2017−目前

研究员, 上海中医药大学 创新中药研究院 手性药物研究中心

2010−2017

副研究员, 中国科学院 上海有机化学研究所 天然产物有机合成化学重点实验室

2006−2009

项目组长, 晟康生物医药技术(上海)有限公司

2005−2006

助研, 中国科学院 上海有机化学研究所 天然产物有机合成化学重点实验室

1999−2005

博士, 中国科学院 上海有机化学研究所 (导师: 林国强 院士)

1995−1999

本科, 武汉大学 化学与分子科学学院 (导师: 李早英 教授)

Thieme Chemistry Journal Awardees 2017

上海市高水平地方高校重点创新团队负责人 2017-2020

上海市优秀学术带头人 2020

12.Chang-Yun Shi, Zhi-Zhou Pan, Ping Tian,* and Liang Yin*  Copper(I)-catalyzed asymmetric 1,6-conjugate allylation. Nat. Commun. 2020, 11, 5480. (IF = 12.121)

11.Xu-Cheng Gan,# Cheng-Yuan Zhang,# Feng Zhong,# Ping Tian,* and Liang Yin* Synthesis of Chiral anti-1,2-Diamine Derivatives through Copper(I)-Catalyzed Asymmetric α-Addition of Ketimines to Aldimines. Nat. Commun. 2020, 11, 4473. (IF = 12.121)

10.Cheng-Yu He,# Yun-Xuan Tan,# Xin Wang, Rui Ding, Yi-Fan Wang, Feng Wang, Dingding Gao,* Ping Tian,* and Guo-Qiang Lin* Copper(I)-catalyzed Diastereo- and Enantio-selective Construction of Optically Pure Exocyclic Allenes. Nat. Commun. 2020, 11, 4293. (IF = 12.121)

9.Peng Yang,# Jian Li,# Li Sun, Ming Yao, Xiang Zhang, Wei-Lie Xiao, Jian-Hua Wang, Ping Tian,* Han-Dong Sun,* Pema-Tenzin Puno,* and Ang Li* Elucidation of the Structure of Pseudorubriflordilactone B by Chemical Synthesis. J. Am. Chem. Soc. 2020, 142, 13701–13708. (IF = 14.612)

8.Yu-Hui Wang,# Zhong-Yan Cao,# Qing-Hua Li, Guo-Qiang Lin, Jian Zhou,* and Ping Tian,* Activating Pronucleophiles with High pKa Values: Chiral Organo‐Superbases. Angew. Chem. Int. Ed. 2020, 59, 8004−8014. (IF = 12.959)

7.Xin Chen, Dingding Gao, Dong Wang, Tong Xu, Wei Liu, Ping Tian,* and Xiaofeng Tong,* Access to Aryl-Naphthaquinone Atropisomers via Phosphine-Catalyzed Atroposelective (4+2) Annulations of δ-Acetoxy Allenoates with 2-Hydroxyquinone Derivatives. Angew. Chem., Int. Ed. 2019, 58, 15334−15338. (IF = 12.959)

6.Yun-Xuan Tan, Fang Zhang, Pei-Pei Xie, Shuo-Qing Zhang, Yi-Fan Wang, Qing-Hua Li, Ping Tian,* Xin Hong,* and Guo-Qiang Lin,* Rhodium(III)-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Dienes: An Experimental and DFT Study. J. Am. Chem. Soc. 2019, 141, 12770−12779. (IF = 14.612)

5.Zhi-Tao He, Xiao-Qi Tang, Li-Bo Xie, Mian Cheng, Ping Tian,* and Guo-Qiang Lin, Efficient Access to Bicyclo[4.3.0]nonanes: Cu-Catalyzed Asymm-etric Silylative Cyclization of Cyclohexadienone-tethered Allenes. Angew. Chem. Int. Ed. 2015, 54, 14815−14818. (IF = 12.959)

4.Yuki Fukui,# Ping Liu,# Qiang Liu, Zhi-Tao He, Nuo-Yi Wu, Ping Tian,* and Guo-Qiang Lin,* Tunable Arylative Cyclization of 1,6-Enynes Triggered by Rhodium(III)-Catalyzed C−H Activation. J. Am. Chem. Soc. 2014, 136, 15607−15614. (IF = 14.612)

3.Ping Liu, Yuki Fukui, Ping Tian,* Zhi-Tao He, Cai-Yun Sun, Nuo-Yi Wu, and Guo-Qiang Lin,* Cu-Catalyzed Asymmetric Borylative Cyclization of Cyclohexadienone-Containing 1,6-Enynes. J. Am. Chem. Soc. 2013, 135, 11700−11704. (IF = 14.612)

2.Zhi-Tao He, Bing Tian, Yuki Fukui, Xiaofeng Tong, Ping Tian,* and Guo-Qiang Lin,* Rhodium-Catalyzed Asymmetric Arylative Cyclization of meso-1,6-Dienynes Leading to Enantioenriched cis-Hydrobenzofurans. Angew. Chem. Int. Ed. 2013, 52, 5314−5318. (IF = 12.959)

1.Ping Tian, Han-Qing Dong, and Guo-Qiang Lin,* Rhodium-Catalyzed Asymmetric Arylation. ACS Catal. 2012, 2, 95−119. (IF = 12.350, Top 1% Cited Papers)