简历模板
| 罗劲 有机化学 实验师 | 邮箱:jinluo@jxnu.edu.cn 电话:15879049575 通讯地址:江西师范大学方荫楼四区 |
研究方向: 有机合成方法学、绿色农药分子设计、合成与化学生物学 学习工作经历(从大学开始):
代表性论文或专利: 1. Lan, J. P.; Li, X. L.; Xu, M. Y.; Zhang, B.; Luo, J.*; Zhou, Y.*; Wang, T.* Visible-Light-Induced Radical Carbon Oximation of Styrenes Using N Nitrosoamine and Organic Halides. J. Org. Chem.2025, 90, 250-258. 2. Jiang, Z.; You, K.; Wu, H. B.; Xu, M. Y.; Luo, J.*;Zhou, Y.*; Wang, T.* Visible-light-promoted thioetherification of aryl diazonium salts with thiols via electron donor-acceptor complexes. Mol. Catal.2025, 572, 114801. 3. Yu, W. J.; Zhang, H. J.; Shen, Z. P.; Yang, L. Y.; Luo, J.*; Li, W. D.; Zhao, K.; Li, X. L.; Xu, J. L.; Zhou, Y.*; Wang, T.* An aryl-to-alkyl radical relay arylation reaction of a remote C(sp3)-H bond using 1,4-dicyanobenzene as an electrochemical redox-mediator. Org. Chem. Front.2024, 11, 4182. 5. Jiang, Z.; You, K.; Wu, H. B.; Xu, M. Y.; Wang, T.*; Luo J.*. Photochemical Halogen-Bonding Promoted Synthesis of Vinyl Sulfones via Vinyl and Sulfonyl Radicals. Org. Lett. 2024, 26, 636-641. 6. Lan, J. P.; Yu, W. J.; You, K.; Xu, M. Y.; Zhang, B.; Wang, Y. Q.; Wang, T.*; Luo J.*. Dehalogenative Arylation of Unactivated Alkyl Halides via Electroreduction. Org. Lett.2023, 25, 7434-7439. 7. Ye, J. F.; Liu, Y. Y.; Luo J.*; Wan, J. P.*. “Alkene-to-Alkene” Difunctionalization of Enaminones for the Synthesis of Polyfunctionalized Alkenes by Transition-Metal-Free C–H and C–N Bond Transformation. Org. Lett.2023, 25, 8451-8456. 8. Luo J.*; Wan, J. L.; Wu, L. L.; Yang, L. Y.; Wang, Tao.*. tert-Butyl Hydroperoxide Promoted the Reaction of Quinazoline-3-oxides with Primary Amines Affording Quinazolin-4(3H)-ones. J. Org. Chem. 2022, 87, 9864-9874. 9. Luo J.*; Nie, H. X.; He, L. H.; Zhao, A. L.; Wang, T.*. New library of pyrimido[5,4-e][1,2,4]triazolo[1,5-c]pyrimidine derivatives: Synthesis, herbicidal activity, and molecular docking study. J. Mol. Struct.2024, 1300, 137246. 10. Yang, L. Y.; Sun, Y.; He, L. H.; Fan, Y. J.; Wang, T. *; Luo J.*. Synthesis and herbicidal activity of novel 1,2,4-triazole derivatives containing fluorine, phenyl sulfonyl and pyrimidine moieties. J. Mol. Struct.2022, 1259, 132722. | ||
