黃漢民，1974年6月生於湖北浠水，教授，博士生導師，英國皇家化學會會士（RSC-Fellow）。2003年於中科院大連化學物理研究所獲得有機化學博士學位，2004年至2008年在日本名古屋大學作JSPS博士後研究。2008年4月到2016年2月在中國科學院蘭州化學物理研究所工作，先後任羰基合成與選擇氧化國家重點實驗室副主任和常務副主任，併入選中科院“百人計畫”。2016年2月調入中國科學技術大學化學系工作。
主要研究方向
導向有機合成的金屬有機化學，均相催化反應及機理研究
獲獎及榮譽
2012年獲得國家自然科學基金“優秀青年基金”的資助；
2013年獲中科院“百人計畫”結題優秀獎，第二屆中國均相催化青年獎；
2015獲中國科學院優秀研究生指導教師獎，入選英國皇家化學會會士（RSC-Fellow）和科技部中青年科技創新領軍人才。
文章及專著
1. Yang Liu, Yinjun Xie, Hongli Wang, and Hanmin Huang*, Enantioselective Aminomethylamination of Conjugated Dienes with Aminals Enabled by Chiral Palladium Complex-Catalyzed C-N Bond Activation, J. Am. Chem. Soc. 2016, 138, ASAP (DOI: 10.1021/jacs.600976).
2. Quanjun Wang, Yijin Su, Lixin Li, and Hanmin Huang*, Transition-Metal-Catalysed C-N Bond Activation, Chem. Soc. Rev. 2016, 45, 1257-1272.
3. Guiping Qin, Lixin Li, Jiawen Li, and Hanmin Huang*, Palladium-Catalyzed Formal Insertion of Carbenoids into Aminals via C-N Bond Activation, J. Am. Chem. Soc. 2015, 137,12490-12493.
4. Hui Yu, Guoying Zhang, and Hanmin Huang*, Palladium-Catalyzed Dearomative Cyclocarbonylation via C-N Bond Activation, Angew. Chem. Int. Ed. 2015, 54,10912-10916.
5. Guoying Zhang, Bao Gao, and Hanmin Huang*, Palladium-Catalyzed Hydroaminocarbonylation of Alkenes with Amines: A Strategy to Overcome Basicity-Barrier Imparted by Aliphatic Amines, Angew. Chem. Int. Ed. 2015, 54, 7657-7661.
6. Yinjun Xie, Shengmei Guo, Longmin Wu, Chungu Xia,and Hanmin Huang*, Metal Bridging for Directing and Accelerating Electron Transfer as Exemplified by Harnessing the Reactivity of AIBN, Angew. Chem. Int. Ed. 2015, 54, 5900-5904.
7. Lei Yang, and Hanmin Huang*, Transition-Metal-Catalyzed Direct Addition of Unactivated C−H Bonds to Polar Unsaturated Bonds, Chem. Rev. 2015, 115, 3468-3517.
8. Jianhua Hu, Yinjun Xie, and Hanmin Huang*, Palladium-Catalyzed Insertion of an Allene into an Aminal: Aminomethylamination of Allenes via C-N Bond Activation, Angew. Chem. Int. Ed. 2014, 53, 7272-7276.
9. Yinjun Xie, Jianhua Hu, Pan Xie, Bo Qian, and Hanmin Huang*, Palladium-Catalyzed Difunctionalization of Enol Ethers to Amino Acetals with Aminals and Alcohols, J. Am. Chem. Soc. 2013, 135, 18327-18330.
10. Guoying Zhang, Lei Yang, Yanyu Wang, Yinjun Xie, and Hanmin Huang*, An Efficient Rh/O2 Catalytic System for Oxidative C-H Activation/Annulation: Evidence for Rh(I) to Rh(III) Oxidation by Molecular Oxygen, J. Am. Chem. Soc. 2013, 135, 8850-8853.
11. Yinjun Xie, Jianhua Hu, Yanyu Wang, Chungu Xia, and Hanmin Huang*, Palladium-Catalyzed Vinylation of Aminals with Simple Alkenes: A New Strategy to Construct Allylamines, J. Am. Chem. Soc. 2012, 134, 20613-20616.
12. Pan Xie, Yinjun Xie, Bo Qian, Han Zhou, Chungu Xia, and Hanmin Huang*, Palladium-CatalyzedOxidative Carbonylation of Benzylic C-H Bonds via Nondirected C(sp3)-H Activation, J. Am. Chem. Soc. 2012, 134, 9902-9905.
13. Dengjian Shi, Yinjun Xie, Han Zhou, Chungu Xia, and Hanmin Huang*, A Highly Diastereo- and Enantioselective Reaction for Constructing Functionalized Cyclohexanes: Six Contiguous Stereocenters in one Step, Angew. Chem. Int. Ed. 2012, 51, 1248-1251.
14. Yinjun Xie, Yingwei Zhao, Bo Qian, Lei Yang, Chungu Xia, and Hanmin Huang*, Enantioselective N-H Functionalization of Indole with α,β-Unsaturated γ-Lactams Catalyzed by Brønsted Acids, Angew. Chem. Int. Ed. 2011, 50, 5682-5686.
15. Shengmei Guo, Yinjun Xie, Xinquan Hu, Chungu Xia, and Hanmin Huang*, Diastereo- and Enantioselective Catalytic Tandem Michael Addition/Mannich Reaction: Access to Chiral Isoindolinones and Azetidines with Multiple Stereocenters, Angew. Chem. Int. Ed. 2010, 49, 2728-2731.
16. Bo Qian, Shengmei Guo, Jianping Shao, Qiming Zhu, Lei Yang, Chungu Xia*, and Hanmin Huang*,Palladium-CatalyzedBenzylic Addition of 2-Methyl Azaarenes to N-Sulfonyl Aldimines via C-H Bond Activation, J. Am. Chem. Soc. 2010, 132, 3650-3651.
17. Hanmin Huang, Tomoko Okuno, Kazuomi Tsuda, Masahiro Yoshimura, Masato Kitamura*, “Enantioselective Hydrogenation of Aromatic Ketones Catalyzed by Ru Complexes of Goodwin-Lions-type sp2N/sp3N hybrid Ligands R-BINAN-R΄-Py”, J. Am. Chem. Soc. 2006, 128, 8716-8717.
