近期论文

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[1] Yunyun Liu*, Hang Wang, Jie-Ping Wan*. Copper-Catalyzed, C–C Coupling-Based One-Pot Tandem Reactions for the Synthesis of Benzofurans Using o-Iodophenols, Acyl Chlorides, and Phosphorus Ylides. J. Org. Chem., 2014, 79, 10599-10604. [2] Zhen Xu, Yangyang Jiang, Shuang Zou, Yunyun Liu.* Bio-based Solvent Mediated Synthesis of Dihydropyrimidinthiones via Biginelli Reaction in Biomass Derived Green Solvent. Phosphorus, Sulfur and Silicon, 2014, 2014, 189, 791-795. [3] Jie-Ping Wan,* Yunfang Lin, Kaikai Hu, Yunyun Liu. Secondary amine-initiated three-component synthesis of 3,4-dihydropyrimidinones and thiones involving alkynes, aldehydes and thiourea/urea. Beilstein J. Org. Chem., 2014, 10, 287-292. [4] Jie-Ping Wan,* Yunfang Lin, Yunyun Liu. Catalytic Asymmetric Biginelli Reaction for the Enantioselective Synthesis of 3,4- Dihydropyrimidinones (DHPMs). Curr. Org. Chem., 2014, 18, 687-699. [5] Jie-Ping Wan,* Youyi Zhou, Yunyun Liu, Zheng Fang, Chengping Wen.* Multicomponent reactions for diverse synthesis of N-substituted and NH 1,4-dihydropyridines. Chin. J. Chem., 2014, 32, 219-226. [6] Shuo, Cao, Yanfeng Jiang, Yunyun Liu, Jie-Ping Wan.* Recent Advances on Multicomponent Reactions Based on the Transamination Process of Electron Deficient Enamines. Chin. J. Org. Chem., 2014, 35, 876-885. [7] Jie-Ping Wan*, Yunfang Lin, Qing Huang, Yunyun Liu. Diastereoselective Construction of Tetrahydropyridine Fused Bicyclic Structures via Three-Component Domino Reaction. J. Org. Chem., 2014, 79, 7232-7238. [8] Yunyun Liu*, Bin Huang, Xiaoji Cao, Dan Wu, Jie-Ping Wan. Synthesis of heteroaryl containing sulfides via enaminone ligand assisted, copper-catalyzed C–S coupling reactions of heteroaryl thiols and aryl halides. RSC Adv., 2014, 4, 37733-37737. [9] Yunyun Liu*, Yi Zhang, Changfeng Hu, Jie-Ping Wan, Chengping Wen*. Synthesis of 3-sulfenylated indoles by a simple NaOH promoted sulfenylation reaction. RSC Adv., 2014, 4, 35528-35530. [10] Jie-Ping Wan*, Yunfang Lin, Yanfeng Jiang, Mengli Xu, Yunyun Liu*. Selectivity tunable divergent synthesis of 1,4- and 1,2-dihydropyridines via three-component reactions. Tetrahedron, 2014, 70, 7874-7880. [11] Jie-Ping Wan*, Yunfang Lin, Kaikai Hu, Yunyun Liu*. Metal-free synthesis of 1,3,5-trisubstituted benzenes by the cyclotrimerization of enaminones or alkynes in water. RSC Adv., 2014, 4, 20499-20505. [12] Jie-Ping Wan*, Hang Wang, Yunyun Liu, Hanfeng Ding*. Synthesis of 2-Vinylbenzofurans via the Copper-Catalyzed Multicomponent Reactions Involving an Oxa-Michael/Arylation/Vinylation Cascade. Org. Lett., 2014, 16, 5160-5163. [13] Yunyun Liu.* Recent advances on diversity oriented heterocycle synthesis via multicomponent tandem reactions based on A3 coupling. ARKIVOC, 2014, I, 1-20. [14] Hang Wang, Guojun Huang, Yang Sun, Yunyun Liu.* Simple conversion of thiols to disulfides in EtOH under ambient aerobic conditions without using any catalyst or additive. J. Chem. Res., 2014, 38, 96-97. [15] Yunyun Liu, Hang Wang, Xiaoji Cao, Zheng Fang, Jie-Ping Wan.* Copper-Catalyzed Selective Single Arylsulfanylation of Aryl Diiodides with Aryl Thiols. Synthesis, 2013, 45, 2977-2982. [16] Yunyun Liu, Hang Wang, Chunping Wang, Jie-Ping Wan,* Chengping Wen.* Bio-based green solvent mediated disulfide synthesis via thiol couplings free of catalyst and additive. RSC Adv., 2013, 3, 21369-21372. [17] 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. [18] Jie-Ping Wan,* Yunyun Liu. Recent Advances in Diversity Oriented Synthesis through Isatin-based Multicomponent Reactions. Asian J. Org. Chem., 2013, 2, 374-386. [19] Yunyun Liu, Rihui Zhou, Jie-Ping Wan.* Water-Promoted Synthesis of Enaminones: Mechanism Investigation and Application in Multicomponent Reactions. Synth. Commun., 2013, 43, 2475-2483. [20] Yunyun Liu,* Chunping Wang, Xiaobo Wang, Jie-Ping Wan. Enaminone ligand-assisted homo- and cross-coupling of terminal alkynes under mild conditions. Tetrahedron Lett., 2013, 54, 3953-3955.