佟硕
副教授，博士生导师
2003-2007，吉林大学化学系，获理学学士学位
2007-2013，中国科学院化学研究所，获理学博士学位
2013-2018，瑞士洛桑联邦理工学院（EPFL），博士后
2018-至今 清华大学化学系 副教授
发表论文：
1. Shuo Tong,* Jiang-Tao Li, Dong-Dong Liang, Yan-E Zhang, Qi-Yun Feng, Xin Zhang, Jieping Zhu, Mei-Xiang Wang.* Catalytic Enantioselective Synthesis and Switchable Chiroptical Property of Inherently Chiral Macrocycles. J. Am. Chem. Soc. 2020, 142, 14432–14436.
DOI: 10.1021/jacs.0c05369
2. Qi-Yun Feng, Jieping Zhu, Mei-Xiang Wang, Shuo Tong.* Organocatalytic Double Ugi Reaction with Statistical Amplification of Product Enantiopurity: A Linker Cleavage Approach To Access Highly Enantiopure Ugi Products. Org. Lett. 2020, 22, 483–487.
DOI: 10.1021/acs.orglett.9b04239
3. Li Zhen, Shuo Tong,* Jieping Zhu, Mei-Xiang Wang.* Fused N‐Heterocycles with Contiguous Stereogenic Centers Accessed by an Asymmetric Catalytic Cascade Reaction of Tertiary Enamides. Chem. Eur. J. 2020, 26, 401-405.
4. Wenju Zhu, Shuo Tong,* Jieping Zhu, and Mei-Xiang Wang.* Intramolecular Arylation of Tertiary Enamides through Pd(OAc)2-Catalyzed Dehydrogenative Cross-Coupling Reaction: Construction of Fused N-Heterocyclic Scaffolds and Synthesis of Isoindolobenzazepine Alkaloids. J. Org. Chem. 2019, 84, 2870–2878.
5. Shuo Tong,* Mei-Xiang Wang.* Catalytic Enantioselective Synthesis of 4-Amino-1,2,3,4-tetrahydropyridine Derivatives from Intramolecular Nucleophilic Addition Reaction of Tertiary Enamides. Synlett. 2019, 30, 483-487.
6. Xin-Ming Xu#, Chuan-Hu Lei#, Shuo Tong,* Jieping Zhu, Mei-Xiang Wang.* Lewis acid catalyst-steered divergent synthesis of functionalized vicinal amino alcohols and pyrroles from tertiary enamides. Org. Chem. Front. 2018, 5, 3138-3142 .
DOI: 10.1039/c8qo00839f
7. Shuo Tong, Qian Wang, Mei-Xiang Wang, Jieping Zhu.* Chiral phosphoric acid-catalyzed enantioselective three-component Mannich reaction of acyclic ketones, aldehydes and anilines. Tetrahedron. 2018, 74, 5143-5149.
DOI: 10.1016/j.tet.2018.05.055
8. Shuo Tong, Aurore Limouni, Qian Wang, Mei-Xiang Wang, Jieping Zhu.* Catalytic Enantioselective Double Carbopalladation/C−H Functionalization with Statistical Amplification of Product Enantiopurity: A Convertible Linker Approach. Angew. Chem., Int. Ed. 2017, 56, 14192-14196.
9. Shuo Tong#, Cyril Piemontesi#, Qian Wang, Mei-Xiang Wang, Jieping Zhu.* Silver‐Catalyzed Three‐Component 1,1‐Aminoacylation of Homopropargylamines: α‐Additions for Both Terminal Alkynes and Isocyanides. Angew. Chem., Int. Ed. 2017, 56, 7958-7962.
10. Shuo Tong, Shun Zhao, Qing He, Qian Wang, Mei-Xiang Wang, Jieping Zhu.* Fluorophores for Excited-State Intramolecular Proton Transfer by an Yttrium Triflate-Catalyzed Reaction of Isocyanides with Thiocarboxylic Acids, Angew. Chem. Int. Ed. 2017, 56, 6599-6603.
11. Shuo Tong, Qian Wang, Mei‐Xiang Wang, Jieping Zhu.* Switchable [3+2] and [4+2] Heteroannulation of Primary Propargylamines with Isonitriles to Imidazoles and 1,6‐Dihydropyrimidines: Catalyst Loading Enabled Reaction Divergence. Chem. Eur. J. 2016, 22, 8332-8338.
12. Shuo Tong#, Zhengren Xu#, Mathias Mamboury, Qian Wang, Jieping Zhu.* Aqueous Titanium Trichloride-Pormoted Reductive Cyclization of o-Nitrostyrenes to Indoles: Development and Application to the Synthesis of Rizatriptan and Aspidospermidine. Angew. Chem. Int. Ed. 2015, 54, 11809-11812.
13. Shuo Tong, Qian Wang, Mei‐Xiang Wang, Jieping Zhu.* Tuning the Reactivity of Isocyano Group: Synthesis of Imidazoles and Imidazoliums from Propargylamines and Isonitriles in the Presence of Multiple Catalysts. Angew. Chem. Int. Ed. 2015, 54, 1293-1927.
14. Shuo Tong, Xu Yang, De-Xian Wang, Liang Zhao, Jieping Zhu, Mei-Xiang Wang.* Synthesis of 4-amino-1,2,3,4-tetrahydropyridine derivatives by intramolecular nucleophilic addition of tertiary enamides to in-situ generated imines. Tetrahedron. 2012, 68, 6492-6497.
DOI: 10.1016/j.tet.2012.05.108
15. Shuo Tong, De‐Xian Wang, Liang Zhao, Jieping Zhu, Mei‐Xiang Wang.* Enantioselective Synthesis of 4-Hydroxytetrahydropyridine Derivatives by Intramolecular Addition of Tetriary Enamides to Aldehydes. Angew. Chem. Int. Ed. 2012, 51, 4417-4420.
