谭伟

姓名：谭伟

系所：化学系

职称：副教授

E-mail：wtan@jsnu.edu.cn

个人简介：

谭伟，理学博士，副教授，硕士生导师。近年来以通讯作者或第一作者在J. Am. Chem. Soc., Org. Lett., Chem. Commun., J. Org. Chem.等国际权威期刊发表SCI学术论文10余篇。

研究领域：

1. 手性药物活性分子的催化不对称合成；

2. 化学实验教学研究与设计。

教育背景：

2015年9月—2019年12月：华东师范大学化学与分子工程学院博士研究生；

2012年9月—2015年6月：江苏师范大学化学化工学院硕士研究生；

2008年9月—2012年6月：江苏师范大学化学化工学院本科生。

部分学术论文：

1. Chun Ma#, Feng-Tao Sheng#, Hai-Qing Wang, Shuang Deng, Yu-Chen Zhang,* Yinchun Jiao, Wei Tan,* Feng Shi*, Atroposelective Access to Oxindole-Based Axially Chiral Styrenes via the Strategy of Catalytic Kinetic Resolution, J. Am. Chem. Soc.2020, 142, 15686−15696.

2. Tian-Zhen Li, Si-Jia Liu, Wei Tan,* Feng Shi*, Catalytic Asymmetric Construction of Axially Chiral Indole-Based Frameworks: An Emerging Area, Chem. Eur. J.2020, 26, 15779-15792.

3. Feng-Tao Sheng, Zhi-Min Li, Yi-Zhu Zhang, Li-Xing Sun, Yu-Chen Zhang, Wei Tan*, Feng Shi*, Atroposelective Synthesis of 3,3’-Bisindoles Bearing Axial and Central Chirality: Using Isatin-Derived Imines as Electrophiles, Chinese Journal of Chemistry,2020, 38, Chin. J. Chem.2020, 38, 583－589.

4. Wei Tan, Niklas Jänsch, Tina Öhlmann, Franz-Josef Meyer-Almes*, Xuefeng Jiang*, Thiocarbonyl Surrogate via Combination of Potassium Sulfide and Chloroform for Dithiocarbamate Construction, Org. Lett.2019‚ 21‚ 7484-7488.

5. Wei Tan, Cuihong Wang*, Xuefeng Jiang*, Visible-Light-Mediated C(sp³)-H Thiocarbonylation for Thiolactam Preparation with Potassium Sulfide, Chin. J. Chem.2019, 37, 1234-1238.

6. Wei Tan, Cuihong Wang*, Xuefeng Jiang*, Green Carbon Disulfide Surrogate via Combination of Potassium Sulfide and Chloroform for Benzothiazine-thione and Benzothiazole-thione Constructions, Org. Chem. Front.2018, 5, 2390-2394.

7. Wei Tan, Jianpeng Wei, Xuefeng Jiang*, Thiocarbonyl Surrogate via Combination of Sulfur and Chloroform for Thiocarbamide and Oxazolidinethione Constructions, Org. Lett.2017‚ 19‚ 2166-2169.

8. Wei Tan, Xin Li, Yu-Xin Gong, Meng-Di Ge, Feng Shi*, Highly diastereo- and enantioselective construction of a spiro[cyclopenta[b]indole-1,3′-oxindole] scaffold via catalytic asymmetric formal [3+2] cycloadditions, Chem. Commun.2014, 50, 15901-15904.