学科成员介绍：
盛文兵，副教授/硕导，邮箱：wbs626@126.com
受教育和工作简历：
1998年6月毕业于湖南科技学院，2004年6月毕业于湖南师范大学有机化学专业，获硕士学位，2016年毕业于湖南大学有机化学专业，获博士学位。2004年7进入湖南中医药大学药学院工作，2014年晋级为副教授。
研究方向：
绿色有机合成方法学，天然小分子药物结构修饰
代表性论文
1. Wen-Bing Sheng,Sumera Yasmin, Chen Chen, Ming Zhang, Yuxin Lei, Caiyun Peng, Bin Li, Yuqing Jian and Wei Wang. Metal-free and base-free decarboxylation of substituted cinnamic acids in a deep eutectic solvent, Synthetic Commun, 2019.12,Published online.
2.Sumera Yasmin, Wen-Bing Sheng(共同第一), Cai-Yun Peng, Atta-ur Rahman, Duan-Fang Liao, M. Iqbal Choudhary*, Wei Wang*, Highly efficient and green esterification of carboxylic acids in deep eutectic solvents without any other additives, Synthetic Commun, 2018, 48(1), 68-75.
3.Sheng Wen-Bing，Chen Tie-Qiao，Zhang Ming-Zhong，Tian Mi，Jiang Guo-Fang，Guo Can-Cheng*, Copper porphyrin-catalyzed aerobic oxidative coupling of terminal alkynes with high TON, Tetrahedron Letters, 2016, 57(15), 1641-1643.
4.Sheng Wen-Bing, Jiang Qing, Luo Wei-Ping, Can-Cheng Guo*, Oxidative rearrangement of internal alkynes to give one-carbon-shorter ketones via manganese porphyrins catalysis, J Org Chem, 2013, 78(11): 5691-5693.
5.Hao-Lin Zhang, Fei Wen, Peng Yin, Chun-Tao Zhang,Wen-Bing Sheng, Cai-Yun Peng, Dong-Ming Peng, Duan-Fang Liao, Rong-Geng Fu, A facile access to thieno[2,3-b]indoles via sulfur-mediated decarboxylative cyclization of a,b-unsaturated carboxylic acids with indoles, Tetrahedron Letters, 2018, 60,80-83.
6.Rong-geng Fu, Yuan Sun, Duan-fang Liao, Wen-bing Sheng. Designing multi-targeted agents: An emerging anticancer drug discovery paradigm, European Journal of Medicinal Chemistry, 2017, 136: 195-211.
7.盛文兵,卿梨红,邓慕雄,陈益瑶,彭彩云,含取代基的β-硝基苯乙烯的合成研究,湖南中医药大学学报, 2014,(06):16-18.
8.Jiang Qing, Guo Cancheng*, Sheng Wenbing. Synthesis of phenacyl bromides via K2S2O8-mediated tandem hydroxybromination and oxidation of styrenes in water, Green Chem, 2013,15(8): 2175-2179.
9.Jiang Qing, Tian Mi, Tang Jie, Guo Cancheng*, Sheng Wenbing. Cobalt(II)-Porphyrin-Catalyzed Aerobic Oxidation: Oxidative Coupling of Phenols, Eur J Org Chem, 2013,10(10):1861-1866.
