永利欢乐娱人城(集团)股份有限公司
     
 
    The current position: Organic Chemistry
Peng Jiao

Published Date: 2017-08-24

 

Peng Jiao中文

 

Associate professor and Supervisor for Ph.D. candidates, Ph. D (Beijing University), Postdoctor (Nagoya University and The University of Chicago)

 

Postal address: College of Chemistry, Beijing Normal University, Xinjiekouwaidajie 19, Beijing, 100875, China

 

Phone: +86-10-58800316; Fax: +86-10-58802075

E-mail: pjiao@bnu.edu.cn

Group homepage: http://jiao.chem.bnu.edu.cn/

 

 

Teaching

Green chemistry, Organic chemistry experiment, Advanced synthetic chemistry experiment

Research Interests

Nature-inspired design of efficient and environmentally benign synthetic procedures; Synthetic methodologies concerning asymmetric synthesis and its applications; Design of O, N, P-containing chiral ligands and the derived catalysts; Transition metal-catalyzed C-CC-N coupling reactions; Asymmetric cycloaddition reactions; Synthesis of biologically active small molecules.

Representative papers

1.      M. Jiang, L. Feng, J. Feng, Peng Jiao* Catalytic asymmetric cycloadditions of silyl nitronates bearing α-aryl group Org. Lett. 2017, 19, 2210–2213.

2.      X. Han, L. Dong, C. Geng, Peng Jiao* Catalytic asymmetric synthesis of isoxazolines from silyl nitronates Org. Lett. 2015, 17, 31943197.

3.      L. Kong, X. Han, Peng Jiao* Catalytic asymmetric Diels-Alder reactions involving aryl vinyl ketones Chem. Commun. 2014, 50, 1411314116.

4.      L. Dong, C. Geng, Peng Jiao* Silyl nitronates cycloadditions catalyzed by Cu(II)-bisoxazoline J. Org. Chem. 2015, 80, 1099211002.

5.      C. Geng, M. Jiang, L. Feng, Peng Jiao* Palladium catalyzed C-H bond acetoxylation: isoxazolinyl as a directing group RSC Adv. 2016, 6, 56971–56976.

6.      G. Zhang, X. Ji, H. Yu, L. Yang, Peng Jiao*, Hanmin Huang* Palladium-catalyzed hydroaminocarbonylation of alkenes with amines promoted by weak acid Tetrahedron Lett. 2016, 57, 383386.

7.      Z. Yang, S. Hou, W. He, B. Cheng, Peng Jiao*, Jiaxi Xu* Regioselectivity of the ortho- and para-semidine, and diphenyline rearrangements Tetrahedron, 2016, 72, 21862195.

8.      Peng Jiao, M. Kawasaki, H. Yamamoto* A sequential O-nitrosoaldol and Grignard addition process: an enantio- and diastereoselective entry to chiral 1,2-diols Angew. Chem. Int. Ed. 2009, 48, 3333–3336.

9.      Peng Jiao, D. Nakashima, H. Yamamoto* Enantioselective 1,3-dipolar cycloaddition of nitrones with ethyl vinyl Ether: the difference between Brønsted and Lewis acid catalysis Angew. Chem. Int. Ed. 2008, 47, 2411–2413.

 

 
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