[1] (a) Neilsen, S. F.; Neilsen, E. O.; Olsen, G. M.; Liljefors, T.; Peters, D. J. Med. Chem. 2000, 43, 2217. (b) Navarro, R.; Perrino, M. P.; Tardajos, M. G.; Reinecke, H. Macromolecules 2010, 43, 2377.[2] Guilarte, V.; Ferna?ndez-Rodríguez, M. A.; García-García, P.; Hernando, E.; Sanz, R. Org. Lett. 2011, 13, 5100. [3] Taniguchi, N. J. Org. Chem. 2004, 69, 6904. [4] (a) Kwong, F. Y.; Buchwald, S. L. Org. Lett. 2002, 4, 3517. (b) Lv, X.; Bao, W.-L. J. Org. Chem.2007, 72, 3863. (c) Sperotto, E.; Klink, G. P. M.; Vries, J. G.; Koten, G. J. Org. Chem. 2008, 73, 5625. [5] (a) Yudin, A. K. Catalyzed Carbon-Heteroatom Bond Formation, Wiley-VCH, Weinheim, 2010, pp. 69~113. (b) Bichler, P.; Love, J. A. Top. Organomet. Chem. 2010, 31, 39. (c) Eichman, C. C.; Stambuli, J. P. Molecules 2011, 16, 590. [6] Jiang, Y.; Qin, Y.; Xie, S.; Zhang, X.; Dong, J.; Ma, D. Org. Lett. 2009, 11,5250. [7] Ke, F.; Qu, Y.; Jiang, Z.; Li, Z.; Wu, D.; Zhou, X. Org. Lett. 2011, 13, 545. [8] (a) Reddy, K. H. V.; Reddy, V. P.; Shankar, J.; Madhav, B.; Kumar, B. S. P. A.; Nageswar, Y. V. D. Tetrahedron Lett. 2011, 52, 2679. (b) Firouzabadi, H.; Iranpoor, N.; Gholinejad, M. Adv. Synth. Catal. 2010, 119. [9] Jiang, Z.; She, J.; Lin, X.-F. Adv. Synth. Catal. 2009, 2558. [10] Kumar, S.; Engman, L. J. Org. Chem. 2006, 71, 5400. [11] Herradura, P. S.; Pendola, K. A.; Guy, R. K. Org. Lett. 2000, 2, 2019. [12] Jammi, S.; Sakthivel, S.; Rout, L.; Mukherje, T.; Mandal, S.; Mitra, R.; Sha, P.; Punniyamurthy, T. J. Org. Chem. 2009, 74, 1971. [13] Savarin, C.; Srogl, J.; Liebeskind, L. S. Org. Lett. 2002, 4, 4309. [14] (a) Taniguchi, N. J. Org. Chem. 2007, 72, 1241. (b) Taniguchi, N. Synlett 2006, 1351. (c) Luo, P.-S.; Wang, F.; Li, J.-H.; Tang, R.-Y.; Zhong, P. Synthesis 2009, 921. [15] Xu, H.; Zhao, Y.; Feng, T.; Feng,Y. J. Org. Chem. 2012, 77, 2878. [16] (a) Yang, M.; Zhu, C.; Yuan, F.; Huang, Y.; Pan, Y. Org. Lett. 2005, 7, 1927. (b) Yang, M.; Liu, F. J. Org. Chem. 2007, 72, 8969. (c) Yang, M.; Yan, G.; Zheng, Y. Tetrahedron Lett. 2008, 49, 6471. (d) Yang, M.; Pei, J.; Yan, G.; Zheng, Y. Lett. Org. Chem. 2011, 8, 587. [17] Hall, D. G.; Suzuki, A. In Boronic Acids, Vol. 2, Ed.: Hall, D. G., Wiley-VCH Verlag, Weinheim, 2011, p. 9. [18] In metal-catalyzed organic reaction using organoboronic acid, water has been added: (a) Miyaura, N.; Suzuki, A. Chem. Rev. 1995, 95, 2457. (b) Hayashi, T.; Yamasaki, K. Chem. Rev. 2003, 103, 2829. Water can improve metal-catalyzed organic reaction using organoboron compounds, see: (c) Guan, B.-T; Wang, Y.; Li, B.-J.; Yu, D.-G.; Shi, Z. -J. J. Am. Chem. Soc. 2008, 130, 14468. And also please see Ref.[14a]. [19] (a) Liu, L.-F.; Zhang, Y.-H.; Wang, Y. G. J. Org. Chem. 2005, 70, 6122. (b) Xin, B.-W. Ph.D. Dissertation, Zhejiang University, Hangzhou, 2010, p. 18 (in Chinese). (辛炳炜, 博士论文, 浙江大学, 杭州, 2010, p. 18.) |