黄吉荣
邮箱：huangjr@hust.edu.cn
ORCID：http://orcid.org/0000-0002-9272-3390
研究领域：药物优势骨架设计合成&杂环化学
地址：武汉市航空路13号华中科技大学同济医学院药学院430030
热忱欢迎对药物化学，有机合成感兴趣的本科生、硕士、博士、博士后加盟课题组！
工作经历
2018.02–今 华中科技大学(HUST)副教授/博士生导师
2015.09–2017.10 德国亚琛工业大学(RWTH)博士后
导师： Prof. Carsten Bolm
2014.08–2015.07 日本冲绳科学技术大学院大学(OIST)博士后
导师： Prof. Fujie Tanaka
教育背景
2009.09–2014.06 四川大学 华西药学院 药物化学 博士 导师: 陈应春教授
2005.09–2009.06 四川大学 华西药学院 药学 学士
主持项目
2022.01-2024.12 国家青年基金
2020.03-2022.03 湖北省青年基金
2018.03-2021.03 华中科技大学人才引进基金
讲授课程
药物化学；药物设计学；药物合成学；新药设计等
所获奖励
湖北省高层次人才计划，2020.
武汉黄鹤英才，2019.
德国亚历山大·冯·洪堡学者，2015.
研究生国家奖学金，2013.
优秀博士毕业生，四川大学，2013.
四川大学第五届研究生学术之星，2013.
四川大学优秀博士研究生，2012,2013.
四川大学复星制药特等奖学金，2012.
四川大学优秀硕士研究生，2011.
卫生部国际交流与合作中心·第一三共医药学奖学金，2011.
泰达·凯莱英奖学金，四川大学，2007.
学术论文
14. Benzo[b]naphtho[1,2-d]thiophene Sulfoxides: Biomimetic Synthesis, Photophysical Properties, and Applications
Xian-Yan Shen, Man Li, Tai-Ping Zhou, and Ji-Rong Huang*
Angew. Chem. Int. Ed. 2022, 10.1002/anie.202203908. (IF 16.823)
13. Organic transformation of benzothiophenes by C–S bond cleavage beyond reductive desulfurization(Review)
Jirong Huang*
EurJOC, 2021,42, 5775-5787.
Selected as “Chinese YoungJOC”
博士及博士后阶段：
12. Microwave-Assisted Synthesis of Heterocycles by Rhodium(III)-Catalyzed Annulation of N-Methoxyamides with α-Chloroaldehydes
Ji-Rong Huang, Carsten Bolm*
Angew. Chem. Int. Ed. 2017,56, 15921-15925 (IF 16.823)
11. Formal (4+1) Cycloaddition and Enantioselective Michael–Henry Cascade Reactions to Synthesize Spiro[4,5]decanes and Spirooxindole Polycycles
Ji-Rong Huangǂ, Muhammad Sohaiǂ, Tohru Taniguchi, Kenji Monde, Fujie Tanaka*
Angew. Chem. Int. Ed. 2017,56, 5853-5857. (IF 16.823)
10. Multi-site cyclization via initial C–H activation using a rhodium(III) catalyst: rapid assembly of frameworks containing indoles and indolines
Ji-Rong Huangǂ, Liu Qinǂ, Yu-Qin Zhu, Qiang Song, Lin Dong*
Chem. Commun. 2015, 51,2844-2847.
9. Rhodium(III)-Catalyzed Three-Component Reaction of Imines, Alkynes, and Aldehydes through C−H Activation
Ji-Rong Huangǂ, Qiang Songǂ, Yu-Qin Zhu, Liu Qin, Zhi-Yong Qian*, Lin Dong*
Chem. Eur. J. 2014, 20,16882-16886.
8. Rhodium(III)-catalyzed Vinylic sp2C–H Bond Functionalization: Efficient Synthesis of Pyrido[1,2-α]benzimidazoles and Imidazo[1,2-α]pyridines
Lin Dong*, Ji-Rong Huang, Chuan-Hua Qu, Qian-Ru Zhang, Wei Zhang, Bo Han, Cheng Peng*
Org. Biomol. Chem. 2013, 11,6142-6149.
7. Rhodium(III)-Catalyzed Direct Selective C(5)–H Oxidative Annulations of 2-Substituted Imidazoles and Alkynes by Double C–H Activation
Ji-Rong Huang, Chuan-Hua Qu, Qian-Ru Zhang, Xun-Hao Sun, Lin Dong*, Ying-Chun Chen*
Org. Lett. 2013,15, 1878-1881.
6. Synthesis of Aza-Fused Polycyclic Quinolines via Double C–H Bond Activations
Ji-Rong Huang, Lin Dong*, Bo Han, Cheng Peng*, Ying-Chun Chen*
Chem. Eur. J. 2012, 18, 8896-8900.
5. Organocatalytic chemoselective asymmetricN-allylic alkylation of enamides
Ji-Rong Huang, Hai-Lei Cui, Jie Lei, Xun-Hao Sun, Ying-Chun Chen*
Chem. Commun. 2011,47, 4784-4786.
4. Rhodium-catalyzed Spirocyclic Sultams Synthesis by [3+2] Annulation with CyclicN-Sulfonyl Ketimines and Alkynes
Lin Dong, *Chuan-Hua Quǂ, Ji-Rong Huangǂ, Wei Zhang, Qian-Ru Zhang, Jin-Gen Deng
Chem. Eur. J. 2013, 19,16537-16540.
3. Highly Functionalized Pyridines Synthesis from N-Sulfonyl Ketimines and Alkynes Using the N−S Bond as an Internal Oxidant
Qian-Ru Zhang, Ji-Rong Huang, Wei Zhang, Lin Dong*
Org. Lett. 2014,16, 1684-1687.
2. Direct Asymmetric Allylic Alkylation of Butenolides with Morita Baylis Hillman Carbonates
Hai-Lei Cui, Ji-Rong Huang, Jie Lei, Zhao-Feng Wang, Shi Chen, Li Wu, Ying-Chun Chen*
Org.Lett. 2010, 12,720-723.
1. The application of Morita-Baylis-Hillman reaction: Synthetic studies on perophoramidine
Lin Wu, Qian-Ru Zhang, Ji-Rong Huang, Yang Li, Fu Su*, Lin Dong*
Tetrahedron, 2017,73, 3966-3972.
ǂCo-first author
