Citation: Zhou Mingdong, Qin Pitao, Jing Like, Sun Jing, Du Haiwu. Progress in Photoinduced Decarboxylative Radical Cross-Coupling of Alkyl Carboxylic Acids and Their Derivatives[J]. Chinese Journal of Organic Chemistry, ;2020, 40(3): 598-613. doi: 10.6023/cjoc201909030 shu

Progress in Photoinduced Decarboxylative Radical Cross-Coupling of Alkyl Carboxylic Acids and Their Derivatives

College of Chemistry, Chemical Engineering and Environmental Engineering, Liaoning Shihua University, Fushun, Liaoning 113001

Corresponding author: Zhou Mingdong, mingdong.zhou@lnpu.edu.cn Sun Jing, sungjing@lnpu.edu.cn
Received Date: 18 September 2019
Revised Date: 1 November 2019
Available Online: 2 December 2019
Fund Project: Project supported by the Doctoral Start-up Foundation of Liaoning Province (No. 20180540085)the Doctoral Start-up Foundation of Liaoning Province 20180540085

Figures(21)

Alkyl carboxylic acids are among the most ubiquitous organic molecules found in nature. The reactions using abundant carboxylic acid and its derivatives as starting materials deserve widespread attention over the world. They are often easy to generate alkyl radical by photoredox catalysis under mild conditions for building various chemical bonds in organic chemistry. Based on the reaction modes, decarboxylation of alkylcarboxylic acids and their derivatives, the recent progress in decarboxylation of alkylcarboxylic acids and their derivatives under visible light is reviewed.
- photocatalysis,
- decarboxylative,
- alkyl radical
1. [1]
  Lunbderg, H.; Tinnis, F.; Selander, N.; Adolfsson, H. Chem. Soc. Rev. 2014, 43, 2714. doi: 10.1039/C3CS60345H
2. [2]
  Morrill, L. C.; Smith, A. D. Chem. Soc. Rev. 2014, 43, 6214. doi: 10.1039/C4CS00042K
3. [3]
  Straathof, A. J. J. Chem. Rev. 2014, 114, 1871. doi: 10.1021/cr400309c
4. [4]
  (a) Sivaguru, P.; Wang, Z.; Zanoni, G.; Bi, X. Chem. Soc. Rev. 2019, 48, 2615.
  (b) Wang, F.; Chen, P.; Liu, G. S. Acc. Chem. Res. 2018, 51, 2036.
  (c) Yi, H.; Zhang, G.; Wang, H.; Huang, Z.; Wang, J.; Singh, A.; Lei, A. Chem. Rev. 2017, 117, 9016.
  (d) Zhao, Y.; Liu, Z. Chin. J. Chem. 2018, 36, 455.
  (e) Tan, F.; Yin, G. Chin. J. Chem. 2018, 36, 545.
  (f) Cao, Y.; He, X.; Wang, N.; Li, H.; He, L.-N. Chin. J. Chem. 2018, 36, 644.
5. [5]
6. [6]
7. [7]
  Sun, A.; C.; McAtee, R. C.; McClain, E. J.; Stephenson, C. R. J. Synthesis 2019, 51, 1063. doi: 10.1055/s-0037-1611658
8. [8]
  Murarka, S. Adv. Synth. Catal. 2018, 360, 1735. doi: 10.1002/adsc.201701615
9. [9]
  Xuan, J.; Zhang, Z. G.; Xiao, W. J. Angew. Chem., Int. Ed. 2015, 54, 15632. doi: 10.1002/anie.201505731
10. [10]
  Chu, L.; Ohta, C.; Zuo, Z.; MacMillan, D. W. C. J. Am. Chem. Soc. 2014, 136, 10886. doi: 10.1021/ja505964r
11. [11]
  Miyake, Y.; Nakajima, K.; Nishibayashi, Y. Chem. Commun. 2013, 49, 7854. doi: 10.1039/c3cc44438d
12. [12]
  Millet, A.; Lefebvre, Q.; Rueping, M. Chem.-Eur. J. 2016, 22, 13464. doi: 10.1002/chem.201602257
13. [13]
  Ramirez, N.; Gonzalez-Gomez, J. Eur. J. Org. Chem. 2017, 2154.
14. [14]
  Chinzei, T.; Miyazawa, K.; Yasu, Y.; Koike, T.; Akita, M. RSC Adv. 2015, 5, 21297. doi: 10.1039/C5RA01826A
15. [15]
  Bloom, S.; Liu, C.; Kölmel, D.; Qiao, J.; Zhang, Y.; Poss, M.; Ewing, W.; MacMillan, D. W. C. Nat. Chem. 2018, 10, 205. doi: 10.1038/nchem.2888
16. [16]
  Kölmel, D. K.; Loach, R. P.; Knauber, T.; Flanagan, M. E. ChemMedChem 2018, 13, 2159. doi: 10.1002/cmdc.201800492
17. [17]
  Chen, J.-Q.; Chang, R.; Wei, Y.-L.; Mo, J.-N.; Wang, Z.-Y.; Xu, P.-F. J. Org. Chem. 2018, 83, 253. doi: 10.1021/acs.joc.7b02628
18. [18]
  Xiao, T.; Li, L.; Zhou, L. J. Org. Chem. 2016, 81, 7908. doi: 10.1021/acs.joc.6b01620
19. [19]
  Noble, A.; Mega, R. S.; Pflästerer, D.; Myers, E.; Aggarwal, V. K. Angew. Chem., Int. Ed. 2018, 57, 2155. doi: 10.1002/anie.201712186
20. [20]
  Guo, T.; Zhang, Y.; Fang, Y.; Jin, X.; Li, Y.; Li, R.; Li, X.; Cen, W.; Liu, X.; Tian, Z. Adv. Synth. Catal. 2018, 360, 1352. doi: 10.1002/adsc.201701285
21. [21]
  Yin, Y.; Dai, Y.; Jia, H.; Li, J.; Bu, L.; Qiao, B.; Zhao, X.; Jiang, Z. J. Am. Chem. Soc. 2018, 140, 6083. doi: 10.1021/jacs.8b01575
22. [22]
  Okada, K.; Okamoto, K.; Morita, N.; Okubo, K.; Oda, M. J. Am. Chem. Soc. 1991, 113, 9401. doi: 10.1021/ja00024a074
23. [23]
  Schnermann, N.; Overman, L. E. Angew. Chem., Int. Ed. 2012, 51, 9576. doi: 10.1002/anie.201204977
24. [24]
  Pratsch, G.; Lackner, G. L.; Overman, L. E. J. Org. Chem. 2015, 80, 6025. doi: 10.1021/acs.joc.5b00795
25. [25]
  Hu, C.; Chen, Y. Org. Chem. Front. 2015, 2, 1352. doi: 10.1039/C5QO00187K
26. [26]
  Schwarz, J.; König, B. Green Chem. 2016, 18, 4743. doi: 10.1039/C6GC01101B
27. [27]
  Jin, Y.; Yang, H.; Fu, H. Org. Lett. 2016, 18, 6400. doi: 10.1021/acs.orglett.6b03300
28. [28]
  Noble, A.; MacMillan, D. W. C. J. Am. Chem. Soc. 2014, 136, 11602. doi: 10.1021/ja506094d
29. [29]
  Cao, H.; Jiang, H.; Feng, H.; Kwan, J.; Liu, X.; Wu, J. J. Am. Chem. Soc. 2018, 140, 16360. doi: 10.1021/jacs.8b11218
30. [30]
  Zheng, C.; Chen, W.; Li, H.; Na, R.; Shang, R. Org. Lett. 2018, 20, 2559. doi: 10.1021/acs.orglett.8b00712
31. [31]
  Till, N. A.; Smith, R. T.; MacMillan, D. W. C. J. Am. Chem. Soc. 2018, 140, 5701. doi: 10.1021/jacs.8b02834
32. [32]
  Zhang, J.; Yang, J.; Guo, L.; Duan, X. Chem.-Eur. J. 2017, 23, 10259. doi: 10.1002/chem.201702200
33. [33]
  Xu, K.; Tan, Z.; Zhang, H.; Liu, J.; Zhang, S.; Wang, Z. Chem. Commun. 2017, 53, 10719. doi: 10.1039/C7CC05910H
34. [34]
  Wang, G.; Shang, R.; Fu, Y. Org. Lett. 2018, 20, 888. doi: 10.1021/acs.orglett.8b00023
35. [35]
  Koy, M.; Sandfort, F.; Tlahuext-Aca, A.; Quach, L.; Daniliuc, C.; Glorius, F. Chem.-Eur. J. 2018, 24, 4552. doi: 10.1002/chem.201800813
36. [36]
  Jin, C.; Yan, Z.; Sun, B.; Yang, J. Org. Lett. 2019, 21, 2064. doi: 10.1021/acs.orglett.9b00327
37. [37]
  Dai, G.; Lai, S.; Luo, Z.; Tang, Z. Org. Lett. 2019, 21, 2269. doi: 10.1021/acs.orglett.9b00558
38. [38]
  Li, Y.; Ge, L.; Qian, B.; Babu, K. R.; Bao, H. Tetrahedron Lett. 2016, 57, 5677. doi: 10.1016/j.tetlet.2016.11.020
39. [39]
  Zhou, Q.; Guo, W.; Ding, W.; Wu, X.; Chen, X.; Lu, L.; Xiao, W. Angew. Chem., Int. Ed. 2015, 54, 11196. doi: 10.1002/anie.201504559
40. [40]
  Yang, J.; Zhang, J.; Qi, L.; Hu, C.; Chen, Y. Chem. Commun. 2015, 51, 5275. doi: 10.1039/C4CC06344A
41. [41]
  Tlahuext-Aca, A.; Garza-Sanchez, R.; Glorius, F. Angew. Chem., Int. Ed. 2017, 56, 3708. doi: 10.1002/anie.201700049
42. [42]
  Ge, L.; Li, Y.; Jian, W.; Bao, H. Chem.-Eur. J. 2017, 23, 11767. doi: 10.1002/chem.201702385
43. [43]
  Quyang, X.; Li, Y.; Song, R.; Li, J. Org. Lett. 2018, 20, 6659. doi: 10.1021/acs.orglett.8b02670
44. [44]
  Tlahuext-Aca, A.; Garza-Sanchez, A.; Schäfer, M.; Glorius, F. Org. Lett. 2018, 20, 1546. doi: 10.1021/acs.orglett.8b00272
45. [45]
  Xia, Z.; Zhang, C.; Gao, Z.; Ye, S. Org. Lett. 2018, 20, 3496. doi: 10.1021/acs.orglett.8b01268
46. [46]
  Kong, W.; Yu, C.; An, H.; Song, Q. Org. Lett. 2018, 20, 349. doi: 10.1021/acs.orglett.7b03587
47. [47]
  Sha, W.; Deng, L.; Ni, S.; Mei, H.; Han, J.; Pan, Y. ACS Catal. 2018, 8, 7489. doi: 10.1021/acscatal.8b01863
48. [48]
  Chen, L.; Chao, C.; Pan, Y.; Dong, S.; Teo, Y.; Wang, J.; Tan, C. Org. Biomol. Chem. 2013, 11, 5922. doi: 10.1039/c3ob41091a
49. [49]
  Shu, C.; Mega, R. S.; Andreassen, B. J.; Noblem A.; Aggarwal, V. K. Angew. Chem., Int. Ed. 2018, 57, 15430. doi: 10.1002/anie.201808598
50. [50]
  He, Z.; Bae, M.; Wu, J.; Jamison, T. F. Angew. Chem., Int. Ed. 2014, 53, 14451. doi: 10.1002/anie.201408522
51. [51]
  Yu, Y.; Yuan, W.; Huang, H.; Cai, Z.; Liu, P.; Sun, P. J. Org. Chem. 2018, 83, 1654. doi: 10.1021/acs.joc.7b03080
52. [52]
  Xie, J.; Xu, P.; Li, H.; Xue, Q.; Jin, H.; Cheng, Y.; Zhu, C. Chem. Commun. 2013, 49, 5672. doi: 10.1039/c3cc42672f
53. [53]
  Tang, Q.; Liu, X.; Liu, S.; Xie, H.; Liu, W.; Zeng, J.; Cheng, P. RSC Adv. 2015, 5, 89009. doi: 10.1039/C5RA17292F
54. [54]
  Sha, W.; Ni, S.; Han, J.; Pan, Y. Org. Lett. 2017, 19, 5900. doi: 10.1021/acs.orglett.7b02899
55. [55]
  Yao, S.; Zhang, K.; Zhou, Q.; Zhao, Y.; Shi, D.; Xiao, W. Chem. Commun. 2018, 54, 8096. doi: 10.1039/C8CC04503H
56. [56]
  Kachkovskyi, G.; Faderl, C.; Reiser, O. Adv. Synth. Catal. 2013, 355, 2240. doi: 10.1002/adsc.201300221
57. [57]
  Yang, J.; Zhang, J.; Zhang, J.; Duan, X.; Gao, L. J. Org. Chem. 2018, 83, 1598. doi: 10.1021/acs.joc.7b02861
58. [58]
  Liu, L.; Dong, J.; Yan, Y.; Yin, S.; Han, L.; Zhou, Y. Chem. Commun. 2019, 55, 233. doi: 10.1039/C8CC08689C
59. [59]
  Garza-Sanchez, A.; Tlahuext-Aca, A.; Glorius, F. ACS Catal. 2017, 56, 12336.
60. [60]
  Koeller, J.; Gandeepan, P.; Ackermann, L. Synthesis 2019, 51, 1284. doi: 10.1055/s-0037-1611633
61. [61]
  Tian, W.-F.; Hu, C.-H.; He, K.-N.; He, X.-Y.; Li, Y. Org. Lett. 2019, 21, 6930. doi: 10.1021/acs.orglett.9b02539
62. [62]
  Wang, B.; Li, P.; Miao, T.; Zou, L.; Wang, L. Org. Biomol. Chem. 2019, 17, 115. doi: 10.1039/C8OB02476F
63. [63]
  Zhang, X.-Y.; Weng, W.-Z.; Liang, H.; Yang, H.; Zhang, B. Org. Lett. 2018, 20, 4686. doi: 10.1021/acs.orglett.8b02016
64. [64]
  Chen, W.; Shang, R.; Fu, Y. ACS Catal. 2017, 7, 907. doi: 10.1021/acscatal.6b03215
65. [65]
  Cheng, W.-M.; Shang, R.; Fu, M.-C.; Fu, Y. Chem.-Eur. J. 2017, 23, 2537. doi: 10.1002/chem.201605640
66. [66]
  Proctor, R. S. J.; Davis, H. J.; Phipps, R. J. Science 2018, 360, 419. doi: 10.1126/science.aar6376
67. [67]
  Liu, X.; Liu, Y.; Chai, G.; Qiao, B.; Zhao, X.; Jiang, Z. Org. Lett. 2018, 20, 6298. doi: 10.1021/acs.orglett.8b02791
68. [68]
  Sherwood, T. C.; Li, N.; Yazdani, A. N.; Murali Dhar, T. G. J. Org. Chem. 2018, 83, 3000. doi: 10.1021/acs.joc.8b00205
69. [69]
  Kammer, L. M.; Rahman, A.; Opatz, T. Molecules 2018, 23, 764. doi: 10.3390/molecules23040764
70. [70]
  Fu, M.-C.; Shang, R.; Zhao, B.; Wang, B.; Fu, Y. Science 2019, 363, 1429. doi: 10.1126/science.aav3200
71. [71]
  Zuo, Z.; MacMillan, D. W. C. J. Am. Chem. Soc. 2014, 136, 5257. doi: 10.1021/ja501621q
72. [72]
  Lang, S.; O'Nele, K.; Tunge, J. J. Am. Chem. Soc. 2014, 136, 13606. doi: 10.1021/ja508317j
73. [73]
  Li, J.; Lefebvre, Q.; Yang, H.; Zhao, Y.; Fu, H. Chem. Commun. 2017, 53, 10299. doi: 10.1039/C7CC05758J
74. [74]
  Yang, H.; Tian, C.; Qiu, D.; Tian, H.; An, G.; Li, G. Org. Chem. Front. 2019, 6, 2365. doi: 10.1039/C9QO00495E
75. [75]
  Guo, J.; Wu, Q.; Xie, Y.; Weng, J.; Lu, G. J. Org. Chem. 2018, 83, 12559. doi: 10.1021/acs.joc.8b01849
76. [76]
  Ren, L.; Cong, H. Org. Lett. 2018, 20, 3225. doi: 10.1021/acs.orglett.8b01077
77. [77]
  Wang, C.; Guo, M.; Qi, R. Shang, Q.; Liu, Q.; Wang, S.; Zhao, L.; Wang, R.; Xu, Z. Angew. Chem., Int. Ed. 2018, 26, 15841.
78. [78]
  Zuo, Z.; Ahneman, D. T.; Chu, L.; Terrett, J. A.; Doyle, A. G.; MacMillan, D. W. C. Science 2014, 345, 437.
79. [79]
  Johnston, C. P.; Smith, R. T.; Allmendinger, S.; MacMillan, D. W. C. Nature 2016, 536, 322. doi: 10.1038/nature19056
80. [80]
  Zuo, Z.; Cong, H.; Li, W.; Choi, J.; Fu, G. C.; MacMillan, D. W. C. J. Am. Chem. Soc. 2016, 138, 1832. doi: 10.1021/jacs.5b13211
81. [81]
  Oderinde, M. S.; Varela-Alvarez, A.; Aquila, B.; Robbins, D. W.; Johannes, J. W. J. Org. Chem. 2015, 80, 7642. doi: 10.1021/acs.joc.5b01193
82. [82]
  Luo, J.; Zhang, J. ACS Catal. 2016, 6, 873. doi: 10.1021/acscatal.5b02204
83. [83]
  McTiernan, C. D.; Leblanc, X.; Scaiano, J. C. ACS Catal. 2017, 7, 2171. doi: 10.1021/acscatal.6b03687
84. [84]
  Suen, L. M.; Wang, C.; Hunter, D. N.; Mitchell, H. J.; Cnverso, A.; ElMarrouni, A. Synthesis 2018, 50, 3177. doi: 10.1055/s-0037-1610155
85. [85]
  Kautzky, J. A.; Wang, T.; Evans, R. W.; MacMillan, D. W. C. J. Am. Chem. Soc. 2018, 10, 6522.
86. [86]
  Zhnag, H.; Zhang, P.; Jiang, M.; Yang, H.; Fu, H. Org. Lett. 2017, 19, 1016. doi: 10.1021/acs.orglett.6b03888
87. [87]
  Mao, R.; Frey, A.; Balon, J.; Hu, X. Nat. Catal. 2018, 1, 120. doi: 10.1038/s41929-017-0023-z
88. [88]
  Liang, Y.; Zhang, X.; MacMillan, D. W. C. Nature 2018, 559, 83. doi: 10.1038/s41586-018-0234-8
89. [89]
  Rueda-Becerril, M.; Mahe, O.; Drouin, M.; Majewski, M. B.; West, J. G.; Wolf, M. O.; Sammis, G. M.; Paquin, J. F. J. Am. Chem. Soc. 2014, 136, 2637. doi: 10.1021/ja412083f
90. [90]
  Ventre, S.; Petronijevi, F. R.; MacMillan, D. W. C. J. Am. Chem. Soc. 2015, 137, 5654. doi: 10.1021/jacs.5b02244
91. [91]
  Wu, X.; Meng, C.; Yuan, X.; Jia, X.; Qian, X.; Ye, J. Chem. Commun. 2015, 51, 11864. doi: 10.1039/C5CC04527D
92. [92]
  Lang, S. B.; Cartwright, K. C.; Welter, R. S.; Locascio, T. M.; Tunge, J. A. Eur. J. Org. Chem. 2016, 3331.
93. [93]
  Davies, J.; Angelini, L.; Alkhalifah, M. A.; Sanz, L. M.; Sheikh, N. S.; Leonori, D. Synthesis 2018, 50, 821. doi: 10.1055/s-0036-1591744
94. [94]
  Hu, D.; Wang, L.; Li, P. Org. Lett. 2017, 19, 2770. doi: 10.1021/acs.orglett.7b01181
95. [95]
  Fawcett, A.; Pradeilles, J.; Wang, Y.; Mutsuga, T.; Myers, E.; Aggarwal, V. K. Science 2017, 357, 283. doi: 10.1126/science.aan3679
96. [96]
  Jiang, M.; Yang, H.; Fu, H. Org. Lett. 2016, 18, 1968. doi: 10.1021/acs.orglett.6b00489
97. [97]
  Jin, Y.; Yang, H.; Fu, H. Chem. Commun. 2016, 52, 12909. doi: 10.1039/C6CC06994K
1. [1]
  Tongyan Yu , Pan Xu . Visible-Light Photocatalyzed Radical Rearrangement Reaction. University Chemistry, 2025, 40(7): 169-176. doi: 10.12461/PKU.DXHX202409070
2. [2]
  Dan Liu . 可见光-有机小分子协同催化的不对称自由基反应研究进展. University Chemistry, 2025, 40(6): 118-128. doi: 10.12461/PKU.DXHX202408101
3. [3]
  Yurong Tang , Yunren Shi , Yi Xu , Bo Qin , Yanqin Xu , Yunfei Cai . Innovative Experiment and Course Transformation Practice of Visible-Light-Mediated Photocatalytic Synthesis of Isoquinolinone. University Chemistry, 2024, 39(5): 296-306. doi: 10.3866/PKU.DXHX202311087
4. [4]
  Bo YANG , Gongxuan LÜ , Jiantai MA . Nickel phosphide modified phosphorus doped gallium oxide for visible light photocatalytic water splitting to hydrogen. Chinese Journal of Inorganic Chemistry, 2024, 40(4): 736-750. doi: 10.11862/CJIC.20230346
5. [5]
  Xinzhe HUANG , Lihui XU , Yue YANG , Liming WANG , Zhangyong LIU , Zhongjian WANG . Preparation and visible light responsive photocatalytic properties of BiSbO₄/BiOBr. Chinese Journal of Inorganic Chemistry, 2025, 41(2): 284-292. doi: 10.11862/CJIC.20240212
6. [6]
  .
  CCS Chemistry | 超分子活化底物为自由基促进高效选择性光催化氧化
  . CCS Chemistry, 2025, 7(10.31635/ccschem.025.202405229): -.
7. [7]
  Zhongyan Cao , Shengnan Jin , Yuxia Wang , Yiyi Chen , Xianqiang Kong , Yuanqing Xu . Advances in Highly Selective Reactions Involving Phenol Derivatives as Aryl Radical Precursors. University Chemistry, 2025, 40(4): 245-252. doi: 10.12461/PKU.DXHX202405186
8. [8]
  Yinjie Xu , Suiqin Li , Lihao Liu , Jiahui He , Kai Li , Mengxin Wang , Shuying Zhao , Chun Li , Zhengbin Zhang , Xing Zhong , Jianguo Wang . Enhanced Electrocatalytic Oxidation of Sterols using the Synergistic Effect of NiFe-MOF and Aminoxyl Radicals. Acta Physico-Chimica Sinica, 2024, 40(3): 2305012-0. doi: 10.3866/PKU.WHXB202305012
9. [9]
  Danqing Wu , Jiajun Liu , Tianyu Li , Dazhen Xu , Zhiwei Miao . Research Progress on the Simultaneous Construction of C—O and C—X Bonds via 1,2-Difunctionalization of Olefins through Radical Pathways. University Chemistry, 2024, 39(11): 146-157. doi: 10.12461/PKU.DXHX202403087
10. [10]
  Baitong Wei , Jinxin Guo , Xigong Liu , Rongxiu Zhu , Lei Liu . Theoretical Study on the Structure, Stability of Hydrocarbon Free Radicals and Selectivity of Alkane Chlorination Reaction. University Chemistry, 2025, 40(3): 402-407. doi: 10.12461/PKU.DXHX202406003
11. [11]
  Xinxin Wu . 基础有机化学教学中自由基重排反应的课程设计及其课程思政元素的融入. University Chemistry, 2025, 40(6): 316-325. doi: 10.12461/PKU.DXHX202408055
12. [12]
  Qin Li , Huihui Zhang , Huajun Gu , Yuanyuan Cui , Ruihua Gao , Wei-Lin Dai . In situ Growth of Cd_0.5Zn_0.5S Nanorods on Ti₃C₂ MXene Nanosheet for Efficient Visible-Light-Driven Photocatalytic Hydrogen Evolution. Acta Physico-Chimica Sinica, 2025, 41(4): 2402016-0. doi: 10.3866/PKU.WHXB202402016
13. [13]
  Bing LIU , Huang ZHANG , Hongliang HAN , Changwen HU , Yinglei ZHANG . Visible light degradation of methylene blue from water by triangle Au@TiO₂ mesoporous catalyst. Chinese Journal of Inorganic Chemistry, 2024, 40(5): 941-952. doi: 10.11862/CJIC.20230398
14. [14]
  Jie Li , Huida Qian , Deyang Pan , Wenjing Wang , Daliang Zhu , Zhongxue Fang . Efficient Synthesis of Anethaldehyde Induced by Visible Light. University Chemistry, 2024, 39(4): 343-350. doi: 10.3866/PKU.DXHX202310076
15. [15]
  Lei Shi . Nucleophilicity and Electrophilicity of Radicals. University Chemistry, 2024, 39(11): 131-135. doi: 10.3866/PKU.DXHX202402018
16. [16]
  Min LIU , Huapeng RUAN , Zhongtao FENG , Xue DONG , Haiyan CUI , Xinping WANG . Neutral boron-containing radical dimers. Chinese Journal of Inorganic Chemistry, 2025, 41(1): 123-130. doi: 10.11862/CJIC.20240362
17. [17]
  Yuanqing Wang , Yusong Pan , Hongwu Zhu , Yanlei Xiang , Rong Han , Run Huang , Chao Du , Chengling Pan . Enhanced Catalytic Activity of Bi₂WO₆ for Organic Pollutants Degradation under the Synergism between Advanced Oxidative Processes and Visible Light Irradiation. Acta Physico-Chimica Sinica, 2024, 40(4): 2304050-0. doi: 10.3866/PKU.WHXB202304050
18. [18]
  Zhen Yao , Bing Lin , Youping Tian , Tao Li , Wenhui Zhang , Xiongwei Liu , Wude Yang . Visible-Light-Mediated One-Pot Synthesis of Secondary Amines and Mechanistic Exploration. University Chemistry, 2024, 39(5): 201-208. doi: 10.3866/PKU.DXHX202311033
19. [19]
  Yanan Fan , Jingjing Huang . Interactive Electronic Courseware Facilitates the Development of Integrated Undergraduate-Graduate Instrumental Analysis Laboratory Courses: A Case Study of UV-Vis Spectroscopy Analysis Experiment. University Chemistry, 2025, 40(10): 282-287. doi: 10.12461/PKU.DXHX202411009
20. [20]
  Jiajia Li , Xiangyu Zhang , Zhihan Yuan , Zhengyang Qian , Jian Zhu . 3D Printing Based on Photo-Induced Reversible Addition-Fragmentation Chain Transfer Polymerization. University Chemistry, 2024, 39(5): 11-19. doi: 10.3866/PKU.DXHX202309073

Get Citation

PDF

XML

Metrics

PDF Downloads(198)
Abstract views(5062)
HTML views(1559)

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