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黄焕明研究员,博士毕业于英国曼彻斯特大学,导师是Prof. David Procter。随后在德国洪堡基金的资助下,在德国明斯特大学开展博士后研究,合作导师为德国科学院院士Prof. Frank Glorius。迄今为止,以(共同)通讯或(共同)第一作者身份发表学术论文数篇,包括:Nature Catalysis,Nature Synthesis,J. Am. Chem. Soc.,Angew. Chem. Int. Ed.,Chem. Soc. Rev.,Nature Rev. Chem.等。2021年,黄焕明研究员加入上海科技大学,组建自由基化学实验室,担任课题组长,获得多个重要项目资助。目前以通讯作者身份在Nature Synthesis,Angew. Chem. Int. Ed.,Acc. Chem. Res.等期刊发表论文数篇。
黄焕明,助理教授、研究员
Address: 上海科技大学物质学院3号楼405-2
Email: huanghm@shanghaitech.edu.cn
ORCiD: orcid.org/0000-0001-9461-6508
Researcher ID: AAB-1528-2019
Website: https://huanminghuang.wixsite.com/huanggroup
Career and education:
2021-now,上海科技大学,助理教授、研究员∣Assistant Professor (Tenure Track), Principal Investigator, ShanghaiTech University
2018-2021,德国明斯特大学,洪堡学者∣Humboldt Fellow, University of Münster (Mentor: Prof. Frank Glorius)
2017-2018,英国曼彻斯特大学,博士后∣EPSRC Postdoc Research Fellow, The University of Manchester (Mentor: Prof. David J. Procter)
2014-2017,英国曼彻斯特大学,哲学博士∣Ph.D. at The University of Manchester (Supervisor: Prof. David J. Procter)
Selected Awards & Honors:
n Alexander von Humboldt Fellowship (2018)
n CSC Chinese National Excellent Self-Funded Students Scholarship (2016)
n Prestigious President's Scholarship of The University of Manchester (2014)
Service:
n Reviewer for Springer Nature, Wiley, Cell Press, Elsevier and Royal Society of Chemistry journals, including:
n Angewandte Chemie n Nature Synthesis n Chem.Commun. n Chemical Science n Chem. Eur. J. n iScience
Research
We are a young research team working in School of Physical Science and Technology at ShanghaiTech University. Our research is focused on radical chemistry and catalysis.
At present, we have two main research directions:
1) Develop novel radical chemistry in the emerging areas, such as photoredox chemistry and electrosynthesis, to rapid construct complex bio-active molecules and provide alternative approaches to the solve the limitations in the area of medicinal, materials, energy and environmental chemistry.
2) Rationally design novel catalysts and ligands in order to discovery novel chemical transformations and contribute the development of develop sustainable chemistry.
Publication
2022
10. Jun-Jie Chen and Huan-Ming Huang*, N2O revalorization, Nature Chem. 2022, DOI: 10.1038/s41557-022-01007-x. (News & Views)
9. Huan-Ming Huang*, "Electrifying cross-electrophile coupling", Nature Synth. 2022, DOI: 10.1038/s44160-022-00102-8. (News & Views)
8. Ying Zhang,+ Jun-Jie Chen+ and Huan-Ming Huang*, "Radical Brook Rearrangement: Concept and Recent Developments", Angew. Chem. Int. Ed. 2022, DOI: 10.1002/anie.202205671.
7. Jun-Jie Chen,+ Ying Zhang+ and Huan-Ming Huang*, Radical umpolung chemistry enabled by dual catalysis: concept and recent advances, Catal. Sci. Technol. 2022, DOI: 10.1039/D2CY01161A.
6. Jun-Jie Chen and Huan-Ming Huang*, Merging Halogen-Atom transfer with transition metal catalysis, Tetrahedron Lett., 2022, 153945.
5. Huan-Ming Huang*,+ Peter Bellotti,+ Suhyeon Kim, Xiaolong Zhang and Frank Glorius*, “Catalytic multicomponent reaction involving a ketyl-type radical”, Nature Synth. 2022, DOI: 10.1038/s44160-022-00085-6.
4. Peter Bellotti,+ Huan-Ming Huang,+ Teresa Faber, Ranjini Laskar and Frank Glorius*, “Catalytic defluorinative ketyl–olefin coupling by halogen-atom transfer”, Chem. Sci. 2022, DOI:10.1039/d2sc02732a.
3. Huan-Ming Huang*,+ Peter Bellotti,+ and Frank Glorius*, “Merging Carbonyl Addition with Photocatalysis”, Acc. Chem. Res. 2022, 55, 1135.
2. Huan-Ming Huang,+ Peter Bellotti,+ Johannes E. Erchinger, Tiffany O. Paulisch and Frank Glorius*, “Radical Carbonyl Umpolung Arylation via Dual Nickel Catalysis”, J. Am. Chem. Soc. 2022, 144, 1899.
1. Huan-Ming Huang,+ Peter Bellotti,+ Pan-Pan Chen,+ Kendall N. Houk* and Frank Glorius*, “Allylic C(sp3)–H arylation of olefins via ternary catalysis”, Nature Synth. 2022, 1, 59.
Before joining ShanghaiTech
12. Huan-Ming Huang,‡ Peter Bellotti,‡ (‡These authors contributed equally) and Frank Glorius*, “Bifunctional Reagents in Organic Synthesis”, Nat. Rev. Chem. 2021, 5, 301.
11. Huan-Ming Huang, Peter Bellotti, Constantin Daniliuc and Frank Glorius*, “Radical Carbonyl Propargylation by Dual Catalysis”, Angew. Chem. Int. Ed. 2021, 60, 2464.
10. Huan-Ming Huang,‡ Peter Bellotti,‡ (‡These authors contributed equally) and Frank Glorius*, “Transition-metal catalysed allylic functionalization reaction involving radicals”, Chem. Soc. Rev. 2020, 49, 6186.
9. Huan-Ming Huang, Peter Bellotti, Philipp Miro Pflueger, J. Luca Schwarz, Bastian Heidrich and Frank Glorius*, “Three-Component, Interrupted Radical Heck/Allylic Substitution Cascade Involving Unactivated Alkyl Bromides”, J. Am. Chem. Soc. 2020, 142, 10173.
8. Huan-Ming Huang, Maximilian Koy, Eloisa Serrano, Philipp Miro Pflüger, J. Luca Schwarz and Frank Glorius*, “Catalytic radical generation of π-allylpalladium complexes”, Nat. Catal. 2020, 3, 393.
7. J. Luca Schwarz,‡Huan-Ming Huang,‡ (‡These authors contributed equally) Tiffany O. Paulisch, and Frank Glorius*, “Dialkylation of 1,3-Dienes by Dual Photoredox and Chromium Catalysis”, ACS Catal. 2020, 10, 1621.
6. Huan-Ming Huang, Monserrat H. Garduño-Castro, Charlotte Morrill and David J. Procter*, “Catalytic Cascade Reactions by Radical Relay”, Chem. Soc. Rev. 2019, 48, 4626.
5. Huan-Ming Huang, J. J. W. McDouall, and David J. Procter*, “SmI2-catalysed Cyclisation Cascades by Radical Relay”,Nat. Catal. 2019, 2, 211.
4. Huan-Ming Huang, J. J. W. McDouall and David J. Procter*, “Radical Anions from Urea-type Carbonyls: Radical Cyclisations and Cyclisation Cascades”,Angew. Chem. Int. Ed. 2018, 57, 4995.
3. Huan-Ming Huang and David J. Procter*, “Dearomatizing Radical Cyclisations and Cyclisation Cascades Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls”, J. Am. Chem. Soc. 2017, 139, 1661.
2. Huan-Ming Huang and David J. Procter*, “Radical Heterocyclisation and Heterocyclisation Cascades Triggered by Electron Transfer to Amide-Type Carbonyls”, Angew. Chem. Int. Ed. 2017, 56, 14262.
1. Huan-Ming Huang and David J. Procter*, “Radical-Radical Cyclisation Cascades of Barbiturates Triggered by Electron-Transfer Reduction of Amide-Type Carbonyls”, J. Am. Chem. Soc. 2016, 138, 7770.
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