陈战国 - 陕西师范大学 - 化学化工学院

研究领域

天然产物化学，有机及药物分析 1 有机合成方法学； 2 天然产物结构改造与全合成；3 中草药有效成分分析。

近期论文

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Wei, Junfa; Chen, Zhanguo; Gao, Yanni; Zhang, Peng; Wang, Chuanning; Zhao, Pengfei; Wang, Yun; Shi, Xianying. A Rapid and Simple Method for Quantitative Aziridination from Aminobrominated Derivatives of Olefins under Solvent-free and Mild Conditions, Chin. J. Chem. 2012, 30, 391—399. Li, Wenli; Chen, Zhanguo; Zhou, Jimei; Hu, Junli; Xia, Wei. Sodium Acetate-catalyzed Regiospecific and High Stereoselective Aminobromination of β,β-Dicyanostyrene Derivatives with NBS as Nitrogen/Bromine Source, Chin. J. Chem. 2012,30，830-836 陈战国, 周继梅, 王芸, 李文丽. K3PO4-催化的β-硝基苯乙烯衍生物与乙酰胺、NBS 的区域专一性氨溴加成反应研究, 化学学报, 2011,69(23): 2851～2858. Jing Li, Jing-jing Cao, Jun-fa Wei, Xian-ying Shi, Li-hui Zhang, Jin-juan Feng, and Zhan-guo Chen. Ionic Liquid Brush as a Highly Efficient and Reusable Catalyst for On-Water Nucleophilic Substitutions, Eur. J. Org. Chem. 2011, 229–233. Jiao Jiao, Xi-Ru Zhang, Ning-Hui Chang, Jie Wang, Jun-Fa Wei, Xian-Ying Shi, and Zhan-Guo Chen. A Facile and Practical Copper Powder-Catalyzed, Organic Solvent- and Ligand-Free Ullmann Amination of Aryl Halides, J. Org. Chem.2011, 76, 1180–1183. Jing Li, Xian-Ying Shi, Yuan-Yuan Bi, Jun-Fa Wei, Zhan-Guo Chen. Pd Nanoparticles in Ionic Liquid Brush: A Highly active and Reusable Heterogeneous Catalytic Assembly for Solvent-free or On-water Hydrogenation of Nitroarene under Mild Conditions, Catal., 2011, 1 (6), 657–664. Zhan-Guo Chen, Peng-Fei Zhao, and Yun Wang. Aminobromination of β-Nitrostyrene Derivatives with N,N-Dibromourethane as the Aminobrominating Reagent, Eur. J. Org. Chem. 2011, 29，5887–5893. Chen, Zhanguo, Wei, Junfa, Li, Wenli, Wang, Yun, Zhao, Pengfei, Shi, Xianying. (＋)-Tartaric Acid-Catalyzed High Regio- and Stereoselective Aminobromination of Olefins, Chin. J. Chem. 2011, 29, 1689—1696. 陈战国，周利燕，李文丽，周继梅，王传宁. 铝粉催化肉桂酸酯衍生物区域选择和立体选择性氨溴加成反应研究,化学学报，2011, 69(9):1093-1100. Junfa Wei, Yanni Gao, Xiaoyan Ma, Xiaowei Jia, Xianying Shi, Zhanguo Chen. A novel class of C3d symmetrical molecules synthesized by a six-fold substitution from 1,4,5,8,9,12-hexabromododecahydrotriphenylenew, Chem. Commun., 2010, 46, 3738–3740.