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黄吉荣
2023-05-11 03:29
  • 黄吉荣
  • 黄吉荣 - 副教授 博导-华中科技大学-同济医学院-个人资料

近期热点

资料介绍

个人简历


教育经历\r
2005.9~2009.6 四川大学 药学 本科毕业\r
2009.9~2014.6 四川大学 药物化学 博士研究生毕业\r
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工作经历\r
2018.2~至今 华中科技大学 同济药学院 副教授\r
2015.11~2017.10 德国亚琛工业大学 有机化学研究所 博士后\r
2014.8~2015.7 日本冲绳科学与技术大学院大学 化学与化学生物工程部门 博士后

研究领域


""药物优势骨架的设计与合成\r
杂环是常见的药物分子优势骨架,课题组利用高价硫介导杂环多样性转化,以发现新的药物或其它功能性分子。""""

近期论文


Xian-Yan Shen,Man Li,Tai-Ping Zhou.Ji-Rong Huang.Benzo[b]naphtho[1,2-d]thiophene Sulfoxides: Biomimetic Synthesis, Photophysical Properties, and Applications.Angew. Chem. Int. Ed. 2022, doi:10.1002/anie.202203908,\r
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Ji-Rong Huang.Organic transformation of benzothiophenes by C–S bond cleavage beyond reductive desulfurization.EurJOC, 2021, 42, 5775-5787,\r
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Ji-Rong Huang,Carsten Bolm.Microwave-Assisted Synthesis of Heterocycles by Rhodium(III)-Catalyzed Annulation of N-Methoxyamides with α-Chloroaldehydes.Angew. Chem. Int. Ed. 2017, 56, 15921-15925,\r
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Ji-Rong Huang,Muhammad Sohai,Kenji Monde,Tohru Taniguchi.Fujie Tanaka.Formal (4+1) Cycloaddition and Enantioselective Michael–Henry Cascade Reactions to Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles.Angew. Chem. Int. Ed. 2017, 56, 5853-5857,\r
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Ji-Rong Huang,Liu Qin,Yu-Qin Zhu,Qiang Song.Lin Dong.Multi-site cyclization via initial C–H activation using a rhodium(III) catalyst: rapid assembly of frameworks containing indoles and indolines.Chem. Commun. 2015, 51, 2844-2847.,\r
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Ji-Rong Huang,Qiang Song,Yu-Qin Zhu,Liu Qin.Zhi-Yong Qian,Lin Dong.Rhodium(III)-Catalyzed Three-Component Reaction of Imines, Alkynes, and Aldehydes through C−H Activation.Chem. Eur. J. 2014, 20, 16882-16886,\r
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Ji-Rong Huang,Chuan-Hua Qu,Qian-Ru Zhang,Wei Zhang,Bo Han.Lin Dong,Cheng Peng.Rhodium(III)-catalyzed Vinylic sp2 C–H Bond Functionalization: Efficient Synthesis of Pyrido[1,2-α]benzimidazoles and Imidazo[1,2-α]pyridines.Org. Biomol. Chem. 2013, 11, 6142-6149,\r
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Ji-Rong Huang,Chuan-Hua Qu,Qian-Ru Zhang,Xun-Hao Sun.Lin Dong,Ying-Chun Chen.Rhodium(III)-Catalyzed Direct Selective C(5)–H Oxidative Annulations of 2-Substituted Imidazoles and Alkynes by Double C–H Activation.Org. Lett. 2013, 15, 1878-1881.,\r
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Ji-Rong Huang,Bo Han.Lin Dong,Cheng Peng,Ying-Chun Chen.Synthesis of Aza-Fused Polycyclic Quinolines via Double C–H Bond Activations.Chem. Eur. J. 2012, 18, 8896-8900.,\r
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Ji-Rong Huang,Hai-Lei Cui,Jie Lei,Xun-Hao Sun.Ying-Chun Chen.Organocatalytic chemoselective asymmetric N-allylic alkylation of enamides.Chem. Commun. 2011, 47, 4784-4786,\r
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Chuan-Hua Qu,Ji-Rong Huang,Wei Zhang,Qian-Ru Zhang,Jin-Gen Deng.Lin Dong.Rhodium-catalyzed Spirocyclic Sultams Synthesis by [3+2] Annulation with Cyclic N-Sulfonyl Ketimines and Alkynes.Chem. Eur. J. 2013, 19, 16537-16540,\r
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Qian-Ru Zhang,Ji-Rong Huang,Wei Zhang.Lin Dong.Highly Functionalized Pyridines Synthesis from N-Sulfonyl Ketimines and Alkynes Using the N−S Bond as an Internal Oxidant.Org. Lett. 2014, 16, 1684-1687,\r
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Hai-Lei Cui,Ji-Rong Huang,Jie Lei,Zhao-Feng Wang,Shi Chen,Li Wu.Ying-Chun Chen.Direct Asymmetric Allylic Alkylation of Butenolides with Morita Baylis Hillman Carbonates.Org. Lett. 2010, 12, 720-723,\r
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Lin Wu,Qian-Ru Zhang,Ji-Rong Huang,Yang Li.Fu Su,Lin Dong.The application of Morita-Baylis-Hillman reaction: Synthetic studies on perophoramidine.Tetrahedron, 2017, 73, 3966-3972,

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