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谭光映     特聘研究员

研究方向:有机化学

联系方式:          Email:guangying@scu.edu.cn(优先)tgy894847413@163.com

个人主页:点击进入

简历:

学习经历

2014.092019.07, 开云全站中国有限公司, 化员工物学, 博士,导师:游劲松教授

2010.092014.07, 开云全站中国有限公司, 应用化学, 学士, 导师:游劲松教授

工作经历

2023.01至今, kaiyun开云官方网站,特聘研究员

2019.082022.12, 德国明斯特大学,博士后,洪堡学者,合作导师:Frank Glorius教授

主要研究方向

光化学合成

电化学合成

过渡金属催化

有机功能材料分子的设计与开发

课题组于20231月刚成立,目前正处于起步发展阶段,诚招硕士、博士研究生、博士后、研究助理以及联合培养员工。欢迎对有机合成化学、光化学、电化学、过渡金属催化、有机功能材料等感兴趣的员工加入课题组!

主要工作业绩

谭光映博士近年来一直致力于有机合成方法学研究,围绕可见光催化和碳氢键活化两个方向,开展了相关研究。主要贡献包括两个方面:1)开发了一类全新的肟酯类双官能化试剂,实现了无金属参与的烯烃或杂芳烃的1,2-胺羧基化反应、1,2-双胺化反应以及多组分烯烃之间高选择性的自由基串联1,4-氧胺化反应和1,4-碳胺化反应,为氨基酸、氨基醇、邻二胺等重要含氮化合物的绿色、高效合成提供了新策略;2)发展了一系列过渡金属催化的()芳烃碳氢键氧化偶联反应,高效构筑了多种结构新颖的荧光分子,为有机发光材料的设计与合成提供了新思路。目前已在国际著名刊物共计发表SCI论文20篇,其中第一作者论文17篇,其中包括Nat. Chem. (1), Nat. Catal. (1), J. Am. Chem. Soc. (2), Angew. Chem. Int. Ed. (6), Adv. Sci. (1), ACS. Catal. (1), Chem. Sci. (1), Org. Lett. (2), Org. Chem. Front. (1)RSC Adv. (1)

主要奖励和荣誉

2019年德国洪堡博士后研究奖学金

2019届四川省优秀大学毕业生

2019届开云全站中国有限公司优秀毕业研究生

2018年博士研究生国家奖学金

2018年开云全站中国有限公司优秀博士

2018年第五届“阿达玛斯”学术论文创新奖

2017年开云全站中国有限公司第九届研究生“优秀学术之星”

2017年第四届“阿达玛斯”学术论文创新奖

2017年开云全站中国有限公司MORESCO二等奖学金

2017年唐敖庆化学奖学金

2017年开云全站中国有限公司优秀博士

2016年开云全站中国有限公司优秀硕士

2016年硕士研究生国家奖学金

20182019年开云全站中国有限公司学业一等奖学金

20162018年开云全站中国有限公司学业一等奖学金

20142016年开云全站中国有限公司学业二等奖学金

2013年国家励志奖学金

2013年开云全站中国有限公司综合二等奖学金

2012年kaiyun开云官方网站“社会实践先进个人”

2012年开云全站中国有限公司单项二等奖学金

2011年开云全站中国有限公司单项二等奖学金

代表性成果(获奖成果、专著、论文、专利)

博士后阶段:

1.Guangying Tan,# Fritz Paulus,# Alessia Petti, Maxim-Aleksa Wiethoff, Anna Lauer, Constantin Daniliuc and Frank Glorius*, Metal-Free Photosensitized Radical Relay 1,4-Carboimination Across Two Distinct Olefins. Chem. Sci. 2023, 14, 2447−2454. (#Equal contribution)

2. Guangying Tan and Frank Glorius*, Stereochemical Editing. Angew. Chem. Int. Ed. 2023, e202217840.

3. Guangying Tan, Fritz Paulus, Ángel Rentería-Gómez,# Remy Lalisse,# Constantin Daniliuc, Osvaldo Gutierrez* and Frank Glorius*, Highly Selective Radical Relay 1,4-Oxyimination of Two Electroni-cally Differentiated Olefins. J. Am. Chem. Soc. 2022, 144, 21664−21673. (#Equal contribution)

4. Guangying Tan, Mowpriya Das, Roman Kleinmans, Felix Katzenburg , Constantin Daniliuc and Frank Glorius*, Energy Transfer-Enabled Unsymmetrical Diamination Using Bifunctional Nitrogen-Radical Precursors. Nat. Catal. 2022, 5, 1120-1130.

5. Guangying Tan, Mowpriya Das, Hyeyun Keum , Peter Bellotti, Constantin Daniliuc and Frank Glorius*, Photochemical Single-Step Synthesis of β-Amino Acid Derivatives from Alkenes and (Hetero)arenes. Nat. Chem. 2022, 14, 1174-1184.

6. Guangying Tan,# Iván Maisuls,# Felix Strieth-Kalthoff, Xiaolong Zhang, Constantin Daniliuc, Cristian A. Strassert* and Frank Glorius*, AIE-Active Difluoroboron Complexes with N,O-Bidentate Ligands: Rapid Construction by Copper-Catalyzed C−H Activation. Adv. Sci. 2021, 8, 202101814. (#Equal contribution)

7. Guangying Tan, Mowpriya Das, Iván Maisuls, Cristian A. Strassert, and Frank Glorius*, Rhodium-Catalyzed Dealkenylative Arylation of Alkenes with Arylboronic Compounds. Angew. Chem. Int. Ed. 2021, 60, 15650–15655.

8. Guangying Tan, Malte L. Schrader, Constantin Daniliuc, Felix Strieth-Kalthoff, and Frank Glorius*, C–H activation based Copper-Catalyzed One-Shot Synthesis of N,O-Bidentate Organic Difluoroboron Complexes. Angew. Chem. Int. Ed. 2020, 59, 21541 –21545.

博士阶段:

9. Guangying Tan, Yimin Wu, Yang Shi and Jingsong You*, Syngas-Free Highly Regioselective Rhodium-Catalyzed Transfer Hydroformylation of Alkynes to α,β-Unsaturated Aldehydes. Angew. Chem. Int. Ed. 2019, 58, 7440–7444.

10. Guangying Tan, Chunhao Ran and Jingsong You*, Iridium-Catalyzed Oxidative Ar–H/Ar–H Cross-Coupling of Primary Benzamides with Thiophenes. Org. Chem. Front. 2018, 5, 2930–2933.

11. Guangying Tan, Qiulin You and Jingsong You*, Iridium-Catalyzed Oxidative Heteroarylation of Arenes and Alkenes: Overcoming the Restriction to Specific Substrates. ACS Catal. 2018, 8, 8709−8714.

12. Guangying Tan, Qiulin You, Jingbo Lan, and Jingsong You*, Iridium-Catalyzed Annulation Reactions of Thiophenes with Carboxylic Acids: Direct Evidence for a Heck-type Pathway. Angew. Chem. Int. Ed. 2018, 57, 6309–6313.

13. Guangying Tan, Lei Zhu, Xingrong Liao, Yu Lan* and Jingsong You*, Rhodium/Copper Co-Catalyzed Highly trans-Selective 1,2-Diheteroarylation of Alkynes with Azoles via C−H Addition/Oxidative Cross-Coupling: A Combined Experimental and Theoretical Study. J. Am. Chem. Soc. 2017, 139, 15724−15737.

14. Guangying Tan and Jingsong You*, Rhodium(III)-Catalyzed Oxidative Cross-Coupling of Unreactive C(sp3)−H Bonds with C(sp2)−H Bonds. Org. Lett. 2017, 19, 4782−4785.

15. Guangying Tan,# Luoqiang Zhang,# Xingrong Liao, Yang Shi, Yimin Wu, Yudong Yang and Jingsong You*, Copper- or Nickel-Enabled Oxidative Cross-Coupling of Unreactive C(sp3)−H Bonds with Azole C(sp2)−H Bonds: Rapid Access to β-Azolyl Propanoic Acid Derivatives. Org. Lett. 2017, 19, 4830−4833. (#Equal contribution)

16. Guangying Tan, Shuang He, Xiaolei Huang, Xingrong Liao, Yangyang Cheng and Jingsong You*, Cobalt-Catalyzed Oxidative C−H/C−H Cross-Coupling between Two Heteroarenes. Angew. Chem. Int. Ed. 2016, 55, 10414–10418.

17. Guangying Tan,# Xiaolei Huang, # Qian Wu, Luo-Qiang Zhang and Jingsong You*, Rh(III)-Catalyzed Annulation of N-Methoxybenzamides with Ynesulfonamides at Room Temperature: A Practical and Efficient Route to 4-Aminoisoquinolone Derivatives. RSC Adv. 2014, 4, 49186–49189. (#Equal contribution)

18. Shuang He, Guangying Tan, Anping Luo and Jingsong You*, Rhodium-Catalyzed Oxidative C–H/C–H Cross-coupling of Aniline with Heteroarene: N-Nitroso Group Enabled Mild Conditions. Chem. Commun. 2018, 54, 7794–7797.

19. Yangyang Cheng, Yimin Wu, Guangyin Tan, and Jingsong You*, Nickel Catalysis Enables Oxidative C(sp2)–H/C(sp2)–H Cross-Coupling Reactions between Two Heteroarenes. Angew. Chem. Int. Ed. 2016, 55, 12275–12279.

20. Kaizhi Li, Guangying Tan, Jingsheng Huang, Feijie Song, and Jingsong You*, Iron-Catalyzed Oxidative C–H/C–H Cross-Coupling: An Efficient Route to a-Quaternary a-Amino Acid Derivatives. Angew. Chem. Int. Ed. 2013, 52, 12942–12945.

 

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