王荣华，理学博士，青年博士生导师。贵州省科技创新青年拔尖人才（2026）、贵州医科大学优秀青年人才（2025）。
教育&工作背景：
2022.8-至今副研究员贵州医科大学（汤磊教授团队）
2016.9-2022.6 理学博士南开大学有机化学（指导教师：叶萌春教授）
2012.8-2016.8 理学学士中国农业大学应用化学
联系方式：wrhchem@163.com
研究方向：有机合成方法学，过渡金属催化；小分子药物合成及活性测试
科研项目情况：
（1）国家自然科学基金青年基金；22401056；基于酰胺C-N活化的不饱和键胺-酰化反应研究；2025.1-2027.12；30万元；在研；主持。
（2）国家自然科学基金地区基金；22361013；面手性1,3-二取代二茂铁的精准构筑；2024.1-2027.12；32万元；在研；主持。
（3）贵州省科技厅一般项目；ZK[2024]-129；镍催化烯丙醇C-C键官能团化反应研究；2024.4-2027.4；10万元；在研；主持。
(4)贵州医科大学优秀青年人才培养计划；100万元；2025,8-2030,7 （5）国重室基础研究项目；“芳烃-金属π活化”促进Ni催化简单芳烃C-H官能化；TS25064; 40万元；在研；主持。
(6)贵州省科技厅科技创新青年拔尖人才计划；KJLYRC-[2026]138；50万元；2026.4-2031.3；在研；主持
（7）贵州省卫生健康委科学技术基金项目；gzwkj2024-511；含烯丙醇骨架生物活性分子的高效构建及其活性研究；2024.4-2026.12；2万元；在研；主持。
（8）贵州医科大学高层次人才启动基金；[2022]033；苯并咪唑非C2位C-H键选择性官能化研究；2022.11-2025.10；10万元；结题；主持。
（9）贵州医科大学国基培育项目；22NSFCP22；面手性1,3-二取代二茂铁的精准构筑；2023.1-2025.12; 5万元；结题；主持。
代表性论著：
(1)R.-H. Wang,#W.-W. Xu,#D. Pan,#Y. Zheng, C. Yu, J.-F. Li, T. Zhang, Y. Li, X.-S. Xue,* Q.-L. Zhou, and M. Ye.* Selective C–C Bond Cleavage-Enabled Annulation betweenβ-Lactams and π-Systems via Ni–Al Bimetallic Catalysis.Nat. Catal.2026. (accepted)
(2)M.-B. Gou, D.-Y. Gou, C.-M. Yang, X.-C. Wei, B. Li, J. Shi,* C. Zhao,* L. Tang,*andR.-H. Wang.*Ni-Catalyzed (A + 2B)-Type Reductive Coupling of Electron-Deficient Alkenes and Alkynes through a Selective Trimerization/1,6-Reduction Cascade.Org. Lett.2026,28, 1766.
(3) B. Li, Q. Peng, J.-X. Wang, M.-B. Gou, H.-J. Zhao, Y.-X. He, Z.-Q. Luo, Q. He, B. Liu, M. Li,* L. Tang, J. Huang,* andR.-H. Wang.* External ligand-free nickel-catalyzed atom-economical coupling of isatins with allyl alcohols via a redox-relay strategy.Chem. Commun.2025,61, 6961.
(4) X. Kong, M.-B. Gou, B. Li, Z.-Q. Luo, Y. Su, Y. Li, C. Yang, B. Liu, Q. He, J.-F. Li,* J. Zhang, J. Wang, L. Tang,* andR.-H. Wang.* Nickel-Catalyzed Rearranged Alkenylation of 2‑Arylaziridines with Aryl Alkenes to Access Allylamines.Org. Lett.2025,27, 2709.
(5)R.-H. Wang,* B. Li, M.-B. Gou, Z.-Q. Luo, B. Liu, Y. Li, X. Kong, Q. He, S. He, J.-F. Li, J. Huang,* J. Wang, J. Zhang, and L. Tang.* Redox-Neutral Coupling of Allyl Alcohols with Trifluoromethyl Ketones via Synergistic Ni−Ti Bimetallic Catalysis.Org. Lett.2024,26, 7408.
(6)R.-H. Wang,* Z. Zhang, B. Li, G.-F. Zhu, J. Shi, L. Tang.*p-Cresol-Enabled Nickel-Catalyzed Intermolecular Redox-Economical Coupling of Allyl Alcohols with Alkynes through Oxa-Nickelacycle.Org. Lett.2023,25, 8463.
(7)R.-H. Wang,#W.-W. Xu,#H. Wu, Y. Li, J.-F. Li, T. Zhang, G. Huang,* and M. Ye.* Ni-catalyzed benzylicβ-C(sp3)–H bond activation of formamides.Nat. Commun.2022,13, 7892.
(8)R.-H. Wang, J.-F. Li, Y. Li, S.-L. Qi, T. Zhang, Y.-X. Luan,* and M. Ye.* Selective C(sp3)−H Cleavage of Enamides for Synthesis of 2-Pyridones via Ligand-Enabled Ni−Al Bimetallic Catalysis.ACS Catal.2021,11, 858.
(9)R.-H. Wang, Y.-X. Luan,* and M. Ye.* Transition Metal-Catalyzed Allylic C(sp3)-H Functionalization viaη3-Allylmetal Intermediate.Chin. J. Chem.2019,37, 720.
(10)R.-H. Wang, M. Ye.* Nickel-Catalyzed Asymmetric C−H Functionalization, Wiley,2022(Handbook of CH-Functionalization)
(11) F.-P. Zhang,R.-H. Wang, J.-F. Li, H. Chen, M. H. Babu, M. Ye.* Intermolecular Carbophosphination of Alkynes with Phosphole Oxides via Ni−Al Bimetal-Catalyzed C−P Bond Activation.Angew. Chem. Int. Ed.2023,62, e2023147.
(12) J.-F. Li, W.-W. Xu,R.-H. Wang, Y. Li, G. Yin, M. Ye.* Construction 7-membered ring via Ni–Al bimetal-enabled C-H cyclization for synthesis of tricyclic imidazoles.Nat. Commun.2021,12, 3070.
(13) G. Yin,#Y. Li,#R.-H. Wang, J.-F. Li, X.-T. Xu, Y.-X. Luan, M. Ye.* Ligand-Controlled Ni(0)−Al(III) Bimetal-Catalyzed C3−H Alkenylation of 2‑Pyridones by Reversing Conventional Selectivity.ACS Catal.2021,11, 4606.
(14) Y. Li, F.-P. Zhang,R.-H. Wang, S.-L. Qi, Y.-X. Luan, M. Ye.* Carbamoyl Fluoride-Enabled Enantioselective Ni-Catalyzed Carbocarbamoylation of Unactivated Alkenes.J. Am. Chem. Soc.2020,142, 19844.
(15) J.-F. Yang,R.-H. Wang, Y.-X. Wang, W.-W. Yao, Q.-S. Liu, M. Ye.* Ligand‐Accelerated Direct C-H Arylation of BINOL: A Rapid One‐Step Synthesis of Racemic 3, 3′-Diaryl BINOLs.Angew. Chem. Int. Ed.2016,55, 14116.
