| [1] Selected review and examples on chloropalladation, please see:(a) Lu, X. In Handbook of Organopalladium Chemistry for Organic Synthesis, Ed.:Negishi, E., Wiley-Interscience, New York, 2002, Vol. 2, pp. 2267~2288.
(b) Huang, L.; Wang Q.; Liu, X.; Jiang, H. Angew. Chem., Int. Ed. 2012, 51, 5696.
(c) Huang, L.; Wang, Q.; Wu, W.; Jiang, H. J. Org. Chem. 2014, 79, 7734.
(d) Zhang, Z.; Ouyang, L.; Wu, W.; Li, J.; Zhang, Z.; Jiang, H. J. Org. Chem. 2014, 79, 10734.
(e) Sun, N.; Li, Y.; Yin, G.; Jiang, S. Eur. J. Org. Chem. 2013, 2541.
(f) Zhang, Z.; Wu, W.; Liao, J.; Li, J.; Jiang, H. Chem.-Eur. J. 2015, 21, 6708.
(g) Derosa, J.; Cantu, A. L.; Boulous, M. N.; O'Duill, M. L.; Turnbull, J. L.; Liu, Z.; Torre, D. L. T.; Engle, K. M. J. Am. Chem. Soc. 2017, 139, 5183.
(h) Li, J.; Hu, W.; Li, C. Yang, S.; Wu, W.; Jiang, H. Org. Chem. Front. 2017, 4, 373.
[2] Selected examples on chloropalladation with CuCl2:(a) Huang, J.; Dong, Y.; Wang, X.; Luo, H. Chem. Commun. 2010, 46, 1035.
(b) An, Y.; Li, J.; Zhang, Z.; Li, C.; Yang, S. Chin. J. Org. Chem. 2016, 36, 2136 (in Chinese).
(安艳妮, 李建晓, 张振明, 李春生, 杨少容, 有机化学, 2016, 36, 2136.)
(c) Li, J.; Li, C.; Yang, S.; Luo, W. Chin. J. Org. Chem. 2015, 35, 898 (in Chinese).
(李建晓, 李春生, 杨少容, 罗维, 有机化学, 2015, 35, 898.)
[3] Review on the reactions with O2:(a) Wu, W.; Jiang, H. Acc. Chem. Res. 2012, 45, 1736.
(b) Wu, W.; Jiang, H. Acc. Chem. Res. 2014, 47, 2483.
(c) Wu, K.; Song, C.; Cui, D. Chin. J. Org. Chem. 2017, 37, 586 (in Chinese).
(吴空, 宋婵, 崔冬梅, 有机化学, 2017, 37, 586.)
(d) Cheng, X.; Hu, X.; Lu, Z. Chin. J. Org. Chem. 2017, 37, 251 (in Chinese).
(程骁恺, 胡新根, 陆展, 有机化学, 2017, 37, 251.)
(e) Xu, J.; Song, Q. Chin. J. Org. Chem. 2016, 36, 1151 (in Chinese).
(许健, 宋秋玲, 有机化学, 2016, 36, 1151.)
[4] For some selected examples, please see:(a) Citta, A.; Folda, A.; Bindoli, A.; Pigeon, P.; Top, S.; Vessières, A.; Salmain, M.; Jaouen, G.; Rigobello, M. P. J. Med. Chem. 2014, 57, 8849.
(b) Tehfe, M.; Dumur, F.; Graff, B.; Gigmes, D.; Fouassier, J.; Lalevée, J. Macromolecules 2013, 46, 3332.
(c) Mróz, W.; Villafiorita-Monteleone, F.; Pasini, M.; Grisci, G.; Paolino, M.; Razzano, V.; Cappelli, A.; Botta, C. Mater. Lett. 2015, 142, 197.
(d) Guerlin, A.; Dumur, F.; Dumas, E.; Miomandre, F.; Wantz, G. C.; Mayer, R. Org. Lett. 2010, 12, 2382.
[5] Selected examples, please see:(a) Mosslemin, M. H.; Shams, N.; Esteghamat, H.; Anaraki-Ardakani, H. Chin. Chem. Lett. 2013, 24, 1095.
(b) Zhou, F.; Yang, M.; Lu, X. Org. Lett. 2009, 11, 1405.
(c) Bu, X.; Hong, J.; Zhou, X. Adv. Synth. Catal. 2011, 353, 2111.
(d) Jia, X.; Petrone, D. A.; Lautens, M. Angew. Chem., Int. Ed. 2012, 51, 9870.
(e) Zeng, Z.; Ilies, L.; Nakamura, E. J. Am. Chem. Soc. 2011, 133, 17638.
(f) Huang, X.; Yang, X.; Song, R.; Li, J. J. Org. Chem. 2014, 79, 1025.
[6] Ye, S.; Gao, K.; Zhou, H.; Yang X.; Wu, J. Chem. Commun. 2009, 5406.
[7] Zhou, P.; Liu, W.; Qiu, H. Chem. Lett. 2015, 44, 1637.
[8] (a) Shi, Z.; Zhang, C.; Li, S.; Pan, D. Ding, S.; Cui, Y.; Jiao, N. Angew. Chem., Int. Ed. 2009, 48, 4572.
(b) Lafrance, M.; Fagnou, K. J. Am. Chem. Soc. 2006, 128, 16496.
[9] Zhou, F.; Han, X.; Lu, X. J. Org. Chem. 2011, 76, 1491. |
