[1] (a) Shi, M.; Wang, F.; Zhao, M.-X.; Wei, Y. The Chemistry of the Morita-Baylis-Hillman Reaction, RSC Catalysis Series, 2011.(b) For a recent example, see: Yi, F.; Zhang, X.; Sun, H.; Chen, S. Acta Chim. Sinica 2012, 70, 741. (易封萍, 张旋, 孙海洋, 陈世洪, 化学学报, 2012, 70, 741.)[2] For selected reviews, see: (a) Basavaiah, D.; Reddy, B. S.; Badsara, S. S. Chem. Rev. 2010, 110, 5447.(b) Singh, V.; Batra, S.;Tetrahedron 2008, 64, 4511.[3] For selected reviews, see: (a) Denmark, S. E.; Beutner, G. L. Angew. Chem., Int. Ed. 2008, 47, 1560.(b) Baidya, M.; Remennikov, G. Y.; Mayer, P.; Mayr, H. Chem. Eur. J. 2010, 16, 1365.(c) Du, Y.; Lu, X.; Zhang, C. Angew. Chem., Int. Ed. 2003, 42, 1035.[4] Steenis, D. J.; Marcelli, T.; Lutz, M.; Spek, A. L.; Maarseveen, J. H.; Hiemstra, H. Adv. Synth. Catal. 2007, 349, 281.[5] (a) Trost, B. M.; Tsui, H.-C.; Toste, F. D. J. Am. Chem. Soc. 2000, 122, 3534.(b) Trost, B. M.; Maehaeek, M. R.; Tsui, H.-C. J. Am. Chem. Soc. 2005, 127, 7014.(c) Trost, B. M.; Thiel, O. R.; Tsui, H.-C. J. Am. Chem. Soc. 2002, 124, 11616.(d) Trost, B. M.; Thiel, O. R.; Tsui, H.-C. J. Am. Chem. Soc. 2003, 125, 13155.[6] (a) Du, Y.; Han, X.; Lu, X. Tetrahedron Lett. 2004, 45, 4967.(b) Peng, J.; Huang, X.; Jiang, L.; Cui, H.-L.; Chen, Y.-C. Org. Lett. 2011, 13, 4584.(c) Sun, X.; Peng, J.; Zhang, S.; Zhou, Q.; Dong, L.; Chen, Y.-C. Acta Chim. Sinica 2012, 70, 1682. (孙峋皓, 彭景, 张叔阳, 周清清, 董琳, 陈应春, 化学学报, 2012, 70, 1682.)[7] Huang, F. C. US 4668694 [Chem. Abstr. 1987, 107, 59027].[8] (a) Brogden, R. N. Drug. 1986, 32, 60.(b) Costa, D.; Marques, A. P.; Reis, R. L.; Lima, J. L. F. C.; Fernandes, E. Free Radical Biol. Med. 2006, 40, 632.[9] Sujatha, K.; Shanthi, G.; Selvam, N. P.; Manoharan, S.; Perumal, P. T.; Rajendran, M. Bioorg. Med. Chem. Lett. 2009, 19, 4501.[10] (a) Casas, J. S.; Castellano, E. E.; Ellena, J.; Garcia-Tasende, M.; Perez-Paralles, M. L.; Sanchez, A.; Sanchez-Gonzalez, A.; Sordo, J.; Touceda, A. J. Inorg. Biochem. 2008, 102, 33.(b) Park, H. J.; Lee, K.; Park, S. J.; Ahn, B.; Lee, J. C.; Cho, H.; Lee, K. I. Bioorg. Med. Chem. Lett. 2005, 15, 3307.(c) Tripathy, R.; Reiboldt, A.; Messina, P. A.; Iqbal, M.; Singh, J.; Bacon, E. R.; Angeles, T. S.; Yang, S. X.; Albmo, M.; Robinson, C.; Chang, H.; Ruggeri, B. A.; Mallamo, J. P. Bioorg. Med. Chem. Lett. 2006, 16, 2158.[11] (a) Bondock, S.; Rabie, R.; Etman, H. A.; Fadda, A. A. Eur. J. Med. Chem. 2008, 43, 2122.(b) Abdel-Aziz, M.; Abuo-Rahma, G. E. A.; Hassan, A. A. Eur. J. Med. Chem. 2009, 44, 3480.[12] Gogoi, S.; Zhao, C.-G. Tetrahedron Lett. 2009, 50, 2252.[13] Gogoi, S.; Zhao, C.-G.; Ding, D. Org. Lett. 2009, 11, 2249.[14] Liao, Y.-H.; Chen, W.-B.; Wu, Z.-J.; Du, X.-L.; Cun, L.-F.; Zhang, X.-M.; Yuan, W.-C. Adv. Synth. Catal. 2010, 352, 827.[15] Alba, A. N.; Zea, A.; Valero, G.; Calbet, T.; Font-Bardia, M.; Mazzanti, A.; Moyano, A.; Rios, R. Eur. J. Org. Chem. 2011, 1318.[16] Mazzanti, A.; Calbet, T.; Font-Bardia, M.; Moyano, A.; Rios, R. Org. Biomol. Chem. 2012, 10, 1645.[17] Yang, Z. G.; Wang, Z.; Bai, S.; Liu, X. H.; Lin, L. L.; Feng, X. M. Org. Lett. 2011, 13, 596.[18] Wang, Z.; Yang, Z. G.; Chen, D. H.; Liu, X. H.; Lin, L. L.; Feng, X. M. Angew. Chem., Int. Ed. 2011, 50, 4928.[19] Wang, Z.; Chen, Z. L.; Bai, S.; Li, W.; Liu, X. H.; Lin, L. L.; Feng, X. M. Angew. Chem., Int. Ed. 2012, 51, 2776.[20] For selected reviews on the MBH reactions, see: (a) Basavaiah, D.; Reddy, B. S.; Badsara, S. S. Chem. Rev. 2010, 110, 5447.(b) Langer, P. Angew. Chem., Int. Ed. 2000, 39, 3049.(c) Basavaiah, D.; Rao, A. J.; Satyanarayana, T. Chem. Rev. 2003, 103, 811.(d) Masson, G.; Housseman, C.; Zhu, J. Angew. Chem., Int. Ed. 2007, 46, 4614.(e) Basavaiah, D.; Rao, K. V.; Reddy, R. J. Chem. Soc. Rev. 2007, 36, 1581.(f) Shi, Y.-L.; Shi, M. Eur. J. Org. Chem. 2007, 2905.(g) Ma, G.-N.; Jiang, J.-J.; Shi, M.; Wei, Y. Chem. Commun. 2009, 5496.(h) Declerck, V.; Martinez, J.; Lamaty, F. Chem. Rev. 2009, 109. For recent reviews on the utilization of MBH adducts, see:(i) Rios, R. Catal. Sci. Technol. 2012, 2, 267.(j) Liu, T.-Y.; Xie, M.; Chen, Y.-C. Chem. Soc. Rev. 2012, 41, 4101.[21] Wang, S.-L. Master Thesis, Lanzhou University, Lanzhou, 2013. (王守磊, 硕士论文, 兰州大学, 兰州, 2013.)[22] (a) Sun, W.; Hong, L.; Liu, C.; Wang, R. Org. Lett. 2010, 12, 3914.(b) Zhong, F.; Luo, J.; Chen, G.-Y.; Dou, X.; Lu, Y. J. Am. Chem. Soc. 2012, 134, 10222.[23]The alkene geometry in the product was determined by NOESY experiment (see supporting information for details). The absolute configurations of the products were not assigned. |