傅滨，男，博士，现为中国农业大学理学院应用化学系教授、博士生导师。
1、主持国家自然基金"基于NQNO村拿的细胞色素c还原酶抑制剂的设计、合成与构效关系研究"，No. 21172255，(2012.1-2015.12)。
2、主持国家"十一五"科技支护概伤世尔阶丰紧啊项撑计划"三噻唑啉化合物的合成与杀菌活性研究"课题，2006BAE01A01，(20来自06.10~2008.10)，15万。
3、主持国家"十一五"科技支撑计划"唑啉类核心物质的研究与开发"，20098AK61804，(2010.8~2012.3)，12万。
4、主持国家"十二五"科技支撑计划"2-取代芳杂环基噻唑啉造因困到衍生物的合成与活性研究"(20360百科11.3~2015.3)，16万。
5两破呀岁否劳、主持教育部课题"氨基噻唑啉化合物的合成与催化性能研究"，2010JS30，2010散断班夜座满今身血.9-2011.9，防乡责听8万
6、主持农业部重点实验室重点基金课题"1医胶孙,3-噻唑啉衍生物的合成与活性研究"，2雨还010.5~2011.5。
1.Ni(II)-Catalyzed e述领养反许西次品状机拉nantioselec气须结tive Mukaiyama-Mannich reaction between silyl enol ethersand cyclic N-sulfonyl α-ketiminoesters，Org. Chem. Front., 2017, 4, 1858–1862(IF=4.95)
2. Enantioselective Conjugate A西获六龙出ddition of 2‑Acetyl Azaarenes toβ,β‑Disubstituted Nitroalkene for the Construction 田候生刑考良of All-Carbon Quaternary Stereocenters，J. Org. Chem. 2017, 82, 7353−7362(IF=4.85)
3.Nickel(II)-Catalyzed Enantioselective 1,3-Dipolar Cycloaddition of Nitrones with α,β-Unsaturated Acylcarboxylates，Eur. J. Org. Chem. 2017静, 657-661(IF= 3.0)
4.Cu(II)-cata安意院率村道责诉刻天使lyzed enantios离苦无曾原常味负河状elective 1,3-dipolar cycloaddition o村时席良误治远植持名f nitrones with a, b-unsaturated acyl phosphonates，Tetrahedron，2017，73，2923-2930.(IF=2.62)
5. An efficie钟七国白五况齐充整妒nt approach for the con款所车给伟机益低减土struction of trifluoromethylated all-carbon quaternary stereocenters:enantioselective Ni(II)-catalyzed Michael addition of 2-acetyl azaarene to disubstituted nitroalkenes,Chem. Commun., 2016, 52, 1470--1473.(IF = 6.8)
6.Enantioselective Copper(II)-Catalyzed Conjugate Addition of Indoles to beta-Substituted Unsaturated Acyl Phosphonates,Adv. Synth. Catal. 2016, 358, 1011 –1016.(IF = 6.3)
7. Synthesis and Fungicidal Activities of Azaindolyl Thiazoline Compounds, Chin. J. Org. Chem. 2016, 36, 158-164
8. Synthesis of a Novel Quinoline Skeleton Introduced Cationic Polyfluorene Derivative for MultimodalAntimicrobial Application, ACS Appl. Mater. Interfaces 2015, 7, 25390−25395.(IF = 7.1)
9. Heteroarylidene-tethered bis(oxazoline) copper complexes catalyzed cascade reaction involving asymmetric F-Calkylation/N-hemiacetalization of indoles with unsaturated ketoester, Tetrahedron, 2015,71, 3625-3631.(IF=2.8)
10.Highly enantioselective F–C alkylation of indoles and pyrrole with β,γ-unsaturated α-ketoesters catalyzedby heteroarylidene-tethered bis(oxazoline) copper complexes, Chem.Commun. 2012, 48, 9281-9283(IF=6.8)
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)
12. Synthesis of heteroarylidene malonate derived bis(thiazolines) and their application in F-C alkylation,Tetrahedron: Asymmetry, 2011, 22, 550-557.(IF = 2.6).
13. Highly enantioselective Friedel–Crafts reaction of indoles with N-sulfonyl aldimines catalyzed by hetero-arylidene malonate-type bis(oxazoline) copper(II) complexes, Tetrahedron: Asymmetry, 2011,22, 1874-1878.
14. Highly enantioselective Friedel-Crafts reaction of indole with alkylidene malonate,Advanced Synthesis & Catalysis, 2009,351, 3113-3117.(IF = 5.66)
15. Synthesis of novel C3 symmetric tris-thiazoline ligands and their application in the allylic oxidation,Tetrahedron: Asymmetry:2008, 19, 2159-2163..(IF = 2.6)
16. Synthesis of novel fluoren-9-ylidene malonate derived bis(oxazoline) ligands and their application inFriedel-Crafts reaction, Molecules, 2010,15, 8582-8592.
17. Synthesis and Fungicidal Activity of 1,3-Thiazoline Derivatives Bearing Nitrophenyl Group on the 2-Position,J. Heterocyclic Chemistry, 2011, 48, 729-732.
18. Synthesis and Biological Activity of 2-Indolyl containing halogenated indolyl moiety,Phos. Sulf. Silicon and Rela. 2011, 186, 1790-1800.19. A convenient one-pot synthesis of arene-centered tris(tiazoline), Heterocycles, 2009, 79, 1031-1039.
1、芳杂环甲叉双恶唑啉化合物的制备及用途，响申请号 200910087763.3, 授权号ZL200910087763.3
2、 2，4-二取代噻唑啉衍生物及系甲其制备方法与应用，申请号200810104850.0, 授权号 ZL200810104850.0
3、2-取代芳杂环基-1,3-噻唑啉衍生物及其制备方法和应用，申请号 201010250887.1
4、手性二苯来自并环庚二烯双恶唑啉配体化合物及其制备与应用，申请号:授360百科权公告号 CN 100364981C。
关注微信