[1] Cheng, X. H.; Hii, K. K. Tetrahedron 2001, 57, 5445.
[2] Kunz, K. R.; Iyengar, B. S.; Dorr, R. T.; Alberts, D. S.; Remers, W. A. J. Med. Chem. 1991, 34, 2281.
[3] Lockhoff, O.; Stadler, P. Carbohydr. Res. 1998, 314, 13.
[4] Takeuchi, Y.; Chang, M. R.; Hashigaki, K.; Yamato, M. Chem. Pharm. Bull. 1991, 39, 1629.
[5] (a) Eliel, E. L.; Daignault, R. A. J. Org. Chem. 1965, 30, 2450~2451.
(b) Glacet, C.; Veron, D. Bull. Soc. Chim. Fr. 1965, 1789.
[6] For selected reviews on visible-light photoredox catalysis, see:
(a) Narayanam, J. M. R.; Stephenson, C. R. J. Chem. Soc. Rev. 2011, 40, 102.
(b) Xuan, J.; Xiao, W. J. Angew. Chem., Int. Ed. 2012, 51, 6828.
(c) Shi, L.; Xia, W. Chem. Soc. Rev. 2012, 41, 7687.
(d) Xi, Y.; Yi, H.; Lei, A. Org. Biomol. Chem. 2013, 11, 2387.
(e) Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Chem. Rev. 2013, 113, 5322.
(f) Dai, X. J.; Xu, X. L.; Li, X. N. Chin. J. Org. Chem. 2013, 33, 2406 (in Chinese).(戴小军, 许孝良, 李小年, 有机化学, 2013, 33, 2406.)
(g) Guan, B. C.; Xu, X. L.; Wang, H; Li, X. N. Chin. J. Org. Chem. 2016, 36, 1564 (in Chinese).(关保川, 许孝良, 王红, 李小年, 有机化学, 2016, 36, 1564.)
(h) Shaw, M. H.; Twilton, J.; MacMillan, D. W. C. J. Org. Chem. 2016, 81, 6898.
(i) Skubi, K. L.; Blum, T. R.; Yoon. T. P. Chem. Rev. 2016, 116, 10035.
(j) Nakajima, K.; Miyake, Y.; Nishibayashi, Y. Acc. Chem. Res. 2016, 49, 1946.
(k) Liu, W.; Zheng, X. Y.; Zeng, J. G.; Cheng, P. Chin. J. Org. Chem. 2017, 37, 1 (in Chinese).(刘薇, 郑昕宇, 曾建国, 程辟, 有机化学, 2017, 37, 1.)
(l) Ruan, L. H.; Dong, Z. C.; Chen, C. X.; Wu, S.; Sun, J. Chin. J. Org. Chem. 2017, 37, 2544 (in Chinese).(阮利衡, 董振诚, 陈春欣, 吴爽, 孙京, 有机化学, 2017, 37, 2544.)
(m) Dai, X. Q.; Zhu, Y. B.; Xu, X. L.; Weng, J. Q. Chin. J. Org. Chem. 2017, 37, 577 (in Chinese).(戴小强, 朱亚波, 许孝良, 翁建全, 有机化学, 2017, 37, 577.)
(n) Xu, W. X.; Dai, X. Q; Xu, H. J.; Weng, J. Q. Chin. J. Org. Chem. 2018, 38, 2807 (in Chinese).(徐雯秀, 戴小强, 徐涵靖, 翁建全, 有机化学, 2018, 38, 2807.)
(o) Bai, Q. F.; He, J. Y.; Zhu, X. Q.; Feng, G. F.; Jin, C. A. Chin. J. Org. Chem. 2019, 39, 527 (in Chinese).(白其凡, 何静耀, 祝小青, 冯高峰, 金城安, 有机化学, 2019, 39, 527.)
[7] For examples of visible-light photoredox catalysis, see:
(a) Nicewicz, D. A.; MacMillan, D. W. C. Science 2008, 322, 77.
(b) DiRocco, D. A.; Rovis, T. J. Am. Chem. Soc. 2012, 134, 8094.
(c) Rono, L. J.; Yayla, H. G.; Wang, D. Y.; Armstrong, M. F.; Knowles, R. R. J. Am. Chem. Soc. 2013, 135, 17735.
(d) Alonso, R.; Bach, T. Angew. Chem., Int. Ed. 2014, 53, 4368.
(e) Huo, H. H.; Shen, X. D.; Wang, C. Y.; Zhang, L. L.; Rose, P.; Chen, L. A.; Harms, K.; Marsch, M.; Hilt, G.; Meggers, E. Nature 2014, 515, 100.
(f) Espelt, L. R.; McPherson, I. S.; Wiensch, E. M. Yoon, T. P. J. Am. Chem. Soc. 2015, 137, 2452.
(g) Ding, W.; Lu, L. Q.; Zhou, Q. Q.; Wei, Y.; Chen, J. R.; Xiao, W. J. J. Am. Chem. Soc. 2017, 139, 63.
(h) Ding, W.; Lu, L. Q.; Zhou, Q. Q.; Wei, Y.; Chen, J. R.; Xiao, W. J. J. Am. Chem. Soc. 2017, 139, 63.
(i) Zhou, Q. Q.; Liu, D.; Xiao, W. J.; Lu, L. Q. Acta Chim. Sinica 2017, 75, 110 (in Chinese).(周泉泉, 刘丹, 肖文精, 陆良秋, 化学学报, 2017, 75, 110.)
(j) Wu, Z. J.; Wang, J. Acta Chim. Sinica 2017, 75, 74 (in Chinese).(吴自俊, 汪舰, 化学学报, 2017, 75, 74.)
(k) Wu, J.; Li, J. W.; Li, H.; Zhu, C. Y. Chin. J. Org. Chem. 2017, 37, 2203 (in Chinese).(吴江, 李嘉雯, 李昊, 朱纯银, 有机化学, 2017, 37, 2203.)
(l) Ye, H; Xiao, C; Lu, L. Q. Chin. J. Org. Chem. 2018, 38, 1897 (in Chinese).(叶辉, 肖聪, 陆良秋, 有机化学, 2018, 38, 1897.)
[8] (a) Kohls, P.; Jadhav, D.; Pandey, G.; Reiser, O. Org. Lett. 2012, 14, 672.
(b) Miyake, Y.; Nakajima, K.; Nishibayashi, Y. J. Am. Chem. Soc. 2012, 134, 3338.
(c) Espelt, L. R.; McPherson, I. S.; Wiensch, E. M.; Yoon, T. P. J. Am. Chem. Soc. 2015, 137, 2452.
[9] Tan, Y. Q.; Yuan, W.; Gong, L.; Meggers, E. Angew. Chem., Int. Ed. 2015, 54, 13045.
[10] (a) Maity, S.; Zhu, M. Z.; Shinabery, R. S.; Zheng, N. Angew. Chem., Int. Ed. 2012, 51, 222.
(b) Nguyen, T. H.; Maity, S.; Zheng, N. Beilstein J. Org. Chem. 2014, 10, 975.
(c) Staveness, D.; Sodano, T. M.; Li, K. J.; Burnham, E. A.; Jackson, K. D.; Stephenson, C. R. J. Chem 2019, 5, 1.
[11] (a) Russell, G. A.; Weiner, S. A. J. Am. Chem. Soc. 1967, 89, 6623.
(b) Ma, J. J.; Rosales, A. R.; Huang, X. Q.; Harms, K.; Riedel R.; Wiest, O.; Meggers, E. J. Am. Chem. Soc. 2017, 139, 17245.
[12] Prier, C. K.; Rankic, D. A.; MacMillan, D. W. C. Chem. Rev. 2013, 113, 5322.
[13] Reger, D.; Haines P.; Heinemann, F. W.; Guldi, D. M.; Jux, N. Angew. Chem., Int. Ed. 2018, 57, 5938.
[14] Cui, W.; Loeppky, R. N. Tetrahedron 2001, 57, 2953.