联系方式：
常州大学药学院
江苏省常州市武进区科教城常州大学测试楼A座802
Email: zhaoshuai@cczu.edu.cn
科研之友（Scholar Mate）主页：https://www.scholarmate.com/P/emIFV3
研究方向：
I. 天然产物以及重要生物活性分子结构导向的有机合成方法学研究
1）惰性C-H键活化
2）可见光催化
II. G蛋白偶联受体相关的药物化学研究
教育及工作经历：
2018.12至2019.12美国Scripps 研究所（The Scripps Research Institute）访问****，导师：余金权教授，研究方向：碳氢活化及DNA编码化合物库
2015.6月至今 常州大学药学院药学系
2010.9至2015.6 兰州大学化学化工学院有机化学专业博士导师：许鹏飞教授，研究方向：不对称有机催化
2006.9至2010.6 兰州大学化学化工学院化学基地专业学士
基金课题：
兰州大学中央高校基本科研业务费专项资金优秀研究生项目，lzujbky-2014-242，有机催化合成吲哚螺环结构的研究，2014/1-2015/6，1万元，已结题，主持
国家自然科学基金面上项目，**，基于不对称有机催化的天然产物全合成研究，2012/1-2015/12，60万元，已结题，参加
常州大学科研启动经费，2015/10-2017/10，已结题，主持
国家自然科学基金青年科学基金项目，**，手性季铵盐氟化物催化非活化羧酸酯的α位不对称烷基化反应研究，2017/1-2019/1, 20万元，已结题，主持
代表性研究成果：
1. Shuai Zhao, Shengchao Guo, Chan Yang, Zheng Gong, Yaomin Wang, Yingli Jia, Xinyu Jiang, Liwei Xu, Li Shi, Xiao Yu, Jinpeng Sun, Yan Zhang, Xin Chen*.Cell active and functionally-relevant small-molecule agonists of calcitoninreceptor. Bioorg. Chem.2020, 96, 103596.
2. Zhoulong Fan,^?Shuai Zhao,^?Tao Liu, Peng-Xiang Shen, Zi-Ning Cui, Zhe Zhuang, Qian Shao, Jason S. Chen, Anokha S. Ratnayake, Mark E. Flanagan, Dominik K. K?lmel, David W. Piotrowski, Paul Richardsond, Jin-Quan Yu*. Merging C(sp3)–H activation with DNA-encoding. Chem. Sci.2020,11,12282.
3. Shuai Zhao, Zhi-Li Chen, Xue Rui, Ming-Mei Gao, Xin Chen*. Asymmetric Allylic Amination of Morita–Baylis–Hillman Adducts with Simple Aromatic Amines by Nucleophilic Amine Catalysis. Synlett. 2019, 30, 703.
4. Shuai Zhao, Lei Jin, Zhi-Li Chen, Xue Rui, Jia-Yi He, Ran Xia, Ke Chen, Xiang-Xiang Chen, Zi-Jian Yin, Xin Chen*. Asymmetric synthesis of multifunctional aryl allyl ethers by nucleophilic catalysis. RSC Adv.2019,9,11585.
5. Lei Jin, Shuai Zhao, Xin Chen*. Synthesis of Both Enantiomers of Chiral Phenylalanine Derivatives Catalyzed by Cinchona Alkaloid Quaternary Ammonium Salts as Asymmetric Phase Transfer Catalysts. Molecules.2018,23,1421.
6. Qinting Wang, Shuai Zhao, Lei Jin, Xin Chen*.Synthesis of Fmoc-protected (S)-3,5-Dibromophenylalanine in the Presence of a Phase Transfer Catalyst or a Chiral Catalyst. Chin. J. Org. Chem.2016,36,2242.
7. Yuan-Yuan Zhao, Shuai Zhao, Ji-Kang Xie, Xiu-Qin Hu, Peng-Fei Xu*. Synthesis of Spirocyclic Oxindole Dihydrothiophenes by DBU Catalyzed [3+2] Annulation of Morita?Baylis?Hillman Carbonates with Isothiocyanates. J. Org. Chem. 2016,81, 10532.
8. Ting Xie, Yu Xiao, Shuai Zhao, Xiu-Qin Hu, Peng-Fei Xu*. Catalyst-Free Chemoselective Synthesis of 3,4-Dihydroquinazoline-2-thiones and 2?Imino[1,3] benzothiazines. J. Org. Chem. 2016, 81, 10499.
9. Shuai Zhao, Yuan-Yuan Zhao, Jun-Bing Lin, Yong-Ming Liang, Peng-Fei Xu*. Organocatalyzed Asymmetric Vinylogous Allylic-Allylic Alkylation of Morita-Baylis-Hillman Carbonates with Olefinic Azlactones: Facile Access to Chiral Multifunctional α-Amino Acid Derivatives. Org. Lett. 2015, 17, 3206.
10. Shuai Zhao, Jun-Bing Lin, Yuan-YuanZhao, Yong-Ming Liang, Peng-Fei Xu*. Hydrogen-bond-directed formal [5+1] annulations of oxindoles with ester-linked bisenones: facile access to chiral spirooxindole δ-Lactones. Org. Lett.2014, 16, 1802.