1 3
Topics in Current Chemistry (2019) 377:37
in one molecule will be developed [25, 26]. In addition, the application of these
asymmetric photochemical reactions to the production of chiral drugs and pesticides
is also expected in the near future.
References
1. Nicewicz DA, MacMillan DWC (2008) Science. 322:77–80
2. Nagib DA, Scott ME, MacMillan DWC (2009) J Am Chem Soc 131:10875–10877
3. Shih H-W, Vander Wal MN, Grange RL, MacMillan DWC (2010) J Am Chem Soc
132:13600–13603
4. Pirnot MT, Rankic DA, Martin DBC, MacMillan DWC (2013) Science 339:1593–1596
5. Zhu Y, Zhang L, Luo S (2014) J Am Chem Soc 136:14642–14645
6. Zhang W, Zhu Y, Zhang L, Luo S (2018) Chin J Chem 36:716–722
7. Welin ER, Warkentin AA, Conrad JC, MacMillan DWC (2015) Angew Chem Int Ed 54:9668–9672
8. Capacci AG, Malinowski JT, McAlpine NJ, Kuhne J, MacMillan DWC (2017) Nat Chem
9:1073–1077
9. Li M, Sang Y, Xue X-S, Cheng J-P (2018) J Org Chem 83:3333–3338
10. Larionov E, Mastandrea MM, Pericàs MA (2017) ACS Catal 7:7008–7013
11. Wang D, Zhang L, Luo S (2017) Org Lett 19:4924–4927
12. Yang Q, Zhang L, Ye C, Luo S, Wu L-Z, Tung C-H (2017) Angew Chem Int Ed 56:3694–3698
13. Zhao J-J, Zhang H-H, Shen X, Yu S (2019) Org Lett 21:913–916
14. Murphy JJ, Bastida D, Paria S, Fagnoni M, Melchiorre P (2016) Nature 532:218–222
15. DiRocco DA, Rovis T (2012) J Am Chem Soc 134:8094–8097
16. Feng Z-J, Xuan J, Xia X-D, Ding W, Guo W, Chen J-R, Zou Y-Q, Lu L-Q, Xiao W-J (2014) Org
Biomol Chem 12:2037–2040
17. Rono L, Yayla J, Wang H-G, Armstrong DY, Knowles MF, Robert R (2013) J Am Chem Soc
135:17735–17738
18. Ding W, Zhou Q-Q, Xuan J, Li T-R, Lu L-Q, Xiao W-J (2014) Tetrahedron Lett 55:4648–4652
19. Hepburna H-B, Melchiorre P (2016) Chem Commun 52:3520–3523
20. Bergonzini G, Schindler CS, Wallentin CJ, Jacobsen EN, Stephenson CR (2014) J Chem Sci
5:112–116
21. Gentry EC, Rono LJ, Hale ME, Matsuura R, Knowles RR (2018) J Am Chem Soc
2018(140):3394–3402
22. Uraguchi D, Kinoshita N, Kizu T, Ooi T (2015) J Am Chem Soc 137:13768–13771
23. Kizu T, Uraguchi D, Ooi T (2016) J Org Chem 81:6953–6958
24. Lenhart D, Bauer A, Pçthig A, Bach T (2016) Chem Eur J 22:6519–6523
25. Ding W, Lu L-Q, Zhou Q-Q, Wei Y, Chen J-R, Xiao W-J (2017) J Am Chem Soc 139:63–66
26. Skubi KL, Kidd JB, Jung H, Guzei IA, Baik M, Yoon TP (2008) J Am Chem Soc 139:17186–17192
Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published
maps and institutional affiliations.
Reprinted from the journal
81
Topics in Current Chemistry (2019) 377:37
in one molecule will be developed [25, 26]. In addition, the application of these
asymmetric photochemical reactions to the production of chiral drugs and pesticides
is also expected in the near future.
References
1. Nicewicz DA, MacMillan DWC (2008) Science. 322:77–80
2. Nagib DA, Scott ME, MacMillan DWC (2009) J Am Chem Soc 131:10875–10877
3. Shih H-W, Vander Wal MN, Grange RL, MacMillan DWC (2010) J Am Chem Soc
132:13600–13603
4. Pirnot MT, Rankic DA, Martin DBC, MacMillan DWC (2013) Science 339:1593–1596
5. Zhu Y, Zhang L, Luo S (2014) J Am Chem Soc 136:14642–14645
6. Zhang W, Zhu Y, Zhang L, Luo S (2018) Chin J Chem 36:716–722
7. Welin ER, Warkentin AA, Conrad JC, MacMillan DWC (2015) Angew Chem Int Ed 54:9668–9672
8. Capacci AG, Malinowski JT, McAlpine NJ, Kuhne J, MacMillan DWC (2017) Nat Chem
9:1073–1077
9. Li M, Sang Y, Xue X-S, Cheng J-P (2018) J Org Chem 83:3333–3338
10. Larionov E, Mastandrea MM, Pericàs MA (2017) ACS Catal 7:7008–7013
11. Wang D, Zhang L, Luo S (2017) Org Lett 19:4924–4927
12. Yang Q, Zhang L, Ye C, Luo S, Wu L-Z, Tung C-H (2017) Angew Chem Int Ed 56:3694–3698
13. Zhao J-J, Zhang H-H, Shen X, Yu S (2019) Org Lett 21:913–916
14. Murphy JJ, Bastida D, Paria S, Fagnoni M, Melchiorre P (2016) Nature 532:218–222
15. DiRocco DA, Rovis T (2012) J Am Chem Soc 134:8094–8097
16. Feng Z-J, Xuan J, Xia X-D, Ding W, Guo W, Chen J-R, Zou Y-Q, Lu L-Q, Xiao W-J (2014) Org
Biomol Chem 12:2037–2040
17. Rono L, Yayla J, Wang H-G, Armstrong DY, Knowles MF, Robert R (2013) J Am Chem Soc
135:17735–17738
18. Ding W, Zhou Q-Q, Xuan J, Li T-R, Lu L-Q, Xiao W-J (2014) Tetrahedron Lett 55:4648–4652
19. Hepburna H-B, Melchiorre P (2016) Chem Commun 52:3520–3523
20. Bergonzini G, Schindler CS, Wallentin CJ, Jacobsen EN, Stephenson CR (2014) J Chem Sci
5:112–116
21. Gentry EC, Rono LJ, Hale ME, Matsuura R, Knowles RR (2018) J Am Chem Soc
2018(140):3394–3402
22. Uraguchi D, Kinoshita N, Kizu T, Ooi T (2015) J Am Chem Soc 137:13768–13771
23. Kizu T, Uraguchi D, Ooi T (2016) J Org Chem 81:6953–6958
24. Lenhart D, Bauer A, Pçthig A, Bach T (2016) Chem Eur J 22:6519–6523
25. Ding W, Lu L-Q, Zhou Q-Q, Wei Y, Chen J-R, Xiao W-J (2017) J Am Chem Soc 139:63–66
26. Skubi KL, Kidd JB, Jung H, Guzei IA, Baik M, Yoon TP (2008) J Am Chem Soc 139:17186–17192
Publisher’s Note Springer Nature remains neutral with regard to jurisdictional claims in published
maps and institutional affiliations.
Reprinted from the journal
81