G. Zhang, X. Zhao, Y. Yan, C. Ding
SHORT COMMUNICATION
4996–4997; d) J. C. Lewis, S. H. Wiedemann, R. G. Bergman,
J. A. Ellman, Org. Lett. 2004, 6, 35–38.
Acknowledgments
[9] For selected examples, see: a) S. Oi, R. Funayama, T. Hattori,
Y. Inoue, Tetrahedron 2008, 64, 6051–6059; b) L. Ackermann,
M. Mulzer, Org. Lett. 2008, 10, 5043–5045; c) L. Ackermann,
A. Althammer, R. Born, Angew. Chem. 2006, 118, 2681–2685;
Angew. Chem. Int. Ed. 2006, 45, 2619–2622; d) S. Oi, S. Fukita,
N. Hirata, N. Watanuki, S. Miyano, Y. Inoue, Org. Lett. 2001,
3, 2579–2581.
We gratefully acknowledge financial support from the National
Natural Science Foundation of China (No. 20702051), Educational
Commission of Zhejiang Province (Y200907685), the New Shoot
Talents Program of Zhejiang Province (2010R403047), and the
Undergraduate Educational Innovation Program of Zhejiang Uni-
versity of Technology (No. 2015).
[10] K. Fujita, M. Nonogawa, R. Yamaguchi, Chem. Commun.
2004, 1926–1927.
[11] For reviews, see: a) E. M. Beck, M. J. Gaunt, Topics in Current
Chemistry Vol. 292: C–H Activation (Eds.: J.-Q. Yu, Z.-J. Shi),
Springer, Berlin, 2010, pp. 85–121; b) O. Daugulis, H.-Q. Do,
D. Shabashov, Acc. Chem. Res. 2009, 42, 1074–1086; c) D. Al-
berico, M. E. Scott, M. Lautens, Chem. Rev. 2007, 107, 174–
238.
[12] For selected examples, see: a) W.-K. Hong, Y.-T. Qiu, Z.-Y.
Yao, Z.-Y. Wang, S. Jiang, Tetrahedron Lett. 2011, 52, 4916–
4919; b) C.-X. Qiu, W.-J. Lu, J. Org. Chem. 2008, 73, 7424–
7427.
[13] For selected examples, see: a) F. Bellina, S. Cauteruccio, R.
Rossi, J. Org. Chem. 2007, 72, 8543–8546; b) F. Bellina, S. Cau-
teruccio, R. Rossi, Eur. J. Org. Chem. 2006, 1379–1382; c) F.
Bellina, S. Cauteruccio, L. Mannina, R. Rossi, S. Viel, Eur. J.
Org. Chem. 2006, 693–703.
[14] For selected examples, see: a) C. B. Bheeter, J. K. Bera, H.
Doucet, J. Org. Chem. 2011, 76, 6407–6413; b) J. Roger, F. Po-
gan, H. Doucet, J. Org. Chem. 2009, 74, 1179–1186; c) J. F. D.
Chabert, L. Joucla, E. David, M. Lemaire, Tetrahedron 2004,
60, 3221–3230; d) C. Gozzi, L. Lavenot, K. Ilg, V. Penalva, M.
Lemaire, Tetrahedron Lett. 1997, 38, 8867–8870.
[15] N. Marion, S. P. Nolan, Acc. Chem. Res. 2008, 41, 1440–1449.
[16] R. Takita, D. Fujita, F. Ozawa, Synlett 2011, 959–963.
[17] For selected examples, see: a) D. A. Alonso, C. Nájera, Chem.
Soc. Rev. 2010, 39, 2891–2902; b) L. Botella, C. Nájera, J. Org.
Chem. 2005, 70, 4360–4369; c) D. A. Alonso, L. Botella, C.
Nájera, M. C. Pacheco, Synthesis 2004, 1713–1718; d) D. A.
Alonso, C. Nájera, M. C. Pacheco, Adv. Synth. Catal. 2003,
345, 1146–1158; e) D. A. Alonso, L. Botella, C. Nájera, M. C.
Pacheco, Adv. Synth. Catal. 2002, 344, 172–183.
[1] For reviews, see: a) D. S. Surry, S. L. Buchwald, Angew. Chem.
2008, 120, 6438–6461; Angew. Chem. Int. Ed. 2008, 47, 6338–
6361; b) J. S. Carey, D. Laffan, C. Thomson, M. T. Williams,
Org. Biomol. Chem. 2006, 4, 2337–2347; c) G. Bringmann, C.
Gunther, M. Ochse, O. Schupp, S. Tasler, Progress in the Chem-
istry of Organic Natural Products (Eds.: W. Herz, H. Falk,
G. W. Kirby, R. E. Moore), Springer, New York, 2001, vol. 82,
pp. 1–293.
[2] For reviews, see: a) C.-L. Shu, B.-J. Li, Z.-J. Shi, Chem. Com-
mun. 2010, 46, 677–685; b) G. P. Chiusoli, M. Catellani, M.
Costa, E. Motti, N. D. CaЈ, G. Maestri, Coord. Chem. Rev.
2010, 254, 456–469; c) L. Ackermann, Modern Arylation Meth-
ods, Wiley-VCH, Weinheim, 2009; d) B.-J. Li, S.-D. Yang, Z.-
J. Shi, Synlett 2008, 949–957.
[3]
a) C.-L. Sun, B.-J. Li, Z.-J. Shi, Chem. Rev. 2011, 111, 1293–
1314; b) W. Liu, H. Cao, A.-W. Lei, Angew. Chem. 2010, 122,
2048–2052; Angew. Chem. Int. Ed. 2010, 49, 2004–2008.
For selected examples, see: a) W. Liu, H. Cao, J. Xin, L.-Q. Jin,
A.-W. Lei, Chem. Eur. J. 2011, 17, 3588–3592; b) B. Sezen, D.
Sames, Org. Lett. 2003, 5, 3607–3610.
[4]
[5] J. Canivet, J. Yamaguchi, I. Ban, K. Itami, Org. Lett. 2009, 11,
1733–1736.
[6] H.-Q. Do, O. Daugulis, J. Am. Chem. Soc. 2007, 129, 12404–
12405.
[7] For selected examples, see: a) J. Roger, F. Pozgan, H. Doucet,
J. Org. Chem. 2009, 74, 1179–1186; b) H. A. Chiong, O. Daug-
ulis, Org. Lett. 2007, 9, 1449–1451; c) F. Bellina, S. Cauteruc-
cio, R. Rossi, Eur. J. Org. Chem. 2006, 1379–1382; d) N.
Gürbüz, I. Özdemir, B. Çetinkaya, Tetrahedron Lett. 2005, 46,
2273–2277; e) J. F. D. Chabert, L. Joucla, E. David, M. Le- [18] C. Baleizão, A. Corma, H. García, A. Leyva, J. Org. Chem.
maire, Tetrahedron 2004, 60, 3221–3230; f) B. S. Lane, D.
Sames, Org. Lett. 2004, 6, 2897–2900; g) B. Hamann-Gaudinet,
J. L. Namy, H. B. Kagan, J. Organomet. Chem. 1998, 567, 49–
55; h) C. Gozzi, L. Lavenot, K. Ilg, V. Penalva, M. Lemaire,
Tetrahedron Lett. 1997, 38, 8867–8870.
2004, 69, 439–446.
[19] For selected examples, see: a) E. Alacid, C. Nájera, J. Org.
Chem. 2009, 74, 2321–2327; b) E. Alacid, C. Nájera, Org. Lett.
2008, 10, 5011–5014; c) E. Alacid, C. Nájera, J. Org. Chem.
2008, 73, 2315–2322; d) E. Alacid, C. Nájera, Adv. Synth. Ca-
tal. 2007, 349, 2572–2584; e) L. Botella, C. Nájera, Angew.
Chem. 2002, 114, 187–189; Angew. Chem. Int. Ed. 2002, 41,
179–181.
[8] For selected examples, see: a) J. C. Lewis, A. M. Berman, R. G.
Bergman, J. A. Ellman, J. Am. Chem. Soc. 2008, 130, 2493–
2500; b) S. H. Wiedemann, J. C. Lewis, J. A. Ellman, R. G.
Bergman, J. Am. Chem. Soc. 2006, 128, 2452–2453; c) X.
Wang, B. S. Lane, D. Sames, J. Am. Chem. Soc. 2005, 127,
Received: September 25, 2011
Published Online: December 20, 2011
672
www.eurjoc.org
© 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim
Eur. J. Org. Chem. 2012, 669–672