Citation: Liu Qianyi, Zhang Lei, Mo Fanyang. Organic Borylation Reactions via Radical Mechanism[J]. Acta Chimica Sinica, ;2020, 78(12): 1297-1308. doi: 10.6023/A20070294 shu

Organic Borylation Reactions via Radical Mechanism

Liu Qianyi ^a ,
Zhang Lei ^a ,
Mo Fanyang ^a,b,,

a.
Department of Energy and Resources Engineering, College of Engineering, Peking University, Beijing 100871, China
b.
Jiangsu Donghai Silicon Industry S & T Innovation Center, Lianyungang 222300, China

Corresponding author: Mo Fanyang, fmo@pku.edu.cn
Received Date: 7 July 2020
Available Online: 31 July 2020
Fund Project: the National Natural Science Foundation of China 21772003the National Natural Science Foundation of China 21933001Project supported by the National Natural Science Foundation of China (Nos. 21772003 and 21933001)

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Organoboronic acids and esters are highly valuable building blocks in cross-coupling reactions and practical intermediates of various functional group transformations. Additionally, organoboronic acids can be utilized directly as small molecule drugs. Therefore, development of efficient methods to synthesize organoboronic compounds is of significant importance. Traditional pathways to synthesize organoboronic compounds mainly rely on electrophilic borylation of organometallic reagent and transition-metal-catalyzed borylation. Radical intermediates have unique chemical properties which are quite different from those of polar intermediates resulted from the heterolysis of chemical bonds and those of the organometallic compounds during transition metal catalysis. As such, borylation based on radical mechanism possesses distinctive reaction process, substrate scope, reaction selectivity, etc., and have great potential in synthesis of organoboronic compounds. In 2010, the Wang's group first reported borylation via a radical mechanism. This method realized an efficient direct conversion of anilines into aryl organoboronic esters. Inspired by this innovative work, more and more borylation methods via radical intermediates have been reported and developed as new avenues for C-B bond formation in the past decade. A series of studies show that organoboronic acids and esters could be efficiently constructed by the reaction of aryl/alkyl radicals with diboron compounds. In this paper, we summarize the recent development of borylation reactions via radical mechanisms, including aryl and alkyl radical borylation. As for aryl radical borylation, the activation of substrates containing C-N, C-O, C-S, C-X (X=halogen) bonds and carboxylic acids to C-B bond is summarized respectively. As for alkyl radical borylation, the activation of substrates containing C-N, C-O, C-X (X=halogen), C-C bonds and carboxylic acids to C-B bond is summarized respectively. Finally, we provide a perspective on the future development direction of this research area.
- radical chemistry,
- borylation reaction,
- diboron compounds,
- aryl radical,
- alkyl radical
1. [1]
  (a) Barth, R. F.; Kabalka, G. W.; Yang, W.; Huo, T.; Nakkula, R. J.; Shaikh, A. L.; Haider, S. A.; Chandra, S. Appl. Radiat. Isotopes 2014, 88, 38; (b) Barth, R. F.; Mi, P.; Yang, W. Cancer Commun. 2018, 38, 35.
2. [2]
  (a) San Miguel, J. F.; Schlag, R.; Khuageva, N. K.; Dimopoulos, M. A.; Shpilberg, O.; Kropff, M.; Spicka, I.; Petrucci, M. T.; Palumbo, A.; Samoilova, O. S.; Dmoszynska, A.; Abdulkadyrov, K. M.; Schots, R.; Jiang, B.; Mateos, M. V.; Anderson, K. C.; Esseltine, D. L.; Liu, K.; Cakana, A.; Van De Velde, H.; Richardson, P. G. New Engl. J. Med. 2008, 359, 906; (b) Beenen, M. A.; An, C.; Ellman, J. A. J. Am. Chem. Soc. 2008, 130, 6910.
3. [3]
  (a) Chemler, S. R.; Trauner, D.; Danishefsky, S. J. Angew. Chem. Int. Ed. 2001, 40, 4544; (b) Moreno-Maas, M.; Pérez, M.; Pleixats, R. J. Org. Chem. 1996, 61, 2346.
4. [4]
  (a) Miyaura, N.; Suzuki, A., J. Chem. Soc. Chem. Commun. 1979, 866; (b) Miyaura, N.; Yamada, K.; Suzuki, A. Tetrahedron Lett. 1979, 20, 3437.
5. [5]
  (a) Schneider, N.; Lowe, D. M.; Sayle, R. A.; Tarselli, M. A.; Landrum, G. A. J. Med. Chem. 2016, 59, 4385; (b) Bostrm, J.; Brown, D. G.; Young, R. J.; Keserü, G. M. Nat. Rev. Drug Discov. 2018, 17, 709.
6. [6]
  Torborg, C.; Beller, M. Adv. Synth. Catal. 2009, 351, 3027.
7. [7]
  (a) Liu, M.; Su, S.-J.; Jung, M.-C.; Qi, Y.; Zhao, W.-M.; Kido, J. Chem. Mater. 2012, 24, 3817; (b) Wong, K.-T.; Hung, T. S.; Lin, Y.; Wu, C.-C.; Lee, G.-H.; Peng, S.-M.; Chou, C. H.; Su, Y. O. Org. Lett. 2002, 4, 513.
8. [8]
  (a) Chan, D. M. T.; Monaco, K. L.; Wang, R.-P.; Winters, M. P. Tetrahedron Lett. 1998, 39, 2933; (b) Evans, D. A.; Katz, J. L.; West, T. R. Tetrahedron Lett. 1998, 39, 2937; (c) Lam, P. Y. S.; Clark, C. G.; Saubern, S.; Adams, J.; Winters, M. P.; Chan, D. M. T.; Combs, A. Tetrahedron Lett. 1998, 39, 2941; (d) Herradura, P. S.; Pendola, K. A.; Guy, R. K. Org. Lett. 2000, 2, 2019.
9. [9]
  Petasis, N. A.; Akritopoulou, I. Tetrahedron Lett. 1993, 34, 583.
10. [10]
  Wu, P.; Givskov, M.; Nielsen, T. E. Chem. Rev. 2019, 119, 11245.
11. [11]
  (a) Brown, H. C.; Cole, T. E. Organometallics. 1983, 2, 1316; (b) Brown, H. C.; Srebnik, M.; Cole, T. E. Organometallics. 1986, 5, 2300.
12. [12]
  Ishiyama, T.; Murata, M.; Miyaura, N. J. Org. Chem. 1995, 60, 7508.
13. [13]
  Li, Z.; Zheng, J.; Li, C.; Wu, W.; Jiang, H. Chin. J. Chem. 2019, 37, 140.
14. [14]
  Yoshida, H. ACS Catal. 2016, 6, 1799.
15. [15]
  Li, S.; Li, J.; Xia, T.; Zhao, W. Chin. J. Chem. 2019, 37, 462.
16. [16]
  He, Z.; Fan, M.; Xu, J.; Hu, Y.; Wang, L.; Wu, X.; Xia, C.; Liu, C. Chin. J. Org. Chem. 2019, 39, 3438.
17. [17]
  Wang, M.; Shi, Z. Chem. Rev. 2020, DOI: 10.1021/acs.chemrev.9b00384. doi: 10.1021/acs.chemrev.9b00384.
18. [18]
  (a) Chen, H.; Schlecht, S.; Semple, T. C.; Hartwig, J. F. Science 2000, 287, 1995; (b) Mkhalid, I. A. I.; Barnard, J. H.; Marder, T. B.; Murphy, J. M.; Hartwig, J. F. Chem. Rev. 2010, 110, 890; (c) Jiang, Z.-T.; Wang, B.-Q.; Shi, Z.-J. Chin. J. Chem. 2018, 36, 950; (d) Zhan, M.; Song, P.; Jiao, J.; Li, P. Chin. J. Chem. 2020, 38, 665.
19. [19]
  (a) (a) Xiao, L. Li, J.-H, Wang, T. Acta Chim. Sinica, 2019, 77, 841(in Chinese). (肖丽, 李嘉恒, 王挺, 化学学报 2019, 77, 841.) (b) Ye, S.-Q, Wu, J. Acta Chim. Sinica, 2019, 77, 814(in Chinese). (叶盛青, 吴劼, 化学学报 2019, 77, 814.)
20. [20]
  Mo, F.; Jiang, Y.; Qiu, D.; Zhang, Y.; Wang, J. Angew. Chem. Int. Ed. 2010, 49, 1846.
21. [21]
  Qiu, D.; Jin, L.; Zheng, Z.; Meng, H.; Mo, F.; Wang, X.; Zhang, Y.; Wang, J. J. Org. Chem. 2013, 78, 1923.
22. [22]
  (a) Yu, J.; Zhang, L.; Yan, G. Adv. Synth. Catal. 2012, 354, 2625; (b) Zhu, C.; Yamane, M. Org. Lett. 2012, 14, 4560; (c) Erb, W.; Hellal, A.; Albini, M.; Rouden, J.; Blanchet, J. Chem. Eur. J. 2014, 20, 6608; (d) Marciasini, L. D.; Vaultier, M.; Pucheault, M. Tetrahedron Lett. 2014, 55, 1702; (e) Zhao, C.-J.; Xue, D.; Jia, Z.-H.; Wang, C.; Xiao, J. Synlett 2014, 25, 1577; (f) Ahammed, S.; Nandi, S.; Kundu, D.; Ranu, B. C. Tetrahedron Lett. 2016, 57, 1551; (g) Qi, X.; Jiang, L.-B.; Zhou, C.; Peng, J.-B.; Wu, X.-F. ChemistryOpen 2017, 6, 345; (h) Xu, Y.; Yang, X.; Fang, H. J. Org. Chem. 2018, 83, 12831.
23. [23]
  Teders, M.; Gómez-Suárez, A.; Pitzer, L.; Hopkinson, M. N.; Glorius, F. Angew. Chem. Int. Ed. 2017, 56, 902.
24. [24]
  Ma, Y.; Pang, Y.; Chabbra, S.; Reijerse, E. J.; Schnegg, A.; Niski, J.; Leutzsch, M.; Cornella, J. Chem. Eur. J. 2020, 26, 3738.
25. [25]
  Chen, K.; Cheung, M. S.; Lin, Z.; Li, P. Org. Chem. Front. 2016, 3, 875.
26. [26]
  Liu, W.; Yang, X.; Gao, Y.; Li, C.-J. J. Am. Chem. Soc. 2017, 139, 8621.
27. [27]
  Jin, S.; Dang, H. T.; Haug, G. C.; He, R.; Nguyen, V. D.; Nguyen, V. T.; Arman, H. D.; Schanze, K. S.; Larionov, O. V. J. Am. Chem. Soc. 2020, 142, 1603.
28. [28]
  Candish, L.; Teders, M.; Glorius, F. J. Am. Chem. Soc. 2017, 139, 7440.
29. [29]
  Cheng, W.-M.; Shang, R.; Zhao, B.; Xing, W.-L.; Fu, Y. Org. Lett. 2017, 19, 4291.
30. [30]
  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.
31. [31]
  Berger, F.; Plutschack, M. B.; Riegger, J.; Yu, W.; Speicher, S.; Ho, M.; Frank, N.; Ritter, T. Nature 2019, 567, 223.
32. [32]
  Huang, C.; Feng, J.; Ma, R.; Fang, S.; Lu, T.; Tang, W.; Du, D.; Gao, J. Org. Lett. 2019, 21, 9688.
33. [33]
  Zhang, J.; Wu, H.-H.; Zhang, J. Eur. J. Org. Chem. 2013, 2013, 6263.
34. [34]
  Hong, J.; Liu, Q.; Li, F.; Bai, G.; Liu, G.; Li, M.; Nayal, O. S.; Fu, X.; Mo, F. Chin. J. Chem. 2019, 37, 347.
35. [35]
  Chen, K.; Zhang, S.; He, P.; Li, P. Chem. Sci. 2016, 7, 3676.
36. [36]
  Mfuh, A. M.; Doyle, J. D.; Chhetri, B.; Arman, H. D.; Larionov, O. V. J. Am. Chem. Soc. 2016, 138, 2985.
37. [37]
  Mukai, K.; de Sant'Ana, D. P.; Hirooka, Y.; Mercado-Marin, E. V.; Stephens, D. E.; Kou, K. G. M.; Richter, S. C.; Kelley, N.; Sarpong, R. Nat. Chem. 2018, 10, 38.
38. [38]
  Zhang, L.; Jiao, L. J. Am. Chem. Soc. 2017, 139, 607.
39. [39]
  Zhang, L.; Jiao, L. Chem. Sci. 2018, 9, 2711.
40. [40]
  Pinet, S.; Liautard, V.; Debiais, M.; Pucheault, M. Synthesis 2017, 49, 4759.
41. [41]
  Hu, D.; Wang, L.; Li, P. Org. Lett. 2017, 19, 2770.
42. [42]
  Fawcett, A.; Pradeilles, J.; Wang, Y.; Mutsuga, T.; Myers, E. L.; Aggarwal, V. K. Science 2017, 357, 283.
43. [43]
  Wang, J.; Shang, M.; Lundberg, H.; Feu, K. S.; Hecker, S. J.; Qin, T.; Blackmond, D. G.; Baran, P. S. ACS Catal. 2018, 8, 9537.
44. [44]
  Wei, D.; Liu, T.-M.; Zhou, B.; Han, B. Org. Lett. 2020, 22, 234.
45. [45]
  (a) Wu, J.; He, L.; Noble, A.; Aggarwal, V. K. J. Am. Chem. Soc. 2018, 140, 10700; (b) Sandfort, F.; Strieth-Kalthoff, F.; Klauck, F. J. R.; James, M. J.; Glorius, F. Chem. Eur. J. 2018, 24, 17210.
46. [46]
  Hu, J.; Wang, G.; Li, S.; Shi, Z. Angew. Chem. Int. Ed. 2018, 57, 15227.
47. [47]
  Friese, F. W.; Studer, A. Angew. Chem. Int. Ed. 2019, 58, 9561.
48. [48]
  Wu, J.; Bär, R. M.; Guo, L.; Noble, A.; Aggarwal, V. K. Angew. Chem. Int. Ed. 2019, 58, 18830.
49. [49]
  Cheng, Y.; Mück-Lichtenfeld, C.; Studer, A. Angew. Chem. Int. Ed. 2018, 57, 16832.
50. [50]
  Liu, Q.; Hong, J.; Sun, B.; Bai, G.; Li, F.; Liu, G.; Yang, Y.; Mo, F. Org. Lett. 2019, 21, 6597.
51. [51]
  Zhang, L.; Wu, Z.-Q.; Jiao, L. Angew. Chem. Int. Ed. 2020, 59, 2095.
52. [52]
  Zhang, J.-J.; Duan, X.-H.; Wu, Y.; Yang, J.-C.; Guo, L.-N. Chem. Sci. 2019, 10, 161.
53. [53]
  Neeve, E. C.; Geier, S. J.; Mkhalid, I. A. I.; Westcott, S. A.; Marder, T. B. Chem. Rev. 2016, 116, 9091.
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