刘承伟 - 上海大学

个人简介

刘承伟，2020年于美国罗格斯新泽西州立大学取得博士学位，师从Michal Szostak教授。2020年至2021年在英国牛津大学Stephen P. Fletcher课题组，开展博士后研究工作。2021年9月至2022年6月在南京信息工程大学工作。2022年6月加入上海大学，开展教学科研工作。先后在新型扭曲酰胺的发现与应用、酰胺的交叉偶联、羧酸的脱羰偶联等领域做出了多项原创性工作，在Angew. Chem. Int. Ed.、ACS Catalysis等期刊上发表高水平学术论文三十余篇。由于研究工作的创新性和重要性，他获得了国际贵金属协会颁发的“2020 International Precious Metals Institute Student Award”、中国国家留学基金委颁发的“2019国家优秀自费留学生奖学金”、美国罗格斯新泽西州立大学颁发的“2021 Outstanding Dissertation Award”和“2019 Dissertation Fellowship”。目前主持上海市海外高层次人才引进项目一项。

研究领域

酰胺键活化、碳硫键活化、碳氧键活化、稀土金属有机、含氟药物分子的设计与合成、新型抗新冠病毒药物分子的全合成等。

近期论文

查看导师新发文章（温馨提示：请注意重名现象，建议点开原文通过作者单位确认）

2022 28. Liu, C.*; Szostak, M.* “Decarbonylative Sonogashira Cross-Coupling: Fruitful Marriage of Alkynes with Carboxylic Acid Electrophiles” Org. Chem. Front. 2022, 9, 216-222. 2021 27. Liu, C.*; Szostak, M.* “Forging C-S Bonds Through Decarbonylation: New Perspectives for the Synthesis of Privileged Aryl Sulfides” ChemCatChem 2021, 13, 4878-4881. 26. Zhang, W.; Bie, F.; Ma, J.; Zhou, F.; Szostak, M.* Liu, C.* “Palladium-Catalyzed Decarbonylative Borylation of Aryl Anhydrides” J. Org. Chem. 2021, 86, 17445-17452. 25. Bie, F.; Liu, X.; Cao, H.; Shi, Y.; Zhou, T.; Szostak, M.* Liu, C.* “Pd-Catalyzed Double-Decarbonylative Aryl Sulfide Synthesis through Aryl Exchange between Amides and Thioesters” Org. Lett. 2021, 23, 8098-8103. 24. Cao, H.; Liu, X.; Bie, F.; Shi, Y.; Han, Y.; Yan, P.; Szostak, M.* Liu, C.* “Rh(I)-Catalyzed Intramolecular Decarbonylation of Thioesters” J. Org. Chem. 2021, 86, 10829-10837. 23. Liu, C.*; Szostak, M.* “Decarbonylative Sulfide Synthesis from Carboxylic Acids and Thioesters via Cross-Over C–S Activation and Acyl Capture” Org. Chem. Front. 2021, 8, 4805-4813. 22. Liu, C.; Szostak, M.* “Decarbonylative Sonogashira Cross-Coupling of Carboxylic Acids” Org. Lett. 2021, 23, 4726-4730. 21. Liu, C.; Ji, C.-L.; Zhou, T.; Hong, X.;* Szostak, M.* “Bimetallic Cooperative Catalysis for Decarbonylative Heteroarylation of Carboxylic Acids via C-O/C-H Coupling” Angew. Chem. Int. Ed. 2021, 60, 10690-10699. 20. Shi, Y.; Liu, X.; Cao, H.; Bie, F.; Yan, P.; Han, Y.; Szostak, R.; Szostak, M.;* Liu, C.* “Conversion of Esters to Thioesters via C–O Bond Cleavage/Weak C–S Bond Formation under Transition-Metal-Free Conditions” Org. Biomol. Chem. 2021, 19, 2991-2996. 19. Cao, H.; Liu, X.; Bie, F.; Shi, Y.; Han, Y.; Yan, P.; Szostak, M.* Liu, C.* “General and Practical Intramolecular Decarbonylative Coupling of Thioesters via Palladium Catalysis” Org. Chem. Front. 2021, 8, 1587-1592. 2020 18. Bie, F.; Liu, X.; Shi, Y.; Cao, H.; Han, Y.; Szostak, M.* Liu, C.* “Rh-Catalyzed Base-Free Decarbonylative Borylation of Twisted Amides” J. Org. Chem. 2020, 85, 15676-15685. Before 2020 17. Liu, C.; Ji, C.-L.; Zhou, T.; Hong, X.; Szostak, M. “Decarbonylative Phosphorylation of Carboxylic Acids via Redox-Neutral Palladium Catalysis” Org. Lett. 2019, 21, 9256-9261. 16. Liu, C.; R.; Lalancette, R.; Szostak, R.; Szostak, M. “Sterically Hindered Ketones via Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Amides by N-C(O) Activation” Org. Lett. 2019, 21, 7976-7981. 15. Liu, C.; Ji, C.-L.; Qin, Z.-X.; Hong, X.; Szostak, M. “Synthesis of Biaryls via Decarbonylative Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of Carboxylic Acids” iScience 2019, 19, 749-759. 14. Liu, C.; Qin, Z.-X.; Ji, C.-L.; Hong, X.; Szostak, M. “Highly-Chemoselective Step-Down Reduction of Carboxylic Acids to Aromatic Hydrocarbons via Palladium Catalysis” Chem. Sci. 2019, 10, 5736-5742. 13. Liu, C.; Shi, S.; Liu, Y.; Liu, R.; Lalancette, R.; Szostak, R.; Szostak, M. “The Most Twisted Acyclic Amides: Structures and Reactivity” Org. Lett. 2018, 20, 7771-7774. 12. Liu, C.; Ji, C.-L.; Hong, X.; Szostak, M. “Palladium-Catalyzed Decarbonylative Borylation of Carboxylic Acids: Tuning Reaction Selectivity by Computation” Angew. Chem. Int. Ed. 2018, 57, 16721-16726. 11. Liu, C.; Li, G.; Shi, S.; Meng, G.; Lalancette, R.; Szostak, R.; Szostak, M. “Acyl and Decarbonylative Suzuki Coupling of N-Acetyl Amides: Electronic Tuning of Twisted, Acyclic Amides in Catalytic Carbon-Nitrogen Bond Cleavage” ACS Catal. 2018, 8, 9131-9139. 10. Liu, C.; Szostak, M. “Decarbonylative Cross-Coupling of Amides” Org. Biomol. Chem. 2018, 16, 7998-8010. 9. Liu, C.; Szostak, M. “Decarbonylative Thioetherification by Nickel Catalysis Using Air- and Moisture-Stable Nickel Precatalysts” Chem. Commun. 2018, 54, 2130-2133. 8. Liu, C.; Szostak, M. “Decarbonylative Phosphorylation of Amides by Palladium and Nickel Catalysis: The Hirao Cross-coupling of Amide Derivatives” Angew. Chem. Int. Ed. 2017, 56, 12718-12722. 7. Liu, C.; Liu, Y.; Liu, R.; Lalancette, R.; Szostak, R.; Szostak, M. “Palladium-Catalyzed Suzuki-Miyaura Cross-Coupling of N-Mesylamides by N-C Cleavage: Electronic Effect of the Mesyl Group” Org. Lett. 2017, 19, 1434-1437. 6. Liu, C.; Szostak, M. “Twisted Amides: From Obscurity to Broadly Useful Transition-Metal- Catalyzed Reactions by N-C Amide Bond Activation” Chem. Eur. J. 2017, 23, 7157-7173. 5. Liu, C.; Meng, G.; Szostak, M. “N-Acylsaccharins as Amide-Based Arylating Reagents via Chemoselective N-C Cleavage: Pd-Catalyzed Decarbonylative Heck Reaction” J. Org. Chem. 2016, 81, 12023-12030. 4. Liu, C.; Meng, G.; Liu, Y.; Liu, R.; Lalancette, R.; Szostak, R.; Szostak, M. “N- Acylsaccharins: Stable Electrophilic Amide-Based Acyl Transfer Reagents in Pd-Catalyzed Suzuki- Miyaura Coupling via N-C Cleavage” Org. Lett. 2016, 18, 4194-4197. 3. Liu, C.; Achtenhagen, M.; Szostak, M. “Chemoselective Ketone Synthesis by the Addition of Organometallics to N-Acylazetidines” Org. Lett. 2016, 18, 2375-2378. 2. Liu, C.; Zhang, Y.; Qian, Q.; Yuan, D.; Yao, Y. “n-BuLi as a Highly Efficient Precatalyst for Hydrophosphonylation of Aldehydes and Unactivated Ketones” Org. Lett. 2014, 16, 6172-6175. 1. Liu, C.; Qian, Q.; Nie, K.; Wang, Y.; Shen, Q.; Yuan, D.; Yao, Y. “Lanthanide Anilido Complexes: Synthesis, Characterization, and Use as Highly Efficient Catalysts for Hydrophosphonylation of Aldehydes and Unactivated Ketones” Dalton Trans. 2014, 43, 8355- 8362.