Citation: Cheng Lei, Zhou Qilin. Advances on Nickel-Catalyzed C(sp3)-C(sp3) Bond Formation[J]. Acta Chimica Sinica, ;2020, 78(10): 1017-1029. doi: 10.6023/A20070335 shu

Advances on Nickel-Catalyzed C(sp3)-C(sp3) Bond Formation

  • Corresponding author: Zhou Qilin, qlzhou@nankai.edu.cn
  • Received Date: 29 July 2020
    Available Online: 15 September 2020

    Fund Project: the National Natural Science Foundation of China 21790330Project supported by the National Natural Science Foundation of China (Nos. 21790332, 21790330)the National Natural Science Foundation of China 21790332

Figures(36)

  • Transition metal-catalyzed coupling reactions are powerful synthetic methods for the C-C bond formation. Many coupling reactions such as Heck reaction, Negishi coupling, and Suzuki coupling have been widely applied in the syntheses of pharmaceuticals, functional materials and fine chemicals. In those coupling reactions, a C(sp2)-C(sp2) bond is formed in high efficiency and selectivity. However, in contrast to the C(sp2)-C(sp2) couplings, the C(sp3)-C(sp3) couplings are more difficult and develop late. Because the C(sp3)-C(sp3) bonds are ubiquitous in organic compound, the C(sp3)-C(sp3) bond formation is the central task of research in organic chemistry. In the past two decades, a great effort has been devoted to the development of cross-coupling reactions between alkyls to construct C(sp3)-C(sp3) bonds and impressive progress has been achieved. Among the transition metal catalysts that have been used in the construction of C(sp3)-C(sp3) bonds, nickel was found to be a preferable one, exhibiting unique activity and selectivity. Nickel catalysts promote the activation of alkyl electrophiles via radical catalytic cycles and inhibit and/or manipulate β-H elimination reactions. Nickel has several variable valence states and can flexibly participate in tandem reactions and reductive cross-coupling reactions. All these characteristic natures contribute to the success of nickel catalysts in the construction of C(sp3)-C(sp3) bonds. In this review, we will describe the advances on the nickel-catalyzed C(sp3)-C(sp3) bond-forming reactions. The main contents of this review include:the cross-coupling of alkyl electrophiles with organometallic reagents; the coupling involving a C(sp3)-H bond activation in the presence of directing group; the coupling co-catalyzed by nickel and photocatalyst; the reductive coupling of two alkyl electrophiles; and the additions of nucleophiles or electrophiles to alkenes such as hydroalkylation and difunctionalization of alkenes. The review will focus on the latest developments of nickel-catalyzed alkyl coupling reactions in the past two decades. The mechanisms of each reaction are discussed in detail for understanding the reactions.
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    1. [1]

      For reviews on nickel catalysis: (a) Tasker, S. Z.; Standley, E. A.; Jamison, T. F. Nature, 2014, 509, 299. (b) Ananikov, V. P. ACS Catal. 2015, 5, 1964. (c) Clevenger, A. L.; Stolley, R. M.; Aderibigbe, J.; Louie, J. Chem. Rev. 2020, 120, 6124. (d) Choi, J.; Fu, G. C. Science 2017, 356, eaaf7230. (e) Modern Organonickel Chemistry, Eds.: Tamaru, Y., Wiley-VCH, Weinheim, 2005. (f) Nickel Catalysis in Organic Synthesis: Methods and Reactions, Eds.: Ogoshi, S., Wiley-VCH, Weinheim, 2020.

    2. [2]

      Devasagayaraj, A.; Stüdemann, T.; Knochel, P. Angew. Chem. Int. Ed. 1996, 34, 2723.  doi: 10.1002/anie.199527231

    3. [3]

      (a) Giovannini, R.; Stüdemann, T.; Dussin, G.; Knochel, P. Angew. Chem. Int. Ed. 1998, 37, 2387. (b) Giovannini, R.; Stüdemann, T.; Devasagayaraj, A.; Dussin, G.; Knochel, P. J. Org. Chem. 1999, 64, 3544. (c) Piber, M.; Jensen, A. E.; Rottl nder, M.; Knochel, P. Org. Lett. 1999, 1, 1323.

    4. [4]

      Terao, J.; Watanabe, H.; Ikumi, A.; Kuniyasu, H.; Kambe, N. J. Am. Chem. Soc. 2002, 124, 4222.  doi: 10.1021/ja025828v

    5. [5]

      Hills, I. D.; Netherton, M. R.; Fu, G. C. Angew. Chem. Int. Ed. 2003, 42, 5749.  doi: 10.1002/anie.200352858

    6. [6]

      Zhou, J.; Fu, G. C. J. Am. Chem. Soc. 2003, 125, 14726.  doi: 10.1021/ja0389366

    7. [7]

      (a) Saito, B.; Fu, G. C. J. Am. Chem. Soc. 2007, 129, 9602. (b) Smith, S. W.; Fu, G. C. Angew. Chem. Int. Ed. 2008, 47, 9334. (c) Vechorkin, O.; Hu, X. Angew. Chem. Int. Ed. 2009, 48, 2937.

    8. [8]

      Fisher, C.; Fu, G. C. J. Am. Chem. Soc. 2005, 127, 4594.  doi: 10.1021/ja0506509

    9. [9]

      Binder, J. T.; Cordier, C. J.; Fu, G. C. J. Am. Chem. Soc. 2012, 134, 17003.  doi: 10.1021/ja308460z

    10. [10]

      (a) Arp, F. O.; Fu, G. C. J. Am. Chem. Soc. 2005, 127, 10482. (b) Son, S.; Fu, G. C. J. Am. Chem. Soc. 2008, 130, 2756. (c) Lundin, P. M.; Esquivias, J.; Fu, G. C. Angew. Chem. Int. Ed. 2009, 48, 154. (d) Smith, S. W.; Fu, G. C. J. Am. Chem. Soc. 2008, 130, 12645. (e) Liang, Y.; Fu, G. C. J. Am. Chem. Soc. 2014, 136, 5520. (f) Owston, N. A.; Fu, G. C. J. Am. Chem. Soc. 2010, 132, 11908. (g) Lu, Z.; Wilsily, A.; Fu, G. C. J. Am. Chem. Soc. 2011, 133, 8154. (h) Wilsily, A.; Tramutola, F.; Owston, N. A.; Fu, G. C. J. Am. Chem. Soc. 2012, 134, 5794. (i) Huo, H.; Gorsline, B. J.; Fu, G. C. Science 2020, 367, 559.

    11. [11]

      Schmidt, J.; Choi, J.; Liu, A. T.; Slusarczyk, M.; Fu, G. C. Science, 2016, 354, 1265.  doi: 10.1126/science.aai8611

    12. [12]

      Schwarzwalder, G. M.; Matier, C. D.; Fu, G. C. Angew. Chem. Int. Ed. 2019, 58, 3571.  doi: 10.1002/anie.201814208

    13. [13]

      Breitenfeld, J.; Ruiz, J.; Wodrich, M. D.; Hu, X. J. Am. Chem. Soc. 2013, 135, 12004.  doi: 10.1021/ja4051923

    14. [14]

      Schley, N. D.; Fu, G. C. J. Am. Chem. Soc. 2014, 136, 16588.  doi: 10.1021/ja508718m

    15. [15]

      Hu, X. Chem. Sci. 2011, 2, 1867.

    16. [16]

      (a) Tollefson, E. J.; Hanna, L. E.; Jarvo, E. R. Acc. Chem. Res. 2015, 48, 2344. (b) Su, B.; Cao, Z.-C.; Shi, Z.-J. Acc. Chem. Res. 2015, 48, 886.

    17. [17]

      (a) Guan, B.-T.; X, S.-K.; Wang, B.-Q.; Sun, Z.-P.; Wang, Y.; Zhao, K.-Q.; Shi, Z.-J. J. Am. Chem. Soc. 2008, 130, 3268. (b) Yu, D.-G.; Wang, X.; Zhu, R.-L.; Luo, S.; Wang, B.-Q.; Wang, L.; Shi, Z.-J. J. Am. Chem. Soc. 2012, 134, 14638.

    18. [18]

      Taylor, B. L. H.; Swift, E. C.; Waetzig, J. D.; Jarvo, E. R. J. Am. Chem. Soc. 2011, 133, 389.  doi: 10.1021/ja108547u

    19. [19]

      Qin, T.; Cornella, J.; Li, C.; Malins, L. R.; Edwards, J. T.; Kawamura, S.; Maxwell, B. D.; Eastgate, M. D.; Baran, P. S. Science 2016, 352, 801.  doi: 10.1126/science.aaf6123

    20. [20]

      Plunkett, S.; Basch, C. H.; Santana, S. O.; Watson, M. P. J. Am. Chem. Soc. 2019, 141, 2257.  doi: 10.1021/jacs.9b00111

    21. [21]

      Zhan, B.-B.; Liu, B.; Hu, F.; Shi, B.-F. Sci. Chin. Chem. 2015, 60, 2097(in Chinese).

    22. [22]

      Wu, X.; Zhao, Y.; Ge, H. J. Am. Chem. Soc. 2014, 136, 1789.  doi: 10.1021/ja413131m

    23. [23]

      (a) Zuo, Z.; Ahneman, D. T.; Chu, L.; Terrett, J. A.; Doyle, A. G.; MacMillan, D. W. C. Science 2014, 345, 437. (b) Tellis, J. C.; Primer, D. N.; Molander, G. A. Science 2014, 345, 433.

    24. [24]

      (a) Twilton, J.; Le, C.; Zhang, P.; Shaw, M. H.; Evans, R. W.; MacMillan, D. W. C. Nat. Rev. Chem. 2017, 1, 0052. (b) Tells, J. C.; Kelly, C. B.; Primer, D.V.; Jouffroy, M.; Patel, N. R.; Molander, G. A. Acc. Chem. Res. 2016, 49, 1429. (c) Milligan, J. A.; Phelan, J. P.; Badir, S. O.; Molander, G. A. Angew. Chem. Int. Ed. 2019, 58, 6152.

    25. [25]

      Johnston, C. P.; Smith, R. T.; Allmendinger, S.; MacMillan, D. W. C. Nature 2016, 536, 322.  doi: 10.1038/nature19056

    26. [26]

      Le, C.; Liang, Y.; Evans, R. W.; Li, X.; MacMillan, D. W. C. Nature 2017, 547, 79.  doi: 10.1038/nature22813

    27. [27]

      Smith, R. T.; Zhang, X.; Rincón, J. A.; Agejas, J.; Mateos, C.; Barberis, M.; García-Cerrada, S.; Frutos, O. D.; MacMillan, D. W. C. J. Am. Chem. Soc. 2018, 140, 17433.  doi: 10.1021/jacs.8b12025

    28. [28]

      For selected reviews of reductive cross-couplings: (a) Knappke, C. E. I.; Grupe, S.; G rtner, D.; Corpet, M.; Gosmini, C.; Jacobi von Wangelin, A. Chem. Eur. J. 2014, 20, 6828. (b) Gu, J.; Wang, X.; Xue, W.; Gong, H. Org. Chem. Front. 2015, 2, 1411. (c) Wang, X.; Dai, Y.; Gong, H. Top. Curr. Chem. 2016, 374, 43. (d) Lucas, E. L.; Jarvo, E. R. Nat. Rev. Chem. 2017, 1, No. 0065. (e) Poremba, K. E.; Dibrell, S. E.; Reisman, S. E. ACS Catal. 2020, 10, 8237.

    29. [29]

      Yu, X.; Yang, T.; Wang, S.; Xu, H.; Gong, H. Org. Lett. 2011, 13, 2138.  doi: 10.1021/ol200617f

    30. [30]

      Xu, H.; Zhao, C.; Qian, Q.; Deng, W.; Gong, H. Chem. Sci. 2013, 4, 4022.  doi: 10.1039/c3sc51098k

    31. [31]

      Komeyama, K.; Michiyuki, T.; Osaka, I. ACS Catal. 2019, 9, 9285.  doi: 10.1021/acscatal.9b03352

    32. [32]

      (a) Hoveyda, A. H.; Evans, D. A.; Fu, G. C. Chem. Rev. 1993, 93, 1307. (b) Kolb, H. C.; VanNieuwenhze, M. S.; Sharpless, K. B. Chem. Rev. 1994, 94, 2483. (c) McDonald, R. I.; Liu, G.; Stahl, S. S. Chem. Rev. 2011, 111, 2981. (d) Dong, Z.; Ren, Z.; Thompson, S. J.; Xu, Y.; Dong, G. Chem. Rev. 2017, 117, 9333. (e) Yan, T.; Guironnet, D. Sci. Chin. Chem. 2020, 63, 755.

    33. [33]

      Wang, X.-X.; Lu, X.; Li. Y.; Wang, J.-W.; Fu, Y. Sci Chin. Chem.10.1007/s11426-020-9838-x.  doi: 10.1007/s11426-020-9838-x

    34. [34]

      Lu, X.; Xiao, B.; Zhang, Z.-Q.; Gong, T.-J.; Su, W.; Yi, J.; Fu, Y.; Liu, L. Nat. Commun. 2016, 7, 11129.  doi: 10.1038/ncomms11129

    35. [35]

      Zhou, F.; Zhu, J.; Zhang, Y.; Zhu, S. Angew. Chem. Int Ed. 2018, 57, 4058.  doi: 10.1002/anie.201712731

    36. [36]

      Wang, Z.-Y.; Wan, J.-H.; Wang, G.-Y.; Wang, R.; Jin, R.-X.; Lan, Q.; Wang, X.-S. Tetrahedron Lett. 2018, 59, 2302.  doi: 10.1016/j.tetlet.2018.05.008

    37. [37]

      (a) Sun, S.-Z.; Borjesson, M.; Martin-Montero, R.; Martin, R. J. Am. Chem. Soc. 2018, 140, 12765. (b) Qian, D.; Hu, X. Angew. Chem. Int. Ed. 2019, 58, 18519.

    38. [38]

      Lu, X.; Xiao, B.; Liu, L.; Fu, Y. Chem. Eur. J. 2016, 22, 11161.  doi: 10.1002/chem.201602486

    39. [39]

      Sun, S.-Z.; Romano, C.; Martin, R. J. Am. Chem. Soc. 2019, 141, 16197.  doi: 10.1021/jacs.9b07489

    40. [40]

      Wang, Z.; Yin, H.; Fu, G. C. Nature 2018, 563, 379.  doi: 10.1038/s41586-018-0669-y

    41. [41]

      Zhou, F.; Zhang, Y.; Xu, X.; Zhu, S. Angew. Chem. Int. Ed. 2019, 58, 1754.  doi: 10.1002/anie.201813222

    42. [42]

      He, S.-J.; Wang, J.-W.; Li, Y.; Xu, Z.-Y.; Wang, X.-X.; Lu, X.; Fu, Y. J. Am. Chem. Soc. 2020, 142, 214.  doi: 10.1021/jacs.9b09415

    43. [43]

      Yang, Z.-P.; Fu, G. C. J. Am. Chem. Soc. 2020, 142, 5870.  doi: 10.1021/jacs.0c01324

    44. [44]

      Green, S. A.; Huffman, T. R.; McCourt, R. O.; van der Puyl, V.; Shenvi, R. A. J. Am. Chem. Soc. 2019, 141, 7709.  doi: 10.1021/jacs.9b02844

    45. [45]

      Cheng, L.; Li, M.-M.; Xiao, L.-J.; Xie, J.-H.; Zhou, Q.-L. J. Am. Chem. Soc. 2018, 140, 11627.  doi: 10.1021/jacs.8b09346

    46. [46]

      Chen, T.; Yang, H.; Yang, Y.; Dong, G.; Xing, D. ACS Catal. 2020, 10, 4238.  doi: 10.1021/acscatal.0c00019

    47. [47]

      (a) Cheng, L.; Li, M.-M.; Wang, B.; Xiao, L.-J.; Xie, J.-H.; Zhou, Q.-L. Chem. Sci. 2019, 10, 10417. (b) Lv, L.; Zhu, D.; Qiu, Z.; Li, J.; Li, C.-J. ACS Catal. 2019, 9, 9199.

    48. [48]

      Ji, D.-W.; He, G.-C.; Zhang, W.-S.; Zhao, C.-Y.; Hu, Y.-C.; Chen, Q.-A. Chem. Commun. 2020, 56, 7431.  doi: 10.1039/D0CC02697B

    49. [49]

      (a) Dhungana, R. K.; KC, S.; Basnet, P.; Giri, R. Chem. Rec. 2018, 18, 1314. (b) Giri, R.; KC, S. J. Org. Chem. 2018, 83, 3013. (c) Derosa, J.; Apolinar, O.; Kang, T.; Tran, V. T.; Engle, K. M. Chem. Sci. 2020, 11, 4287. (d) Luo, Y.-C.; Xu, C.; Zhang, X. Chin. J. Chem. 2020, 38, 1371. (e) Qi, X.; Diao, T. ACS Catal. 2020, 10, 8542.

    50. [50]

      Qin, T.; Cornella, J.; Li, C.; Malins, L. R.; Edwards, J. T.; Kawamura, S.; Maxwell, B. D.; Eastage, M. D.; Baran, P. S. Science, 2016, 352, 801.  doi: 10.1126/science.aaf6123

    51. [51]

      KC, S.; Dhungana, R. K.; Shrestha, B.; Thapa, S.; Khanal, N.; Basnet, P.; Lebrun, R. W.; Giri, R. J. Am. Chem. Soc. 2018, 140, 9801.  doi: 10.1021/jacs.8b05374

    52. [52]

      Chierchia, M.; Xu, P.; Lovinger, G. J.; Morken, J. P. Angew. Chem. Int. Ed. 2019, 58, 14245.  doi: 10.1002/anie.201908029

    53. [53]

      García-Domínguez, A.; Li, Z.; Nevado, C. J. Am. Chem. Soc. 2017, 139, 6835.  doi: 10.1021/jacs.7b03195

    54. [54]

      Shu, W.; García-Domínguez, A.; Quirós, M. T.; Mondal, R.; Cárdenas, D. J.; Nevado, C. J. Am. Chem. Soc. 2019, 141, 13812.  doi: 10.1021/jacs.9b02973

    55. [55]

      (a) Guo, L.; Tu, H.-Y.; Zhu, S.; Chu, L. Org. Lett. 2019, 21, 4771. (b) García-Domínguez, A.; Mondal, R.; Nevado, C. Angew. Chem. Int. Ed. 2019, 58, 12286. (c) Campbell, M. W.; Compton, J. S.; Kelly, C. B.; Molander, G. A. J. Am. Chem. Soc. 2019, 141, 20069.

    56. [56]

      Derosa, J.; Tran, V. T.; Boulous, M. N.; Chen, J. S.; Engle, K. M. J. Am. Chem. Soc. 2017, 139, 10657.  doi: 10.1021/jacs.7b06567

    57. [57]

      Derosa, J.; van der Puyl, V. A.; Tran, V. T.; Liu, M.; Engle, K. M. Chem. Sci. 2018, 9, 5278.  doi: 10.1039/C8SC01735B

    58. [58]

      (a) Nattmann, L.; Saeb, R.; N thling, N.; Cornella, J. Nat. Catal. 2020, 3, 6. (b) Tran, V. T.; Li, Z.-Q.; Apolinar, O.; Derosa, J.; Joannou, . W. V.; Wisniewski, S. R.; Eastgate, M. D.; Engle, K. M. Angew. Chem. Int. Ed. 2020, 59, 7409.

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