Citation: Junsong Zhong, Yi Yu, Dongliang Zhang, Keyin Ye. Merging cobalt catalysis and electrochemistry in organic synthesis^☆[J]. Chinese Chemical Letters, ;2021, 32(3): 963-972. doi: 10.1016/j.cclet.2020.08.011 shu

Merging cobalt catalysis and electrochemistry in organic synthesis^☆

Key Laboratory of Molecule Synthesis and Function Discovery (Fujian Province University), College of Chemistry, Fuzhou University, Fuzhou 350108, China

Author Bio: Junsong Zhong obtained his BSc degree in chemical biology from Xiamen University in 2019. Then he continued his research at Fuzhou University under the guidance of Prof. Ke-Yin Ye. His research interests focuse on electrochemical synthesis
Yi Yu obtained her master degree in organic chemistry in 2019 from Jiangxi Normal University. Then she moved to the Fuzhou University for her doctoral studies under the guidance of Prof. Ke-Yin Ye. Her research interests focuse on electrochemical synthesis
Dongliang Zhang is an undergraduate student at Fuzhou University. At present, he is studying and working in Prof. Ke-Yin Ye's research group. His research focuses on electrochemical synthesis
Prof. Dr. Keyin Ye obtained his bachelor degree from Xiamen University (mentors: Prof. Pei-Qiang Huang and Prof. Hong-Kui Zhang) and PhD from Shanghai Institute of Organic Chemistry (mentors: Prof. Li-Xin Dai and Prof. Shu-Li You). He then conducted his postdoctoral research with Prof. Gerhard Erker (Universität Münster) and Prof. Song Lin (Cornell University), respectively. Since June 2019 he started his independent career at Fuzhou University as a Minjiang Professor. His research interests include organometallics, asymmetric catalysis and electrosynthesis

^☆

^th

kyye@fzu.edu.cn

Received Date: 28 June 2020
Revised Date: 24 July 2020
Accepted Date: 10 August 2020
Available Online: 12 August 2020

Figures(23)

There is an increasing demand of using the low-cost and sustainable cobalt to replace its noble congeners (rhodium and iridium) as reflected by the recent upsurge of cobalt catalysis in the diverse organic transformations. Since all the redox reactivity of cobalt catalysis highly relies on the capability of the interconversion between their oxidation states (most frequently +1, +2 and +3), electrochemistry perfectly meets such a requirement owing to its outstanding performance in the redox manipulation. In this review, we highlight the recent advances in the merger of cobalt catalysis and electrochemistry in organic synthesis.
- Cobalt,
- Catalysis,
- Electrochemistry,
- Organic synthesis,
- Sustainable chemistry
1. [1]
  M. Hapke, G. Hilt, Cobalt Catalysis in Organic Synthesis: Methods and Reactions, 1st. ed., Wiley, Weinheim, 2020.
2. [2]
  C.K. Rofer-DePoorter, Chem. Rev. 81(1981) 447-474. doi: 10.1021/cr00045a002
3. [3]
  H. Schulz, Appl. Catal. A: Gen. 186(1999) 3-12. doi: 10.1016/S0926-860X(99)00160-X
4. [4]
  K.L. Brown, Chem. Rev. 105(2005) 2075-2149. doi: 10.1021/cr030720z
5. [5]
  M. Giedyk, K. Goliszewska, D. Gryko, Chem. Soc. Rev. 44(2015) 3391-3404. doi: 10.1039/C5CS00165J
6. [6]
  J. Cheng, L. Wang, P. Wang, L. Deng, Chem. Rev. 118(2018) 9930-9987. doi: 10.1021/acs.chemrev.8b00096
7. [7]
  Y. Liu, J. Cheng, L. Deng, Acc. Chem. Res. 53(2019) 244-254.
8. [8]
  K. Gao, N. Yoshikai, Acc. Chem. Res. 47(2014) 1208-1219. doi: 10.1021/ar400270x
9. [9]
  T. Michiyuki, K. Komeyama, Asian J. Org. Chem. 9(2019) 343-358.
10. [10]
  S. Mohle, M. Zirbes, E. Rodrigo, et al., Angew. Chem. Int. Ed. 57(2018) 6018-6041. doi: 10.1002/anie.201712732
11. [11]
  A. Wiebe, T. Gieshoff, S. Mohle, et al., Angew. Chem. Int. Ed. 57(2018) 5594-5619. doi: 10.1002/anie.201711060
12. [12]
  S. Tang, Y. Liu, A. Lei, Chem 4(2018) 27-45. doi: 10.1016/j.chempr.2017.10.001
13. [13]
  J. Yoshida, K. Kataoka, R. Horcajada, A. Nagaki, Chem. Rev. 108(2008) 2265-2299. doi: 10.1021/cr0680843
14. [14]
  Z. Li, Q. Sun, P. Qian, et al., Chin. Chem. Lett. 31(2020) 1855-1858. doi: 10.1016/j.cclet.2020.02.030
15. [15]
  J. Zhang, H. Wang, Y. Chen, et al., Chin. Chem. Lett. 31(2020) 1576-1579. doi: 10.1016/j.cclet.2019.11.037
16. [16]
  M. Yan, Y. Kawamata, P.S. Baran, Chem. Rev. 117(2017) 13230-13319. doi: 10.1021/acs.chemrev.7b00397
17. [17]
  R. Francke, R.D. Little, Chem. Soc. Rev. 43(2014) 2492-2521. doi: 10.1039/c3cs60464k
18. [18]
  K.J. Jiao, Y.K. Xing, Q.L. Yang, H. Qiu, T.S. Mei, Acc. Chem. Res. 53(2020) 300-310. doi: 10.1021/acs.accounts.9b00603
19. [19]
  J.C. Siu, N. Fu, S. Lin, Acc. Chem. Res. 53(2020) 547-560. doi: 10.1021/acs.accounts.9b00529
20. [20]
  P. Gandeepan, L.H. Finger, T.H. Meyer, L. Ackermann, Chem. Soc. Rev. 49(2020) 4254-4272. doi: 10.1039/D0CS00149J
21. [21]
  T.H. Meyer, L.H. Finger, P. Gandeepan, L. Ackermann, Trends Analyt. Chem. 1(2019) 63-76. doi: 10.1016/j.trechm.2019.01.011
22. [22]
  Y. Jiang, K. Xu, C. Zeng, Chem. Rev. 118(2018) 4485-4540. doi: 10.1021/acs.chemrev.7b00271
23. [23]
  P. Xiong, H.C. Xu, Acc. Chem. Res. 52(2019) 3339-3350. doi: 10.1021/acs.accounts.9b00472
24. [24]
  N. Sauermann, T.H. Meyer, C. Tian, L. Ackermann, J. Am. Chem. Soc. 139(2017) 18452-18455. doi: 10.1021/jacs.7b11025
25. [25]
  X.R. Chen, S.Q. Zhang, T.H. Meyer, et al., Chem. Sci. 11(2020) 5790-5796. doi: 10.1039/D0SC01898H
26. [26]
  T.H. Meyer, J.C.A. Oliveira, D. Ghorai, L. Ackermann, Angew. Chem. Int. Ed. 59(2020) 10955-10960. doi: 10.1002/anie.202002258
27. [27]
  L. Ackermann, Acc. Chem. Res. 53(2020) 84-104. doi: 10.1021/acs.accounts.9b00510
28. [28]
  N. Sauermann, T.H. Meyer, L. Ackermann, Chem. Eur. J. 24(2018) 16209-16217. doi: 10.1002/chem.201802706
29. [29]
  C. Tian, U. Dhawa, J. Struwe, L. Ackermann, Chin. J. Chem. 37(2019) 552-556. doi: 10.1002/cjoc.201900050
30. [30]
  X. Gao, P. Wang, L. Zeng, S. Tang, A. Lei, J. Am. Chem. Soc. 140(2018) 4195-4199. doi: 10.1021/jacs.7b13049
31. [31]
  N. Sauermann, R. Mei, L. Ackermann, Angew. Chem. Int. Ed. 57(2018) 5090-5094. doi: 10.1002/anie.201802206
32. [32]
  U. Dhawa, C. Tian, W. Li, L. Ackermann, ACS Catal. 10(2020) 6457-6462. doi: 10.1021/acscatal.0c01436
33. [33]
  T.H. Meyer, G.A. Chesnokov, L. Ackermann, ChemSusChem 13(2020) 668-671. doi: 10.1002/cssc.202000057
34. [34]
  C. Tian, L. Massignan, T.H. Meyer, L. Ackermann, Angew. Chem. Int. Ed. 57(2018) 2383-2387. doi: 10.1002/anie.201712647
35. [35]
  Y. Cao, Y. Yuan, Y. Lin, et al., Green Chem. 22(2020) 1548-1552. doi: 10.1039/D0GC00289E
36. [36]
  R. Mei, N. Sauermann, J.C.A. Oliveira, L. Ackermann, J. Am. Chem. Soc. 140(2018) 7913-7921. doi: 10.1021/jacs.8b03521
37. [37]
  R. Mei, X. Fang, L. He, et al., Chem. Commun. 56(2020) 1393-1396. doi: 10.1039/C9CC09076B
38. [38]
  T.H. Meyer, J.C.A. Oliveira, S.C. Sau, N.W.J. Ang, L. Ackermann, ACS Catal. 8(2018) 9140-9147. doi: 10.1021/acscatal.8b03066
39. [39]
  S. Tang, D. Wang, Y. Liu, L. Zeng, A. Lei, Nat. Commun. 9(2018) 798. doi: 10.1038/s41467-018-03246-4
40. [40]
  L. Zeng, H. Li, S. Tang, et al., ACS Catal. 8(2018) 5448-5453. doi: 10.1021/acscatal.8b00683
41. [41]
  J. Chen, L. Jin, J. Zhou, X. Jiang, C. Yu, Tetrahedron Lett. 60(2019) 2054-2058. doi: 10.1016/j.tetlet.2019.06.060
42. [42]
  S.C. Sau, R. Mei, J. Struwe, L. Ackermann, ChemSusChem 12(2019) 3023-3027. doi: 10.1002/cssc.201900378
43. [43]
  Y.L. Lai, J.S. Ye, J.M. Huang, Chem. Eur. J. 22(2016) 5425-5429. doi: 10.1002/chem.201505074
44. [44]
  Y. Yu, P. Zheng, Y. Wu, X. Ye, Org. Biomol. Chem. 16(2018) 8917-8921. doi: 10.1039/C8OB02485E
45. [45]
  S. Tian, S. Lv, X. Jia, et al., Adv. Synth. Catal. 361(2019) 5626-5633. doi: 10.1002/adsc.201901260
46. [46]
  S. Lin, R.A. DiStasio Jr., M.O. Frederick, et al., Nat. Chem. (2020), doi:http://dx.doi.org/10.1038/s41557-020-0469-5. doi: 10.1038/s41557-020-0469-5
47. [47]
  J.M. Hammann, M.S. Hofmayer, F.H. Lutter, L. Thomas, P. Knochel, Synthesis 49(2017) 3887-3894. doi: 10.1055/s-0036-1588430
48. [48]
  T. Fujihara, Y. Tsuji, Beilstein J. Org. Chem. 14(2018) 2435-2460. doi: 10.3762/bjoc.14.221
49. [49]
  E. Le Gall, C. Gosmini, J.Y. Nédélec, J. Périchon, Tetrahedron Lett. 42(2001) 267-269. doi: 10.1016/S0040-4039(00)01936-5
50. [50]
  P. Gomes, H. Fillon, C. Gosmini, E. Labbé, J. Périchon, Tetrahedron 58(2002) 8417-8424. doi: 10.1016/S0040-4020(02)01030-X
51. [51]
  P. Gomes, C. Gosmini, J. Périchon, Tetrahedron 59(2003) 2999-3002. doi: 10.1016/S0040-4020(03)00404-6
52. [52]
  L. Polleux, E. Labbé, O. Buriez, J. Périchon, Chem. Eur. J. 11(2005) 4678-4686. doi: 10.1002/chem.200400971
53. [53]
  P. Gomes, C. Gosmini, J. Périchon, Org. Lett. 5(2003) 1043-1045. doi: 10.1021/ol0340641
54. [54]
  P. Gomes, C. Gosmini, J. Périchon, J. Org. Chem. 68(2003) 1142-1145. doi: 10.1021/jo026421b
55. [55]
  C. Gosmini, Y. Rollin, J.Y. Nédélec, J. Périchon, J. Org. Chem. 65(2000) 6024-6026. doi: 10.1021/jo000459b
56. [56]
  E.L. Gall, C. Gosmini, J. -Y. Nédélec, J. Périchon, Tetrahedron 57(2001) 1923-1927. doi: 10.1016/S0040-4020(01)00015-1
57. [57]
  H. Fillon, C. Gosmini, J. Périchon, Tetrahedron 59(2003) 8199-8202. doi: 10.1016/j.tet.2003.08.032
58. [58]
  Y. Shen, S. Inagi, M. Atobe, T. Fuchigami, Res. Chem. Intermed. 39(2013) 89-99. doi: 10.1007/s11164-012-0634-6
59. [59]
  M. Tokuda, A. Hayashi, H. Suginome, Bull. Chem. Soc. Jpn. 64(1991) 2590-2592. doi: 10.1246/bcsj.64.2590
60. [60]
  R. Scheffold, M. Dike, S. Dike, T. Herold, L. Walder, J. Am. Chem. Soc. 102(1980) 3642-3644. doi: 10.1021/ja00530a064
61. [61]
  L. Auer, C. Weymuth, R. Scheffold, Helv. Chim. Acta 76(1993) 810-818. doi: 10.1002/hlca.19930760205
62. [62]
  R. Orlinski, T. Stankiewicz, Tetrahedron Lett. 29(1988) 1601-1602. doi: 10.1016/S0040-4039(00)80364-0
63. [63]
  R. Scheffold, R. Orlinski, J. Am. Chem. Soc. 105(1983) 7200-7202. doi: 10.1021/ja00362a047
64. [64]
  L. Walder, G. Rytz, K. Meier, R. Scheffold, Helv. Chim. Acta 61(1978) 3013-3017. doi: 10.1002/hlca.19780610826
65. [65]
  P. Gomes, C. Gosmini, J.Y. Nédélec, J. Périchon, Tetrahedron Lett. 41(2000) 3385-3388. doi: 10.1016/S0040-4039(00)00420-2
66. [66]
  P. Gomes, C. Gosmini, J.Y. Nédélec, J. Périchon, Tetrahedron Lett. 43(2002) 5901-5903. doi: 10.1016/S0040-4039(02)01286-8
67. [67]
  S. Torii, T. Inokuchi, T. Yukawa, J. Org. Chem. 50(1985) 5875-5877. doi: 10.1021/jo00350a090
68. [68]
  E. Duñach, A.P. Esteves, M.J. Medeiros, D. Pletcher, S. Olivero, J. Electroanal. Chem. 566(2004) 39-45. doi: 10.1016/j.jelechem.2003.10.045
69. [69]
  C. Floriani, G. Fachinetti, J. Chem. Soc., Chem. Commun. (1974) 615-616.
70. [70]
  J.C. Folest, J.M. Duprilot, J. Perichon, Y. Robin, J. Devynck, Tetrahedron Lett. 26(1985) 2633-2636. doi: 10.1016/S0040-4039(00)98122-X
71. [71]
  G. Zheng, M. Stradiotto, L. Li, J. Electroanal. Chem. 453(1998) 79-88. doi: 10.1016/S0022-0728(98)00173-9
72. [72]
  P. -L. Fabre, O. Reynes, Electrochem. Commun. 12(2010) 1360-1362. doi: 10.1016/j.elecom.2010.07.020
73. [73]
  D.J. Weix, Acc. Chem. Res. 48(2015) 1767-1775. doi: 10.1021/acs.accounts.5b00057
74. [74]
  B. -L. Chen, H. -W. Zhu, Y. Xiao, et al., Electrochem. Commun. 42(2014) 55-59. doi: 10.1016/j.elecom.2014.02.009
75. [75]
  H.P. Yang, Y.N. Yue, Q.L. Sun, et al., Chem. Commun. 51(2015) 12216-12219. doi: 10.1039/C5CC04554A
76. [76]
  N.W.J. Ang, J.C.A. Oliveira, L. Ackermann, Angew. Chem. Int. Ed. (2020), doi:http://dx.doi.org/10.1002/anie.202003218. doi: 10.1002/anie.202003218
77. [77]
  L. Capaldo, L.L. Quadri, D. Ravelli, Angew. Chem. Int. Ed. 58(2019) 17508-17510. doi: 10.1002/anie.201910348
78. [78]
  Y. Yu, P. Guo, J.S. Zhong, Y. Yuan, K.Y. Ye, Org. Chem. Front. 7(2020) 131-135. doi: 10.1039/C9QO01193E
79. [79]
  J.P. Barham, B. König, Angew. Chem. Int. Ed. 59(2020) 11732-11747. doi: 10.1002/anie.201913767
80. [80]
  T. Hardwick, A. Qurashi, B. Shirinfar, N. Ahmed, ChemSusChem 13(2020) 1967-1973. doi: 10.1002/cssc.202000032
81. [81]
  Y.C. Wu, R.J. Song, J.H. Li, Org. Chem. Front. 7(2020) 1895-1902. doi: 10.1039/D0QO00486C
82. [82]
  J. Liu, L. Lu, D. Wood, S. Lin, ACS Cent. Sci. (2020), doi:http://dx.doi.org/10.1021/acscentsci.0c00549. doi: 10.1021/acscentsci.0c00549
1. [1]
  Uttam Pandurang Patil . Porous carbon catalysis in sustainable synthesis of functional heterocycles: An overview. Chinese Chemical Letters, 2024, 35(8): 109472-. doi: 10.1016/j.cclet.2023.109472
2. [2]
  Fangling Cui , Zongjie Hu , Jiayu Huang , Xiaoju Li , Ruihu Wang . MXene-based materials for separator modification of lithium-sulfur batteries. Chinese Journal of Structural Chemistry, 2024, 43(7): 100337-100337. doi: 10.1016/j.cjsc.2024.100337
3. [3]
  Peng Guo , Shicheng Dong , Xiang-Gui Zhang , Bing-Bin Yang , Jun Zhu , Ke-Yin Ye . Cobalt-catalyzed migratory carbon-carbon cross-coupling of borabicyclo[3.3.1]nonane (9-BBN) borates. Chinese Chemical Letters, 2025, 36(4): 110052-. doi: 10.1016/j.cclet.2024.110052
4. [4]
  Jia-Cheng Hou , Wei Cai , Hong-Tao Ji , Li-Juan Ou , Wei-Min He . Recent advances in semi-heterogenous photocatalysis in organic synthesis. Chinese Chemical Letters, 2025, 36(2): 110469-. doi: 10.1016/j.cclet.2024.110469
5. [5]
  Manoj Kumar Sarangi , L․D Patel , Goutam Rath , Sitansu Sekhar Nanda , Dong Kee Yi . Metal organic framework modulated nanozymes tailored with their biomedical approaches. Chinese Chemical Letters, 2024, 35(11): 109381-. doi: 10.1016/j.cclet.2023.109381
6. [6]
  Longlong Geng , Huiling Liu , Wenfeng Zhou , Yong-Zheng Zhang , Hongliang Huang , Da-Shuai Zhang , Hui Hu , Chao Lv , Xiuling Zhang , Suijun Liu . Construction of metal-organic frameworks with unsaturated Cu sites for efficient and fast reduction of nitroaromatics: A combined experimental and theoretical study. Chinese Chemical Letters, 2024, 35(8): 109120-. doi: 10.1016/j.cclet.2023.109120
7. [7]
  Xiao-Hong Yi , Chong-Chen Wang . Metal-organic frameworks on 3D interconnected macroporous sponge foams for large-scale water decontamination: A mini review. Chinese Chemical Letters, 2024, 35(5): 109094-. doi: 10.1016/j.cclet.2023.109094
8. [8]
  Shuai Li , Liuting Zhang , Fuying Wu , Yiqun Jiang , Xuebin Yu . Efficient catalysis of FeNiCu-based multi-site alloys on magnesium-hydride for solid-state hydrogen storage. Chinese Chemical Letters, 2025, 36(1): 109566-. doi: 10.1016/j.cclet.2024.109566
9. [9]
  Xue Xin , Qiming Qu , Islam E. Khalil , Yuting Huang , Mo Wei , Jie Chen , Weina Zhang , Fengwei Huo , Wenjing Liu . Hetero-phase zirconia encapsulated with Au nanoparticles for boosting electrocatalytic nitrogen reduction. Chinese Chemical Letters, 2024, 35(5): 108654-. doi: 10.1016/j.cclet.2023.108654
10. [10]
  Zixuan Guo , Xiaoshuai Han , Chunmei Zhang , Shuijian He , Kunming Liu , Jiapeng Hu , Weisen Yang , Shaoju Jian , Shaohua Jiang , Gaigai Duan . Activation of biomass-derived porous carbon for supercapacitors: A review. Chinese Chemical Letters, 2024, 35(7): 109007-. doi: 10.1016/j.cclet.2023.109007
11. [11]
  Qiang Cao , Xue-Feng Cheng , Jia Wang , Chang Zhou , Liu-Jun Yang , Guan Wang , Dong-Yun Chen , Jing-Hui He , Jian-Mei Lu . Graphene from microwave-initiated upcycling of waste polyethylene for electrocatalytic reduction of chloramphenicol. Chinese Chemical Letters, 2024, 35(4): 108759-. doi: 10.1016/j.cclet.2023.108759
12. [12]
  Yuemin Chen , Yunqi Wu , Guoao Wang , Feihu Cui , Haitao Tang , Yingming Pan . Electricity-driven enantioselective cross-dehydrogenative coupling of two C(sp³)-H bonds enabled by organocatalysis. Chinese Chemical Letters, 2024, 35(9): 109445-. doi: 10.1016/j.cclet.2023.109445
13. [13]
  Li Li , Zhi-Xin Yan , Chuan-Kun Ran , Yi Liu , Shuo Zhang , Tian-Yu Gao , Long-Fei Dai , Li-Li Liao , Jian-Heng Ye , Da-Gang Yu . Electro-reductive carboxylation of CCl bonds in unactivated alkyl chlorides and polyvinyl chloride with CO₂. Chinese Chemical Letters, 2024, 35(12): 110104-. doi: 10.1016/j.cclet.2024.110104
14. [14]
  Yan-Jiang Li , Shu-Lei Chou , Yao Xiao . Detecting dynamic structural evolution based on in-situ high-energy X-ray diffraction technology for sodium layered oxide cathodes. Chinese Chemical Letters, 2025, 36(2): 110389-. doi: 10.1016/j.cclet.2024.110389
15. [15]
  Haodong Wang , Xiaoxu Lai , Chi Chen , Pei Shi , Houzhao Wan , Hao Wang , Xingguang Chen , Dan Sun . Novel 2D bifunctional layered rare-earth hydroxides@GO catalyst as a functional interlayer for improved liquid-solid conversion of polysulfides in lithium-sulfur batteries. Chinese Chemical Letters, 2024, 35(5): 108473-. doi: 10.1016/j.cclet.2023.108473
16. [16]
  Mengxiang Zhu , Tao Ding , Yunzhang Li , Yuanjie Peng , Ruiping Liu , Quan Zou , Leilei Yang , Shenglei Sun , Pin Zhou , Guosheng Shi , Dongting Yue . Graphene controlled solid-state growth of oxygen vacancies riched V₂O₅ catalyst to highly activate Fenton-like reaction. Chinese Chemical Letters, 2024, 35(12): 109833-. doi: 10.1016/j.cclet.2024.109833
17. [17]
  Fengxing Liang , Yongzheng Zhu , Nannan Wang , Meiping Zhu , Huibing He , Yanqiu Zhu , Peikang Shen , Jinliang Zhu . Recent advances in copper-based materials for robust lithium polysulfides adsorption and catalytic conversion. Chinese Chemical Letters, 2024, 35(11): 109461-. doi: 10.1016/j.cclet.2023.109461
18. [18]
  Shiyan Cheng , Yonghong Ruan , Lei Gong , Yumei Lin . Research Advances in Friedel-Crafts Alkylation Reaction. University Chemistry, 2024, 39(10): 408-415. doi: 10.12461/PKU.DXHX202403024
19. [19]
  Wei Chen , Pieter Cnudde . A minireview to ketene chemistry in zeolite catalysis. Chinese Journal of Structural Chemistry, 2024, 43(11): 100412-100412. doi: 10.1016/j.cjsc.2024.100412
20. [20]
  Aidang Lu , Yunting Liu , Yanjun Jiang . Comprehensive Organic Chemistry Experiment: Synthesis and Characterization of Triazolopyrimidine Compounds. University Chemistry, 2024, 39(8): 241-246. doi: 10.3866/PKU.DXHX202401029

Get Citation

PDF

XML

Metrics

PDF Downloads(59)
Abstract views(1513)
HTML views(306)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

Merging cobalt catalysis and electrochemistry in organic synthesis☆

Metrics

通讯作者: 陈斌, bchen63@163.com

Merging cobalt catalysis and electrochemistry in organic synthesis^☆