研究队伍
姓名: 苏毅进 性别:
学科类别: 资源化学 职务:
学历: 博士 职称: 研究员
电话: 传真:
电子邮件: suyj@licp.cas.cn
通讯地址: 甘肃省兰州市天水中路18号

简  历:

教育经历 

2009.9 – 2012.7 北京大学药学院,博士 (导师: 焦宁教授) 

2007.9 – 2009.7 北京大学药学院,硕士 (导师: 焦宁教授) 

2003.9 – 2007.7 北京大学药学院,学士 

工作经历 

2015.3 – 中科院兰州化学物理研究所,研究员 

2012.8 – 2015.8 美国西弗吉尼亚大学化学系,博士后 (Supervisor: Prof. Xiaodong Mike Shi)  

招生专业:

有机化学专业的硕士、博士研究生,博士后和职工

研究方向:

均相催化、可见光促进的羰基合成和选择氧化

获奖及荣誉:

承担科研项目:

代表论著:

1Su, Y., Petersen, J. L.,Gregg, T. L.,Shi, X.*, “Ambient 1,2,3-Triazole Ring Opening through Intermolecular Radical Addition to Vinyl-Triazole.” Org. Lett., 2015, 17, 1208-1211. 

2Dong, B.?, Su, Y.?, Ye, X., Petersen, J. L., Shi, X.*, “Synthesis and Characterization of Fluorescent-Active Triazole-Gold Complexes.” Sci. China Chem., 2015, 58, 1-4. 

3Su, Y., Lu, M., Dong, B., Chen, H.*, Shi, X.* “Silver Catalyzed Alkyne Activation: the Surprising Ligand Effect” Adv. Syn. Cat., 2014, 356, 692-696. 

4Su, Y., Zhang, Y., Akhmedov, N. G., Petersen, J. L., Shi, X.*, “Ambient Intermolecular [2 + 2] Cycloaddition: An Example of Carbophilicity and Oxophilicity Competition in Au/Ag Catalysis.” Org. Lett., 2014, 16, 2478-2481. 

5Xi, Y.?, Su, Y.?, Yu, Z., Dong, B., McClain, E. J., Yu, L.*, Shi, X.*, “Chemoselective Carbophilic Addition of α-Diazoesters through Ligand-Controlled Gold Catalysis.” Angew. Chem. Int. Ed., 2014, 53, 9817-9821 

6) Su, Y.?, Sun, X.?, Wu, G., Jiao, N.*, “Catalyst-Controlled Highly Selective Coupling and Oxygenation of Olefins: A Direct Approach to Alcohols, Ketones, and Diketone.” Angew. Chem. Int. Ed., 2013, 52, 9808-9812  

7Su, Y., Jiao, N.*, “Palladium-Catalyzed Oxidative Heck Reaction.” Curr. Org. Chem., 2011, 15, 3362-3388 

8Su, Y., Jia, W., Jiao, N.*, “Inexpensive Copper/Iron-Cocatalyzed Reactions.” Synthesis, 2011, 1678-1690. 

9Su, Y., Zhang, L., Jiao, N.*, “Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides.” Org. Lett., 2011, 13, 2168-2171 

10Su, Y., Jiao, N.*, “Control of Chemo-, Regio-, and Stereoselectivities in Ligand-Free Pd-Catalyzed Oxidative Heck Reactions of Arylboronic Acids or Alkenylboronate with Allyl Esters.” Org. Lett., 2009, 11, 2980-2983.

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