Communication
Organic & Biomolecular Chemistry
(c) J. A. Labinger and J. E. Bercaw, Nature, 2002, 417, 507;
(d) H. M. L. Davies and J. R. Manning, Nature, 2008, 451,
417; (e) J. F. Hartwig, Nature, 2008, 455, 314; (f) X. Chen,
K. M. Engle, D.-H. Wang and J.-Q. Yu, Angew. Chem.,
Int. Ed., 2009, 48, 5094; (g) L. Ackermann, Chem. Rev.,
2011, 111, 1315; (h) J. Wencel-Delord, T. Dröge, F. Liu and
F. Glorius, Chem. Soc. Rev., 2011, 40, 4740; (i) P. B. Arockiam,
D. H. Wang and J.-Q. Yu, J. Am. Chem. Soc., 2010, 132, 460;
(c) K. Ueura, T. Satoh and M. Miura, J. Org. Chem., 2007, 72,
5362; (d) K. Ueura, T. Satoh and M. Miura, Org. Lett., 2007,
9, 1407; (e) N. Umeda, K. Hirano, T. Satoh and M. Miura,
J. Org. Chem., 2009, 74, 7094; (f) T. Ueyama, S. Mochida,
T. Fukutani, K. Hirano, T. Satoh and M. Miura, Org. Lett.,
2011, 13, 706.
C. Bruneau and P. H. Dixneuf, Chem. Rev., 2012, 112, 5879; 13 F. Chao and T. P. Loh, Chem. Commun., 2011, 47, 10458.
( j) K. M. Engle, T.-S. Mei, M. Wasa and J.-Q. Yu, Acc. Chem. 14 L. Ackermann, J. Pospech and H. K. Potukuchi, Org. Lett.,
Res., 2012, 45, 788; (k) D. A. Colby, A. S. Tsai, R. G. Bergman
and J. A. Ellman, Acc. Chem. Res., 2012, 45, 814.
3 (a) Y. Fujiwara, I. Moritani, S. Danno, R. Asano and
2012, 14, 2146.
15 J. Shao, W. Chen, M. A. Giulianotti, R. A. Houghten and
Y. Yu, Org. Lett., 2012, 14, 5452.
S. Teranishi, J. Am. Chem. Soc., 1969, 91, 7166; (b) Y. Fujiwara, 16 B. Liu, Y. Fan, Y. Gao, C. Sun, C. Xu and J. Zhu, J. Am.
I. Moritani and M. Matsuda, Tetrahedron, 1968, 24, 4819; Chem. Soc., 2013, 135, 468.
(c) I. Moritani and Y. Fujiwara, Tetrahedron Lett., 1967, 8, 17 R. C. Larock, Comprehensive Organic Transformations. A
1119.
Guide to Functional Group Preparations, VCH Publishers,
New York, 1989.
4 (a) S. Oi, Y. Ogino, S. Fukita and Y. Inoue, Org. Lett., 2002,
4, 1783; (b) L. Ackermann, Org. Lett., 2005, 7, 2229.
5 (a) R. B. Bedford, S. J. Coles, M. B. Hursthouse and
M. E. Limmert, Angew. Chem., Int. Ed., 2003, 42, 112;
(b) R. B. Bedford and M. E. Limmert, J. Org. Chem., 2003,
68, 8669; (c) T. Satoh and M. Miura, Chem. – Eur. J., 2010,
16, 11212.
6 S. Oi, E. Aizawa, Y. Ogino and Y. Inoue, J. Org. Chem., 2005,
70, 3113.
7 (a) F. Kakiuchi, S. Kan, K. Igi, N. Chatani and S. Murai,
18 (a) M. I. Fernandez-Bachiller, C. Perez, L. Monjas,
J. Rademann and M. I. Rodríguez-Franco, J. Med.
Chem., 2012, 55, 1303; (b) S. G. Das, B. Srinivasan,
D. L. Hermanson, N. P. Bleeker, J. M. Doshi, R. Tang,
W. T. Beck and C. Xing, J. Med. Chem., 2011, 54, 5937.
19 G. Aromí, L. A. Barrios, O. Roubeau and P. Gamez, Coord.
Chem. Rev., 2011, 255, 485.
20 R. F. Shuman, A. O. King and R. K. Anderson, US 5039814,
1991.
J. Am. Chem. Soc., 2003, 125, 1698; (b) F. Kakiuchi, 21 N. Yasuda, L. Xavier, D. L. Rieger, Y. Li, A. E. DeCamp and
Y. Matsuura, S. Kan and N. Chatani, J. Am. Chem. Soc.,
2005, 127, 5936.
8 X. Chen, J. J. Li, X. S. Hao, C. E. Goodhue and J.-Q. Yu,
J. Am. Chem. Soc., 2006, 128, 78.
9 Z. Shi, B. Li, X. Wan, J. Cheng, Z. Fang, B. Cao, C. Qin and
Y. Wang, Angew. Chem., Int. Ed., 2007, 46, 5554.
U. H. Dolling, Tetrahedron Lett., 1993, 34, 3211.
22 (a) M. Seki, ACS Catal., 2011, 1, 607; (b) M. Seki and
M. Nagahama, J. Org. Chem., 2011, 76, 10198; (c) M. Seki,
Synthesis, 2012, 3231; (d) E. Diers, N. Y. P. Kumar,
T. Mejuch, I. Marek and L. Ackermann, Tetrahedron, 2013,
69, 4445.
10 L. V. Desai, K. J. Stower and M. S. Sanford, J. Am. Chem. 23 H. Wang, R. Hu, H. Zhang, A. Zhou and S. Yang, Org. Lett.,
Soc., 2008, 130, 13285. 2013, 15, 5302.
11 V. S. Thirunavukkarasu, K. Parthasarathy and C. H. Cheng, 24 T. Iitsuka, P. Schaal, K. Hirano, T. Satoh, C. Bolm and
Chem. – Eur. J., 2010, 16, 1436. M. Miura, J. Org. Chem., 2013, 78, 7216.
12 (a) D. H. Wang, K. M. Engle, B. F. Shi and J.-Q. Yu, Science, 25 K. Parthasarathy, A. R. Azcargorta, Y. Cheng and C. Bolm,
2010, 327, 315; (b) B. F. Shi, Y. H. Zhang, J. K. Lam, Org. Lett., 2014, 16, 2538.
7926 | Org. Biomol. Chem., 2014, 12, 7923–7926
This journal is © The Royal Society of Chemistry 2014