江西师范大学化学化工学院导师介绍：刘云云

　　刘云云，女，2005年7月毕业于曲阜师范大学，获工学学士学位；2010年6月毕业于浙江大学理学院化学系，获理学博士学位。同年7月到江西师范大学化学化工学院从事教学科研工作，担任《有机化学》以及《有机化学实验》本科课程教学；现主要研究方向为金属催化的偶联反应、C-H活化反应及其在串联反应中的应用研究，目的是为具有生物药物活性的功能小分子化合物提供简捷高效的新合成方法。目前已在国际知名刊物Organic Letters(IF=5.8), Advanced Synthesis & Catalysis(IF=6.0), Chemistry-An Asian Journal (IF=4.5), Organic & Biomolecular Chemistry(IF=3.7), European Journal of Organic Chemistry(IF=3.21), Tetrahedron Letters(IF=2.6)以及Synthesis(IF=2.3)等发表具有高影响力的SCI论文多篇，获得国内外同行的关注和认可，并被广泛引用。目前主持国家自然科学基金青年基金一项(经费25万元)，江西省教育厅基金一项(经费1万元)，江西师大博士启动基金以及江西师大青年成长基金各一项，参与国家自然科学基金以及江西省自然科学基金多项。

　　欢迎广大对有机合成化学感兴趣的同学加入研究小组！

　　联系方式：chemliuyunyun@gmail.com

　　近期发表部分论文如下：

　　[1] Yunyun Liu, Rihui Zhou, Jie-Ping Wan.* Water promoted synthesis of enaminones, mechanism investigation and application in multicomponent reactions. Synth. Commun., 2013, DOI: 10.1080/00397911.2012.715712.

　　[2] Yunyun Liu, Hang Wang, Jie-Ping Wan.* Recent advances in diversity oriented synthesis through isatin-based multicomponent reactions. Asian J. of Org. Chem., 2013, in press, DOI: 10.1002/ajoc.201200180.

　　[3] Jie-Ping Wan, Chunping Wang, Rihui Zhou, Yunyun Liu.* Sustainable H2O/ethyl lactate system for ligand-free Suzuki–Miyaura reaction. RSC Adv., 2012, 2, 8789-8792.

　　[4] Jie-Ping Wan,* Yunyun Liu. Recent advances in new multicomponent synthesis of structurally diversified 1,4-dihydropyridines. RSC Adv., 2012, 2, 9763-9771.

　　[5] Jie-Ping Wan,* Chunping Wang, Yunyun Liu. Chemo-selective copper-catalyzed C-O coupling reactions of phenols with aryl/vinyl halides using enaminone as efficient ligand. Appl. Organometal. Chem., 2012, 26, 445-447.

　　[6] Jie-Ping Wan,* Rihui Zhou, Yunyun Liu, Mingzhong Cai. A “byproduct–intermediate–product” recycling strategy for multicomponent synthesis of 1,4-dihydropyridines. RSC Adv., 2013, 3, 2477-2482.

　　[7] Yunyun Liu, Jie-Ping Wan.* Advances in Copper-Catalyzed C-C Coupling Reactions as Well as Related Domino Reactions Based on Active Methylene Compounds. Chem. Asian J., 2012, 7, 1488-1501.

　　[8] Yunyun Liu,* Jie-Ping Wan. Tandem reactions initiated by copper-catalyzed cross-coupling: A new strategy towards heterocycle synthesis. Org. Biomol. Chem.,2011, 9, 6873-6894. (Review)

　　[9] Yunyun Liu, Weiliang Bao.* Copper-catalyzed tandem process: An efficient approach to 2-substituted-1,4-benzodioxanes. Org. Biomol. Chem.,2010, 8, 2700-2703.

　　[10] Yunyun Liu, Jianguo, Yang, Weiliang Bao.* Palladium free synthesis of conjugated enynes by direct olefination of terminal alkynes using vinyl bromides. Eur. J. Org. Chem.,2009, 5317-5320.

　　[11] Weiliang Bao,* Yunyun Liu, Xin Lv, Weixing Qian.Cu2O-catalyzed tandem ring-opening/coupling cyclization process for the synthesis of 2, 3-dihydro-1, 4-benzodioxins.Org. Lett., 2008, 10, 3899-3902.

　　[12] Weiliang Bao,* Yunyun Liu, Xin Lv. Mild copper(I) iodide/β-keto ester catalyzed coupling reactions of styryl bromides with phenols, thiophenols, and imidazoles. Synthesis, 2008, 1911-1917.

　　[13] Yunyun Liu, Weiliang Bao.* New method for the synthesis of dithiocarbamates by CuI-catalyzed coupling reaction. Tetrahedron Lett., 2007, 48, 4785-4788.

　　[14] Yunyun Liu,* Chunping Wang.A clean method for the synthesis of 1,2-disubstituted benzimidazoles through a redox reaction of o-phenylenediamine and aldehydes. J. Chem. Res. 2012, 36, 61-62.

　　[15] Jie-Ping Wan,* Yunyun Liu. Multicomponent Reactions Promoted by Organosilicon Reagents. Curr. Org. Chem., 2011, 15, 2758-2773.

　　[16] Jie-Ping Wan,* Yunyun Liu.Synthesis of dihydropyrimidinones and thiones by multicomponent reactions: Strategies beyond the classical biginelli reactiondihydropyrimidinones and thiones by multicomponent reactions. Synthesis, 2010, 3943-3953.

　　[17] Xin Lv, Yunyun Liu,Weixing Qian, Weiliang Bao.* Copper(I)-catalyzed one-pot synthesis of 2-iminobenzo-1,3-oxathioles from ortho-iodophenols and isothiocyanates. Adv. Synth. Catal., 2008, 350, 2507-2512.

　　[18] Jie-Ping Wan,* Chunping Wang, Yunyun Liu. Direct Synthesis of Enaminone Functionalized Biaryl Ethers by CuI-Catalyzed O-Arylation of Enaminone Functionalized Phenols. Org. Biomol. Chem., 2011, 9, 6481-6483.

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