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田平 研究员, 博导, 副院长

手性药物研究中心

创新中药研究院

上海中医药大学

地址:上海市浦东新区蔡伦路1200号

电话:(+86)-21-5132 2765

邮箱:tianping@shutcm.edu.cn

          or tianping@sioc.ac.cn

  • 研究内容

    • 合成方法导向多样性分子的生理活性研究

    • 基于靶点或计算机辅助的药物设计

    • 利用化学生物学阐述中药单体的作用机制研究

    • 整合现代分子工程技术创制源于中药的新药研究

  • 工作经历

    • 2022−目前

      研究员, 博导,上海中医药大学 创新中药研究院 副院长

    • 2017−目前

      研究员, 博导,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

      高级研究员, SynChem, Inc.

    • 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

  • 教育背景

    • 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)

  • 学术荣誉

    • 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

    • 上海中医药大学第三届“我心目中的好老师”2022

  • 代表性论文

    • 13.Hao Xu,# Yun-Xuan Tan,# Pei-Pei Xie,# Rui Ding, Qi Liao, Jian-Wei Zhang, Qing-Hua Li,* Yu-Hui Wang,* Xin Hong,* Guo-Qiang Lin, and Ping Tian*  Rhodium(III)-Catalyzed Asymmetric Reductive Cyclization of Cyclohexadienone-Containing 1,6-Dienes via an Anti-Michael/ Michael Cascade Process. ACS Catal. 2021, 11, 8015−8022. (IF = 12.350)

    • 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. 201958, 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. 2019141, 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. 201554, 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. 2013135, 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. 201352, 5314−5318. (IF = 12.959)

    • 1.Ping Tian, Han-Qing Dong, and Guo-Qiang Lin,* Rhodium-Catalyzed Asymmetric Arylation. ACS Catal. 20122, 95−119. (IF = 12.350, Top 1% Cited Papers)