教育经历 PhD in Organic Chemistry, The University of Edinburgh Jan 07 – Jun 10 Research Supervisor: Dr Hon Wai Lam Thesis Title: Synthesis of multisubstituted alkenes via ring-opening of cyclopropenes. Msc in Organic Chemistry, The University of Edinburgh Sep 05 – Sep 06 Research Supervisor: Dr Trent H. Galow Thesis Title: Towards the synthesis of new triimide-based supramolecular synthons. BSc in Chemistry, Nanjing University, China Sep 01 – Jun 05 Dissertation Title: Enantioselective synthesis of camphor-derived sulfur ylides. 工作经历 Associate Professor, Nanjing University, China Jun 14 – present Research Collaborator: Professor Yi Pan, Deputy Vice-Chancellor Research interests: Iridium Chemistry, fluorine chemistry, PET radiolabels.
Research Associate, Nanjing University, China Jan 13 – Jun 14 Research Advisor: Professor Yi Pan, Deputy Vice-Chancellor Research interests: Organometallic Chemistry, fluorine chemistry, PET radiolabels.
ERC Research Fellow, The University of St Andrews, UK Jan 11 – Dec 12 Research Advisor: Professor David O’Hagan Research interests: fluorine chemistry, enzyme chemistry, PET radiolabels. 科研方向 金属催化方法学、氟化学、放射性同位素标定、金属配合物发光材料 海外求学期间主要从事研究金属催化的小分子开环反应研究。研究着重于新型环丙烯的合成和立体选择开环反应。本人通过条件摸索和机理研究,揭示了这种小环在铁催化下选择性开环的反应机制,并阐释了此种独特的beta-碳消去机理对于立体化学控制的重要性。此课题在《Angew. Chem. Int. Ed.》、《Chem. Comm》和《J. Org. Chem》上发表论文各1篇。博士后期间主要从事含氟有机物的合成和构型研究,开展了一系列含氟药物的实验研究和应用探索。研究的重心集中于多氟取代的药物和材料的合成与开发,制备了一系列多氟取代环十二烷和氟代棕榈酸的链状和环状单体化合物,通过研究其晶体排列和分子极性之间的联系,发现此类氟化物分子由于氟原子之间的相互排斥而保持链状构型定向排列,并且分子内的偶极弛豫则使这种构型更加稳定。在《Angew. Chem. Int. Ed.》、《Pure and Applied Chemistry》等国际期刊上发表论文4篇。同时开展了天然氨基酸和异黄酮类化合物的氟-18放射性同位素标定和生理活性的研究,用于其机理探索和临床医学PET/MRI研究,其成果发表在《Beilstain J. Org. Chem》上。回国后开展了一系列含氮化合物碳氢活化方法学的研究工作,包括:1.酰胺上的自由基硫化反应;2.糖精的自由基活化反应;3.新型磷酸配位的铱配合物有机光电材料合成。通过对过氧化物自由基产生途径的探索,发展了两项新型邻氮甲基的自由基机理硫化反应,尤其是糖精和邻苯二甲酰亚胺衍生物的合成,具有一定的创新意义。此课题已撰写论文5篇,分别发表在《Org. Biomol. Chem.》和《J.Org.Chem》等期刊上。于2011年获得欧洲研究学会ERC Fellowship。多年来担任《Org. Biomol. Chem.》和《Stud. Nat. Prod. Chem.》等国际期刊的审稿人。 科研项目 1.环丙烯立体选择开环反应合成不对称烯烃 英国政府EaStCHEM研究基金 2.“多氟取代药物和材料的合成与构型研究“ 欧洲研究协会ERC基金 3.”极大规模集成电路高K关键材料的研究与开发” 国家02专项 4.“有机小分子氟化开环反应在含氟聚合物材料中的应用“ 国家自然科学基金 5.”放射性碳标的鸟氨酸合成及其在PET/MRI下的生物显影应用” 国家留学基金委 科研成果 “Metal-Free Catalytic Approach for Allylic C–H Amination Using N-Heterocycles via sp3 C–H Bond Activation”, J. Sun, Y. Wang* and Y. Pan, J. Org. Chem., 2015, 80, 8945-8950.
“Manganese Catalysed sulfenylation of N-methyl Amides with Arenesulfonyl Hydrazides”, J. Sun, Y. Wang*, Y. Pan, Org. Biomol. Chem., 2015, 13, 3878-3881.
“A convenient enantioselective decarboxylative aldol reaction to access chiral α-hydroxy esters using β-keto acids”, Z. Duan, J. Han, P. Qian, Z. Zhang, Y. Wang* and Y. Pan, Beilstein J. Org. Chem. 2014, 10, 969-974.
“The difluoromethylene (CF2) group in aliphatic chains: Synthesis and conformational preference of palmitic acids and nonadecane containing CF2 groups”, Y. Wang, R. Callejo, A. M. Z. Slawin and D. O’Hagan*. Beilstein J. Org. Chem., 2014, 10, 18-25.
“Enantioselective Synthesis of 3-Hydroxy Oxindoles by Ytterbium-Catalysed Decarboxylative Addition of β-Ketoacids to Isatins”, Z. Duan, J. Han, P. Qian, Z. Zhang, Y. Wang* and Y. Pan. Org. Biomol. Chem., 2013, 11, 6456-6459.
The preferred conformation of erythro- and threo-1,2-difluorocyclododecanes, Y. Wang, P. Kirsch, T. Lebl, A. M. Z. Slawin and D. O’Hagan*, Beilstein J. Org. Chem., 2012, 8, 1271-1278.
The influence of the difluoromethylene group (CF2) on the conformation of selected organic compounds, D. O’Hagan*, Y. Wang, M. Skibinski, A. M. Z. Slawin and T. Lebl, Pure and Applied Chemistry, 2012, 7, 1587-1595.
Alicyclic ring structure: Conformational influence of the CF2 group in cyclododecanes, M. Skibinski, Y. Wang, A. M. Z. Slawin, T. Lebl, P. Kirsch and D. O’Hagan*, Agnew. Chem. Int. Ed, 2011, 50, 10581-10584.
Fluorescence Enhancement by Symmetry Breaking in a Twisted Triphenylene Derivative, J. Levell, A. Ruseckas, J. Henry, A. Stretton, A. Mount, I. Samuel, Y. Wang and T. Galow*, J. Phys. Chem., 2010, 114, 13291-13295.
“Stereoselective Formation of Alkenyl Halides via Magnesium Halide Promoted Ring Opening of Bis-Activated Cyclopropenes”, Y. Wang and H.W. Lam*, J. Org. Chem. 2009, 74, 1353-1355.
“Stereoselective Synthesis of Tri- and Tetrasubstituted Alkenes via Iron-Catalysed Carbometalation–Ring-Opening Reactions of Cyclopropenes”, Y. Wang, F. Y. Chen, E.A.F. Fordyce, and H.W. Lam*, Agnew. Chem. Int. Ed, 2008, 47, 7350-7353.
“Copper-Catalysed Silylation of Cyclopropenes Using (Trifluoromethyl)trimethylsilane”, E. A. F. Fordyce, Y. Wang, T. Luebbers, H. Lam*, Chem. Comm, 2008, 1124-1126.
“1,4,5,8,9,12-Hexamethyltriphenylene. A Molecule with a Flipping Twist”, Y. Wang, A.D. Stretton, M.C. McConnell, P.A. Wood, S. Parsons, J.B. Henry, A.R. Mount and T.H. Galow*. J. Am. Chem. Soc, 2007, 129(43), 13193-13200.
“New Camphor-Derived Selenonium Ylides: Enantioselective Synthesis of Chiral Epoxides”, X. L. Li, Y. Wang and Z. Z. Huang*, Aust. J. Chem, 2005, 58 (10), 749–752.
2011 欧洲研究协会青年研究奖 ERC Fellowship 环科有机化学 有机化学实验 |