Citation: Feng Zhao, Hongyu Ding, Ting Sun, Chao Shen, Zu-Li Wang, Wei Wei, Dong Yi. Visible-light-promoted multi-component carbene transfer reactions of diazo compounds via ring-opening of cyclic ethers[J]. Chinese Chemical Letters, ;2026, 37(2): 111834. doi: 10.1016/j.cclet.2025.111834 shu

Visible-light-promoted multi-component carbene transfer reactions of diazo compounds via ring-opening of cyclic ethers

Feng Zhao ^{a, 1} ,
Hongyu Ding ^{b, c, 1} ,
Ting Sun ^a ,
Chao Shen ^{b, *,} ,
Zu-Li Wang ^e ,
Wei Wei ^{c, *,} ,
Dong Yi ^{d, *,}

a.
School of Chemistry and Materials Science, Guizhou Integrated Research Center of Polymer Electromagnetic Materials, Key Laboratory of Functional Organic Molecule, Guizhou Education University, Guiyang 550018, China
b.
Zhejiang Collaborative Innovation Center for Full-Process Monitoring and Green Governance of Emerging Contaminants, College of Biology and Environmental Engineering, Zhejiang Shuren University, Hangzhou 310015, China
c.
School of Chemistry and Chemical Engineering, Qufu Normal University, Qufu 273165, China
d.
Green Pharmaceutical Technology Key Laboratory of Luzhou City, School of Pharmacy, Southwest Medical University, Luzhou 646000, China
e.
College of Chemical Engineering, Nanjing Forestry University, Nanjing 210037, China

shenchaozju@zjsru.edu.cn

weiweiqfnu@163.com

yidong@swmu.edu.cn

Received Date: 19 July 2025
Revised Date: 1 September 2025
Accepted Date: 11 September 2025
Available Online: 13 September 2025

Figures(37)

Carbenes as one of the most important class of intermediates have been widely utilized in various organic synthetic transformations. Carbene insertion-initiated ring-opening reactions of cyclic ethers offer a valuable strategy for constructing new carbon-oxygen bonds. In comparison with traditional thermal or metal-mediated carbene transfer reactions, visible-light-promoted multi-component reaction strategy provides a mild and eco-friendly approach to access densely functionalized molecules. Recently, visible-light-induced multi-component carbene transfer reactions of diazo compounds have been rapidly developed and attracted a great deal of research interest of chemists owing to their advantages of simple operation, mild condition, high atom economy and rich structural diversity. This paper summarizes the recent research progress on the visible-light-promoted multi-component carbene transfer reactions of diazo compounds via ring-opening of cyclic ethers with various nucleophiles. The reaction patterns of different nucleophiles and their corresponding mechanism are described in this review. The future research direction and challenges in this area are also discussed.
- Visible-light,
- Multi-component reaction,
- Carbene insertion,
- Diazo compounds,
- Ring-opening reaction
1. [1]
  C. Empel, S. Jana, R.M. Koenigs, Molecules 25 (2020) 880. doi: 10.3390/molecules25040880
2. [2]
  S.T. Liu, K.R. Reddy, Chem. Soc. Rev. 28 (1999) 315–322.
3. [3]
  T.R. Roose, D.S. Verdoorn, P. Mampuys, et al., Chem. Soc. Rev. 51 (2022) 5842–5877. doi: 10.1039/d1cs00305d
4. [4]
  D. Zhu, L. Chen, H. Fan, et al., Chem. Soc. Rev. 49 (2020) 908–950. doi: 10.1039/c9cs00542k
5. [5]
  M.Y. Huang, S.F. Zhu, Chem. Sci. 12 (2021) 15790–15801. doi: 10.1039/d1sc03328j
6. [6]
  X. Shen, Acc. Chem. Res. 58 (2025) 1519–1533. doi: 10.1021/acs.accounts.5c00136
7. [7]
  Y. Zhang, G. Zhou, S. Liu, X. Shen, Chem. Soc. Rev. 54 (2025) 1870–1904. doi: 10.1039/d4cs01275e
8. [8]
  C. Damiano, P. Sonzini, E. Gallo, Chem. Soc. Rev. 49 (2020) 4867–4905. doi: 10.1039/d0cs00221f
9. [9]
  X. Zhang, L. Li, P. Sivaguru, et al., Chem. Commun. 58 (2022) 13699–13715. doi: 10.1039/d2cc04845k
10. [10]
  D. Qiu, J. Wang, Recent Developments of Diazo Compounds in Organic Synthesis, World Scientific, 2021.
11. [11]
  J. Wang, C.M. Che, M.P. Doyle, Transition Metal-Catalyzed Carbene Transformations, John Wiley & Sons, 2021.
12. [12]
  Y. He, Z. Huang, K. Wu, et al., Chem. Soc. Rev. 51 (2022) 2759–2852. doi: 10.1039/d1cs00895a
13. [13]
  C. Jing, Q.Q. Cheng, Y. Deng, et al., Org. Lett. 18 (2016) 4550–4553. doi: 10.1021/acs.orglett.6b02192
14. [14]
  C. Qin, H.M.L. Davies, J. Am. Chem. Soc. 135 (2013) 14516–14519. doi: 10.1021/ja4069003
15. [15]
  W. Zhang, S. Chen, Y. Zhang, et al., Angew. Chem. Int. Ed. 64 (2025) e202422020.
16. [16]
  D.M. Hodgson, F.Y.T.M. Pierard, P.A. Stupple, Chem. Soc. Rev. 30 (2001) 50–61.
17. [17]
  F. Tan, X. Liu, X. Hao, et al., ACS Catal. 6 (2016) 6930–6934. doi: 10.1021/acscatal.6b02184
18. [18]
  S.F. Zhu, B. Xu, G.P. Wang, et al., J. Am. Chem. Soc. 134 (2012) 436–442. doi: 10.1021/ja2084493
19. [19]
  C. Qin, H.M.L. Davies, J. Am. Chem. Soc. 136 (2014) 9792–9796. doi: 10.1021/ja504797x
20. [20]
  Y. Xia, D. Qiu, J.B. Wang, Chem. Rev. 117 (2017) 13810–13889. doi: 10.1021/acs.chemrev.7b00382
21. [21]
  Y. Xia, Y. Zhang, J.B. Wang, ACS Catal. 3 (2013) 2586–2598. doi: 10.1021/cs4006666
22. [22]
  S. Gupta, A. Kundu, S. Ghosh, et al., Green Chem. 25 (2023) 8459–8493. doi: 10.1039/d3gc03291d
23. [23]
  Q. Feng, J. Hao, Y. Hu, et al., Chin. Chem. Lett. 36 (2025) 110582.
24. [24]
  H.C. Li, M. Zhang, Q. Lv, et al., Chin. Chem. Lett. 36 (2025) 110579.
25. [25]
  Q. Zhao, Q. Zhang, X. Wu, et al., Chin. Chem. Lett. 36 (2025) 110167.
26. [26]
  Y. Wang, J. Wang, C. Chen, et al., Chem. Commun. 61 (2025) 10812–10815. doi: 10.1039/d5cc02744f
27. [27]
  Y.H. Lu, C. Wu, J.C. Hou, et al., ACS Catal. 13 (2023) 13071–13076. doi: 10.1021/acscatal.3c02268
28. [28]
  H.T. Ji, K.L. Wang, W.T. Ouyang, et al., Green Chem. 25 (2023) 7983–7987. doi: 10.1039/d3gc02575f
29. [29]
  L.W. Ciszewski, K. Rybicka-Jasinska, D. Gryko, Org. Biomol. Chem. 17 (2019) 432–448. doi: 10.1039/c8ob02703j
30. [30]
  Z. Yang, M.L. Stivanin, I.D. Jurberg, et al., Chem. Soc. Rev. 49 (2020) 6833–6847. doi: 10.1039/d0cs00224k
31. [31]
  W.T. Ouyang, J. Jiang, Y.F. Jiang, et al., Chin. Chem. Lett. 35 (2024) 110038.
32. [32]
  H.Y. Song, J. Jiang, C. Wu, et al., Green Chem. 25 (2023) 3292–3296. doi: 10.1039/d2gc04843d
33. [33]
  N. Meng, Y. Lv, Q. Liu, et al., Chin. Chem. Lett. 32 (2021) 258–262.
34. [34]
  M. Zhang, G. Nan, X. Zhao, et al., Chin. J. Org. Chem. 42 (2022) 4315–4322. doi: 10.6023/cjoc202209013
35. [35]
  Y.H. Lu, S.Y. Mu, J. Jiang, et al., ChemSusChem 16 (2023) e202300523.
36. [36]
  X. Cheng, B.G. Cai, H. Mao, et al., Org. Lett. 23 (2021) 4109–4114. doi: 10.1021/acs.orglett.1c00979
37. [37]
  H.B. Ye, X.Y. Zhou, L. Li, et al., Org. Lett. 24 (2022) 6018–6023. doi: 10.1021/acs.orglett.2c02313
38. [38]
  S. Li, J. Ling, L. Zhou, Org. Lett. 26 (2024) 5220–5225. doi: 10.1021/acs.orglett.4c01876
39. [39]
  I.D. Jurberg, H.M.L. Davies, Chem. Sci. 9 (2018) 5112–5118. doi: 10.1039/c8sc01165f
40. [40]
  T. Xiao, M. Mei, Y. He, L. Zhou, Chem. Commun. 54 (2018) 8865–8868. doi: 10.1039/c8cc04609c
41. [41]
  R. Hommelsheim, Y. Guo, Z. Yang, et al., Angew. Chem. Int. Ed. 58 (2019) 1203–1207. doi: 10.1002/anie.201811991
42. [42]
  B.G. Cai, S.S. Luo, L. Li, et al., CCS Chem. 2 (2020) 2764–2771.
43. [43]
  R. Cheng, C. Qi, L. Wang, et al., Chem. Soc. Rev. 49 (2020) 6833–6847.
44. [44]
  S. Zhou, B. Cai, C. Hu, et al., Chin. Chem. Lett. 32 (2021) 2577–2581.
45. [45]
  Z. Chen, J. Chen, J. Xuan, Chin. Chem. Lett. 33 (2022) 2763–2764.
46. [46]
  P. Duan, H. Zhao, J. Yang, et al., Org. Lett. 24 (2022) 608–612. doi: 10.1021/acs.orglett.1c04048
47. [47]
  Y. Guo, G. Zhou, X. Shen, Chin. J. Chem. 42 (2024) 887–902. doi: 10.1002/cjoc.202300569
48. [48]
  G. Zhou, X. Shen, Angew. Chem. Int. Ed. 61 (2022) e202115334.
49. [49]
  S. Chen, Y. Zhang, S. Liu, X. Shen, Sci. China Chem. 66 (2023) 3141–3147. doi: 10.1007/s11426-023-1676-y
50. [50]
  R.D.C. Gallo, G. Cariello, T.A.C. Goulart, I.D. Jurberg, Chem. Commun. 59 (2023) 7346–7360. doi: 10.1039/d3cc00988b
51. [51]
  Z. Zhang, V. Gevorgyan, Chem. Rev. 124 (2024) 7214–7261. doi: 10.1021/acs.chemrev.3c00869
52. [52]
  D. Qi, J. Bai, H. Zhang, et al., Green Chem. 24 (2022) 5046–5051. doi: 10.1039/d2gc01362b
53. [53]
  D.K. Jha, S. Acharya, N. Sakkani, et al., Org. Lett. 26 (2024) 172–177. doi: 10.1021/acs.orglett.3c03805
54. [54]
  Y.N. Wang, X. Wang, S.J. Li, Y. Lan, Org. Chem. Front. 9 (2022) 1247–1253. doi: 10.1039/d1qo01730f
55. [55]
  T. Wang, N. Jiao, Acc. Chem. Res. 47 (2014) 1137–1145. doi: 10.1021/ar400259e
56. [56]
  F.F. Fleming, L. Yao, P.C. Ravikumar, et al., J. Med. Chem. 53 (2010) 7902–7917. doi: 10.1021/jm100762r
57. [57]
  J.M. Crance, N. Scaramozzino, A. Jouan, D. Garin, Antiviral Res. 58 (2003) 73–79.
58. [58]
  J. Liu, Y. Gong, J. Shi, et al., Eur. J. Med. Chem. 194 (2020) 112244.
59. [59]
  W. Yuan, K.J. Szabó, ACS Catal. 6 (2016) 6687–6691. doi: 10.1021/acscatal.6b01760
60. [60]
  F. He, C. Pei, R.M. Koenigs, Chem. Commun. 56 (2020) 599–602. doi: 10.1039/c9cc08888a
61. [61]
  D. Maiti, R. Das, S. Sen, Green Chem. 23 (2021) 8533–8544. doi: 10.1039/d1gc02797b
62. [62]
  S.K. Hota, S. Murarka, Chem. Asian J. (2023) e202301027.
63. [63]
  M.L. Stivanin, R.D.C. Gallo, J.P.M. Spadeto, et al., Org. Chem. Front. 9 (2022) 1321–1326. doi: 10.1039/d1qo01780b
64. [64]
  S. Xia, Y. Jian, L. Zhang, et al., RSC Adv. 13 (2023) 14501–14505. doi: 10.1039/d3ra02407e
65. [65]
  Z. Wang, J. Hao, Y. Lv, et al., Asian J. Org. Chem. 11 (2022) e202200484.
66. [66]
  B.G. Cai, G.Y. Xu, J. Xuan, Chin. Chem. Lett. 34 (2023) 108335.
67. [67]
  S. Fustero, M. Sánchez-Roselló, P. Barrio, A. Simón-Fuentes, Chem. Rev. 111 (2011) 6984–7034. doi: 10.1021/cr2000459
68. [68]
  M.F. Khan, M.M. Alam, G. Verma, et al., Eur. J. Med. Chem. 120 (2016) 170–201.
69. [69]
  V. Kumar, K. Kaur, G.K. Gupta, A.K. Sharma, Eur. J. Med. Chem. 69 (2013) 735–753.
70. [70]
  H. Ding, Z. Wang, C. Qu, et al., Org. Chem. Front. 9 (2022) 5530–5535. doi: 10.1039/d2qo01082h
71. [71]
  J. Klankermayer, S. Wesselbaum, K. Beydoun, W. Leitner, Angew. Chem. Int. Ed. 55 (2016) 7296–7343. doi: 10.1002/anie.201507458
72. [72]
  S.S. Yan, Q. Fu, L.L. Liao, et al., Coord. Chem. Rev. 374 (2018) 439–463.
73. [73]
  R. Cheng, C. Qi, L. Wang, et al., Green Chem. 22 (2020) 4890–4895. doi: 10.1039/d0gc00910e
74. [74]
  B. Rong, G. Xu, H. Yan, et al., Chem. Commun. 57 (2021) 7272–7275. doi: 10.1039/d1cc02422a
75. [75]
  M. Murakami, N. Ishida, Chem. Rev. 121 (2021) 264–299. doi: 10.1021/acs.chemrev.0c00569
76. [76]
  Q. Li, B.G. Cai, L. Li, J. Xuan, Org. Lett. 23 (2021) 6951–6955. doi: 10.1021/acs.orglett.1c02555
77. [77]
  M.L. Stivanin, M. Duarte, L.P.M.O. Leão, et al., J. Org. Chem. 86 (2021) 17528–17532. doi: 10.1021/acs.joc.1c02411
78. [78]
  B.-G. Cai, Q. Li, Q. Zhang, et al., Org. Chem. Front. 8 (2021) 5982–5987. doi: 10.1039/d1qo01102b
79. [79]
  C. Qu, J. Hao, H. Ding, et al., J. Org. Chem. 87 (2022) 12921–12931. doi: 10.1021/acs.joc.2c01499
80. [80]
  S. Bertrand, J.J. Helesbeux, G. Larcher, O. Duval, Mini-Rev. Med. Chem. 13 (2013) 1311–1326. doi: 10.2174/13895575113139990007
81. [81]
  A. Citarella, D. Moi, L. Pinzi, et al., ACS Omega 6 (2021) 21843–21849. doi: 10.1021/acsomega.1c03628
82. [82]
  B.G. Cai, Li Q, C. Empel, et al., ACS Catal. 12 (2022) 11129–11136. doi: 10.1021/acscatal.2c02875
83. [83]
  R. Liu, S. Fu, X. Chu, et al., Chin. J. Org. Chem. 42 (2022) 2462–2470. doi: 10.6023/cjoc202204014
84. [84]
  K. Zhu, W.J. Yu, X. Zhou, et al., Chem. Commun. 59 (2023) 12605–12608. doi: 10.1039/d3cc03317a
85. [85]
  P. Li, X. Jia, Synthesis (2018) 711–722.
86. [86]
  R. Bag, D. Sar, T. Punniyamurthy, ACS Omega 2 (2017) 6278–6290. doi: 10.1021/acsomega.7b01111
87. [87]
  B.A. Mir, S. Rajamanickam, P. Begum, B.K. Patel, Eur. J. Org. Chem. (2020) 2617–2625. doi: 10.1002/ejoc.202000149
88. [88]
  Y. Lv, J. Hao, J. Huang, et al., Chem. Commun. 60 (2024) 9801–9804. doi: 10.1039/d4cc03272a
89. [89]
  S. Dutta, H. Abe, S. Aoyagi, et al., J. Am. Chem. Soc. 127 (2005) 15004–15005. doi: 10.1021/ja053735i
90. [90]
  M. Burow, A. Bergner, J. Gershenzon, U. Wittstock, Plant Mol. Biol. 63 (2006) 49–61. doi: 10.1007/s11103-006-9071-5
91. [91]
  R. Ding, S. Shi, C. Ma, et al., Chin. J. Org. Chem. 44 (2024) 2216–2222. doi: 10.6023/cjoc202403029
92. [92]
  X.M. Chen, L. Song, J. Pan, et al., Chin. Chem. Lett. 35 (2024) 110112.
93. [93]
  X. Chen, J. Huang, J. Pan, et al., Org. Lett. 26 (2024) 3883–3888. doi: 10.1021/acs.orglett.4c01038
94. [94]
  J. Li, C. Chen, X. Li, et al., Chin. Chem. Lett. 35 (2024) 109732.
95. [95]
  J. Hao, Y. Lv, S. Tian, et al., Chin. Chem. Lett. 35 (2024) 109513.
96. [96]
  C. Wu, S. Wu, Q. Huang, et al., Chin. Chem. Lett. 36 (2025) 110250.
97. [97]
  Y. Lv, R. Liu, H. Ding, et al., Org. Chem. Front. 9 (2022) 3486–3492. doi: 10.1039/d2qo00311b
98. [98]
  C. Qu, R. Liu, Z. Wang, et al., Green Chem. 24 (2022) 4915–4920. doi: 10.1039/d2gc00903j
99. [99]
  Z. Wang, R. Liu, C. Qu, et al., Org. Chem. Front. 9 (2022) 3565–3570. doi: 10.1039/d2qo00539e
100. [100]
  Z. Wang, N. Meng, Y. Lv, et al., Chin. Chem. Lett. 34 (2023) 107599.
101. [101]
  Y. Lv, Z. Wang, J. Hao, et al., Asian J. Org. Chem. 12 (2023) e202300290.
102. [102]
  Y. Lv, H. Ding, J. You, et al., Chin. Chem. Lett. 35 (2024) 109107.
1. [1]
  Jun Huang , Jiangping Qin , Caijin Ban , Jingmei Yuan , Jing Yang , Guoping Yang . Visible-light induced cascade sulfonation/cyclization reaction in water towards sulfonated dihydroisoquinolino[1,2-b]quinazolinones. Chinese Chemical Letters, 2026, 37(2): 111379-. doi: 10.1016/j.cclet.2025.111379
2. [2]
  Qiang Feng , Jindong Hao , Ya Hu , Rong Fu , Wei Wei , Dong Yi . Photocatalytic multi-component synthesis of ester-containing quinoxalin-2(1H)-ones using water as the hydrogen donor. Chinese Chemical Letters, 2025, 36(6): 110582-. doi: 10.1016/j.cclet.2024.110582
3. [3]
  Hua Tian , Xin Yang , Ge Shi , Heng Xu , Yi Dong . Rhodium-catalyzed site-selective cross-couplings of indoles and pyridotriazoles through carbene insertion. Chinese Chemical Letters, 2025, 36(7): 110434-. doi: 10.1016/j.cclet.2024.110434
4. [4]
  Sixiao Liu , Tianyi Wang , Lei Zhang , Chengyin Wang , Huan Pang . Cerium-based metal-organic framework-modified natural mineral vermiculite for photocatalytic nitrogen fixation under visible-light irradiation. Chinese Chemical Letters, 2025, 36(3): 110058-. doi: 10.1016/j.cclet.2024.110058
5. [5]
  Yi Luo , Lin Dong . Multicomponent remote C(sp²)-H bond addition by Ru catalysis: An efficient access to the alkylarylation of 2H-imidazoles. Chinese Chemical Letters, 2024, 35(10): 109648-. doi: 10.1016/j.cclet.2024.109648
6. [6]
  Chunyan Yang , Qiuyu Rong , Fengyin Shi , Menghan Cao , Guie Li , Yanjun Xin , Wen Zhang , Guangshan Zhang . Rationally designed S-scheme heterojunction of BiOCl/g-C₃N₄ for photodegradation of sulfamerazine: Mechanism insights, degradation pathways and DFT calculation. Chinese Chemical Letters, 2024, 35(12): 109767-. doi: 10.1016/j.cclet.2024.109767
7. [7]
  Guoju Guo , Xufeng Li , Jie Ma , Yongjia Shi , Jian Lv , Daoshan Yang . Photocatalyst/metal-free sequential C–N/C–S bond formation: Synthesis of S-arylisothioureas via photoinduced EDA complex activation. Chinese Chemical Letters, 2024, 35(11): 110024-. doi: 10.1016/j.cclet.2024.110024
8. [8]
  Dong-Sheng Deng , Su-Qin Tang , Yong-Tu Yuan , Ding-Xiong Xie , Zhi-Yuan Zhu , Yue-Mei Huang , Yun-Lin Liu . C-F insertion reaction sheds new light on the construction of fluorinated compounds. Chinese Chemical Letters, 2024, 35(8): 109417-. doi: 10.1016/j.cclet.2023.109417
9. [9]
  Rong-Nan Yi , Wei-Min He . Visible light/copper catalysis enabled radial type ring-opening of sulfonium salts. Chinese Chemical Letters, 2025, 36(4): 110787-. doi: 10.1016/j.cclet.2024.110787
10. [10]
  Qinghong Zhang , Qiao Zhao , Xiaodi Wu , Li Wang , Kairui Shen , Yuchen Hua , Cheng Gao , Yu Zhang , Mei Peng , Kai Zhao . Visible-light-induced ring-opening cross-coupling of cycloalcohols with vinylazaarenes and enones via β-C-C scission enabled by proton-coupled electron transfer. Chinese Chemical Letters, 2025, 36(2): 110167-. doi: 10.1016/j.cclet.2024.110167
11. [11]
  Xuhui Fan , Fan Wang , Mengjiao Li , Faiza Meharban , Yaying Li , Yuanyuan Cui , Xiaopeng Li , Jingsan Xu , Qi Xiao , Wei Luo . Visible light excitation on CuPd/TiN with enhanced chemisorption for catalyzing Heck reaction. Chinese Chemical Letters, 2025, 36(1): 110299-. doi: 10.1016/j.cclet.2024.110299
12. [12]
  Ting Zhang , Baojing Huang , Hong Huang , Ailing Yan , Shiqiang Lu , Xufang Qian . Visible light boosted Fenton-like reaction of carbon dot-Fe(Ⅲ) complex: Kinetics and mechanism insights. Chinese Chemical Letters, 2025, 36(11): 110885-. doi: 10.1016/j.cclet.2025.110885
13. [13]
  Qiongqiong Wan , Yanan Xiao , Guifang Feng , Xin Dong , Wenjing Nie , Ming Gao , Qingtao Meng , Suming Chen . Visible-light-activated aziridination reaction enables simultaneous resolving of C=C bond location and the sn-position isomers in lipids. Chinese Chemical Letters, 2024, 35(4): 108775-. doi: 10.1016/j.cclet.2023.108775
14. [14]
  Shifang Song , Chenyu Wu , Li Zhang , Dezhi Yang , Yang Lu , Zhengzheng Zhou . Unpacking phase transitions in multi-component drug systems: A case study. Chinese Chemical Letters, 2025, 36(7): 110911-. doi: 10.1016/j.cclet.2025.110911
15. [15]
  Nana Yang , Rui Yuan , Xinyue Fu , Xiao Tian , Jin Yu , Shengzhou Ma , Liuqing Wen , Jiabin Zhang . Concise synthesis of NDP-activated uronic acid by an oxidation reaction insertion strategy. Chinese Chemical Letters, 2025, 36(8): 110757-. doi: 10.1016/j.cclet.2024.110757
16. [16]
  Yue Sun , Liming Yang , Yaohang Cheng , Guanghui An , Guangming Li . Pd(I)-catalyzed ring-opening arylation of cyclopropyl-α-aminoamides: Access to α-ketoamide peptidomimetics. Chinese Chemical Letters, 2024, 35(6): 109250-. doi: 10.1016/j.cclet.2023.109250
17. [17]
  Pei Xu , Tian-Zi Hao , Zhi-Tao Liu , Yi-Qin Liu , Hui-Xian Jiang , Dong Guo , Xu Zhu . Visible-light-induced dual catalysis for divergent reduction of nitro compounds with CO₂ radical anion. Chinese Chemical Letters, 2025, 36(10): 110899-. doi: 10.1016/j.cclet.2025.110899
18. [18]
  Tian-Yu Gao , Xiao-Yan Mo , Shu-Rong Zhang , Yuan-Xu Jiang , Shu-Ping Luo , Jian-Heng Ye , Da-Gang Yu . Visible-light photoredox-catalyzed carboxylation of aryl epoxides with CO₂. Chinese Chemical Letters, 2024, 35(7): 109364-. doi: 10.1016/j.cclet.2023.109364
19. [19]
  Jing Wang , Zenghui Li , Xiaoyang Liu , Bochao Su , Honghong Gong , Chao Feng , Guoping Li , Gang He , Bin Rao . Fine-tuning redox ability of arylene-bridged bis(benzimidazolium) for electrochromism and visible-light photocatalysis. Chinese Chemical Letters, 2024, 35(9): 109473-. doi: 10.1016/j.cclet.2023.109473
20. [20]
  Yao Zou , Difei Gong , Haiguang Yang , Hongmei Yu , Guorong He , Ningbo Gong , Lianhua Fang , Guanhua Du , Yang Lu . Prediction, screening, characterization, antioxidant and antihypoxic effects of multi-component zwitterionic cocrystals of dietary flavonoids with picolinic acid. Chinese Chemical Letters, 2025, 36(9): 110768-. doi: 10.1016/j.cclet.2024.110768

Get Citation

PDF

XML

Metrics

PDF Downloads(0)
Abstract views(9)
HTML views(0)

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