jinnian(金字招牌)诚信至上·金年会官网

博士/教授/硕士生导师

E-mail:shenguodong33@163.com

招生专业：有机化学

科研方向：过渡金属与多酸催化、C-H活化、医药中间体合成

讲授课程

本科生：高等有机、有机基础实验、有机专论实验

研究生：研究生现代仪器技术分析、高等有机

教育经历

2002.09-2006.07   金年会   学士

2006.09-2011.07   浙江大学    博士

2011.10-2013.08   the Catholic University of America    博士后

2011.11-2013.08   the Combi-blocks .Int                项目负责人

2013.11-至今      金年会      教授

科研项目

1. 国家自然科学青年基金：廉价过渡金属铜催化的偶联与C-H活化反应在合成5-8元含氮杂环化合物中的应用，主持；

2. 山东省自然科学基金：铜、钯催化的偶联与C-H活化反应在合成及修饰苯并杂环化合物中的研究，主持；

3. 横向项目 2项，到账210万。

获奖情况

科研成果(第一作者或通讯作者、专利)

1. Guodong Shen,* Kun Bi, Dehe Wang, Zhirong Zhao, Xuan Tang, Xianqiang Huang,* Xin Lv. Condition-Controlled Divergent Selective Synthesis of (Z)-N-Vinyl and N-Allenyl Benzimidazoles by Pd- or Bi-Catalyzed Direct N-Alkenylation Reactions. J. Org. Chem. 2025, 90, 2602-2612.

2. Lirong Jiang, Jiayang Zhang, Xiaolu Li, Xuan Tang, Shuwen Gong,* Xianqiang Huang,* Guodong Shen.* TfOH-Catalyzed PPh3-Promoted Nucleophilic Cyclization Reactions for the Synthesis of Functionalized (Z)-2-Imino-Benzo[e][1,3]Thiazin-4-ones. Tetrahedron 2025, 180, 134676.

3. Wenjing Lu, Yongjun Zhang, Kun Bi, Zhirong Zhao, Xianqiang Huang,* and Guodong Shen.* Hydrogen-Bond-Induced Aza-Michael Addition of Imidazoles and Quinones without Additional Base and DFT Calculations. Tetrahedron 2025, 184, 134748.

4. Guodong Shen,* Zhirong Zhao, Kun Bia, Yi Mana, Juntong Liua, Xianqiang Huang*, Xin Lv. Room temperature natural light promoted DMSO/O2‑catalyzed N‑acylation reaction of imidazoles/triazoles with cyclopropenones. Mol. Divers. 2024, 29, 4371-4386.

5. Zhanjun Li, Yalin Zhang, Manman Sun, Ye Zhang, Zhaoxiang Lu, Yupeng Deng, Xianqiang Huang,* Guodong Shen.* La(OTf)3-Catalyzed [3+2] Cycloaddition Reactions for the Synthesis of Benzo[d]oxazoles/Benzofurans. J. Org. Chem. 2024, 89, 3809-3820.

6. Guodong Shen,* Zhanjun Li, Lingyu Zhao, Ye Zhang, Yalin Zhang, Zhen Li, Xianqiang Huang,* Xin Lv. Room-Temperature Cascade Electrophilic Addition/Cyclization/Oxidation Reactions: Divergent Selective Synthesis of Brominated 2H-Chromenes, 2H-Chromen-2-ols and 2H-Chromen-2-ones. Chem. A Eur. J. 2024, 30, e202401011.

7. Zhanjun Li, Lingyu Zhao, Yalin Zhang, Hui Yan, Xianqiang Huang,* Guodong Shen.* Cascade Nucleophilic Attack/Addition Cyclization Reactions to Synthesize Oxazolidin-2-imines via (Z)‑2-Bromo-3-phenylprop-2-en-1-ols/3-phenylprop-2-yn-1-ols and Diphenyl Carbodiimides. J. Org. Chem. 2022, 87, 12721-12732.

8. Guodong Shen,* Zeyou Wang, Xianqiang Huang,* Min Hong,* Shuhua Fan, and Xin Lv. Palladium/Copper Cocatalyzed C-H Activation and C-C Bond Regioselective Cleavage Reaction for the Synthesis of Fused Chromeno Quinolines. Org. Lett. 2022, 22, 8860-8865.

9. Dehe Wang, Qichao Lu, Zhanjun Li, Chen Fang, Ran Liu, Bingchuan Yang,* and Guodong Shen.* "One-Pot" CuCl2-Mediated Condensation/C-S Bond Coupling Reactions to Synthesize Dibenzothiazepines by Bi-Functional-Reagent N, N'-Dimethylethane-1,2-Diamine. Molecules 2022, 27, 7392.

10. Yuquan Qi, Xiaoyu Gu, Xianqiang Huang,* Guodong Shen,* Bingchuan Yang, Qingpeng He, Zechun Xue, Mengcheng Du, Lilong Shi, Bing Yu, Microwave-assisted controllable synthesis of 2-acylbenzothiazoles and bibenzo[b][1,4]thiazines from aryl methyl ketones and disulfanediyldianilines. Chin. Chem. Lett. 2021, 32, 3544-3547.

11. Xianqiang Huang,* Xiaoyu Gu, Yuquan Qi, Yanru Zhang, Guodong Shen,* Bingchuan Yang, Wenzeng Duan, Shuwen Gong, Zechun Xue, Yifa Chen*. Decavanadate-based Transition Metal Hybrids as Bifunctional Catalysts for Sulfide Oxidation and C-C Bond Construction. Chin. J. Chem. 2021, 39, 2495-2503.

12. Xianqiang Huang,* Xiaoyu Gu, Haichao Zhang, Guodong Shen,* Shuwen Gong, Bingchuan Yang, Yanlan Wang, Yifa Chen*. Decavanadate-based clusters as bifunctional catalysts for efficient treatment of carbon dioxide and simulant sulfur mustard. J. CO2 Util. 2021, 45, 101419.

13. Guodong Shen,* Zeyou Wang, Xianqiang Huang,* Min Hong,* Shuhua Fan, and Xin Lv. Palladium/Copper Cocatalyzed C-H Activation and C-C Bond Regioselective Cleavage Reaction for the Synthesis of Fused Chromeno Quinolines. Org. Lett. 2020, 22, 8860-8865.