Topics in Current Chemistry (2019) 377:23
1 3
Acknowledgements Financial support from the National Natural Science Foundation of China
(Nos 21722203, 21831002, and 21801116) and Shenzhen Nobel Prize Scientists Laboratory Project
(C17783101) is greatly appreciated.
References
1. Mlynarski J (ed) (2017) Chiral Lewis acids in organic synthesis. Wiley, Weinheim
2. Akiyama T (2007) Chem Rev 107:5744–5758
3. Parmar D, Sugiono E, Raja S, Rueping M (2014) Chem Rev 114:9047–9153
4. Parmar D, Sugiono E, Raja S, Rueping M (2017) Chem Rev 117:10608–10620
5. Maji R, Mallojjala SC, Wheeler SE (2018) Chem Soc Rev 47:1142–1158
6. Akiyama T, Itoh J, Yokota K, Fuchibe K (2004) Angew Chem Int Ed 43:1566–1568
7. Uraguchi D, Terada M (2004) J Am Chem Soc 126:5356–5357
8. Terada M (2008) Chem Commun 35:4097–4112
9. Terada M (2010) Synthesis 12:1929–1982
10. Masahiro T (2010) Bull Chem Soc Jpn 83:101–119
11. Schenker S, Zamfir A, Freund M, Tsogoeva SB (2011) Eur J Org Chem 12:2209–2222
12. Stemper J, Isaac K, Duret V, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2013) Chem Commun 49:6084–6086
13. Stemper J, Isaac K, Ghosh N, Lauwick H, Le Duc G, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2017) Adv Synth Catal 359:519–526
14. Stemper J, Isaac K, Pastor J, Frison G, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2013)
Adv Synth Catal 355:3613–3624
15. Zhu J-C, Cui D-X, Li Y-D, Jiang R, Chen W-P, Wang P-A (2018) ChemCatChem 10:907–919
16. Isaac K, Stemper J, Servajean V, Retailleau P, Pastor J, Frison G, Kaupmees K, Leito I, Betzer J-F,
Marinetti A (2014) J Org Chem 79:9639–9646
17. Yang C, Xue X-S, Jin J-L, Li X, Cheng J-P (2013) J Org Chem 78:7076–7085
18. Rueping M, Kuenkel A, Atodiresei I (2011) Chem Soc Rev 40:4539–4549
19. Chen D-F, Han Z-Y, Zhou X-L, Gong L-Z (2014) Acc Chem Res 47:2365–2377
20. Allen AE, MacMillan DWC (2012) Chem Sci 3:633–658
21. Du Z, Shao Z (2013) Chem Soc Rev 42:1337–1378
22. Shao Z, Zhang H (2009) Chem Soc Rev 38:2745–2755
23. Zhong C, Shi X (2010) Eur J Org Chem 16:2999–3025
24. Inamdar SM, Shinde VS, Patil NT (2015) Org Biomol Chem 13:8116–8162
25. Yang Z-P, Zhang W, You S-L (2014) J Org Chem 79:7785–7798
26. Rueping M, Koenigs RM, Atodiresei I (2010) Chem Eur J 16:9350–9365
27. Phipps RJ, Hamilton GL, Toste FD (2012) Nat Chem 4:603–614
28. Brak K, Jacobsen EN (2013) Angew Chem Int Ed 52:534–561
29. Mayer S, List B (2006) Angew Chem Int Ed 45:4193–4195
30. Parra A, Reboredo S, Martín Castro AM, Alemán J (2012) Org Biomol Chem 10:5001–5020
31. Mahlau M, List B (2013) Angew Chem Int Ed 52:518–533
32. Lv J, Luo S (2013) Chem Commun 49:847–858
33. Mukherjee S, List B (2007) J Am Chem Soc 129:11336–11337
34. Yan S-Y, Han Y-Q, Yao Q-J, Nie X-L, Liu L, Shi B-F (2018) Angew Chem Int Ed 57:9093–9097
35. Lin H-C, Wang P-S, Tao Z-L, Chen Y-G, Han Z-Y, Gong L-Z (2016) J Am Chem Soc
138:14354–14361
36. Rueping M, Antonchick AP, Brinkmann C (2007) Angew Chem Int Ed 46:6903–6906
37. Terada M, Li F, Toda Y (2014) Angew Chem Int Ed 53:235–239
38. Hu W, Xu X, Zhou J, Liu W-J, Huang H, Hu J, Yang L, Gong L-Z (2008) J Am Chem Soc
130:7782–7783
39. Jiang J, Xu H-D, Xi J-B, Ren B-Y, Lv F-P, Guo X, Jiang L-Q, Zhang Z-Y, Hu W-H (2011) J Am
Chem Soc 133:8428–8431
40. Alamsetti SK, Spanka M, Schneider C (2016) Angew Chem Int Ed 55:2392–2396
41. Li C, Wang C, Villa-Marcos B, Xiao J (2008) J Am Chem Soc 130:14450–14451
42. Miura T, Nishida Y, Morimoto M, Murakami M (2013) J Am Chem Soc 135:11497–11500
Reprinted from the journal
182
1 3
Acknowledgements Financial support from the National Natural Science Foundation of China
(Nos 21722203, 21831002, and 21801116) and Shenzhen Nobel Prize Scientists Laboratory Project
(C17783101) is greatly appreciated.
References
1. Mlynarski J (ed) (2017) Chiral Lewis acids in organic synthesis. Wiley, Weinheim
2. Akiyama T (2007) Chem Rev 107:5744–5758
3. Parmar D, Sugiono E, Raja S, Rueping M (2014) Chem Rev 114:9047–9153
4. Parmar D, Sugiono E, Raja S, Rueping M (2017) Chem Rev 117:10608–10620
5. Maji R, Mallojjala SC, Wheeler SE (2018) Chem Soc Rev 47:1142–1158
6. Akiyama T, Itoh J, Yokota K, Fuchibe K (2004) Angew Chem Int Ed 43:1566–1568
7. Uraguchi D, Terada M (2004) J Am Chem Soc 126:5356–5357
8. Terada M (2008) Chem Commun 35:4097–4112
9. Terada M (2010) Synthesis 12:1929–1982
10. Masahiro T (2010) Bull Chem Soc Jpn 83:101–119
11. Schenker S, Zamfir A, Freund M, Tsogoeva SB (2011) Eur J Org Chem 12:2209–2222
12. Stemper J, Isaac K, Duret V, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2013) Chem Commun 49:6084–6086
13. Stemper J, Isaac K, Ghosh N, Lauwick H, Le Duc G, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2017) Adv Synth Catal 359:519–526
14. Stemper J, Isaac K, Pastor J, Frison G, Retailleau P, Voituriez A, Betzer J-F, Marinetti A (2013)
Adv Synth Catal 355:3613–3624
15. Zhu J-C, Cui D-X, Li Y-D, Jiang R, Chen W-P, Wang P-A (2018) ChemCatChem 10:907–919
16. Isaac K, Stemper J, Servajean V, Retailleau P, Pastor J, Frison G, Kaupmees K, Leito I, Betzer J-F,
Marinetti A (2014) J Org Chem 79:9639–9646
17. Yang C, Xue X-S, Jin J-L, Li X, Cheng J-P (2013) J Org Chem 78:7076–7085
18. Rueping M, Kuenkel A, Atodiresei I (2011) Chem Soc Rev 40:4539–4549
19. Chen D-F, Han Z-Y, Zhou X-L, Gong L-Z (2014) Acc Chem Res 47:2365–2377
20. Allen AE, MacMillan DWC (2012) Chem Sci 3:633–658
21. Du Z, Shao Z (2013) Chem Soc Rev 42:1337–1378
22. Shao Z, Zhang H (2009) Chem Soc Rev 38:2745–2755
23. Zhong C, Shi X (2010) Eur J Org Chem 16:2999–3025
24. Inamdar SM, Shinde VS, Patil NT (2015) Org Biomol Chem 13:8116–8162
25. Yang Z-P, Zhang W, You S-L (2014) J Org Chem 79:7785–7798
26. Rueping M, Koenigs RM, Atodiresei I (2010) Chem Eur J 16:9350–9365
27. Phipps RJ, Hamilton GL, Toste FD (2012) Nat Chem 4:603–614
28. Brak K, Jacobsen EN (2013) Angew Chem Int Ed 52:534–561
29. Mayer S, List B (2006) Angew Chem Int Ed 45:4193–4195
30. Parra A, Reboredo S, Martín Castro AM, Alemán J (2012) Org Biomol Chem 10:5001–5020
31. Mahlau M, List B (2013) Angew Chem Int Ed 52:518–533
32. Lv J, Luo S (2013) Chem Commun 49:847–858
33. Mukherjee S, List B (2007) J Am Chem Soc 129:11336–11337
34. Yan S-Y, Han Y-Q, Yao Q-J, Nie X-L, Liu L, Shi B-F (2018) Angew Chem Int Ed 57:9093–9097
35. Lin H-C, Wang P-S, Tao Z-L, Chen Y-G, Han Z-Y, Gong L-Z (2016) J Am Chem Soc
138:14354–14361
36. Rueping M, Antonchick AP, Brinkmann C (2007) Angew Chem Int Ed 46:6903–6906
37. Terada M, Li F, Toda Y (2014) Angew Chem Int Ed 53:235–239
38. Hu W, Xu X, Zhou J, Liu W-J, Huang H, Hu J, Yang L, Gong L-Z (2008) J Am Chem Soc
130:7782–7783
39. Jiang J, Xu H-D, Xi J-B, Ren B-Y, Lv F-P, Guo X, Jiang L-Q, Zhang Z-Y, Hu W-H (2011) J Am
Chem Soc 133:8428–8431
40. Alamsetti SK, Spanka M, Schneider C (2016) Angew Chem Int Ed 55:2392–2396
41. Li C, Wang C, Villa-Marcos B, Xiao J (2008) J Am Chem Soc 130:14450–14451
42. Miura T, Nishida Y, Morimoto M, Murakami M (2013) J Am Chem Soc 135:11497–11500
Reprinted from the journal
182