Citation: Xin Wang, Jianping Meng, Dongyang Zhao, Shi Tang, Kai Sun. Synthesis and applications of thiosulfonates and selenosulfonates as free-radical reagents[J]. Chinese Chemical Letters, ;2023, 34(4): 107736. doi: 10.1016/j.cclet.2022.08.016 shu

Synthesis and applications of thiosulfonates and selenosulfonates as free-radical reagents

Xin Wang ^{a, *,} ,
Jianping Meng ^a ,
Dongyang Zhao ^a ,
Shi Tang ^b ,
Kai Sun ^{a, *,}

a.
College of Chemistry and Chemical Engineering, Yantai University, Yantai 264005, China
b.
College of Chemistry and Chemical Engineering, Jishou University, Jishou 416000, China

Author Bio: Xin Wang was born in Heilongjiang, China and received her MS degree from Northeast Normal University in 2012. In July 2013, she joined the College of Chemistry and Chemical Engineering, Anyang Normal University. In 2019, she pursued her Ph.D. degree in Zhengzhou University. Her research program is drug design, structural identification and structural modification of natural products
Jianping Meng was born in Heilongjiang Province, China in 1994. In 2014, she began her studies at the School of Science of Heihe University. In 2019, she pursued her MS degree under the supervision of Kai Sun in YanTai University. Her current research is focused on green synthetic chemistry

Kai Sun was born in Shanxi, China in 1983. He received his Ph.D. degree in organic chemistry from Northeast Normal University in 2013 under the supervision of Prof. Qian Zhang. In July 2020, he joined the College of Chemistry and Chemical Engineering, YanTai University, where he is an associate professor. His current research is focused on radical C–H functionalization and green synthetic chemistry

wangx933@nenu.edu.cn

sunk468@nenu.edu.cn

Received Date: 13 June 2022
Revised Date: 26 July 2022
Accepted Date: 5 August 2022
Available Online: 11 August 2022

Figures(32)

Chalcogenative sulfones (thiosulfonates and selenosulfonates), as reactants for organic transformations, are widely used and interesting because of their potential to react with nucleophiles, electrophiles, and free radicals. As stable radical reagents, the synthesis and applications of chalcogenative sulfones have opened up a novel pathway to synthesize many kinds of compounds containing sulfur or selenium motifs. However, despite the numerous recent works on the synthesis and applications of thiosulfonates and selenosulfonates as radical reagents, no review has yet provided a summary of the literature. In this paper, we aim to review the synthesis and applications strategies of chalcogenative sulfones as radical reagents reported over the past several decades. Different types of catalysis are discussed in this review: (ⅰ) metal catalysis; (ⅱ) visible-light catalysis; (ⅲ) synergistic catalysis; and (ⅲⅰ) other types. Concurrently, in visible-light catalysis and metallaphotoredox catalysis sections, we highlight that developing relatively environmentally friendly synthetic methods in this area is always a great challenge, but also a persistent pursuit. Finally, the scopes, limitations, mechanisms, and existing problems of some reactions are described briefly.
- Chalcogenative sulfones,
- Radical,
- Synthesis,
- Applications,
- Mechanisms
1. [1]
  T. Kondo, T. Mitsudo, Chem. Rev. 100 (2000) 3205–3220. doi: 10.1021/cr9902749
2. [2]
  M. Mellah, A. Voituriez, E. Schulz, Chem. Rev. 107 (2007) 5133–5209. doi: 10.1021/cr068440h
3. [3]
  J.E. Taylor, S.D. Bull, J.M.J. Williams, Chem. Soc. Rev. 41 (2012) 2109–2121. doi: 10.1039/c2cs15288f
4. [4]
  B. Mandal, B. Basu, RSC Adv. 4 (2014) 13854–13881. doi: 10.1039/c3ra45997g
5. [5]
  E.A. Ilardi, E. Vitaku, J.T. Njardarson, J. Med. Chem. 57 (2014) 2832–2842. doi: 10.1021/jm401375q
6. [6]
  C. Ni, M. Hu, J. Hu, Chem. Rev. 115 (2015) 765–825. doi: 10.1021/cr5002386
7. [7]
  D. Wang, P. Cao, B. Wang, et al., Org. Lett. 17 (2015) 2420–2423. doi: 10.1021/acs.orglett.5b00934
8. [8]
  X.X. Shao, C.F. Xu, L. Lu, Q.L. Shen, Acc. Chem. Res. 48 (2015) 1227–1236. doi: 10.1021/acs.accounts.5b00047
9. [9]
  M.H. Feng, B.Q. Tang, S.H. Liang, X.F. Jiang, Curr. Top. Med. Chem. 16 (2016) 1200–1216. doi: 10.2174/1568026615666150915111741
10. [10]
  X. Xiao, M. Feng, X. Jiang, Angew. Chem. Int. Ed. 55 (2016) 14121–14125. doi: 10.1002/anie.201608011
11. [11]
  Y. Li, M. Wang, X. Jiang, ACS Catal. 7 (2017) 7587–7592. doi: 10.1021/acscatal.7b02735
12. [12]
  C. Fortugno, G. Varchi, A. Guerrini, et al., Biomed. Anal. 95 (2014) 151–157. doi: 10.1016/j.jpba.2014.03.002
13. [13]
  G. Mugesh, W.W. du Mont, H. Sies, Chem. Rev. 101 (2001) 2125–2180. doi: 10.1021/cr000426w
14. [14]
  C.W. Nogueira, G. Zeni, J.B.T. Rocha, Chem. Rev. 104 (2004) 6255–6286. doi: 10.1021/cr0406559
15. [15]
  J.J. Ai, J. Li, S.J. Ji, S.Y. Wang, Chin. Chem. Lett. 32 (2021) 721–724. doi: 10.1016/j.cclet.2020.07.007
16. [16]
  X.Z. Li, P. Liu, J. He, et al., Green Synth. Catal. 2 (2021) 381–384. doi: 10.1016/j.gresc.2021.08.006
17. [17]
  O. Foss, J. Am. Chem. Soc. 69 (1947) 2236–2237.
18. [18]
  B.M. Trost, Chem. Rev. 78 (1978) 363–382. doi: 10.1021/cr60314a002
19. [19]
  D.H.R. Barton, B. Lacher, B. Misterkiewics, S.Z. Zard, Tetrahedron 44 (1988) 1153–1158. doi: 10.1016/S0040-4020(01)85895-6
20. [20]
  K. Fujiki, E. Yoshida, Synth. Commun. 29 (1999) 3289–3294. doi: 10.1080/00397919908085956
21. [21]
  S. Kim, S. Kim, N. Otsuka, I. Ryu, Angew. Chem. Int. Ed. 44 (2005) 6183–6186. doi: 10.1002/anie.200501606
22. [22]
  F. Kopp, P. Knochel, Org. Lett. 9 (2007) 1639–1641. doi: 10.1021/ol063136w
23. [23]
  S.H. Wunderlich, P. Knochel, Angew. Chem. Int. Ed. 46 (2007) 7685–7688. doi: 10.1002/anie.200701984
24. [24]
  V. Girijavallabhan, C. Alvarez, F.G. Njoroge, J. Org. Chem. 76 (2011) 6442–6446. doi: 10.1021/jo201016z
25. [25]
  P. Saravanan, P. Anbarasan, Org. Lett. 16 (2014) 848–851. doi: 10.1021/ol4036209
26. [26]
  S. Yoshida, Y. Sugimura, Y. Hazamam, et al., Chem. Commun. 51 (2015) 16613–16616. doi: 10.1039/C5CC07463K
27. [27]
  P.K. Shyam, H.Y. Jang, J. Org. Chem. 82 (2017) 1761–1767. doi: 10.1021/acs.joc.6b03016
28. [28]
  N. Wang, P. Saidhareddy, X. Jiang, Nat. Prod. Rep. 37 (2020) 246–275. doi: 10.1039/C8NP00093J
29. [29]
  H. Haruki, M.G. Pedersen, K.I. Gorska, F. Pojer, K. Johnsson, Science 340 (2013) 987–991. doi: 10.1126/science.1232972
30. [30]
  T.J. Deming, Bioconjugate Chem. 28 (2017) 691–700. doi: 10.1021/acs.bioconjchem.6b00696
31. [31]
  M. Yan, J.C. Lo, J.T. Edwards, P.S. Baran, J. Am. Chem. Soc. 138 (2016) 12692–12714. doi: 10.1021/jacs.6b08856
32. [32]
  S. Crespi, M. Chem. Rev. 120 (2020) 9790–9833. doi: 10.1021/acs.chemrev.0c00278
33. [33]
  A. Studer, D.P. Curran, Angew. Chem. Int. Ed. 55 (2016) 58–102. doi: 10.1002/anie.201505090
34. [34]
  K. Sun, Z.D. Shi, Z.H. Liu, et al., Org. Lett. 20 (2018) 6687–6690. doi: 10.1021/acs.orglett.8b02733
35. [35]
  K. Sun, S.N. Wang, R.R. Feng, et al., Org. Lett. 21 (2019) 2052–2055. doi: 10.1021/acs.orglett.9b00240
36. [36]
  K. Sun, G.F. Li, Y.Y. Li, et al., Adv. Synth. Catal. 362 (2020) 1947–1954. doi: 10.1002/adsc.202000040
37. [37]
  X. Wang, Q.L. Wang, Y.R. Xue, et al., Chem. Commun. 56 (2020) 4436–4439. doi: 10.1039/D0CC01079K
38. [38]
  K. Sun, X. Wang, C. Li, H. Wang, L. Li, Org. Chem. Front. 7 (2020) 3100–3119. doi: 10.1039/D0QO00849D
39. [39]
  X. Wang, S. Guo, Y. Zhang, et al., Adv. Synth. Catal. 363 (2021) 3290–3296. doi: 10.1002/adsc.202100208
40. [40]
  Y. Xing, C. Li, J.P. Meng, et al., Adv. Synth. Catal. 363 (2021) 3913–3936. doi: 10.1002/adsc.202100446
41. [41]
  X. Wang, Y. Zhang, K. Sun, J.P. Meng, B. Zhang, Chin. J. Org. Chem. 41 (2021) 4588–4609. doi: 10.6023/cjoc202109046
42. [42]
  S. Guo, X. Wang, D.Y. Zhao, et al., Asian J. Org. Chem. 11 (2022) e20210081.
43. [43]
  X. Wang, J. Lei, S. Guo, et al., Chem. Commun. 58 (2022) 1526–1529. doi: 10.1039/D1CC06323E
44. [44]
  C. Ghiazza, T. Billard, Eur. J. Org. Chem. 2021 (2021) 5571–5584. doi: 10.1002/ejoc.202100944
45. [45]
  S. Huang, Z.H. Xia, K. Lu, et al., Chin. J. Chem. 38 (2020) 1625–1628. doi: 10.1002/cjoc.202000279
46. [46]
  P. Mampuys, C.R. McElroy, J.H. Clark, R.V.A. Orru, B.U.W. Maes, Adv. Synth. Catal. 362 (2020) 3–64. doi: 10.1002/adsc.201900864
47. [47]
  M.D. Bentley, I.B. Douglass, J.A. Lacadie, J. Org. Chem. 37 (1972) 333–334. doi: 10.1021/jo00967a040
48. [48]
  G.G. Liang, J. Chen, J.L. Chen, et al., Tetrahedron Lett. 53 (2012) 6768–6770. doi: 10.1016/j.tetlet.2012.09.132
49. [49]
  N. Taniguchi, Eur. J. Org. Chem. 2014 (2014) 5691–5694. doi: 10.1002/ejoc.201402847
50. [50]
  P. Natarajan, Tetrahedron Lett. 56 (2015) 4131–4134. doi: 10.1016/j.tetlet.2015.05.050
51. [51]
  Y. Zheng, F.L. Qing, Y. Huang, X.H. Xu, Adv. Synth. Catal. 358 (2016) 3477–3481. doi: 10.1002/adsc.201600633
52. [52]
  X.J. Li, C. Zhou, P.H. Diao, Y.Q. Ge, C. Guo, Tetrahedron Lett. 58 (2017) 1296–1300. doi: 10.1016/j.tetlet.2017.02.042
53. [53]
  G.Y. Zhang, S.S. Lv, A. Shoberu, J.P. Zou, J. Org. Chem. 82 (2017) 9801–9807. doi: 10.1021/acs.joc.7b01121
54. [54]
  Z.Z. Yang, Y.S. Shi, Z. Zhan, et al., ChemElectroChem 5 (2018) 3619–3623. doi: 10.1002/celc.201801058
55. [55]
  X. Zhang, T. Cui, Y. Zhang, et al., Adv. Synth. Catal. 361 (2019) 2014–2019. doi: 10.1002/adsc.201900047
56. [56]
  A.K. Pandey, A. Kumar, N. Verma, S.K. Srivastava, Beilstein Arch (2021) 202115.
57. [57]
  X.C. Wang, C.M. Zhang, Y.D. Zhang, Z.H. Ren, Z.H. Guan, Chin. J. Org. Chem. 40 (2020) 1618–1624. doi: 10.6023/cjoc202002009
58. [58]
  H. Li, Y.X. Han, Z. Yang, et al., Chin. Chem. Lett. 32 (2021) 1709–1712. doi: 10.1016/j.cclet.2020.12.027
59. [59]
  P. Zhang, W.J. Chang, H.Y. Jiao, et al., Chin. Chem. Lett. 32 (2021) 1717–1720. doi: 10.1016/j.cclet.2021.01.024
60. [60]
  Z. Zhang, W.X. Chang, Chin. J. Org. Chem. 41 (2021) 1835–1850.
61. [61]
  S.P. Wu, D.K. Wang, Q.Q. Kang, et al., Chem. Commun. 57 (2021) 8288–8291. doi: 10.1039/D1CC03252F
62. [62]
  Y. Liu, S.Y. Xing, J. Zhang, et al., Org. Chem. Front. 9 (2022) 1375–1382. doi: 10.1039/D1QO01873F
63. [63]
  Y.H. Lv, J.P. Meng, C. Li, et al., Adv. Synth. Catal. 363 (2021) 5235–5265. doi: 10.1002/adsc.202101184
64. [64]
  K. Sun, Y. Li, Q. Zhang, Sci. China Chem. 58 (2015) 1354–1358. doi: 10.1007/s11426-015-5385-y
65. [65]
  K. Sun, X. Wang, L.L. Liu, et al., ACS Catal. 5 (2015) 7194–7198. doi: 10.1021/acscatal.5b02411
66. [66]
  D.H. Zhu, X.X. Shao, X. Hong, L. Lu, Q.L. Shen, Angew. Chem. 128 (2016) 16039–16043. doi: 10.1002/ange.201609468
67. [67]
  P.K. Shyam, S. Son, H.Y. Jang, Eur. J. Org. Chem. 2017 (2017) 5025–5031. doi: 10.1002/ejoc.201700971
68. [68]
  S. Huang, N. Thirupathi, C.H. Tung, Z.H. Xu, J. Org. Chem. 83 (2018) 9449–9455. doi: 10.1021/acs.joc.8b01161
69. [69]
  Q.J. Liang, P.J. Walsh, T.Z. Jia, ACS Catal. 10 (2020) 2633–2639. doi: 10.1021/acscatal.9b04887
70. [70]
  C.K. Prier, D.A. Rankic, D.W. MacMillan, Chem. Rev. 113 (2013) 5322–5363. doi: 10.1021/cr300503r
71. [71]
  M.N. Hopkinson, A. Tlahuext-Aca, F. Glorius, Acc. Chem. Res. 49 (2016) 2261–2272. doi: 10.1021/acs.accounts.6b00351
72. [72]
  N.A. Romero, D.A. Nicewicz, Chem. Rev. 116 (2016) 10075–10166. doi: 10.1021/acs.chemrev.6b00057
73. [73]
  X.Y. Yu, J.R. Chen, W.J. Xiao, Chem. Rev. 121 (2020) 506–561.
74. [74]
  T. Rawner, E. Lutsker, C.A. Kaiser, O. Reiser, ACS Catal. 8 (2018) 3950–3956. doi: 10.1021/acscatal.8b00847
75. [75]
  B. Lipp, L.M. Kammer, M. Kücükdisli, et al., Chem. Eur. J. 25 (2019) 8965–8969. doi: 10.1002/chem.201901175
76. [76]
  L.M. Kammer, M. Krumb, B. Spitzbarth, et al., Org. Lett. 22 (2020) 3318–3322. doi: 10.1021/acs.orglett.0c00614
77. [77]
  J.K. Liu, H. Yao, X.N. Li, et al., Org. Chem. Front. 7 (2020) 1314–1320. doi: 10.1039/D0QO00343C
78. [78]
  J. Li, X.E. Yang, S.L. Wang, et al., Org. Lett. 22 (2020) 4908–4913. doi: 10.1021/acs.orglett.0c01776
79. [79]
  K. Gadde, P. Mampuys, A. Guidetti, et al., ACS Catal. 10 (2020) 8765–8779. doi: 10.1021/acscatal.0c02159
80. [80]
  C.M. Huang, J. Li, J.J. Ai, et al., Org. Lett. 22 (2020) 9128–9132. doi: 10.1021/acs.orglett.0c03562
81. [81]
  Y. Dong, P. Ji, Y.T. Zhang, et al., Org. Lett. 22 (2020) 9562–9567. doi: 10.1021/acs.orglett.0c03624
82. [82]
  H. Chen, Y.Y. Yan, N.N. Zhang, et al., Org. Lett. 23 (2021) 376–381. doi: 10.1021/acs.orglett.0c03876
83. [83]
  F. Wang, S.Y. Wang, Org. Chem. Front. 8 (2021) 1976–1982. doi: 10.1039/D1QO00085C
84. [84]
  W.Y. Li, L. Zhou, Green Chem. 23 (2021) 6652–6658. doi: 10.1039/D1GC02036F
85. [85]
  W.Z. Bi, W.J. Zhang, Z.J. Li, et al., Org. Biomol. Chem. 19 (2021) 8701–8705. doi: 10.1039/D1OB01592C
86. [86]
  X.Y. Liu, S.Y. Tian, Y.F. Jiang, W.D. Rao, S.Y. Wang, Org. Lett. 23 (2021) 8246–8251. doi: 10.1021/acs.orglett.1c02981
87. [87]
  Y. Liu, N.N. Zhang, Y.L. Xu, Y.Y. Chen, J. Org. Chem. 86 (2021) 16882–16891. doi: 10.1021/acs.joc.1c02082
88. [88]
  J. Xuan, Z. Zhang, W. Xiao, Angew. Chem. Int. Ed. 54 (2015) 15632–15641. doi: 10.1002/anie.201505731
89. [89]
  C.K. Prier, D.A. Rankic, D.W.C. MacMillan, Chem. Rev. 113 (2013) 5322–5363. doi: 10.1021/cr300503r
90. [90]
  J. Xuan, W. Xiao, Angew. Chem. Int. Ed. 51 (2012) 6828–6838. doi: 10.1002/anie.201200223
91. [91]
  J.M.R. Narayanam, C.R.J. Stephenson, Chem. Soc. Rev. 40 (2011) 102–113. doi: 10.1039/B913880N
92. [92]
  T.P. Yoon, M.A. Ischay, J. Du, Nat. Chem. 2 (2010) 527–532. doi: 10.1038/nchem.687
93. [93]
  T. Chatterjee, N. Iqbal, Y. You, E.J. Cho, Acc. Chem. Res. 49 (2016) 2284–2294. doi: 10.1021/acs.accounts.6b00248
94. [94]
  K.L. Skubi, T.R. Blum, T.P. Yoon, Chem. Rev. 116 (2016) 10035–10074. doi: 10.1021/acs.chemrev.6b00018
95. [95]
  D. Kalyani, K.B. McMurtrey, S.R. Neufeldt, M.S. Sanford, J. Am. Chem. Soc. 133 (2011) 18566–18569. doi: 10.1021/ja208068w
96. [96]
  S.R. Neufeldt, M.S. Sanford, Adv. Synth. Catal. 354 (2012) 3517–3522. doi: 10.1002/adsc.201200738
97. [97]
  J. Zoller, D.C. Fabry, M.A. Ronge, M. Rueping, Angew. Chem. Int. Ed. 53 (2014) 13264–13268. doi: 10.1002/anie.201405478
98. [98]
  J. Xuan, T. Zeng, Z. Feng, et al., Angew. Chem. Int. Ed. 54 (2015) 1625–1628. doi: 10.1002/anie.201409999
99. [99]
  J.A. Terrett, J.D. Cuthbertson, V.W. Shurtleff, D.W.C. MacMillan, Nature 524 (2015) 330–334. doi: 10.1038/nature14875
100. [100]
  Z. Zuo, H. Cong, W. Li, et al., J. Am. Chem. Soc. 138 (2016) 1832–1835. doi: 10.1021/jacs.5b13211
101. [101]
  Y. Ye, M.S. Sanford, J. Am. Chem. Soc. 134 (2012) 9034–9037. doi: 10.1021/ja301553c
102. [102]
  A.Y. Chan, I.B. Perry, N.B. Bissonnette, et al., Chem. Rev. 122 (2022) 1485–1542. doi: 10.1021/acs.chemrev.1c00383
103. [103]
  H.Y. Li, C.C. Shan, C.H. Tung, Z.H. Xu, Chem. Sci. 8 (2017) 2610–2615. doi: 10.1039/C6SC05093J
104. [104]
  T.T. Song, H.Y. Li, F. Wei, C.H. Tung, Z.H. Xu, Tetrahedron Lett. 60 (2019) 916–919. doi: 10.1016/j.tetlet.2019.02.039
105. [105]
  R. Zhang, P. Xu, S.Y. Wang, S.J. Ji, J. Org. Chem. 84 (2019) 12324–12333. doi: 10.1021/acs.joc.9b01626
106. [106]
  X. Zhou, Z.Y. Peng, P.G. Wang, Q.C. Liu, T.Z. Jia, Org. Lett. 23 (2021) 1054–1059. doi: 10.1021/acs.orglett.0c04254
107. [107]
  T.G. Back, S. Collins, R.G. Kerr, J. Org. Chem. 48 (1983) 3077–3084. doi: 10.1021/jo00166a030
108. [108]
  P. Mampuys, Y.P. Zhu, S. Sergeyev, et al., Org. Lett. 18 (2016) 2808–2811. doi: 10.1021/acs.orglett.6b01023
109. [109]
  N. Taniguchi, Tetrahedron 73 (2017) 2030–2035. doi: 10.1016/j.tet.2017.02.047
110. [110]
  S.J. Hwang, P.K. Shyam, H.Y. Jang, Bull. Korean Chem. Soc. 39 (2018) 535–539. doi: 10.1002/bkcs.11426
111. [111]
  S. Son, P.K. Shyam, H. Park, I. Jeong, H.Y. Jang, Eur. J. Org. Chem. 2018 (2018) 3365–3371. doi: 10.1002/ejoc.201800778
112. [112]
  Y. Fang, C. Liu, F. Wang, et al., Org. Chem. Front. 6 (2019) 660–663.
113. [113]
  Y. Fang, C. Liu, W.D. Rao, S.Y. Wang, S.J. Ji, Org. Lett. 21 (2019) 7687–7691. doi: 10.1021/acs.orglett.9b01886
114. [114]
  L. Cao, C. Jimeno, P. Renaud, Adv. Synth. Catal. 362 (2020) 3644–3648. doi: 10.1002/adsc.202000657
115. [115]
  F. Wang, B.X. Liu, W.D. Rao, S.Y. Wang, Org. Lett. 22 (2020) 6600–6604. doi: 10.1021/acs.orglett.0c02370
116. [116]
  K.M. Mao, M.W. Bian, L. Dai, et al., Org. Lett. 23 (2021) 218–224. doi: 10.1021/acs.orglett.0c03946
117. [117]
  A. Shankar, M. Waheed, R.J. Reddy, SynOpen 5 (2021) 91–99. doi: 10.1055/a-1422-9411
1. [1]
  Hangwen Zheng , Ziqian Wang , HuiJie Zhang , Jing Lei , Rihui Li , Jian Yang , Haiyan Wang . Synthesis and applications of B, N co-doped carbons for zinc-based energy storage devices. Chinese Chemical Letters, 2025, 36(3): 110245-. doi: 10.1016/j.cclet.2024.110245
2. [2]
  Zhengzhong Zhu , Shaojun Hu , Zhi Liu , Lipeng Zhou , Chongbin Tian , Qingfu Sun . A cationic radical lanthanide organic tetrahedron with remarkable coordination enhanced radical stability. Chinese Chemical Letters, 2025, 36(2): 109641-. doi: 10.1016/j.cclet.2024.109641
3. [3]
  Hao Lv , Zhi Li , Peng Yin , Ping Wan , Mingshan Zhu . Recent progress on non-metallic carbon nitride for the photosynthesis of H₂O₂: Mechanism, modification and in-situ applications. Chinese Chemical Letters, 2025, 36(1): 110457-. doi: 10.1016/j.cclet.2024.110457
4. [4]
  Xiao-Bo Liu , Ren-Ming Liu , Xiao-Di Bao , Hua-Jian Xu , Qi Zhang , Yu-Feng Liang . Nickel-catalyzed reductive formylation of aryl halides via formyl radical. Chinese Chemical Letters, 2024, 35(12): 109783-. doi: 10.1016/j.cclet.2024.109783
5. [5]
  Zhongjie Li , Xiangyue Kong , Yuhao Liu , Huayu Qiu , Lingling Zhan , Shouchun Yin . Progress of additives for morphology control in organic photovoltaics. Chinese Chemical Letters, 2024, 35(6): 109378-. doi: 10.1016/j.cclet.2023.109378
6. [6]
  Yulong Shi , Fenbei Chen , Mengyuan Wu , Xin Zhang , Runze Meng , Kun Wang , Yan Wang , Yuheng Mei , Qionglu Duan , Yinghong Li , Rongmei Gao , Yuhuan Li , Hongbin Deng , Jiandong Jiang , Yanxiang Wang , Danqing Song . Chemical construction and anti-HCoV-OC43 evaluation of novel 10,12-disubstituted aloperine derivatives as dual cofactor inhibitors of TMPRSS2 and SR-B1. Chinese Chemical Letters, 2024, 35(5): 108792-. doi: 10.1016/j.cclet.2023.108792
7. [7]
  Huiju Cao , Lei Shi . sp¹-Hybridized linear and cyclic carbon chain. Chinese Chemical Letters, 2025, 36(4): 110466-. doi: 10.1016/j.cclet.2024.110466
8. [8]
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9. [9]
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10. [10]
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11. [11]
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12. [12]
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13. [13]
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14. [14]
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15. [15]
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16. [16]
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17. [17]
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18. [18]
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19. [19]
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20. [20]
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沈阳化工大学材料科学与工程学院沈阳 110142