College of Chemistry ,BEIJING NORMAL UNIVERSITY

The current position: Organic Chemistry

Peng Jiao

Published Date： 2017-08-24

Peng Jiao

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-C、C-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, 3194–3197.

3. L. Kong, X. Han, Peng Jiao* Catalytic asymmetric Diels-Alder reactions involving aryl vinyl ketones Chem. Commun. 2014, 50, 14113–14116.

4. L. Dong, C. Geng, Peng Jiao* Silyl nitronates cycloadditions catalyzed by Cu(II)-bisoxazoline J. Org. Chem. 2015, 80, 10992–11002.

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, 383–386.

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, 2186–2195.

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.