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导师简介

申国栋老师简介

作者: 发布时间:2021-11-19



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申国栋老师简介

shenguodong.lcu.edu.cn

博士/教授

TEL/ 13793094893

EMAIL/shenguodong@lcu.edu.cn

科研方向/有机化学

  • 讲授课程

有机基础实验、研究生现代仪器技术分析(原波谱分析)、基础有机化学、高等有机

  • 教育经历

2002.09-2006.07   伟德国际betvlctor1946   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                研究员

2013.11-至今      伟德国际betvlctor1946     副教授

  • 科研项目

结题青年国家自然科学基金一项201402079、正在主持山东省青年科学基金一项(ZR2019QB022)伟德国际betvlctor1946博士启动基金1项

  • 论著一览

1. 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.

2. Guodong Shen, Zeyou Wang, Xianqiang Huang, huwen Gong, Jiangong Zhang, Zhenfei Tang, Manman Sun and Xin Lv Bonded- and discreted-Lindqvist hexatungstate-based copper hybrids as heterogeneous catalysts for the one-pot synthesis of 2-phenylquinoxalines via 2-haloanilines with vinyl azides or 3-phenyl-2H-azirines. Dalton Trans. 2020, 49, 1399313998.

3. Zeyou Wang, Guodong Shen, Xianqiang, Huang, Shuwen Gong, Bingchuan Yang, Zhenzhe Sun, Zuhao Zhang and Wanxing Liu. Ball-milling Synthesis of Tetrahydroquinolines via One-pot Three-component Diels-Alder Reaction Catalyzed by Phosphotungstic Acid. Chem. Res. Chinese Universities, 2020, 36(5), 835-842.

4. Guodong Shen,* Bingchuan Yang, Xianqiang Huang, Yaxin Hou, Huan Gao, Jichun Cui, Chuansheng Cui, and Tongxin Zhang*. Copper and Palladium Catalyzed Cross-Coupling Reactions for the Synthesis of N-Fused Benzo[4,5]imidazo[2,1-b]thiazole Derivatives via Substituted trans-1,2-Diiodoalkenes, 1H-Benzo[d]imidazole-2-thiols and Halobenzenes. J. Org. Chem. 2017, 82, 3798-3805.

5. Guodong Shen,* Lingyu Zhao, Xiliang Zhao, Xinlei Huangfu, Zhe Li, Rui Wang, and Tongxin Zhang*. Synthesis of quinoxaline derivatives via copper(I)-catalyzed cross-coupling reaction of 1,2-dihalobenzenes with N, N'-disubstituted ethane-1,2-diamines under “ligand and solvent-free” condition. Synlett., 2017, 28, 1111-1115.

6. Guodong Shen*, Yichen Wang, Xiliang Zhao, Xinlei Huangfu, Yanmeng Tian, Tongxin Zhang, and Bingchuan Yang*. Pd/C-Catalyzed Homocoupling Reaction for the Synthesis of Symmetrical Biaryl Diamides. Synlett., 2017, 28, 2030-2035.

7. Guodong Shen*, Lingyu Zhao, Wanxing Liu, Xianqiang Huang, Huina Song, and Tongxin Zhang*. Convenient, metal-free ipso-nitration of arylboronic acids using nitric acid and trifluoroacetic acid. SYNTHETIC COMMUNICATIONS., 2017, 47, 10-14.

8. Synthesis of quinoxaline derivatives via copper(I)-catalyzed cross-coupling reaction of 1,2-dihalobenzenes with N, N'-disubstituted ethane-1,2-diamines under ligand and solvent-free condition. Synlett, 2017, 28, 111-1115.

9. Guodong Shen,* Lingyu zhao, Yichen Wang and Tongxin Zhang*. Room temperature copper-catalyzed oxidative amidation of terminal alkynes for the synthesis of a-ketoamides using O-benzoyl hydroxylamines as aminating reagent and oxidant. RSC Adv., 2016, 6, 78307-78310.

10. Guodong Shen,* Lingyu Zhao, Yichen Wang, Wenfang Xia, Mingsen Yang and Tongxin Zhang*. Palladium-copper catalyzed C(sp3)-C(sp2) bond C-H activation cross-coupling reaction: selective arylation to synthesize 9-aryl-9H-xanthene and 9,9-diaryl-xanthene derivatives. RSC Adv., 2016, 6, 84748-84751.

11. Guodong Shen*, Lingyu Zhao, and Weiliang Bao. 1,1′-Binaphthyl-2,2′-diamine Dihydrochloride: an Efficient Ligand for the N-Arylation of Imidazole with Aryl/heteroaryl Halides Catalyzed by CuI. Chem. Res. Chin. Univ., 2016, 32(6), 947-51.

12. Manman Sun, Guodong Shen, and Weiliang Bao*. Regioselective Cleavage of Unstrained C-C Bond and C-H Bond: Palladium-Copper Catalyzed Deacetophenonylative Arylation of Coumarin Derivatives. Adv. Synth. Catal. 2012, 354, 3468-3474.

13. Guodong Shen, and Weiliang Bao*. Synthesis of Benzoxazole and Benzimidazole Derivatives via Ligand-Free Copper(I)-Catalyzed Cross-Coupling Reaction of o-Halophenols or o-Haloanilines with Carbodiimides. Adv. Synth. Catal., 2010, 352, 981-986.






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