姓名 |
张震 |
2寸照片:

|
职称 |
副教授 |
邮箱 |
zhangz@ytu.edu.cn |
研究领域 |
1、温和条件下的杂环药物中间体的转化及合成; 2、高性能液晶单体和功能染料分子的合成开发; 课题组网站:https://www.x-mol.com/groups/zhangz_zhen |
个人简介:
张震,男,2018年入职烟台大学从事教学科研工作,主要围绕温和条件下的杂环药物中间体的转化及合成开展研究工作,承担省级项目2项,企业横向课题3项,以第一或通讯作者在Angew. Chem. Int. Ed.,Org. Lett. ,Chem. Commun.,Org. Chem. Front.等期刊发表SCI论文20余篇,授权国家发明专利3项。
教育经历:
2009年09月–2013年07月,河南农业大学,植物科学与技术,学士
2013年09月–2018年07月,中国农业大学,化学,博士(硕博连读)
工作经历:
2018年11月– 2025年1月,烟台大学,化学化工学院,讲师
2025年1月– 至今,烟台大学,化学化工学院,副教授
项目经历:
(1) 碳二酰亚胺为前体的脒基化合物的合成及应用研究,山东省自然科学基金青年项目,2021.01-2023.12,15.0万,主持
(2) 基于C1源插入策略构建药物Normorphan桥环及其衍生物,山东省自然科学基金面上项目,2025.01-2027.12,10.0万,主持
(3) 基于氮宾化学的新型自由基或单电子转移反应研究,烟台大学青年博士启动基金,2019.01-2024.01,20.0万,主持
(4) 高效紫外吸收剂开发,企业横向,2021.04-2022.04,5.0万,主持
(5) 二色性染料的开发,企业横向,2023.10-2025.10,15万,主持
(6) TFT新单晶材料开发,企业横向,2024.6-2026.10,10万,主持
代表性论文:
(1)Guiling Li; Mengshuang Guo; Yijia Zhang; Xiubin Zhang; Xiaowei Dong; Xiaotong Deng; Zijuan Liang; Zongyuan Su; Zhen Zhang*, Fe(iii)/NaBD4-mediated regioselective deuteration/cyclization of 1,7-enynes and 1,7-dienes. Chem. Commun. 2025, 61 (83), 16266–16269(自然指数期刊)
(2)Pengpeng Tan, Shilong Wang, Guiling Li, Huichao Wang, Ziheng Zhao, Haochen Jiang, Lei Xie, Liru Yang, Jinchun Chen*, and Zhen Zhang* Oxidative Cascade Iodocyclization of 1,n-Dienes: Synthesis of Iodinated Benzo[b]azepine and Benzo[b]azocine Derivatives J. Org. Chem.2024, 89(9), 6405–6415. (SCI二区)
(3)Zhen Zhang,* Lichao Lu, Guiling Li, Xiaoyu Sheng, Yijia Zhang, Lin Yang, Jiaqi Zhao, Lei Xie, Jiazhu Li* and Kai Sun*Radical cascade silylation/cyclization of 1,7-dienes to access silyl-substituted benzo[b]azepin-2-ones, Chem. Commun. 2024, 60(31), 4206-4209. (自然指数期刊)
(4)Zhen Zhang,* Xiangshan Fang, Ayimnisa Aili, Shilong Wang, Junhong Tang, Wanjun Lin, Lei Xie, Jinchun Chen,* and Kai Sun* Cascade Radical Trifluoromethylthiolation/Cyclization of Dienes To Access SCF3‑Containing Medium-Sized Heterocycles Org. Lett.2023, 25(24), 4598–4602. (SCI一区)
(5)Zhen Zhang,* Pengpeng Tan, Shilong Wang, Huichao Wang, Lei Xie, Yue Chen, Liangliang Han, Shubin Yang, and Kai Sun*Visible-Light-Promoted Selective Sulfonylation and Selenylation of Dienes to Access Sulfonyl-/Seleno-benzazepine Derivatives Org. Lett.2023, 25(22), 4208–4213. (SCI一区)
(6)Kai Sun,* Yan Zhang, Miao Tian, Zhichuan Wang, Dongyang Zhao, Shilong Wang, Shi Tang, Zhen Zhang* Radical annulation of a designed diene system: access to nitro-benzo[b]azepines, Chem. Commun.
2022, 58(69), 9658-9661. (自然指数期刊)
(7)Zhen Zhang*, Shilong Wang, Pengpeng Tan, Xiaowen Gu, Wenjie Sun, Chang Liu, Jinchun Chen, Jiazhu Li, and Kai Sun* K2S2O8/I2-Promoted Electrophilic Selenylative Cyclization To Access Seleno-Benzo[b]azepines Org. Lett.2022, 24(12), 2288–2293. (SCI一区)
(8) Shilong Wang, Yuanyuan Zhang, Guixin Liu, Hui Xu, Lijuan Song, Jinchun Chen, Jiazhu Li and Zhen Zhang *. Transition-metal-free synthesis of 5-amino-1,2,3-triazoles via nucleophilic addition/cyclization of carbodiimides with diazo compounds Org. Chem. Front., 2021, 8, 599. (SCI一区)
(9) Shilong Wang, Xiangqi Xie, Xingchen Zhao, Jixin Liu, Ziling Zhao, Jinchun Chen, Jiazhu Li, Kai Sun and Zhen Zhang* Ceric ammonium nitrate (CAN) enabled concerted nitration/ureation of carbodiimides to synthesize o-nitroaryl ureas Org. Chem. Front., 2021, 8, 5771-5776. (SCI一区)
(10) Zhen Zhang,* Pengpeng Tan, Wenxu Chang, and Zhenhua Zhang*. Transition-Metal-Catalyzed Cross-Coupling and Sequential Reactions of Azides with Isocyanides, Adv. Synth. Catal. 2021, 363, 5344. (SCI二区)
(11)Zhen Zhang,* Ziqiang Qin, Wenxu Chang, Jiazhu Li,* Ruoqian Fan, Xing Wu, Rongrong Guo, Xiangqi Xie, and Lanxin Zhou. Nickel-Catalyzed Decarboxylative Cyclization of Isatoic Anhydrides with Carbodiimides: Synthesis of 2,3- Dihydroquinazolin-4(1H)-ones. Adv. Synth. Catal. 2020, 362, 2864. (SCI二区)
(12)Z. Zhang, B. Huang, G. Qiao, L. Zhu, F. Xiao, F. Chen, B. Fu, Z. Zhang*, Angew. Chem. Int. Ed., 2017, 56, 4320. (SCI一区)
授权发明专利:
1.一种5-氨基-1,2,3-三氮唑类化合物的制备方法,张震,张媛媛,刘桂辛,等;专利号: ZL202010767433.5
2.一种2-亚氨基二氢喹唑啉酮类化合物的制备方法,张震,范若骞,吴星,等;专利号: ZL 201910901786.7
3.一种邻硝基芳基脲类化合物的制备方法,张震,王世龙,赵星辰,等;专利号: ZL 202110430592.0