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个人简介

学习工作经历 1998-2002 南开大学,获得理学学士学位 2002-2007 上海有机化学研究所,获得理学博士学位 2008-2013 上海应用技术大学,讲师、副教授 2014-2016 复旦大学,博士后研究 2017-2018 美国斯克里普斯研究所(The Scripps Research Institute),访问学者研究 2019-至今 复旦大学,青年副研究员

研究领域

非活化碳氢键氧化偶联 新型聚苯胺材料合成及性能研究 光催化碳氢键氧化 新型生物正交反应

近期论文

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Y. Liao, Y. Zhou, Z. Zhang, J. Fan, F. Liu, Z. Shi. Intramolecular Oxidative Coupling between Unactivated Aliphatic C-H and Aryl C-H Bonds. Org. Lett. 23, 1251-1257 (2021). H. Diao, Z. Shi, F. Liu. Biaryl Construction Base on Nickel-Catalyzed C-O Bond Activation. Syn. lett. 32, A-S (2021). C. Wang, F. Liu, Z. Shi. Homogeneous functionalization of light alkanes. Sci. Sin. Chem. 50, 756-765 (2020). F. Liu, H. Jiang, Y. Zhou, Z. Shi. Direct Transformation of Arenols Based on C-O Activation. Chin. J. Chem. 38, 855-863 (2020). F. Liu, H. Wang, S. Li, G. Bare, J. Moses, P. Wu, K. Sharpless. Biocompatible SuFEx Click Chemistry: Thionyl Tetrafluoride (SOF4) Derived Connective Hubs For Bioconjugation to DNA and Proteins. Angew. Chem. Int. Ed. 58, 8029-8033 (2019). R. Gou, Y. Zhang, S. W. Wu, F. Liu. Synthesis of Polysubstituted 3-Chalcogenated Indoles through Copper(I)-Catalyzed Three Component Domino-Reactions. Syn. Lett. 30, 207-212 (2019). Z. P. Chen, Y. Zhou, M.Z. Shui, F. Liu. CuI Catalyzed Domino Coupling-Cyclization of 2-Iodo-Phenols and 1-Alkynes to the Synthesis of 2-Substituted Benzo[b]furans/furo-pyridines. Tetrahedron Lett. 60, 133-136 (2019). X.H. Pan, S.P. Bai, W.S. Yu, D. Ding, D.X. Zhao, F. Liu. Efficient Synthesis of 3-R-Boc-amino-4-(245-trifluorophenyl)butyric Acid. Synth. Commun. 45, 1451-1456 (2015). D. Ding, X.H. Pan, W.S. Yu, X.J. Li, S.K. Chen, F. Liu. An Cost-Effective and Safe Process of L-cis-45-Methanoproline Amide The Key Synthetic Intermediate of Saxagliptin via an Improved Simmons-Smith Reaction. Heterocycles 91, 719-725 (2015). X.H. Pan, S.Y. Xu, R. Huang, W.S. Yu, F. Liu. A Facile Six-Step Process for the Synthesis of (3S5S)‑3-Isopropyl-5-((2S4S)‑4-isopropyl- 5-oxo-tetra- hydrofuran-2-yl)-2-oxopyrrolidine-1-carboxylic Acid tert- Butyl Ester The Key Synthetic Intermediate of Aliskiren. Org. Pro. Res. Dev. 19, 611-617 (2015).

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