姓名: | 苏毅进 | 性别: | 男 |
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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:
获奖及荣誉:
承担科研项目:
代表论著:
1)Su, 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.;
2)Dong, 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.;
3)Su, Y., Lu, M., Dong, B., Chen, H.*, Shi, X.* “Silver Catalyzed Alkyne Activation: the Surprising Ligand Effect” Adv. Syn. Cat., 2014, 356, 692-696.;
4)Su, 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.;
5)Xi, 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;
7)Su, Y., Jiao, N.*, “Palladium-Catalyzed Oxidative Heck Reaction.” Curr. Org. Chem., 2011, 15, 3362-3388;
8)Su, Y., Jia, W., Jiao, N.*, “Inexpensive Copper/Iron-Cocatalyzed Reactions.” Synthesis, 2011, 1678-1690.;
9)Su, Y., Zhang, L., Jiao, N.*, “Utilization of Natural Sunlight and Air in the Aerobic Oxidation of Benzyl Halides.” Org. Lett., 2011, 13, 2168-2171;
10)Su, 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.;社会任职:
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