文章
2024年
74. Progress in Photocatalyzed Trifluoromethylthiolation and Trifluoromethylselenolation Reactions
F. Li (co-first author), J.-W. Song (co-first author), X. Han, C.-P. Zhang*, Synthesis, 2024, DOI: 10.1055/a-2335-8627
Review article invited by Prof. Martin Oestreich.
73. Pd-catalyzed relay Heck arylation of alkenyl alcohols with arylsulfonium salts
J.-W. Song, F. Xia, X.-L. Zhang, C.-P. Zhang*, Org. Chem. Front. 2024, DOI: 10.1039/D4QO00618F.
72. Group VIII metal difluorocarbene complexes: Synthesis and applications
X. Ding, Y.-F. Yao, W. Lin, Z. Ye*, C.-P. Zhang*, J. Fluorine Chem. 2024, 273, 110238
Review article invited by Prof. Jun-an Ma and Prof. René M. Koenigs for the Special Issue "Fluorinated carbenes and diazo reagents for the synthesis of organofluorine compounds"
2023年
71. Photoinduced Trifluoromethylselenolation of Aryl Halides with [Me4N][SeCF3]
F. Li, X. Han, Z. Xu, C.-P. Zhang*, Org. Lett. 2023, 25, 7884-7889.
Highlighted by CBG (https://www.chembeango.com/zixun/59027c5)
70. Trifluoromethyltellurolation of Indole Derivatives with [Me4N][TeCF3] and NIS
J.-Y. Dong, H.-N. Wang, C.-P. Zhang*, ChemistrySelect 2023, 8, e202302350.
69. Photoinduced Copper-Promoted Decarboxylative Trifluoromethylselenolation of Aromatic Carboxylic Acids with [Me4N][SeCF3]
L. Liu, Y.-C. Gu, C.-P. Zhang*, J. Org. Chem. 2023, 88, 9372-9380.
68. Recent Advances in the Synthesis and Transformation of Carbamoyl Fluorides, Fluoroformates, and Their Analogues
L. Liu, Y.-C. Gu, C.-P. Zhang*, Chem. Rec. 2023, e202300071. https://doi.org/10.1002/tcr.202300071.
Review article invited by Prof. Norio Shibata.
This article also appears in Hot Topic: Fluorine Chemistry.
67. Divergent dehydroxyfluorination and carbonation of alcohols with trifluoromethyl trifluoromethanesulfonate
L.-Y. Ran, X. Ding, X.-P. Yan, C.-P. Zhang*, Org. Biomol. Chem. 2023, 21, 1235-1241. https://doi.org/10.1039/D2OB02028A.
2022年
66. Copper-Mediated Aerobic Trifluoromethyltelluration of Boronic Acids with [Me4N][TeCF3]
J.-Y. Dong, H.-N. Wang, Y.-Q. Xie, C.-P. Zhang*, iScience, 2022, 25, 105566. https://doi.org/10.1016/j.isci.2022.105566.
Article invited by Dr. Michelle Muzzio.
65. Deuteration of Arylthianthren-5-ium Salts in CD3OD
Z.-H. Lin, Y.-F. Yao, C.-P. Zhang*, Org. Lett. 2022, 24, 8417-8422. https://doi.org/10.1021/acs.orglett.2c03541.
Highlighted by CBG (https://www.chembeango.com/zixun/57506)
64. Palladium-catalyzed C–H trifluoromethylselenolation of arenes with [Me4N][SeCF3] and an oxidant
L. Liu, Y.-C. Gu, C.-P. Zhang*, Chem. Commun. 2022, 58, 9238-9241. doi: 10.1039/d2cc02897b.
63. An Overview of the Reactions with Trifluoromethyl Trifluoromethanesulfonate
L.-Y. Ran, C.-P. Zhang*, Youji Huaxue, 2022, 42, 2045-2054. doi: 10.6023/cjoc202202025.
62. Visible-light-initiated catalyst-free trifluoromethylselenolation of arylsulfonium salts with [Me4N][SeCF3]
Z.-Y. Tian, C.-P. Zhang*, Org. Chem. Front. 2022, 9, 2220-2227. doi: 10.1039/d2qo00235c.
61. Cu-Catalyzed Allylation of Amines with Cyclopropyldiphenylsulfonium Trifluoromethanesulfonate
Y. Ma, Z.-Y. Tian, S.-Y. Zheng, C.-P. Zhang*, Synthesis 2022, 54, 2350-2360. doi: 10.1055/a-1730-2540.
Feature Article invited by Prof. Paul Knochel.
60. Alkylation Reactions with Alkylsulfonium Salts
Z.-Y. Tian, Y. Ma, C.-P. Zhang*, Synthesis 2022, 54, 1478-1502. doi: 10.1055/a-1677-5971.
Short Review invited by Prof. Hideki Yorimitsu.
2021年
59. Trifluoromethylselenolation reactions using the versatile [Me4N][SeCF3] reagent
H.-N. Wang, J.-Y. Dong, J. Shi, C.-P. Zhang*, Tetrahedron 2021, 132476. https://doi.org/10.1016/j.tet.2021.132476
Invited contribution for the Special Issue "Fluorine and Chalcogens"
58. Pd/Cu-Catalyzed Vinylation of Terminal Alkynes with (2-Bromoethyl)diphenylsulfonium Triflate
X.-X. Ming, S. Wu, Z.-Y. Tian, J.-W. Song, C.-P. Zhang*, Org. Lett. 2021, 23, 6795-6800.
Highlighted by CBG (https://www.chembeango.com/zixun/55403)
Highlighted by Organic Chemistry Portal
57. Facile Synthesis of Selenocarbamyl Fluorides, Selenoureas and Their Derivatives with [Me4N][SeCF3]
L. Liu, L.-Y. Ran, Y. Gu, C.-P. Zhang*, Org. Chem. Front. 2021, 8, 5736-5743.
56. Revisiting the Balz–Schiemann Reaction of Aryldiazonium Tetrafluoroborate in Different Solvents under Catalyst- and Additive-Free Conditions.
L. Yang, C.-P. Zhang*, ACS Omega, 2021, 6, 21595-21603.
55. Synthesis and Biological Evaluation of CF3Se-Substituted α-Amino Acid Derivatives
Z.-Z. Han, T. Dong, X.-X. Ming, F. Kuang*, C.-P. Zhang*, ChemMedChem, 2021, 16, 3177-3180.
54. Additive-Free Visible-Light-Mediated Hydro-/Deuterodediazoniation of Arenediazonium Tetrafluoroborates in THF/THF-d8
L. Yang, C.-P. Zhang*, Asian J. Org. Chem. 2021, 10, 2157-2160.
53. Trifluoromethylselenolation and N-acylation of indoles with [Me4N][SeCF3]
K.-L. Tan, H.-N. Wang, T. Dong, C.-P. Zhang*, Org. Biomol. Chem. 2021, 19, 5368-5376.
52. Pd/Cu-Catalyzed C−H/C−H Cross Coupling of (Hetero)Arenes with Azoles through Arylsulfonium Intermediates
Z.-Y. Tian, Z.-H. Lin, C.-P. Zhang*, Org. Lett. 2021, 23, 4400-4405.
51. Phenyl(trifluoroethyl)iodonium-triflate-initiated ring-opening polymerization of tetrahydrofuran
Z.-Z. Han, C.-P. Zhang*, Tetrahedron Lett. 2021, 73, 153146.
2020年
50. Markovnikov-Type Hydrotrifluoromethylchalcogenation of Unactivated Terminal Alkenes with [Me4N][XCF3] (X = S, Se) and TfOH
J. Shi, C.-P. Zhang*, Molecules 2020, 25, 4535, https://doi.org/10.3390/molecules25194535
Invited contribution for the special issue "Halogen-Controlled Synthesis of Useful Organic Molecules"
49. Tertiary‐Amine‐Initiated Synthesis of Acyl Fluorides from Carboxylic Acids and CF3SO2OCF3
H.-X. Song (co-first author), Z.-Y. Tian (co-first author), J.-C. Xiao, C.-P. Zhang*, Chem. Eur. J. 2020, 26, 16261-16265.
Highlighted by WileyChem (https://mp.weixin.qq.com/s/i9GVOS1hseeMWVck3m5Dvw)
48. Fluorination and Fluoroalkylation Reactions Mediated by Hypervalent Iodine Reagents
Z.-Z. Han, C.-P. Zhang*, Adv. Synth. Catal. 2020, 362, 4256-4292.
Selected as VIP paper
47. CaCl2-Promoted Dehydroxytrifluoromethylselenolation of Alcohols with [Me4N][SeCF3]
S. Wu, T.-H. Jiang, C.-P. Zhang*, Org. Lett. 2020, 22, 6016-6020.
Highlighted by CBG (https://www.chembeango.com/zixun/50772)
46. Fluoroalkylation of Diazo Compounds with Diverse Rfn Reagents
S. Wu, H.-X. Song, C.-P. Zhang*, Chem Asian J. 2020, 15, 1660-1677.
Highlighted by ASNChina (https://mp.weixin.qq.com/s/t2h9YKvxH-dTmzG3oLXx9w)
45. Oxidative trifluoromethylselenolation of 1,3-dicarbonyls with [Me4N][SeCF3]
K.-L. Tan, T. Dong, X.-Q. Zhang*, C.-P. Zhang*, Org. Biomol. Chem. 2020, 18, 1769-1779.
44. Fluorine-Containing Inhalation Anesthetics: Chemistry, Properties and Pharmacology
Y. Wang, X.-X. Ming, C.-P. Zhang*, Curr. Med. Chem. 2020, 27, 5599-5652. (Invited contribution)
2019年
43. Q.-Y. Han, K.-L. Tan, H.-N. Wang, C.-P. Zhang*, Org. Lett. 2019, 21, 10013-10017.
42. Z.-Y. Tian, C.-P. Zhang*, Chem. Commun. 2019, 55, 11936-11939.
41. C.-L. Zhao#, J. Shi#, X.-Q. Lu, X. Wu, C.-P. Zhang*, J. Fluorine Chem. 2019, 226, 109360.
40. X.-X. Ming, Z.-Y. Tian, C.-P. Zhang*, Chem. Asian J. 2019, 14, 3370-3379.
39. S. Wu, J. Shi, C.-P. Zhang*, Org. Biomol. Chem. 2019, 17, 7468-7473.
38. Q.-Y. Han, C.-L. Zhao, T. Dong, J. Shi, K.-L. Tan, C.-P. Zhang*, Org. Chem. Front, 2019, 6, 2732-2737.
37. H.-X. Song, Z.-Z. Han, C.-P. Zhang*, Chem. Eur. J. 2019, 25, 10907-10912. (Selected as “hot paper”)
36. Q.-Y. Han, X.-X. Hu, X.-S. Xue*, C.-L. Zhao, C.-P. Zhang*, Asian J. Org. Chem. 2019, 8, 665-670. (Invited contribution for the special “Organofluorine Chemistry” issue)
35. L. Yang, Z.-Y. Tian, C.-P. Zhang*, ChemistrySelect 2019, 4, 311-315.
34. Q.-Y. Han, C.-L. Zhao, C.-P. Zhang*, Chin. J. Org. Chem. 2019, 39, 84-94. (Invited contribution to celebrate Prof. Qing-Yun Chen’s 90th birthday)
2018年
33. C.-L. Zhao, Q.-Y. Han, C.-P. Zhang*, Org. Lett. 2018, 20, 6480-6484.
32. T. Dong, J. Nie, C.-P. Zhang*, Tetrahedron 2018, 74, 5642-5649. (Invited contribution for the "Organo Fluorine Chemistry"
issue)
31. Z.-Y. Tian, X.-X. Ming, H.-B. Teng*, Y.-T. Hu, C.-P. Zhang*, Chem. Eur. J. 2018, 24, 13744-13748. (Highlighted by CBG)
30. H.-X. Song, Q.-Y. Han, C.-L. Zhao, C.-P. Zhang*, Green. Chem. 2018, 20, 1662-1731. (Featured in front cover and highlighted by X-MOL)
29. J. Yang, H.-W. Zhao*, J. He, C.-P. Zhang*, Catalysts 2018, 8, 23/1-23/35. (Invited contribution)
28. Z.-Y. Tian, Y.-T. Hu, H.-B. Teng, C.-P. Zhang*, Tetrahedron Lett. 2018, 59, 299-309. (Invited contribution for digest)
27. T. Dong, J. He*, Z.-H. Li, C.-P. Zhang*, ACS Sustainable Chem. Eng. 2018, 6, 1327-1335. (Invited contribution for the Festschrift in Honor of Prof. István T. Horváth)
2017年
26. C.-L. Zhao, J. Yang, Z.-Z. Han, C.-P. Zhang*, J. Fluorine Chem. 2017, 204, 23-30.
25. Z.-Y. Tian, S.-M. Wang, S.-J. Jia, H.-X. Song, C.-P. Zhang*, Org. Lett. 2017, 19, 5454-5457. (Highlighted by Organic Chemistry Portal)
24. L. Yang, T. Dong, H. M. Revankar, C.-P. Zhang*, Green Chem. 2017, 19, 3915-3992. (Highlighted by X-MOL)
23. J.-Bin Han, T. Dong, D. A. Vicic, C.-P. Zhang*, Org. Lett. 2017, 19, 3919-3922.
22. Q.-Y. Han#, C.-L. Zhao#, J. Yang, C.-P. Zhang*, Green Chem. Lett. Rev. 2017, 10, 162-170 (Open access).
21. X.-Q. Hu, J.-B. Han, C.-P. Zhang*, Eur. J. Org. Chem. 2017, 324-331.
2016年
20. W.-Y. Fang, T. Dong, J.-B. Han, G.-F. Zha, C.-P. Zhang*, Org. Biomol. Chem. 2016, 14, 11502-11509.
19. H.-X. Song, S.-M. Wang, X.-Y. Wang, J.-B. Han, Y. Gao, S.-J. Jia, C.-P. Zhang*, J. Fluorine Chem. 2016, 192, 131-140.
18. X.-Y. Wang, H.-X. Song, S.-M. Wang, J. Yang, H.-L. Qin, X. Jiang, C.-P. Zhang*, Tetrahedron, 2016, 72, 7606-7612.
17. J.-B. Han, L. Yang, X. Chen, G.-F. Zha, C.-P. Zhang*, Adv. Synth. Catal. 2016, 358, 4119-4124.
16. S.-M. Wang, H.-X. Song, X.-Y. Wang, N. Liu, H.-L. Qin, C.-P. Zhang*, Chem. Commun. 2016, 52, 11893-11896. (Featured in back cover and highlighted by Atlas of Science)
15. J. Yang, Q.-Y. Han, C.-L. Zhao, T. Dong, Z.-Y. Hou, H.-L. Qin, C.-P. Zhang*, Org. Biomol. Chem. 2016, 14, 7654-7658. (Featured in front cover and highlighted by Atlas of Science）
14. X.-H. Liu#, J. Leng#, S.-J. Jia, J.-H. Hao, F. Zhang, H.-L. Qin, C.-P. Zhang*, J. Fluorine Chem. 2016, 189, 59-67.
13. G.-F. Zha, J.-B. Han, X.-Q. Hu, H.-L. Qin, W.-Y. Fang, C.-P. Zhang*, Chem. Commun. 2016, 52, 7458-7461. (Featured in back cover)
12. G.-F. Zha#, C.-P. Zhang#, H.-L. Qin, I. Jantan, M. Sher, M. W. Amjad, M. A. Hussain, Z. Hussain, S. N. A. Bukhari, Bioorg. Med. Chem. 2016, 24, 2352-2359.
11. C.-B. Yue, J.-H. Lin, J. Cai, C.-P. Zhang, G. Zhao, J.-C. Xiao, H. Li, RSC Adv. 2016, 6, 35705-35708.
10. H. Qin, J. Leng, C.-P. Zhang, I. Jantan, M. W. Amjad, M. Sher, M. Naeemul Hassan, M. A. Hussain, S. N. A. Bukhari, J. Med. Chem. 2016, 59, 3549-3561.
9. L. Zhu*, L.-S. Wang, B. Li, B. Fu, C.-P. Zhang*, W. Li, Chem. Commun. 2016, 52, 6371-6374. (Featured in back cover and highlighted by X-MOL)
8. S.-M. Wang, X.-Y. Wang, H.-L. Qin, C.-P. Zhang*, Chem. Eur. J. 2016, 22, 6542-6546.
7. J.-B. Han, H.-L. Qin, S.-H. Ye, L. Zhu*, C.-P. Zhang*, J. Org. Chem. 2016, 81, 2506-2512. (Highlighted by X-MOL)
6. C.-P. Zhang, "(1,3-dimesitylimidazolin-2-ylidene)Cu(trifluoromethyl)" Encyclopedia of Reagents for Organic Synthesis (EROS), 2016, DOI: 10.1002/047084289X.rn01964. (Invited contribution).
2015年
5. C.-P. Zhang, Z. Xi, K. M. Mueller, B. J. Holliday, H. S. Bazzi, J. A. Gladysz, Dalton Trans. 2015, 44, 19615-19624.
4. S.-M. Wang, J.-B. Han, C.-P. Zhang*, H.-L. Qin*, Tetrahedron Lett. 2015, 56, 6219-6222.
3. S.-M. Wang, J.-B. Han, C.-P. Zhang*, H.-L. Qin*, J.-C. Xiao*, Tetrahedron, 2015, 71, 7949-7976.
2. K.-C. Zhu#, J.-H. Hao#, C.-P. Zhang, Y. Feng, H.-L. Qin, RSC Adv. 2015, 5, 11132-11135.
1. J.-B. Han#, J.-H. Hao#, C.-P. Zhang*, H.-L. Qin*, Curr. Org. Chem. 2015, 19, 1554-1565. (Invited contribution).
以上文章为成立独立课题组后发表
独立工作前以第一作者身份发表的文章
19. C.-P. Zhang, Q.-Y. Chen, Y. Guo, J.-C, Xiao, Y.-C. Gu, Coord. Chem. Rev. 2014, 261, 28-72.
18. C.-P. Zhang, Q.-Y. Chen, Y. Guo, J.-C. Xiao, Tetrahedron, 2013, 69, 10955-10989.
17. C.-P. Zhang, H. Wang, A. Klein, C. Biewer, K. Stirnat, Y. Yamaguchi, L. Xu, V. Gomez-Benitez, D.A. Vicic, J. Am. Chem. Soc. 2013, 135, 8141-8144.
16. C.-P. Zhang, D.A. Vicic, J. Am. Chem. Soc. 2012, 134, 183-185.
15. C.-P. Zhang, Q.-Y. Chen, Y. Guo, J.-C. Xiao, Y.-C. Gu, Chem. Soc. Rev. 2012, 41, 4536-4559.
14. C.-P. Zhang, D.A. Vicic, Organometallics, 2012, 31, 7812-7815.
13. C.-P. Zhang, D.A. Vicic, Chem. Asian J. 2012, 7, 1756-1758.
12. C.-P. Zhang, W.W. Brennessel, D.A. Vicic, J. Fluorine Chem. 2012, 140, 112-115.
11. C.-P. Zhang, Z.-L. Wang, Q.-Y. Chen, C.-T. Zhang, Y.-C. Gu, J.-C. Xiao, Angew. Chem. Int. Ed. 2011, 50, 1896-1900.
10. C.-P. Zhang, Z.-L. Wang, Q.-Y. Chen, C.-T. Zhang, Y.-C. Gu, J.-C. Xiao, Chem. Commun., 2011, 47, 6632-6634.
9. C.-P. Zhang, J. Cai, C.-B. Zhou, X.-P. Wang, X. Zheng, Y.-C. Gu, J.-C. Xiao, Chem. Commun., 2011, 47, 9516-9518.
8. C.-P. Zhang, Z.-L. Wang, Q.-Y. Chen, C.-T. Zhang, J.-C. Xiao, J. Fluorine Chem. 2010, 131, 433-438.
7. C.-P. Zhang, Z.-L. Wang, Q.-Y. Chen, C.-T. Zhang, Y.-C. Gu, J.-C. Xiao, J. Fluorine Chem. 2010, 131, 761-766.
6. C.-P. Zhang, H.-P. Cao, Z.-L. Wang, C.-T. Zhang, Q.-Y. Chen, J.-C. Xiao, Synlett, 2010, 7, 1089-1092.
5. C.-P. Zhang, Z.-L. Wang, Q.-Y. Chen, C.-T. Zhang, Y.-C. Gu, J.-C. Xiao, Eur. J. Inorg. Chem., 2010, 3419-3422.
3. C.-P. Zhang, Z.-W. Qiang, J.-H. Lin, J.-C. Xiao, Chin. J. Chem. 2009, 27, 202-204.
2. C.-P. Zhang, Q.-Y. Chen, J.-C. Xiao, Y.-C. Gu, J. Fluorine Chem. 2009, 130, 671-673.
1. C.-P. Zhang, Q.-Y. Chen, J.-C. Xiao, J. Fluorine Chem. 2008, 129, 424-428.
代表性专利
1. 肖吉昌，张成潘，严冲，强震卫，CN 101503382A, 2009
2. 肖吉昌，张成潘，张忠，绍伟，严冲，强震卫，CN 101591296A, 2009
3. 肖吉昌，张成潘，CN 101973829A, 2010
4. 张成潘，汪诗梦，董涛，韩家斌，CN 105017320 A, 2015
5. 张成潘，查高峰，韩秋燕，胡潇谦，韩家斌，方莞茵，王云芳，董涛，CN 105753695 A, 2016
6. 张成潘，宋海霞，汪诗梦，王晓燕，韩家斌，高颖，贾苏娇，CN 106349134 A, 2017
7. 张成潘，韩秋燕，杨静，赵成龙，CN 106349071 A, 2017
8. 张成潘，宋海霞，韩家斌，杨炼，查高峰，胡潇谦，CN 106432009 A, 2017
9. 张成潘，韩家斌，杨炼，董涛，CN 107118143 A, 2017
10. 张成潘，韩周州，董涛，CN 109053536 A, 2018
11. 焦关胜，张成潘，CN 109111376 A, 2019
12. 焦关胜，张成潘，CN 109160888 A, 2019
13. 张成潘，宋海霞，黄言新，韩周洲，CN 109824548 A, 2019
14. 张成潘，施进，赵成龙，吴勋，CN 110294708 A, 2019
15. 张成潘，谭凯丽，韩秋燕，施进，CN 110372565 A, 2019.
16. 张成潘，韩秋燕，施进，谭凯丽，CN 110407727 A, 2019.
17. 张成潘，明小霞，韩周洲，施进，CN 110452146 A, 2019.
18. 张成潘，吴帅，张杰，CN 111018765 A, 2020.
