姓名：袁勇

职称：副教授/硕士生导师

出生年月：1989年8月

学科专业：有机化学

通讯地址：威尼斯9499登录入口新校区综合实验楼E-422

Email: yuanyong@nwnu.edu.cn; yuanyong1989@outlook.com

【个人简介】

2013年6月在威尼斯9499登录入口获理学学士学位。2016年6月在威尼斯9499登录入口获理学硕士学位，导师为霍聪德教授。2020年6月在武汉大学获理学博士学位，导师为雷爱文教授。2020年10月进入威尼斯9499登录入口工作。近几年以（共同）第一作者，（共同）通讯作者身份在Angew. Chem. Int. Ed., Chem. Soc. Rev., Acc. Chem. Res., Sci. Adv., Nat. Commun., ACS Catal., Green. Chem., Chem. Commun.等高水平学术期刊发表论文20余篇，引用次数累计超过1500次，单篇最高引用达到380次。

【主讲课程】

1. 有机化学（本科生）

2. 有机化学实验（本科生）

3. 化学基础实验（本科生）

4. 高等有机化学（研究生）

【研究兴趣】

1. 电化学有机合成

2. 光催化有机合成

3. 二氧化碳的转化与利用

【代表性论文】

(1) Wang, D.; Jiang, T.; Wan, H.; Chen, Z.; Qi, J.; Yang, A.; Huang, Z*.; Yuan, Y*.; Lei, A*. Alternating Current Electrolysis Enabled Formal C−O/O−H Cross-Metathesis of 4-Alkoxy Anilines with Alcohols. Angew. Chem. Int. Ed. 2022, 61, e202201543 (IF = 16.832).

(2) Yuan, Y.; Yang, J.; Lei, A*. Recent advances in electrochemical oxidative cross-coupling with hydrogen evolution involving radicals. Chem. Soc. Rev. 2021, 50, 10058-10086 (IF = 60.615).

(3) Yuan, Y.; Lei, A*. Electrochemical Oxidative Cross-Coupling with Hydrogen Evolution Reactions. Acc. Chem. Res. 2019, 52, 3309-3324 (IF = 24.466).

(4) Yuan, Y.; Chen, Y.; Tang, S.; Huang, Z.; Lei, A*. Electrochemical oxidative oxysulfenylation and aminosulfenylation of alkenes with hydrogen evolution. Sci. Adv. 2018, 4, eaat5312 (IF = 14.957).

(5) Yuan, Y.; Lei, A*. Is electrosynthesis always green and advantageous compared to traditional methods? Nat. Commun. 2020, 11, 802 (IF = 17.694).

(6) Yuan, Y.; Cao, Y.; Lin, Y.; Li, Y.; Huang, Z.; Lei, A*. Electrochemical Oxidative Alkoxysulfonylation of Alkenes Using Sulfonyl Hydrazines and Alcohols with Hydrogen Evolution. ACS Catal. 2018, 8, 10871-10875 (IF = 13.7).

(7) Yuan, Y.; Zheng, Y.; Xu, B.; Liao, J.; Bu, F.; Wang, S.; Hu, J.-G.; Lei, A*. Mn-Catalyzed Electrochemical Radical Cascade Cyclization toward the Synthesis of Benzo[4,5]imidazo[2,1-a]isoquinolin-6(5H)-one Derivatives. ACS Catal. 2020, 10, 6676-6681 (IF = 13.7).

(8) Yuan, Y.; Liu, X.; Hu, J.; Wang, P.; Wang, S.; Alhumade, H.; Lei, A. Electrochemical oxidative N–H/P–H cross-coupling with H2 evolution towards the synthesis of tertiary phosphines. Chem. Sci. 2022, 13, 3002-3008 (IF = 9.969).

(9) Yuan, Y.; Yao, A.; Zheng, Y.; Gao, M.; Zhou, Z.; Qiao, J.; Hu, J.; Ye, B.; Zhao, J.; Wen, H.; Lei, A*. Electrochemical Oxidative Clean Halogenation Using HX/NaX with Hydrogen Evolution. iScience 2019, 12, 293-303.

(10) Yuan, Y.; Qi, J.; Wang, D.; Chen, Z.; Wan, H.; Zhu, J.; Yi, H.; Chowdhury, A. D.; Lei, A*. Radical–Radical Cross-Coupling Assisted N–S Bond Formation Using Alternating Current Protocol. CCS Chem. 2021, 3, 3027–3038.

(11) Yuan, Y.; Yu, Y.; Qiao, J.; Liu, P.; Yu, B.; Zhang, W.; Liu, H.; He, M.; Huang, Z*.; Lei, A*. Exogenous-oxidant-free electrochemical oxidative C–H sulfonylation of arenes/heteroarenes with hydrogen evolution. Chem. Commun. 2018, 54, 11471-11474.

(12) Yuan, Y.; Qiao, J.; Cao, Y.; Tang, J.; Wang, M.; Ke, G.; Lu, Y.; Liu, X.; Lei, A*. Exogenous-oxidant-free electrochemical oxidative C–H phosphonylation with hydrogen evolution. Chem. Commun. 2019, 55, 4230-4233.

(13) Yuan, Y.; Jiang, M.; Wang, T.; Xiong, Y.; Li, J.; Guo, H.; Lei, A*. Synergy of anodic oxidation and cathodic reduction leads to electrochemical deoxygenative C2 arylation of quinoline N-oxides. Chem. Commun. 2019, 55, 11091-11094.

(14) Yuan, Y.; Li, L.-S.; Zhang, L.; Wang, F.; Jiang, L.; Zuo, L.; Wang, Q.; Hu, J.-G.; Lei, A. Electrochemical synthesis of versatile ammonium oxides under metal catalyst-, exogenous-oxidant-, and exogenous-electrolyte-free conditions. Chem. Commun. 2021, 57, 2768-2771.

(15) Yuan, Y.; Zhou, Z.; Zhang, L.; Li, L.-S.; Lei, A. Electrochemical Oxidative C3 Acyloxylation of Imidazo[1,2-a]pyridines with Hydrogen Evolution. Org. Lett. 2021, 23, 5932-5936.

(16) Yuan, Y.; Cao, Y.; Qiao, J.; Lin, Y.; Jiang, X.; Weng, Y.; Tang, S.; Lei, A*. Electrochemical Oxidative C—H Sulfenylation of Imidazopyridines with Hydrogen Evolution. Chin. J. Chem. 2019, 37, 49-52.

(17) Lu, F.; Yuan, Y*. An Electrochemical Synthesis Approach for Tetrasubstituted Olefins. Chin. J. Chem. 2019, 37, 744-745.