Citation: Dai Hongxue, Wu Fen, Bai Dachang. Recent Advances in Ni-Catalyzed C—C Bond Activation Reactions[J]. Chinese Journal of Organic Chemistry, ;2020, 40(6): 1423-1436. doi: 10.6023/cjoc202002035 shu

Recent Advances in Ni-Catalyzed C—C Bond Activation Reactions

Dai Hongxue ^a ,
Wu Fen ^a ,
Bai Dachang ^a,,

a.
School of Chemistry and Chemical Engineering, Henan Normal University, Xinxiang, Henan 453007

Corresponding author: Bai Dachang, baidachang@htu.edu.cn
Received Date: 25 February 2020
Revised Date: 3 April 2020
Available Online: 13 April 2020
Fund Project: the Start-Up Fund from Henan Normal University 2019QK01the Natural Science Research Program of Education Department of Henan Province 18A150010the Start-Up Fund from Henan Normal University qd17108the National Natural Science Foundation of China 21801067Project supported by the National Natural Science Foundation of China (No. 21801067), the Natural Science Research Program of Education Department of Henan Province (No. 18A150010) and the Start-Up Fund from Henan Normal University (Nos. qd17108, 2019QK01)

Figures(30)

Transition-metal catalyzed C-C bond cleavage reaction is one of the most challenge topics, and has drawn considerable attention in recent years. This process has not only emerged as a useful strategy for syntheses of complex molecular skeletons, but also satisfied atom economy. Compared to the noble transition metals catalysis such as Rh, Pd and Ir, the nickel catalysis offered a more cost effective option and exhibited unique activity or selectivity. This recent advances on the Ni-catalyzed C-C bond activations are summarized.
- nickel,
- C-C bond activation,
- transition-metal
1. [1]
  Reviews: (a) Song, F.-J.; Gou, T.; Wang, B.-Q.; Shi, Z.-J. Chem. Soc. Rev. 2018, 47, 7078.
  (b) Deng, L.; Jin, L.; Dong, G. Angew. Chem., Int. Ed. 2018, 57, 2702.
  (c) Fumagalli, G.; Stanton, S.; Bower, J. F. Chem. Rev. 2017, 117, 9404.
  (d) Chen, P.-H.; Billett, B. A.; Tsukamoto, T.; Dong, G.-B. ACS Catal. 2017, 7, 1340.
  (e) Souillart, L.; Cramer, N. Chem. Rev. 2015, 115, 9410.
  (f) Liu, H.; Feng, M.-H.; Jiang, X.-F. Chem.-Asian J. 2014, 9, 3360.
  (g) Jun, C.-H. Chem. Soc. Rev. 2004, 33, 610.
  (h) Liang, Y.-F.; Jiao, N. Acc. Chem. Res. 2017, 50, 1640.
  (i) Liu, J.-Z.; Qiu, X.; Huang, X.-Q.; Luo, X.; Zhang, C.; Wei, J.-L.; Pan, J.; Liang, Y.-J.; Zhu, Y.-C.; Qin, Q.-X.; Son, S.; Jiao, N. Nat. Chem. 2019, 11, 94.
  (j) Sivaguru, P.; Wang, Z.-K.; Zanoni, G.; Bi, X.-H. Chem. Soc. Rev. 2019, 48, 2615.
  (k) Wu, X.-X.; Zhu, C. Chem. Rec. 2018, 18, 587.
2. [2]
  (a) Murakami, M.; Ishida, N. J. Am. Chem. Soc. 2016, 138, 13759.
  (b) Marek, I.; Masarwa, A.; Delaye, P.-O.; Leibeling, M. Angew. Chem., Int. Ed. 2015, 54, 414.
  (c) Li, T.-F.; Xu, F.; Li, X.-C.; Wang, C.-X.; Wan, B.-S. Angew. Chem., Int. Ed. 2016, 55, 2861.
  (d) Chen, F.; Wang, T.; Jiao, N. Chem. Rev. 2014, 114, 8613.
  (e) Chen, W.-L.; Wu, S.-Y.; Mo, X.-L.; Wei, L.-X.; Liang, C.; Mo, D.-L. Org. Lett. 2018, 20, 3527.
  (f) Zhao, H.-P; Liang, G.-C.; Nie, S.-M.; Lu, X.; Pan, C.-X.; Zhong, X.-X.; Su, G.-F.; Mo, D.-L. Green Chem. 2020, 22, 404.
3. [3]
  (a) Dai, P.-F.; Ning, X.-S.; Wang, H.; Cui, X.-C.; Liu, J.; Qu, J.-P.; Kang, Y.-B. Angew. Chem., Int. Ed. 2019, 58, 5392.
  (b) Sun, T.-W.; Zhang, Y.-N.; Qiu, B.; Wang, Y.-F.; Qin, Y.-T.; Dong, G.-B.; Xu, T. Angew. Chem., Int. Ed. 2018, 57, 2859.
  (c) Cao, J.; Fang, R.; Liu, J.-Y.; Lu, H.; Luo, Y.-C.; Xu, P.-F. Chem.-Eur. J. 2018, 24, 18863.
  (d) Liu, L.-T.; Guo, Z.-H.; Xu, K.; Hui, S.-S.; Zhao, X.-F.; Zhao, B.-L.; Tan, H.; Chen, C.; Jiao, N.; Shi, Z.-Z. Chin. J Chem. 2018, 36, 995.
  (e) Yu, X.-Y.; Chen, J.-R.; Wang, P.-Z.; Yang, M.-N.; Liang, D.; Xiao, W.-J. Angew. Chem., Int. Ed. 2018, 57, 738.
  (f) Mao, W.-B.; Zhu, C. J. Org. Chem. 2017, 82, 9133.
4. [4]
  Selected examples on nickel catalyzed C—C cleavage: (a) Fan, C.; Lv, X.-Y.; Xiao, L.-J.; Xie, J.-H.; Zhou, Q.-L. J. Am. Chem. Soc. 2019, 141, 2889.
  (b) Zhao, T.-T.; Xu, W.-H.; Zheng, Z.-J.; Xu, P.-F.; Wei, H. J. Am. Chem. Soc. 2018, 140, 586.
  (c) Morioka, T.; Nishizawa, A.; Furukawa, T.; Tobisu, M.; Chatani, N. J. Am. Chem. Soc. 2017, 139, 1416.
  (d) Liu, L.; Montgomery, J. J. Am. Chem. Soc. 2006, 128, 5348.
  (e) Lloyd-Jones, G. C. Angew. Chem., Int. Ed. 2006, 45, 67880.
  (f) Ogoshi, S.; Nagata, M.; Kurosawa, H. J. Am. Chem. Soc. 2006, 128, 5350.
  (g) Jiang, L.-H.; Huang, F.; Wang, Q.; Sun, C.-Z.; Liu, J.-B.; Chen, D.-Z. Org. Chem. Front. 2018, 5, 2332.
5. [5]
  (a) Wiberg, K.; Waddell, S. T. J. Am. Chem. Soc. 1990, 112, 2194.
  (b) Yu, S. J.; Noble, A.; Bedford, R. B.; Aggarwal, V. K. J. Am. Chem. Soc. 2019, 141, 20325.
6. [6]
  (a) Nakamura, M.; Isobe, H.; Nakamura, E. Chem. Rev. 2003, 103, 1295.
  (b) Yang, Y.; Zhang, Z.; Zhang, X.; Wang, D.; Wei, Y.; Shi, M. Chem. Commun. 2014, 50, 115.
  (c) Li, X.; Han, C.; Yao, H.; Lin, A. Org. Lett. 2017, 19, 778.
7. [7]
  Noyori, R.; Umeda, I.; Takaya H. Chem. Lett. 1972, 1, 1189. doi: 10.1246/cl.1972.1189
8. [8]
  (a) Baba, A.; Ohshiro, Y.; Agawa, T. Chem. Lett. 1976, 5, 11.
  (b) Baba, A.; Ohshiro, Y.; Agawa. T. J. Organomet. Chem. 1976, 110, 121.
9. [9]
  Zhao, W.-T.; Gao, F.; Zhao, D.-B. Angew. Chem., Int. Ed. 2018, 57, 6329. doi: 10.1002/anie.201803156
10. [10]
  Huang, J. Q.; Ho, C. Y. Angew. Chem., Int. Ed. 2019, 58, 5702. doi: 10.1002/anie.201901255
11. [11]
  (a) Noyori, R.; Odagi, T.; Takaya, H. J. Am. Chem. Soc. 1970, 92, 5780.
  (b) Noyori, R.; Kumagai, Y.; Umeda, I.; Takaya, H. J. Am. Chem. Soc. 1972, 94, 4018.
  (c) Ma, X.-P.; Nong, C.-M.; Zhao, J.; Lu, X.; Liang, C.; Mo, D.-L. Adv. Synth. Catal. 2020, 362, 478.
12. [12]
  (a) Saito, S.; Masuda, M.; Komagawa, S. J. Am. Chem. Soc. 2004, 126, 10540.
  (b) Saito, S.; Komagawa, S.; Azumaya, I.; Masuda, M. J. Org. Chem. 2007, 72, 9114.
  (c) Komagawa, S.; Saito, S. Angew. Chem., Int. Ed. 2006, 45, 2446.
  (d) Maeda, K.; Saito, S. Tetrahedron Lett. 2007, 48, 3173.
  (e) Saito, S.; Takeuchi, K. Tetrahedron Lett. 2007, 48, 595.
13. [13]
  Saito, S.; Maeda, K.; Yamasaki, R.; Kitamura, T.; Nakagawa, M.; Kato, K.; Azumaya, I.; Masu, H. Angew. Chem., Int. Ed. 2010, 49, 1830. doi: 10.1002/anie.200907052
14. [14]
  Saito, S.; Yoshizawa, T.; Ishigami, S.; Yamasaki, R. Tetrahedron Lett. 2010, 51, 6028. doi: 10.1016/j.tetlet.2010.09.031
15. [15]
  (a) Saya, L.; Bhargava, G.; Navarro, M. A.; Gulías, M.; López, F.; Fernández, I.; Castedo, L.; Mascareñas, J. L. Angew. Chem., Int. Ed. 2010, 49, 9886.
  (b) Saya, L.; Fernández, I.; López, F.; Mascareñas, J. L. Org. Lett. 2014, 16, 5008.
16. [16]
  Yao, B.; Li, Y.; Liang, Z.; Zhang, Y. Org. Lett. 2011, 13, 640. doi: 10.1021/ol1028628
17. [17]
  (a) Ogata, K.; Shimada, D.; Furuya, S.; Fukuzawa, S.-I. Org. Lett. 2013, 15, 1182.
  (b) Ogata, K.; Atsuumi, Y.; Fukuzawa, S.-I. Org. Lett. 2010, 12, 4536.
  (c) Pan, B.; Wang, C.; Wang, D.; Wu, F.; Wan, B. Chem. Commun. 2013, 49, 5073.
18. [18]
  (a) Yamamoto, K.; Ishida, T.; Tsuji, J. Chem. Lett. 1987, 16, 1157.
  (b) Wang, Q.; Wang, C.; Shi, W.; Xiao, Y.; Guo, H. Org. Biomol. Chem. 2018, 16, 4881.
  (c) Parsons, A. T.; Campbell, M. J.; Johnson, J. S. Org. Lett. 2008, 10, 2541.
  (d) Liu, C.-H.; Yu, Z.-X. Angew. Chem., Int. Ed. 2017, 56, 8667.
  (e) Wang, Y.-Y.; Wang, J.-H.; Su, J.-C.; Huang, F.; Jiao, L.; Liang, Y.; Yang, D.-Z.; Zhang, S.-W.; Wender, P.-A.; Yu, Z.-X. J. Am. Chem. Soc. 2007, 129, 10060.
19. [19]
  (a) Sumida, Y.; Yorimitsu, H.; Oshima, K. Org. Lett. 2008, 10, 4677.
  (b) Bowman, R. K.; Johnson, J. S. Org. Lett. 2006, 8, 573.
20. [20]
  (a) Tombe, R.; Iwamoto, T.; Kurahashi, T.; Matsubara, S. Synlett. 2014, 25, 2281.
  (b) Mori, T.; Nakamura, T.; Kimura, M. Org. Lett. 2011, 13, 2266.
  (c) Mita, T.; Tanaka, H.; Higuchi, Y.; Sato, Y. Org. Lett. 2016, 18, 2754.
  (d) Tombe, R.; Kurahashi, T.; Matsubara, S. Org. Lett. 2013, 15, 1791.
21. [21]
  Ogoshi, S.; Nagata, M.; Kurosawa, H. J. Am. Chem. Soc. 2006, 128, 5350. doi: 10.1021/ja060220y
22. [22]
  (a) Liu, L.; Montgomery, J. J. Am. Chem. Soc. 2006, 128, 5348.
  (b) Lloyd-Jones, G. C. Angew. Chem., Int. Ed. 2006, 45, 6788.
  (c) Liu, L.; Montgomery, J. Org. Lett. 2007, 9, 3885.
  (d) Tamaki, T.; Ohashi, M.; Ogoshi, S. Angew. Chem., Int. Ed. 2011, 50, 12067.
23. [23]
  (a) Zuo, G.; Louie, J. Angew. Chem., Int. Ed. 2004, 43, 2277.
  (b) Nečas, D.; Kotora, M. Org. Lett. 2008, 10, 5261.
  (c) Wender, P. A.; Takahashi, H.; Witulski, B. J. Am. Chem. Soc. 1995, 117, 4720.
24. [24]
  Schwager, H.; Spyroudis, S.; Vollhardt, K. P. C. J. Organomet. Chem. 1990, 382, 191. doi: 10.1016/0022-328X(90)85227-P
25. [25]
  (a) Edelbach, B. L.; Lachicotte, R. J.; Jones, W. D. Organometallics 1999, 18, 4660.
  (b) Edelbach, B. L.; Lachicotte, R. J.; Jones, W. D. Organometallics 1999, 18, 4040.
  (c) Müller, C.; Lachicotte, R. J.; Jones, W. D. Organometallics 2002, 21, 1975.
  (d) Schaub, T.; Radius, U. Chem.-Eur. J. 2005, 11, 5024.
  (e) Schaub, T.; Backes, M.; Radius, U. Organometallics 2006, 25, 4196.
  (f) Iverson, C. N.; Jones, W. D. Organometallics 2001, 20, 5745.
26. [26]
  Ho, K. Y. T.; Aïssa, C. Chem.-Eur. J. 2012, 18, 3486. doi: 10.1002/chem.201200167
27. [27]
  (a) Kumar, P.; Zhang, K.; Louie, J. Angew. Chem., Int. Ed. 2012, 51, 8602.
  (b) Thakur, A.; Facer, M. E.; Louie, J. Angew. Chem., Int. Ed. 2013, 52, 12161.
28. [28]
  (a) Juliá-Hernández, F.; Ziadi, A.; Nishimura, A.; Martin, R. Angew. Chem., Int. Ed. 2015, 54, 9537.
  (b) Yang, S.; Xu, Y.; Li, J. Org. Lett. 2016, 18, 6244.
29. [29]
  Auvinet, A.-L.; Harrity, J. P. A. Angew. Chem., Int. Ed. 2011, 50, 2769. doi: 10.1002/anie.201007598
30. [30]
31. [31]
  Gerlach, D. H.; Kane, A. R.; Parshall, G. W.; Jesson, J. P.; Muetterties, E. L. J. Am. Chem. Soc. 1971, 93, 3543. doi: 10.1021/ja00743a050
32. [32]
  Nakao, Y.; Oda, S.; Hiyama, T. J. Am. Chem. Soc. 2004, 126, 13904. doi: 10.1021/ja0448723
33. [33]
  (a) Nakao, Y.; Oda, S.; Yada, A.; Hiyama, T. Tetrahedron 2006, 62, 7567.
  (b) Ohnishi, Y.-Y.; Nakao, Y.; Sato, H.; Nakao, Y.; Hiyama, T.; Sakaki, S. Organometallics 2009, 28, 2583.
  (c) Hirata, Y.; Yukawa, T.; Kashihara, N.; Nakao, Y.; Hiyama, T. J. Am. Chem. Soc. 2009, 131, 10964.
  (d) Nakao, Y.; Yada, A.; Ebata, S.; Hiyama, T. J. Am. Chem. Soc. 2007, 129, 2428.
  (e) Yada, A.; Yukawa, T.; Nakao, Y.; Hiyama, T. Chem. Commun. 2009, 3931.
  (f) Yada, A.; Yukawa, T.; Idei, H.; Nakao, Y.; Hiyama, T. Bull. Chem. Soc. Jpn. 2010, 83, 619.
  (g) Nakao, Y.; Yada, A.; Hiyama, T. J. Am. Chem. Soc. 2010, 132, 10024.
  (h) Nakao, Y.; Hirata, Y.; Tanaka, M.; Hiyama, T. Angew. Chem., Int. Ed. 2008, 47, 385.
  (i) Hirata, Y.; Tanaka, M.; Yada, A.; Nakao, Y.; Hiyama, T. Tetrahedron 2009, 65, 5037.
  (j) Nakao, Y.; Ebata, S.; Yada, A.; Hiyama, T.; Ikawa, M.; Ogoshi, S. J. Am. Chem. Soc. 2008, 130, 12874.
  (k) Minami, Y.; Yoshiyasu, H.; Nakao, Y.; Hiyama, T. Angew. Chem., Int. Ed. 2013, 52, 883.
  (l) Nakai, K.; Kurahashi, T.; Matsubara, S. Org. Lett. 2013, 15, 856.
34. [34]
  (a) Nakao, Y.; Hirata, Y.; Tanaka, M.; Hiyama, T. Angew. Chem., Int. Ed. 2008, 47, 385.
  (b) Hirata, Y.; Tanaka, M.; Yada, A.; Nakao, Y.; Hiyama, T. Tetrahedron 2009, 65, 5037.
  (c) Hirata, Y.; Yada, A.; Morita, E.; Nakao, Y.; Hiyama, T.; Ohashi, M.; Ogoshi, S. J. Am. Chem. Soc. 2010, 132, 10070.
  (d) Hirata, Y.; Inui, T.; Nakao, Y.; Hiyama, T. J. Am. Chem. Soc. 2009, 131, 6624.
  (e) Nakao, Y.; Hirata, Y.; Hiyama, T. J. Am. Chem. Soc. 2006, 128, 7420.
  (f) Hirata, Y.; Inui, T.; Nakao, Y.; Hiyama, T. J. Am. Chem. Soc. 2009, 131, 6624.
35. [35]
  (a) Yu, D.-G.; Yu, M.; Guan, B.-T.; Li, B.-J.; Zheng, Y.; Wu, Z.-H.; Shi, Z.-J. Org. Lett. 2009, 11, 3374.
  (b) Sun, M.; Zhang, H.-Y.; Han, Q.; Yang, K.; Yang, S.-D. Chem.-Eur. J. 2011, 17, 9566.
36. [36]
  Zhang, J.-S.; Chen, T.-Q.; Zhou, Y.-B.; Yin, S.-F.; Han, L.-B. Org. Lett. 2018, 20, 6746. doi: 10.1021/acs.orglett.8b02854
37. [37]
  Chen, H.; Sun, S.-H.; Liu, Y.-H.; Liao, X.-B. ACS Catal. 2020, 10, 1397. doi: 10.1021/acscatal.9b04586
38. [38]
  Morioka, T.; Nishizawa, A.; Furukawa, T.; Tobisu, M.; Chatani, O. J. Am. Chem. Soc. 2017, 139, 1416. doi: 10.1021/jacs.6b12293
39. [39]
  Zhao, T.-T.; Xu, W.-H.; Zheng, Z.-J.; Xu, P.-F.; Wei, H. J. Am. Chem. Soc. 2018, 140, 586. doi: 10.1021/jacs.7b11591
40. [40]
  Fan, C.; Lv, X.-Y.; Xiao, L.-J.; Xie, J.-H.; Zhou, Q.-L. J. Am. Chem. Soc. 2019, 141, 7, 2889.
41. [41]
  Jiang, C.; Lu, H.; Xu, W.-H.; Wu, J.-N.; Yu, T.-Y.; Xu, P.-F.; Wei, H. ACS Catal. 2020, 10, 1947. doi: 10.1021/acscatal.9b04112
42. [42]
  Tombe, R.; Kurahashi, T.; Matsubara, S. Org. Lett. 2013, 15, 1791. doi: 10.1021/ol4005068
43. [43]
  (a) Liu, Q.-S.; Wang, D.-Y.; Yang, Z.-J.; Luan, Y.-X.; Yang, J.-F.; Li, J.-F.; Pu, Y.-G.; Ye, M.-C. J. Am. Chem. Soc. 2017, 139, 18150.
  (b) Wang, Y.-X.; Ye, M.-C. Sci. China, Chem. 2018, 61, 1004.
44. [44]
  Bai, D.-C.; Yu, Y.-J.; Guo, H.-M.; Chang, J.-B.; Li, X.-W. Angew. Chem., Int. Ed. 2020, 59, 2740. doi: 10.1002/anie.201913130
45. [45]
  (a) Liu, L.; Ishida, N.; Murakami, M. Angew. Chem., Int. Ed. 2012, 51, 2485.
  (b) Zhou, X.; Dong, G.-B. Angew. Chem., Int. Ed. 2016, 55, 15091.
  (c) Murakami, M.; Ashida, S.; Matsuda, T. J. Am. Chem. Soc. 2005, 127, 6932.
46. [46]
  (a) Watson, M. P.; Jacobsen, E. N. J. Am. Chem. Soc. 2008, 130, 12594.
  (b) Nakao, Y.; Ebata, S.; Yada, A.; Hiyama, T.; Ikawa, M.; Ogoshi, S. J. Am. Chem. Soc. 2008, 130, 12874.
  (c) Hsieh, J.-C.; Ebata, S.; Nakao, Y.; Hiyama, T. Synlett 2010, 1709.
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沈阳化工大学材料科学与工程学院沈阳 110142