榮子強，男，博士，西北工業大學柔性電子研究院教授。
基本介紹
- 中文名：榮子強
- 學位/學歷：博士
- 職業：教師
- 任職院校：西北工業大學
- 職稱：教授
個人經歷,榮譽獎項,研究方向,學術成果,
個人經歷
教育經歷 Education Experience
2012-2013：新加坡國立大學，Research Associate (導師：Zhao Yu教授)
2008-2011：瀋陽化工大學與中科院上海有機所聯合培養碩士研究生（導師：游書力 研究員）
工作經歷 Work Experience
2018.10-至今，西北工業大學柔性電子研究院，教授
2017-2018：芝加哥大學 (博士後合作導師：Dong Guangbin 教授)
榮譽獎項
2019 陝西省特聘青年人才計畫（原陝西省百人計畫）
2018 西北工業大學翱翔海外學者
2016 國家優秀留學生獎學金
研究方向
研究工作主要集中於有機合成方法學，涉及領域包括過渡金屬催化、有機小分子催化、不對稱催化等。
學術成果
主持的基金
2019年 陝西省特聘青年人才基金（主持）
2019年 國家自然科學基金青年基金（主持）
2018年 西北工業大學翱翔海外青年學者基金（主持）
1: Rong, Z.-Q.; Lim, H. N.; Dong, G.* Intramolecular Acetyl Transfer to Olefins via Catalytic C-C Bond Activation of Unstrained Ketones. Angew. Chem. Int. Ed. 2018, 57, 475-479.
2: Rong, Z.-Q.;# Yang, L.-C.;# Liu, S.; Yu, Z.; Wang, Y.-N.; Tan, Z. Y.; Huang, R.-Z.; Lan, Y.; Zhao, Y.* Nine-Membered Benzofuran-Fused Heterocycles: Enantio-selective Synthesis by Pd-Catalysis and Rearrangement via Transannular Bond Formation. J. Am. Chem. Soc. 2017, 139, 15304-15307. (Highlighted in Synfacts and X-MOL)
3: Yang, L.-C.;# Rong, Z.-Q.;# Wang, Y.-N.; Tan, Z. Y.; Wang, M.; Zhao, Y.* Construction of Nine-Membered Heterocycles through Palladium-Catalyzed Formal [5 + 4] Cycloaddition. Angew. Chem. Int. Ed. 2017, 56, 2927？2931. (#Co-First author). (ESI高被引論文，Highlighted in Synfacts and X-MOL)
4: Rong, Z.-Q.; Wang, M.; Zhao, Y.* Diastereodivergent organocatalytic asymmetric aza-Diels-Alder reaction: complementarity of N-heterocyclic carbene and chiral amine. Chem. Eur. J. 2016, 22, 9483-9487. (被選為後封面文章和熱點文章)
5: Rong, Z.-Q.; Zhang, Y.; Chua, R. H. B.; Pan, H.-J.; Zhao, Y.* Dynamic Kinetic Asymmetric Amination of Alcohols: From A Mixture of Four Isomers to Diastereo- and Enantiopure a-Branched Amines. J. Am. Chem. Soc. 2015, 137, 4944-4947.
6: Wang, M.;# Rong, Z.-Q.;# Zhao, Y.* Stereoselective Synthesis of ε-Lactones or Spiro-Heterocycles through NHC-Catalyzed Annulation: Divergent Reactivity by Catalyst Control. Chem. Comm. 2014, 50, 15309-15312. (#Co-First author).
7: Rong, Z.-Q.; Pan, H.-J.; Yan, H.-L.; Zhao, Y.* Enantioselective Oxidation of 1,2-Diols with Quinine-derived Urea Organocatalyst. Org. Lett. 2014, 16, 208-211.
8: Rong, Z.-Q.; Jia, M.-Q.; You, S.-L.* Enantioselective N-Heterocyclic Carbene-Catalyzed Michael Addition to α,β-Unsaturated Aldehydes by Redox Oxidation. Org. Lett. 2011, 13, 4080-4083.
9: Rong, Z.-Q.; Li, Y.; Yang, G.-Q.; You, S.-L.* D-Camphor-derived Triazolium Salts for Enantioselective Intramolecular Stetter Reactions. Synlett 2011, 1033-1037. (紀念陸熙炎院士和戴立信院士從教60周年應邀專刊).
10: Rong, Z.-Q.; Zhang, W.; Yang, G.-Q.;* You, S.-L.* N-Heterocyclic Carbene-Catalyzed Redox Reactions of α-Functionalized Aldehydes. Curr. Org. Chem. 2011, 15, 3077-3090.
11: Rong, Z.-Q.; Jia, M.-Q.; You, S.-L.* (1R,2R)-DPEN-Derived Triazolium Salts for Enantioselective Oxodiene Diels-Alder Reactions. Tetrahedron 2011, 67, 9329-9333.
12: Yang, L.-C.; Tan, Z. Y.; Rong, Z.-Q.; Liu, R.; Wang, Y.-N.; Zhao, Y.* Pd-Titanium Relay Catalysis Enables Switch of Alkoxide-π-Allyl to Dienolate Reactivity for Spiro-Heterocycle Synthesis. Angew. Chem. Int. Ed. 2018, 57, 7860-7864.
13: Wang, Y.-N.; Yang, L.- C.; Rong, Z.-Q.; Liu, T.-L.; Liu, R.; Zhao, Y.* Pd-Catalyzed Enantioselective [6+4] Cycloaddition of Vinyl Oxetanes with Azadienes to Access Ten-Membered Heterocycles. Angew. Chem. Int. Ed. 2018, 57, 1596-1600. （ESI高被引論文, Highlighted in Synfacts）
14: Paderes, M. C.;* Siau, W. Y.; Rong, Z.-Q.; Zhao, Y.* Catalytic and Enantioselective Direct α-Alkylation of 3-Aryl and 3-Alkyl Oxindole Using Quinine-Derived Urea Catalyst. Chem. Select 2018, 3, 6160-6164.
15: Gu, Q.; Rong, Z.-Q.; Zheng, C.; You, S.-L.* Desymmetrization of Cyclohexadienones via Br？nsted Acid-Catalyzed Enantioselective Oxo-Michael Reaction. J. Am. Chem. Soc. 2010, 132, 4056-4057.
16: Jia, M.-Q.; Li, Y.; Rong, Z.-Q.; You, S.-L.* Synthesis of (1R,2R)-DPEN-Derived Triazolium Salts and Their Application in Asymmetric Intramolecular Stetter Reactions. Org. Biomol. Chem. 2011, 9, 2072-2074.
17: Wu, Q.-F.; Liu, W.-B.; Zhuo, C.-X.; Rong, Z.-Q.; Ye, K.-Y.; You, S.-L.* Iridium-Catalyzed Intramolecular Asymmetric Allylic Dearomatization of Phenols. Angew. Chem. Int. Ed. 2011, 50, 4455-4458.
