[1] (a) Jie, M. S. F. L. K.; Pasha, M. K.; Syed-Rahmatulla, M. S. K. Nat. Prod. Rep. 1997, 14, 163.
(b) Fürstner, A.; Nevado, C.; Waser, M.; Tremblay, M.; Chevrier, C.; Teplý, F.; Aïssa, C.; Moulin, E.; Müller, O. J. Am. Chem. Soc. 2007, 129, 9150.
(c) Wilson, M. C.; Nam, S.-J.; Gulder, T. A. M.; Kauffman, C. A.; Jensen, P. R.; Fenical, W.; Moore, B. S. J. Am. Chem. Soc. 2011, 133, 1971.
[2] (a) Macklin, T. K.; Micalizio, G. C. Nat. Chem. 2010, 2, 638.
(b) Sharma, R. K.; RajanBabu, T. V. J. Am. Chem. Soc. 2010, 132, 3295.
(c) Trost, B. M.; Luan, X. J. Am. Chem. Soc. 2011, 133, 1706.
(d) McCammant, M. S.; Liao, L.; Sigman, M. S. J. Am. Chem. Soc. 2013, 135, 4167.
(e) Jin, W.; Yang, Q.; Wu, P.; Chen, J.; Yu, Z. Adv. Synth. Catal. 2014, 360, 2097.
[3] (a) Miyaura, N.; Yano, T.; Suzuki, A. Tetrahedron Lett. 1980, 21, 2865.
(b) Kabalka, G. W.; Al-Masum, M. Org. Lett. 2006, 8, 11.
(c) Lee, Y.; Akiyama, K.; Gillingham, D. G.; Brown, M. K.; Hoveyda, A. H. J. Am. Chem. Soc. 2008, 130, 446.
(d) Akiyama, K.; Gao, F.; Hoveyda, A. H. Angew. Chem., Int. Ed. 2010, 49, 419.
(e) Gao, F.; Lee, K. P.; McGrath, Y.; Hoveyda, A. H. J. Am. Chem. Soc. 2010, 132, 14315.
(f) Gao, F.; Carr, J. L.; Hoveyda, A. H. Angew. Chem., Int. Ed. 2012, 51, 6613.
(g) Huang, Y.; Fañanás-Mastral, M.; Minnaard, A. J.; Feringa, B. L. Chem. Commun. 2013, 49, 3309.
(h) Hamilton, J. Y.; Sarlah, D.; Carreira, E. M. J. Am. Chem. Soc. 2013, 135, 994.
(i) Gao, F.; Carr, J. L.; Hoveyda, A. H. J. Am. Chem. Soc. 2014, 136, 2149.
(j) Sidera, M.; Fletcher, S. P. Chem. Commun. 2015, 51, 5044.
(k) Zhurkin, F. E.; Hu, X. J. Org. Chem. 2016, 81, 5795.
(l) Yang, B.; Wang, Z.-X. J. Org. Chem. 2017, 82, 4542.
[4] (a) Cornella, J.; Zarate, C.; Martin, R. Chem. Soc. Rev. 2014, 43, 8081.
(b) Matsubara, R.; Jamison, T. F. J. Am. Chem. Soc. 2010, 132, 6880.
(c) Matsubara, R.; Jamison, T. F. Chem. Asian J. 2011, 6, 1860.
(d) Ye, K.-Y.; He, H.; Liu, W.-B.; Dai, L.-X.; Helmchen, G.; You, S.-L. J. Am. Chem. Soc. 2011, 133, 19006.
(e) Hamilton, J. Y.; Sarlah, D.; Carreira, E. M. J. Am. Chem. Soc. 2014, 13 6, 2006.
(f) Gumrukcu, Y.; de Bruin, B.; Reek, J. N. H. Chem.-Eur. J. 2014, 20, 10905.
[5] (a) Thadani, A. N.; Rawal, V. H. Org. Lett. 2002, 4, 4317.
(b) Chen, X.; Chen, D.; Lu, Z.; Kong, L.; Zhu, G.-G. J. Org. Chem. 2011, 76, 6338.
(c) Wen, Y.; Jiang, H.-F. Tetrahedron Lett. 2013, 54, 4034.
(d) Todd, D. P.; Thompson, B. B.; Nett, A. J.; Montgomery, J. J. Am. Chem. Soc. 2015, 137, 12788
(e) Mateos, J.; Rivera-Chao, E.; Fañanás-Mastral, M. ACS Catal. 2017, 7, 5340.
[6] For rare examples for terminal skipped dienes synthesis, see:(a) Basavaiah, D.; Kumaragurubaran, N.; Sharada, D. S. Tetrahedron Lett. 2001, 42, 85.
(b) Basavaiah, D.; Sharada, D. S.; Kumaragurubaran, N.; Reddy, R. M. J. Org. Chem. 2002, 67, 7135.
(c) Li, Y.-Q.; Wang, H.-J.; Huang, Z.-Z. J. Org. Chem. 2016, 81, 4429.
[7] For reviews, see:(a) Edmonds, M.; Abell, A. In Modern Carbonyl Olefination, Ed.:Takeda, T., Wiley-VCH, Weinheim, Germany, 2004, pp. 1~17.
(b) Ju, Y. In Modern Organic Reactions, Vol. 3, Eds.:Hu, Y.-F.; Lin, G.-Q., Chemical Industry Press, Beijing, 2008, pp. 413~460(in Chinese). (巨勇, 现代有机反应, 主编:胡跃飞, 林国强, 第3卷, 化学工业出版社, 北京, 2008, pp. 413~460.)
(c) Gu, Y.; Tian, S.-K. Top. Curr. Chem. 2012, 327, 197.
[8] (a) Liu, W.-B.; He, H.; Dai, L.-X.; You, S.-L. Chem.-Eur. J. 2010, 16, 7376.
(b) Ma, X.-T.; Wang, Y.; Dai, R.-H.; Liu, C.-R.; Tian, S.-K. J. Org. Chem. 2013, 78, 11071.
[9] For reviews, see:(a) Bandini, M. Angew. Chem., Int. Ed. 2011, 50, 994.
(b) Sundararaju, B.; Achard, M.; Bruneau, C. Chem. Soc. Rev. 2012, 41, 4467.
(c) Butta, N. A.; Zhang, W. Chem. Soc. Rev. 2015, 44, 7929.
(d) Ferraccioli, R.; Pignataro, L. Curr. Org. Chem. 2015, 19, 106. For selected recent examples:
(e) Shen, D.; Chen, Q.; Yan, P.; Zeng, X.; Zhong, G. Angew. Chem., Int. Ed. 2017, 129, 3290.
(f) Wu, F.-P.; Peng, J.-B.; Fu, L.-Y.; Qi, X.; Wu, X.-F. Org. Lett 2017, 19, 5474.
(g) Su, Y.-L.; Han, Z.-Y.; Li, Y.-H.; Gong, L.-Z. ACS Catal. 2017, 7, 7917.
(h) Jia, X.-G.; Guo, P.; Duan, J.; Shu, X.-Z. Chem. Sci. 2018, 9, 640.
[10] Ma, X.; Yu, J.; Han, C.; Zhou, Q.; Ren, M.; Li, L.; Tang, L. Adv. Synth. Catal. 2019, https://doi.org/10.1002/adsc.201801266.
[11] (a) Ma, X.-T.; Dai, R.-H.; Zhang, J.; Gu, Y.; Tian, S.-K. Adv. Synth. Catal. 2014, 356, 2984.
(b) Ma, X.; Yu, L.; Su, C.; Yang, Y.; Li, H.; Xu, Q. Adv. Synth. Catal. 2017, 359, 1649.
(c) Ma, X.; Xu, Q.; Li, H.; Su, C.; Yu, L.; Zhang, X.; Cao, H.; Han, L.-B. Green Chem. 2018, 20, 3408.
(d) Ma, X.; Su, C.; Xu, Q. Top. Curr. Chem. 2016, 374, 27.
[12] Kaszynski, P.; Friedli, A. C.; Michl, J. J. Am. Chem. Soc. 1992,114, 601.
[13] Liu, H.-J.; Wynn, H. Tetrahedron Lett. 1982, 23, 3151. |