个人简历

傅滨，教授，博士生导师，主要研究方向为农药创制和不对称合成，致力于杂环化学应用于新农药创制与不对称合成，同时承担国家化学理科基地《有机化学》教学工作。已指导毕业硕士6名和博士5名。现指导博士生3名，硕士生2名。先后6次获得 “校级百篇优秀本科毕业设计”优秀指导教师称号，3次获得 “国家大学生创新性实验计划”优秀指导教师称号。2012年获“宝钢优秀教师奖”。先后指导和推荐十几名本科生保送到港大、北大、清华、上海有机所及中科院化学所等国内外著名科研机构。

研究领域

""主要研究方向为农药创制和不对称合成，致力于杂环化学应用于新农药创制与不对称合成""""

近期论文

1.Ni(II)-Catalyzed enantioselective Mukaiyama-Mannich reaction between silyl enol ethers\r
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and cyclic N-sulfonyl α-ketiminoesters，Org. Chem. Front., 2017, 4, 1858–1862（IF=4.95)\r
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2. Enantioselective Conjugate Addition of 2‑Acetyl Azaarenes toβ,β‑Disubstituted Nitroalkene for the Construction of All-Carbon Quaternary Stereocenters，J. Org. Chem. 2017, 82, 7353−7362（IF=4.85)\r
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3.Nickel(II)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Nitrones with α,β-Unsaturated \r
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Acylcarboxylates，Eur. J. Org. Chem. 2017, 657-661(IF= 3.0)\r
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4.Cu(II)-catalyzed enantioselective 1,3-dipolar cycloaddition of nitrones with a, b-unsaturated acyl phosphonates，\r
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Tetrahedron，2017，73，2923-2930.（IF=2.62)\r
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5. An efficient approach for the construction of trifluoromethylated all-carbon quaternary stereocenters: \r
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enantioselective Ni(II)-catalyzed Michael addition of 2-acetyl azaarene to disubstituted nitroalkenes,\r
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Chem. Commun., 2016, 52, 1470--1473.(IF = 6.8)\r
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6.Enantioselective Copper(II)-Catalyzed Conjugate Addition of Indoles to beta-Substituted Unsaturated Acyl Phosphonates,\r
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Adv. Synth. Catal. 2016, 358, 1011 –1016.(IF = 6.3)\r
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7. Synthesis and Fungicidal Activities of Azaindolyl Thiazoline Compounds, Chin. J. Org. Chem. 2016, 36, 158-164\r
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8. Synthesis of a Novel Quinoline Skeleton Introduced Cationic Polyfluorene Derivative for Multimodal\r
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Antimicrobial Application, ACS Appl. Mater. Interfaces 2015, 7, 25390−25395.(IF = 7.1)\r
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9. Heteroarylidene-tethered bis(oxazoline) copper complexes catalyzed cascade reaction involving asymmetric F-C \r
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alkylation/N-hemiacetalization of indoles with unsaturated ketoester, Tetrahedron, 2015,71, 3625-3631.(IF=2.8)\r
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10.Highly enantioselective F–C alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters catalyzed\r
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by heteroarylidene-tethered bis(oxazoline) copper complexes, Chem.Commun. 2012, 48, 9281-9283(IF=6.8)\r
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11. Malonate-type bis(oxazoline) ligands with sp2 hybridized bridge carbon: synthesis and application in Friedele-Crafts alkylation and allylic alkylation, Tetrahedron 2011,67, 9602-9608(.(IF = 2.8)\r
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12. Synthesis of heteroarylidene malonate derived bis(thiazolines) and their application in F-C alkylation,\r
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Tetrahedron: Asymmetry, 2011, 22, 550-557.(IF = 2.6).\r
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13. Highly enantioselective Friedel–Crafts reaction of indoles with N-sulfonyl aldimines catalyzed by hetero-\r
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arylidene malonate-type bis(oxazoline) copper(II) complexes, Tetrahedron: Asymmetry, 2011,22, 1874-1878.\r
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14. Highly enantioselective Friedel-Crafts reaction of indole with alkylidene malonate,Advanced Synthesis & Catalysis, 2009,351, 3113-3117.(IF = 5.66)\r
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15. Synthesis of novel C3 symmetric tris-thiazoline ligands and their application in the allylic oxidation,\r
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Tetrahedron: Asymmetry:2008, 19, 2159-2163..(IF = 2.6)\r
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16. Synthesis of novel fluoren-9-ylidene malonate derived bis(oxazoline) ligands and their application in\r
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Friedel-Crafts reaction, Molecules, 2010,15, 8582-8592.\r
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17. Synthesis and Fungicidal Activity of 1,3-Thiazoline Derivatives Bearing Nitrophenyl Group on the 2-Position,\r
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J. Heterocyclic Chemistry, 2011, 48, 729-732.\r
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18. Synthesis and Biological Activity of 2-Indolyl containing halogenated indolyl moiety,\r
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Phos. Sulf. Silicon and Rela. 2011, 186, 1790-1800.\r
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19. A convenient one-pot synthesis of arene-centered tris(tiazoline), Heterocycles, 2009, 79, 1031-1039.