李亚军
李亚军
更新日期:2021-09-19  

李亚军,博士,副研究员,硕士生导师。分别于2009年6月、20146月年华中科技大学学士、博士学位,博士研究生在上海有机所进行联合培养,2014年9月至2016年8月海外留学。2016年9月入职澳门银银河并入选福建省高层次人才引进(境外C类)计划。主要从事含氟有机化合物的合成及应用、自由基化学在有机合成中的应用等研究。先后主持了国家自然科学基金青年基金、福建省科技厅青年基金、中科院重点实验室开放基金、中科院STS项目子课题等多项项目,迄今已发表SCI论文60余篇,授权专利1项。

 

研究方向:(1)含氟有机化合物的合成及应用; (2)自由基化学在有机合成中的应用

招生专业:有机化学

办公地点:澳门银银河 1#1324

电子邮箱:liyajun@fjirsm.ac.cn

 

代表性论文

1. L. Ge, H. Zhou, M.-F. Chiou, H. Jiang, W. Jian, C. Ye, X. Li, X. Zhu, H. Xiong, Y. Li, L. Song, X. Zhang,* H. Bao*, Iron-catalysed Asymmetric Carboazidation of Styrenes, Nat. Catal. 2021, 4, 2835.

2. D. Lv, Q. Sun, H. Zhou, L. Ge, Y. Qu, T. Li, X. Ma, Y. Li, H. Bao*, Iron-Catalyzed Radical Asymmetric Aminoazidation and Diazidation of Styrenes. Angew. Chem. Int. Ed., 2021, 60, 12455–12460.

3. Y. Zeng, M.-F. Chiou, X. Zhu, J. Cao, D. Lv, W. Jian, Y. Li (李亚军), X. Zhang*, H. Bao*, Copper-Catalyzed Enantioselective Radical 1,4-Difunctionalization of 1,3-Enynes, J. Am. Chem. Soc., 2020, 142, 18014–18021.

4. Q. Zhang, M. T. Muhammad, M.-F. Chiou, Y. Jiao, H. Bao, Y. Li*, 1,4-Fluoroamination of 1,3-Enynes en Route to Fluorinated Allenes, Org. Lett., 2020, 22, 5261–5265.

5. X. Zhu, M. Su, Q. Zhang, Y. Li*, H. Bao*, Cu-Catalyzed Alkylarylation of Vinylarenes with Masked Alkyl Electrophiles. Org. Lett., 2020, 22, 620–625.

6. X. Zhu, W. Deng, M.-F. Chiou, C. Ye, W. Jian, Y. Zeng, Y. Jiao, L. Ge, Y. Li, X. Zhang*, H. Bao*, Copper-catalyzed radical 1,4-difunctionalization of 1,3-enynes with alkyl diacyl peroxides and N-fluorobenzenesulfonimide, J. Am. Chem. Soc., 2019. 141, 548–559.

7. R. Wei, L. Ge, H. Bao, S. Liao*, Y. Li*, Copper-catalyzed Nitrogenation of Aromatic and Aliphatic Aldehydes: A Direct Route to Carbamoyl Azides, Synthesis, 2019, 54, 4645–4649.

8. W. Deng, W. Feng, Y. Li*, H. Bao*, Merging visible-light photocatalysis and transition-metal catalysis in three-component alkyl-fluorination of olefins with a fluoride ion, Org. Lett., 2018, 20, 4245–4249.

9. Y. Li, F. Fleming*, Direct conversion of nitriles into alkene “isonitriles”, Angew. Chem. Int. Ed., 2016, 55, 14770–14773.

 

Baidu
sogou