K. Park, J. Jeong, Tetrahedron 2005, 61, 545;
b) C. Y. Chen, T. Andreani, H. Li, Org. Lett. 2011, 13,
6300; c) M. M. Johnson, J. M. Naidoo, M. A. Fernandes,
E. M. Mmutlane, W. A. L. van Otterlo, C. B. de Koning,
J. Org. Chem. 2010, 75, 8701; d) D. Tsvelikhovsky, S. L.
Buchwald, J. Am. Chem. Soc. 2011, 133, 14228.
[18] a) R. A. Joshi, M. K. Gurjar, N. K. Tripathy, M. S. Chor-
ghade, Org. Process Res. Dev. 2001, 5, 176; b) R. D.
Weinstein, J. J. Gribbin, K. R. Muske, J. Chem. Eng.
Data 2005, 50, 226; c) D. J. Lowes, W. A. Guiguemde,
M. C. Connelly, F. Zhu, M. S. Sigal, J. A. Clark, A. S.
Lemoff, J. L. Derisi, E. B. Wilson, R. K. Guy, J. Med.
Chem. 2011, 54, 7477; d) D. Lowes, A. Pradhan, L. V.
Iyer, T. Parman, J. Gow, F. Zhu, A. Furimsky, A.
Lemoff, W. A. Guiguemde, M. Sigal, J. A. Clark, E.
Wilson, L. Tang, M. C. Connelly, J. L. DeRisi, D. E.
Kyle, J. Mirsalis, R. K. Guy, J. Med. Chem. 2012, 55,
6087.
[19] a) L. Niu, H. Yang, R. Wang, H. Fu, Org. Lett. 2012,
14, 2618; b) J. H. Chu, P. S. Lin, M. J. Wu, Organome-
tallics 2010, 29, 4058; c) L. Ackermann, E. Diers, A.
Manvar, Org. Lett. 2012, 14, 1154.
[20] a) J. M. Anderson, J. K. Kochi, J. Am. Chem. Soc. 1970,
92, 1651; b) F. Fontana, F. Minisci, M. C. Nogueira Bar-
bosa, E. Vismara, J. Org. Chem. 1991, 56, 2866; c) S.
Seo, M. Slater, M. F. Greaney, Org. Lett. 2012, 14, 2650.
[21] CCDC 930446 contains the supplementary crystallo-
graphic data for this paper (palladacyle A). These data
can be obtained free of charge from The Cambridge
data_request/cif.
[6] R. Shang, Y. Fu, J. B. Li, S. L. Zhang, Q. X. Guo, L.
Liu, J. Am. Chem. Soc. 2009, 131, 5738.
[7] a) M. Yamashita, K. Hirano, T. Satoh, M. Miura, Org.
Lett. 2010, 12, 592; b) Z. Cui, X. Shang, X. F. Shao,
Z. Q. Liu, Chem. Sci. 2012, 3, 2853; c) Z. Wang, Q.
Ding, X. He, J. Wu, Org. Biomol. Chem. 2009, 7, 863.
[8] L. J. Gooßen, F. Rudolphi, C. Oppel, N. Rodrꢃguez,
Angew. Chem. 2008, 120, 3085; Angew. Chem. Int. Ed.
2008, 47, 3043.
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