专家人才库
陈庆安 研究员

学历:博士研究生

学科:有机化学

电话:0411-82463702

邮箱:qachen@dicp.ac.cn

地址:大连市中山路457号

邮编:116023

简历介绍

 陈庆安,男,福建泉州人。2007年于中国科学技术大学化学系获学士学位,导师:尤田耙教授。2012年于中国科学院大连化学物理研究所获博士学位,师从周永贵研究员。2012年到美国加州大学欧文分校(University of California, Irvine)化学系从事博士后研究,合作导师:Vy M. Dong教授。2015年至2017年作为德国洪堡学者在德国柏林工业大学(Technische Universitat Berlin)化学系工作,合作导师:Martin Oestreich教授。2017年聘为仿生催化合成课题组组长,研究员,博导,张大煜青年学者。

 研究方向主要为过渡金属催化和不对称有机合成。目前研究兴趣包括:1)基于生物代谢的原理的仿生催化合成;2)过渡金属催化烯烃和炔烃的高效不对称转化;3)发展新的有机合成方法学。详情请见课题组主页

      开展研究工作以来,先后在Chem. Rev., Chem. Soc. Rev., J. Am. Chem. Soc.等国际权威期刊上发表文章44篇,总引用次数为2482次,H-因子为22 (截止20209)2017年获得辽宁省自然科学一等奖(排名第二),2020年获得“Thieme  Chemistry Journal Award”国际学术奖。

研究方向
 
职务
社会任职
获奖及荣誉
 
代表论著

1. Wen-Shuang Jiang+, Ding-Wei Ji+, Wei-Song Zhang, Gong Zhang, Xiang-Ting Min, Yan-Cheng Hu, Xu-Liang Jiang*, and Qing-An Chen.* Orthogonal Regulation of Nucleophilic and Electrophilic Sites in Pd-Catalyzed Regiodivergent Couplings between Indazoles and Isoprene. Angew. Chem. Int. Ed. 2021, Accepted.

2. Yan-Cheng Hu+, Yingying Zhao+, Boshun Wan*, Qing-An Chen.* Reactivity of Ynamides in Catalytic Intermolecular Annulations. Chemical Society Reviews. 2020, Accepted.

3. Xiang-Ting Min, Ding-Wei Ji, Yu-Qing Guan, Shi-Yu Guo, Yan-Cheng Hu, Boshun Wan, Qing-An Chen.* Visible Light-Induced Bifunctional Rhodium Catalysis for Decarbonylative Coupling of Imides with Alkynes. Angew. Chem. Int. Ed. 2021, 60, 1583-1587.

4. Chang-Sheng Kuai+, Ding-Wei Ji+, Chao-Yang Zhao, Heng Liu, Yan-Cheng Hu, Qing-An Chen.* Ligand Regulated Regiodivergent Hydrosilylation of Isoprene under Iron Catalysis. Angew. Chem. Int. Ed. 2020, 59, 19115-19120.

5. Chao-Yang Zhao, Hao Zheng, Ding-Wei Ji, Xiang-Ting Min, Yan-Cheng Hu, and Qing-An Chen.* Copper-Catalyzed Asymmetric Carboboronation of Allenes to Access α-Quaternary Amino Esters with Adjacent Stereocenters. Cell Reports Physical Science 2020, 1, 100067.

6. Jun Yang, Ding-Wei Ji, Yan-Cheng Hu, Xiang-Ting Min, Xiang-Ge Zhou,* Qing-An Chen.* Cobalt-Catalyzed Hydroxymethylarylation of Terpenes with Formaldehyde and Arenes. Chem. Sci. 2019, 10, 9560-9564.        

7. Ding-Wei Ji, Yan-Cheng Hu, Hao Zheng, Chao-Yang Zhao, Qing-An Chen.* and Vy M. Dong. Catalytic Regioselectivity Switch in Pd-Catalyzed Hydroallylation of Alkynes. Chem. Sci. 2019, 10, 6311-6315.

8. Yan-Cheng Hu, Ding-Wei Ji, Chao-Yang Zhao, Hao Zheng, Qing-An Chen.* Catalytic Prenylation and Reverse-Prenylation of Indoles with Isoprene: Regioselectivity Manipulation by Metal-Hydride. Angew. Chem. Int. Ed. 2019, 58, 5438-5442.

9. Qing-An Chen, Hendrik F. T. Klare, and Martin Oestreich.* Bronsted Acid-Promoted Formation of Stabilized Silylium Ions for Catalytic Friedel-Crafts C-H Silylation. J. Am. Chem. Soc. 2016, 138, 7868-7871.

10. Qing-An Chen, Zhiwei Chen, Vy M. Dong.* Rhodium-Catalyzed Enantioselective Hydroamination of Alkynes with Indolines. J. Am. Chem. Soc. 2015, 137, 8392-8395.

11. Qing-An Chen, Faben A. Cruz, Vy M. Dong.* Alkyne Hydroacylation: Switching Regioselectivity by Tandem Ruthenium Catalysis. J. Am. Chem. Soc. 2015, 137, 3157-3160.

12. Qing-An Chen, Daniel K. Kim, Vy M. Dong.* Regioselective Hydroacylation of 1,3-Dienes by Cobalt-Catalysis. J. Am. Chem. Soc. 2014, 136, 3772-3775.

13. Qing-An Chen, Zhi-Shi Ye, Ying Duan and Yong-Gui Zhou.* Homogeneous Palladium Catalyzed Asymmetric Hydrogenation. Chem. Soc. Rev. 2013, 42, 497-511.

14. Qing-An Chen, Kai Gao, Ying Duan, Zhi-Shi Ye, Lei Shi, Yan Yang and Yong-Gui Zhou.* Dihydrophenanthridine: A New and Easily Regenerable NAD(P)H Model for Biomimetic Asymmetric Hydrogenation. J. Am. Chem. Soc. 2012, 134, 2442-2448.

15. Qing-An Chen, Mu-Wang Chen, Chang-Bin Yu, Lei Shi, Duo-Sheng Wang, Yan Yang and Yong-Gui Zhou.* Biomimetic Asymmetric Hydrogenation: In Situ Regenerable Hantzsch Esters for Asymmetric Hydrogenation of Benzoxazinones. J. Am. Chem. Soc. 2011, 133, 16432-16435.

16.Qing-An Chen, Duo-Sheng Wang, Yong-Gui Zhou,* Ying Duan, Hong-Jun Fan,* Yan Yang, Zhang Zhang. Convergent Asymmetric Disproportionation Reactions: Metal/Bronsted Acid Relay Catalysis for Enantioselective Reduction of Quinoxalines. J. Am. Chem. Soc. 2011, 133, 6126-6129.

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