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个人简介

2003年至今,在Chem. Rev., J. Am. Chem. Soc., Nature Commun., Chem. Sci., ACS Catal., Org. Lett., Chem. Commun., Adv. Synth. Catal., Chem. Eur. J., J. Org. Chem., Tetrahedron, Synlett/Synthesis等期刊上发表学术论文80余篇,其中以第一作者、通讯联系人发表论文六十余篇。2006年-2007年度苏州市自然科学论文一等奖;2007年苏州大学优秀博士论文、2008年江苏省优秀博士论文、2009年全国百篇优秀博士论文提名奖;2010年第六届亚欧金属促进反应会议优秀墙报奖;作为主要完成人参与的项目“功能性有机分子的合成、性质及应用研究”获得2010年中国石油和化学工业协会科技进步二等奖、2013年教育部高等学校科学研究优秀成果奖(科学技术)自然科学奖二等奖。目前主持、完成国家自然科学基金面上项目一项、国家自然科学基金应急项目一项、江苏省教育厅重大项目一项、国家自然科学基金青年基金一项、江苏省自然科学基金青年基金一项、江苏省有机合成重点实验室开放基金一项。 1998.9-2002.6苏州大学化学化工学院 学士 2002.9-2007.6 苏州大学化学化工学院 博士 2007.8-2011.2 新加坡南洋理工大学博士后研究员 (Research Fellow, 马来西亚科学院院士) 2011.3-2011.12 德国慕尼黑大学博士后研究员 (Research Fellow, 德国科学院院士Prof. Paul Knochel) 2012.1-2015.06 苏州大学材料与化学化工学部副教授 2015.06-至今 苏州大学材料与化学化工学部教授

研究领域

异腈化学反应研究;氧化脱氢反应研究;自由基参与的新反应研究

近期论文

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Yi Fang, Torben Rogge, Lutz Ackermann, Shun-Yi Wang,* and Shun-Jun Ji* Nickel-catalyzed reductive thiolation and selenylation of unactivated alkyl bromides Nature Communications 2018, 9, 2240. (SCI12.353) Rong Zhang, Zheng-Yang Gu, Shun-Yi Wang,* and Shun-Jun Ji* Co(II)/Ag(I) Synergistically Catalyzed Mono-insertion Reaction of Isocyanide to Terminal Alkynes with H2O: Synthesis of Alkynamides Derivatives Organic Letters 2018, 20, DOI: 10.1021/acs.orglett.8b02516 (SCI6.492) Jing-Hao Li, Qi Huang,Shun-Yi Wang,* and Shun-Jun Ji* Trisulfur Radical Anion (S3•−) Involved [1+2+2] and [1+3+1] Cycloaddition with Aromatic Alkynes: Synthesis of Tetraphenylthiophene and 2-Benzylidenetetrahydrothiophene Derivatives Organic Letters 2018, 20, 4704-4708. (SCI6.492) Huan Liu, Yi Fang, Shun-Yi Wang,* and Shun-Jun Ji* TEMPO-catalyzed aerobic oxidative selenium insertion reaction:synthesis of 3-selenylindole derivatives by multicomponent reaction of isocyanides, selenium powder, amines and indoles under transition metal-free conditions Organic Letters 2018, 20, 930-933. (SCI6.492) Fei Wang, Pei Xu,Shun-Yi Wang,* and Shun-Jun Ji* Cu(II)/Ag(I)-Catalyzed Cascade Reaction of Sulfonylhydrazone with Anthranils: Synthesis of 2-Aryl-3-sulfonyl Substituted Quinoline Derivatives Organic Letters 2018, 20, 2204-2207. (SCI6.492) Bei-Bei Liu, Hui-Wen Bai, Huan Liu, Shun-Yi Wang,* and Shun-Jun Ji* [4+1] Cycloaddition Reaction of ,-alkynic Hydrazones and KSCN under Transition-Metal Free Conditions: Synthesis of N-Iminoisothiazolium Ylides The Journal of Organic Chemistry2018, 84, DOI: 10.1021/acs.joc.8b01725.(SCI4.805) Bei-Bei Liu, Hui-Wen Bai, Huan Liu, Shun-Yi Wang,* and Shun-Jun Ji* A cascade trisulfur radical anion (S3•−) addition / electron de-tosylation process for the synthesis of 1,2,3-thiadiazoles and isothiazoles The Journal of Organic Chemistry2018, 84, 10281-10288.(SCI4.805) Zheng-Yang Gu, Rong Zhang, Shun-Yi Wang,* and Shun-Jun Ji* Cobalt(II)-Catalyzed Bis-isocyanides Insertion Reactions with Boric acids and Sulfonyl Azides via Nitrene Radical Coupling Chinese Journal of Chemistry2018, 36, 1011-1016. (SCI2.378) Fei Wang, Tian-Qi Wei, Pei Xu, Shun-Yi Wang * and Shun-Jun Ji* Mn(III)-mediated radical cascade reaction of boronic acids with isocyanides: synthesis of diimide derivatives Chinese Chemistry Letters2018, in press.(SCI2.631) Zheng-Yang Gu,Yuan Liu,Fei Wang,Xiaoguang Bao,*Shun-Yi Wang,*and Shun-Jun Ji* Cobalt(II)-Catalyzed Synthesis of Sulfonyl Guanidines via Nitrene Radical Coupling with Isonitriles: A Combined Experimental and Computational Study ACS Catalysis2017, 7, 3893−3899.(SCI11.384) Yi Fang, Zheng-Lin Zhu, Pei Xu, Shun-Yi Wang,* and Shun-Jun Ji* Aerobic Radical-Cascade Cycloaddition of Isocyanides, Selenium and Imidamides: Facile Access to 1,2,4-Selenadiazoles under Metal-Free Conditions, Green Chemistry 2017, 19, 1613-1618. (SCI8.506) Pei Xu, Fei Wang, Tian-Qi Wei, Ling Yin, Shun-Yi Wang,* and Shun-Jun Ji* Palladium-catalyzed Incorporation of Two C1 Building Blocks: The Reaction of Atmospheric CO2 and Isocyanides with 2-Iodoanilines Leading to an Synthesis of Quinazoline-2,4(1H,3H)-diones Organic Letters 2017, 19, 4484-4487. (SCI6.492) Zheng-Yang Gu, Jing-Hao Li, Shun-Yi Wang,* and Shun-Jun Ji* Cobalt(II)-Catalyzed Bis-isocyanides Insertion Reactions with Sulfonyl Azides via Nitrene Radical:Chemoselective Synthesis of The Sulfonylamidyl amide and 3-Imine Indole Derivatives Chemical Communications 2017, 53, 11713-11716. (SCI5.123) Fang-Hui Li, Zhong-Jian Cai, Ling Yin, Jian Li, Shun-Yi Wang,* and Shun-Jun Ji*Silver-Catalyzed Regioselective Fluorination of Carbonyl Directed Alkynes: Synthesis of α-Fluoroketones Organic Letters 2017, 19, 1662-1665. (SCI6.492) Tian Jiang,Zheng-Yang Gu,Ling Yin,Shun-Yi Wang*and Shun-Jun Ji* Cobalt(II)-Catalyzed Isocyanide Insertion Reaction with Sulfonyl Azides in Alcohols: Synthesis of Sulfonyl Isoureas The Journal of Organic Chemistry2017, 82, 7913–7919.(SCI4.805) Huan Liu, YiFang,Ling Yin,Shun-Yi Wang* and Shun-Jun Ji* Copper(I)-Catalyzed Ligand-Promoted Multicomponent Reactions of Isocyanides, Selenium, Amines and Iodoarenes: Access to Highly Functionalized Carbamimidoselenoates The Journal of Organic Chemistry2017, 82, 10866-0874. (SCI4.805) Bei-Bei Liu,Xue-Qiang Chu, Huan Liu, Ling Yin,Shun-Yi Wang*and Shun-Jun Ji* Aqueous reaction of alcohols, organohalides and odourless sodium thiosulfate under transition metal-free conditions: synthesis of unsymmetrical aryl sulfides via dual C-S bond formation The Journal of Organic Chemistry2017, 82, 10174-10180. (SCI4.805) Zheng-Yang Gu, Cheng-Guo Liu, Shun-Yi Wang,* and Shun-Jun Ji* Cobalt-Catalyzed Annulation of Amides with Isocyanides via C(sp2)−H Activation, Journal of Organic Chemistry2017, 82, 2223−2230.(SCI4.805) Zheng-Yang Gu, Jia-Jia Cao, Shun-Yi Wang,* and Shun-Jun Ji*,The Involvement of the Trisulfur Radical Anion in Electron-Catalyzed Sulfur Insertion Reactions: Facile Synthesis of Benzothiazine Derivatives under Transition Metal-free Conditions, Chemical Science2016, 7, 4067-4072. (SCI9.063) Zheng-Yang Gu, Cheng-Guo Liu, Shun-Yi Wang,* and Shun-Jun Ji* Pd-Catalyzed Intramolecular Heck Reaction, C(sp2)−H Activation, 1,4-Pd Migration and Aminopalladation: Chemoselective Synthesis of Dihydroindeno[1,2,3-kl]acridines and 3-Arylindoles, Organic Letters 2016, 18, 2379-2382. (SCI6.492)

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