[1] (a) Tucker. C. E.; Vries, de J. G. Top. Catal. 2002, 19, 111.
(b) Nicolaou, K. C.; Bulger, P. G.; Sarlah, D. Angew. Chem., Int. Ed. 2005, 44, 4442.
(c) Johnson, J. B.; Rovis, T. Angew. Chem., Int. Ed. 2008, 47, 840.
(d) Torborg, C.; Beller, M. Adv. Synth. Catal. 2009, 351, 3027.
(e) Wu, X.-F.; Anbarasan, P.; Neumann, H.; Beller, M. Angew. Chem., Int. Ed. 2010, 49, 9047.
(f) Li, H.-B.; Johansson Seechurn, C. C. C.; Colacot, T. J. ACS Catal. 2012, 2, 1147.
(g) Sun, F.-Y.; Lv, L.-L.; Huang, M.; Zhou, Z.-H.; Fang, X.-D. Org. Lett. 2014, 16, 5024.
(h) Greco, R.; Goessler, W.; Cantillo, D.; Kappe, C. O. ACS Catal. 2015, 5, 1303.
(i) Ruiz-Castillo, P.; Buchwald, S. L. Chem. Rev. 2016, 116, 12564.
(j) Jedinak, L.; Zatopkova, R.; Zemankova, H.; Sustkova, A.; Cankar, P. J. Org. Chem. 2017, 82, 157.
(k) Liu, C.-W.; Liu, Y.-M.; Liu, R.-Z.; Lalancette, R.; Szostak, R.; Szostak, M. Org. Lett. 2017, 19, 1434.
(l) Halima, T. B.; Vandavasi, J. K.; Shkoor, M.; Newman, S. G. ACS Catal. 2017, 7, 2176.
[2] (a) Yu, D.-G.; Shi, Z.-J. Angew. Chem., Int. Ed. 2011, 50, 7079.
(b) Hirner, J. J.; Blum, S. A. Organometallics 2011, 30, 1299.
(c) Greene, M. A.; Yonova, I. M.; Williams, F. J.; Jarvo, E. R. Org. Lett. 2012, 14, 4293.
(d) Zhang, X.-Q.; Wang, Z.-X. Synlett 2013, 24, 2081.
(e) Everson, D. A.; Buonomo, J. A.; Weix, D. J. Synlett 2014, 25, 233.
(f) Li, Q.-H.; Ding, Y.; Yang, X. J. Chin. Chem. Lett. 2014, 25, 1296.
(g) Magano, J.; Monfette, S. ACS Catal. 2015, 5, 3120.
(h) Tarui, A.; Shinohara, S.; Sato, K.; Omote, M.; Ando, A. Org. Lett. 2016, 18, 1128.
(i) Li, Q.-H.; Ding, Y.; Zhang, G.; Zhang, Z.; Mo, S. Chin. J. Org. Chem. 2016, 36, 83(in Chinese). (李清寒, 丁勇, 张刚, 张震, 莫松, 有机化学, 2016, 36, 83.)
(j) Matsubara, K.; Yamamoto, H.; Miyazaki, S.; Inatomi, T.; Nonaka, K.; Koga, Y.; Yamada, Y.; Veiros, L. F.; Kirchner, K. Organometallics 2017, 36, 255.
[3] (a) Kang, S.-K.; Yamaguchi, T.; Kim, T.-H.; Ho, P.-S. J. Org. Chem. 1996, 61, 9082.
(b) Mao, Z.-F.; Wang, Z.; Xu, Z.-Q.; Huang, F.; Yu, Z.-K.; Wang, R. Org. Lett. 2012, 14, 3854.
(c) Hornillos, V.; Perez, M.; Fananas-Mastral, M.; Feringa, B. L. J. Am. Chem. Soc. 2013, 135, 2140.
(d) Santandrea, J.; Bedard, A. C.; Collins, S. K. Org. Lett. 2014, 16, 3892.
(e) Anima Bose, A.; Mal, P. J. Org. Chem. 2015, 80, 11219.
(f) Ding, S.-Y.; Xu, L.; Li, P.-F. ACS Catal. 2016, 6, 1329.
(g) Singh, S. K.; Chandna, N.; Jain, N. Org. Lett. 2017, 19, 1322.
(h) Sahoo, H.; Mukherjee, S.; Grandhi, G. S.; Selvakumar, J.; Baidya, M. J. Org. Chem. 2017, 82, 2764.
(i) Li, Q.-H.; Ding, Y.; Zhang, G.; Zhang, Z.; Mo, S. Curr. Org. Synth. 2017, 14, 462.
[4] (a) Baba, S.; Negishi, E.-I. J. Am. Chem. Soc. 1976, 98, 6729.
(b) Negishi, E-i.; Baba, S. J. Chem. Soc., Chem Commun. 1976, 596.
[5] (a) Negishi, E-i.; Zeng, X.; Tan, Z.; Qian, M.; Hu, Q.; Huang, Z. In Metal-catalyzed Cross-Coupling Reactions, Eds.:de Meijere, A.; Diederich, F., Vol. 2, WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim, 2004.
(b) Haas, D.; Hammann, J. M.; Greiner, R.; Knochel, P. ACS Catal. 2016, 6, 1540.
[6] (a) Andrus, M. B.; Meredith, E. L.; Hicken, E. J.; Simmons, B. L.; Glancey, R. R.; Ma, W. J. Org. Chem. 2003, 68, 8162.
(b) Liu, B.; Zhou, W.-S. Org. Lett. 2004, 6, 71.
(c) Elkhayat, Z.; Safir, I.; Dakir, M.; Arseniyadis, S. Tetrahedron Asymmetry 2007, 18, 1589.
(d) Chanu, A.; Safir, I.; Basak, R.; Chiaroni, A.; Arseniyadis, S. Org. Lett. 2007, 9, 1351.
[7] Woodward, S.; Dagorne, S. Topics in Organometallic Chemistry, Vol. 41, Springer, Berlin, 2013, pp. 1~322. For the synthesis of organoaluminum compounds, see pp. 173~186, in the chapter on Preparation of organoalanes for organic synthesis, by Knochel, P.; Blimke, T.; Groll, K.; Chen, Y.-H.; For cross-coupling reactions of organoaluminum compounds, see pp. 267~276, in chapter on Organoaluminum couplings to carbonyls, imines, and halides, by Kolb, A.; Zezschwitz, P.
[8] Hallwachs, W.; Schafarik, A. Justus Liebigs Ann. Chem. 1859, 109, 206.
[9] Maruoka, K.; Yamamoto, H. Tetrahedron 1988, 44, 5001.
[10] Wang, C.; Xi, Z. Chem. Soc. Rev. 2007, 36, 1395.
[11] Uhl, W. Coord. Chem. Rev. 2008, 252, 1540.
[12] (a) Mo, S.; Shao, X.-B.; Zhang, G.; Li, Q.-H. RSC Adv. 2017, 7, 27248.
(b) Zhang, Z.; Shao, X.-B.; Zhang, G.; Li, Q.-H.; Li, X.-Y. Synthesis 2017, 49, 3643.
(c) Zhang, Z.; Mo, S.; Zhang, G.; Shao, X.-B.; Li, Q.-H.; Zhong, Y. Synlett 2017, 28, 611.
[13] Blîmke, T.; Chen, Y. H.; Peng, Z.; Knochel, P. Nat. Chem. 2010, 2, 313.
[14] (a) Ohta, A.; Inoue, A.; Watanabe, T. Heterocycles 1984, 22, 2317.
(b) Ohta, A.; Inoue, A.; Ohtsuka, K.; Watanabe, T. Heterocycles 1985, 23, 133.
[15] Hirota, K.; Isobe, Y.; Maki, Y. J. Chem. Soc., Perkin Trans. 1 1989, 2513.
[16] Crisp, G. T.; Papadopoulos, S. Aust. J. Chem. 1989, 42, 279.
[17] Hirota, K.; Kitade, Y.; Kanbe, Y.; Maki, Y. J. Org. Chem. 1992, 57, 5268.
[18] Mangalagiu, I.; Benneche, T.; Undheim, K. Tetrahedron Lett. 1996, 37, 1309.
[19] Blum, J.; Gelman, D.; Baidossi, W.; Shakh, E.; Rosenfeld, A.; Aizenshtat, Z.; Wassermann, B. C.; Frick, M.; Heymer, B.; Schutte, S.; Wernik, S.; Herbert, S. H. J. Org. Chem. 1997, 62, 8681.
[20] Biswas, K.; Chapron, A.; Cooper, T.; Fraser, P. K, Novak, A.; Prieto, O.; Woodward, S. Pure Appl. Chem. 2006, 78, 511.
[21] Vinogradov, A.; Woodward, S. Org. Synth. 2010, 87, 104.
[22] Cooper, T.; Novak, A.; Humphreys, L. D.; Walker, M. D.; Woodward, S. Adv. Synth. Catal. 2006, 348, 686.
[23] Conte, V.; Fiorani, G.; Floris, B.; Galloni, P.; Woodward, S. Appl. Catal. A:Gen. 2010, 381, 161.
[24] Baba, S.; Negishi, E.-I. J. Am. Chem. Soc. 1976, 98, 6729.
[25] Negishi, E-i.; Baba, S. J. Chem. Soc., Chem. Commun. 1976, 596.
[26] Negishi, E.-I.; Okukado, N.; King, A. O.; Van Horn, D. E.; Spiegel, B. I. J. Am. Chem. Soc. 1978, 100, 2254.
[27] Zeng, F.; Negishi, E.-I. Org. Lett. 2001, 3, 719.
[28] Qian, M.; Huang, Z.; Negishi, E.-I. Org. Lett. 2004, 6, 1531.
[29] Chen, Q.-Y.; He, Y.-B. Chin. J. Chem. 1990, 8, 451.
[30] Zweifel, G.; Miller, R. L. Organic Reactions, Vol. 32, John Wileys, New York, 1984, p. 375.
[31] Samaritani, S.; Signore, G.; Malanga, C.; Menicagli, R. Tetrahedron 2005, 61, 14475.
[32] Andrews, P.; Latham, C. M.; Magre, M.; Willcox, D.; Woodward, S. Chem. Commun. 2013, 49, 1488.
[33] Fang, H.; Yang, Z.-Y.; Zhang, L.-J.; Wang, W.; Li, Y.-M.; Xu, X.-L.; Zhou, S.-L. Org. Lett. 2016, 18, 6022.
[34] Feuvrie, C.; Blanchet, J.; Bonin, M.; Micouin, L. Org. Lett. 2004, 6, 2333.
[35] Wang, B.; Bonin, M.; Micouin, L. Org. Lett. 2004, 6, 3481.
[36] Ku, S.-L.; Hui, X.-P.; Chen, C.-A.; Kuo, Y.-Y.; Gau, H.-M. Chem Commun. 2007, 3847.
[37] Shu, W.-T.; Zhou, S.-L.; Gau, H.-M. Synthesis 2009, 4075.
[38] Gao, H. J.; Knochel, P. Synlett 2009, 1321.
[39] Blümke, T.; Chen, Y.-H. Peng, Z.; Knochel, P. Nat. Chem. 2010, 2, 313.
[40] Groll, K.; Blümke, T. D.; Unsinn, A.; Haas, D.; Knochel, P. Angew. Chem., Int. Ed. 2012, 51, 11157.
[41] Chen, X.; Zhou, L.-M.; Li, Y.-M.; Xie, T.; Zhou, S.-L. J. Org. Chem. 2014, 79, 230.
[42] (a) Necas, D.; Kotora, M.; Clsarova, I. Eur. J. Org. Chem. 2004, 6, 1280.
(b) Necas, D.; Drabina, P.; Sedlak, M.; Kotora, M. Tetrahedron Lett. 2007, 48, 4539.
(c) Kawamura, S.; Ishizuka, K.; Takaya, H.; Nakamura, M. Chem. Commun. 2010, 46, 6054.
(d) Kawamura, S.; Kawabata, T.; Ishizuka, K.; Nakamura, M. Chem. Commun. 2012, 48, 9376.
[43] (a) Wunderlich, S. H.; Knochel, P. Angew. Chem., Int. Ed. 2009, 48, 1501.
(b) Blümke, T. D.; Groll, K.; Karaghiosoff, K.; Knochel, P. Org Lett. 2011, 13, 6440.
(c) Zhou, S.-L.; Yang, Z.-Y.; Chen, X.; Li, Y.-M.; Zhang, L.-J.; Fang, H.; Wang, W.; Zhu, X.-C.; Wang, S. W. J. Org. Chem. 2015, 80, 6323.
(d) Shrestha, B.; Thapa, S.; Gurung, S. K.; Pike, R. A. S.; Giri, R. J. Org. Chem. 2016, 81, 787.
[44] (a) Biradar, D. B.; Gau, H.-M. Chem. Commun. 2011, 47, 10467.
(b) Biradar, D. B.; Gau, H.-M. Org. Biomol. Chem. 2012, 10, 4243.
(c) He, F.; Wang, Z.-X. Tetrahedron 2017, 73, 4450.
(d) Mo, S.; Shao, X.-B.; Zhang, G.; Li, Q.-H. RSC Adv. 2017, 7, 27243. |