School of Pharmaceutical Sciences, South-Central University of Nationalities,
182 Minzu Road, Hongshan District, Wuhan, Hubei Province Wuhan, 430074, China
Mobile phone: +86-15172336102
Email:zhysh@mail.scuec.edu.cn
Education
2013-2015 Postdoctoral associate
University of Central Florida, Orlando, Florida
Supervisor: Yuan Yu
2010-2013 PH.D. in Organic Chemistry
Chengdu Institute of Organic Chemistry, Chinese Academy of Sciences
Supervisor: Professor Xiao-Mei Zhang and Professor Wei-Cheng Yuan
2007-2010 M.S. in Medicinal Chemistry
West China School of Pharmacy, Sichuan University, Chengdu, China.
Supervisor: Associate Professor Li Cheng
2002-2006 B.S. in Pharmaceutical Engineering
Xihua University, Chengdu, China
Fundings
1、National Natural Science Foundation of China (81973208，2020/01-2023/12，Principal Investigator)
2、Hubei Provincial Natural Science Foundation of China (2019CFB624，2019/01-2020/12，Principal Investigator)
3、Fundamental Research Funds for the Central Universities (CZQ17010, Principal Investigator)
4、National Natural Science Foundation of China (21172217，2012/01-2015/12)
Publications
(1) Yongsheng Zheng, Liang Tu, Na Li, Rong Huang, Tao Feng, Huan Sun, Zhenghui Li, Jikai Liu*, Inverse-Electron-Demand [4+2]-Cycloaddition of 1,3,5-triazinanes: Facile Approaches to Tetrahydroquinazolines, Adv. Synth. Catal., 2019, 361, 44-48.
(2) Liang Tu, Zhenghui Li, Tao Feng, Shuyan Yu, Rong Huang, Jing Li, Wenxuan Wang, Yongsheng Zheng*, Jikai Liu*，Access to Imidazolidines via 1,3-Dipolar Cycloadditions of 1,3,5-Triazinanes with Aziridines, J. Org. Chem., 2019, 84, 11161-11169.
(3) Yongsheng Zheng, Liang Tu, Limei Gao, Rong Huang, Tao Feng, Huan Sun, Wenxuan Wang, Zhenghui Li, Jikai Liu. Accessing benzooxadiazepines via formal [4+3] cycloadditions of aza-o-quinone methides with nitrones, Org. Biomol. Chem., 2018, 16, 2639-2642.
(4) Zhiyao Chu, Na Li, Dan Liang, Zhenghui Li, Yongsheng Zheng*, Jikai Liu. Accessing Substituted Pyrrolidines via Formal [3+2] Cycloaddition of 1,3,5-Triazinanes and Donor-acceptor Cyclopropanes, Tetrahedron Lett., 2018, 59, 715-718.
(5) Yongsheng Zheng, Ebrahim H. Ghazvini Zadeh, Yu Yuan. One-Pot, Enantioselective Synthesis of 2,3-Dihydroazulen-6(1H)-one: A Concise Access to the Core Structure of Cephalotaxus Norditerpenes, Eur. J. Org. Chem., 2016, 12, 2115-2119.
(6) M. W. Logan, A. L. Yuen, Y. S. Zheng, E. A. Hall, M. A. Hettinger, R. M. Marks, M. L. Hosler, F. M. Rossi, Y. Yuan, F. Uribe-Romo. Heterogeneous Photoredox Synthesis of N-hydroxy-oxazolidinones Catalyzed by Metal-Organic Frameworks. Catal. Sci. Technol., 2016, 5647-5655.
(7) Yongsheng Zheng, Jacob Cleaveland, David Richardson, Yu Yuan. An Oganocatalysis Based Carbocyclic Spiroindoline Synthesis Enables Facile SAR Study at C-2 Position, Org. Lett., 2015, 17, 4240-4243.
(8) Yongsheng Zheng, Muqiong Liu, Yu Yuan. A Very Mild and Selective Method for O-benzoylation of Hydroxamic Acids, Tetrahedron Lett., 2014, 55, 4404-4406.
(9) Bracken F. Roberts, Yongsheng Zheng, Jacob Cleaveleand, Sukjun Lee, Eunyoung Lee, Lawrence Ayong, Yu Yuan, Debopam Chakrabarti. 4-Nitro Styrylquinoline is an Antimalarial Inhibiting Multiple Stages of Plasmodium Falciparum Asexual Life Cycle, Int J Parasitol., 2017, 7, 120-129.
(10) Lixin Liu, Yongsheng Zheng, Xiaoyan Hu, Chunxia Lian, Weicheng Yuan, Xiaomei Zhang. Lewis Base Organocatalyzed Enantioselective Hydrosilylation of α-Keto Ketimines, Chemical Research in Chinese Universities, 2014, 30, 235-241.
(11) Yongsheng. Zheng, Zhouyang Xue, Lixi Liu, Chang. Shu, Weicheng. Yuan, Xiaomei Zhang. “Highly enantioselective hydrosilylation of N-(1,2-diphenylethylidene)arylamines”. Org. Biomol. Chem., 2013, 11, 412-415.
(12) Xing Chen, Yongsheng Zheng, Chang Shu, Weicheng Yuan, Bo Liu, Xiaomei Zhang. Enantioselective Synthesis of 4-substituted-4,5-dihydro-1H- [1,5]benzodiazepine -2(3H)-ones by the Lewis Base Catalyzed Hydrosilylation, J. Org. Chem., 2011, 21, 9109-9115.
(13) Yan Jiang, Xing Chen, Yongsheng Zheng, Zhouyang Xue, Chang Shu, Weicheng Yuan, Xiaomei Zhang. Highly Diastereoselective and Enantioselective Synthesis of α-Hydroxy β-Amino Acid Derivatives: Lewis Base Catalyzed Hydrosilylation of α-Acetoxy β-Enamino Esters, Angew. Chem. Int. Ed., 2011, 50, 7304-7307.
