(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.
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.
(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.
