郭昌
郭昌 教授合肥微尺度物质科学国家实验室(筹)
- 中文名:
介绍
姓名: 郭昌
生日: 1987年6月
地址: 合肥微尺度物质科学国家实验室(筹)
中国科学技术大学
邮编: 230026
电话: 15155932590
邮箱: guochang@ustc.edu.cn
教育与科研经历
2018.03 - 至今 特任教授,博士生导师,合肥微尺度物质科学国家研究中心,中组部“青年**计划”入选者
2017.02-2018.02 特任研究员,中国科学技术大学,合肥微尺度物质科学国家研究中心
2013.08-2017.01 博士后,德国明斯特大学
2007.09-2013.06 博士,中国科学技术大学
2003.08-2007.06 学士,中国科学技术大学
研究方向
研究工作主要集中在不对称合成方向,以新型不对称催化研究为基础,发展惰性化学键的直接手性官能团化反应,建立手性催化模型,提高反应活性与选择性,并将这些方法学用于天然产物的合成,发展高效、原子经济性和环境友好的现代有机合成化学。
代表性论文
1) Guo, C.*; Janssen-Müller, D.; Fleige, M.;Lerchen, A.; Daniliuc, C. G.; Glorius, F.*Mechanistic studies on a cooperative NHC organocatalysis/palladium catalysis system: uncovering significant lessons for mixed chiral Pd(NHC)(PR3) catalyst design. J. Am. Chem. Soc. 2017,ASAP, DOI: 10.1021/jacs.7b00462.
2) Guo, C.; Fleige, M.; Janssen-Müller, D.; Daniliuc, C. G.; Glorius, F.* Cooperative N-heterocyclic carbene/palladium-catalyzed enantioselective umpolungannulations, J. Am. Chem. Soc. 2016, 138, 7840-7843.
3) Guo, C.; Fleige, M.; Janssen-Müller, D.; Daniliuc, C. G.; Glorius, F. *Switchable selectivity in an NHC-catalyseddearomatizing annulation reaction, Nat. Chem.2015, 7, 842-847.
4) Guo,C.;Sahoo, B.;Daniliuc,C. G.;Glorius,F.*N-Heterocyclic carbenecatalyzed switchable reactions of enals with azoalkenes: formal [4+3] and [4+1] annulations for the synthesis of 1,2-diazepines and pyrazoles, J. Am. Chem. Soc. 2014, 136,17402-17405.
5) Guo, C.;Schedler, M.;Daniliuc, C. G.;Glorius,F.*N-Heterocyclic carbenecatalyzed formal [3+2] annulation reaction of enals: an efficient enantioselective access to spiro-heterocycles, Angew. Chem. Int. Ed. 2014, 53, 10232-10236.
6) Guo, C.; Song, J.; Huang, J.-Z.; Chen, P.-H.; Luo, S.-W.; Gong, L.-Z. *Core-structure-oriented asymmetric organocatalyticsubstitution of3-hydroxyoxindoles: application in the enantioselective total synthesis of (+)-folicanthine. Angew. Chem. Int. Ed. 2012, 51, 1046-1050.
7) Guo, C.; Song, J.; Luo, S.-W.; Gong, L.-Z. *Enantioselective oxidative cross-coupling reaction of 3-indolylmethyl C-H bonds with 1,3-dicarbonyls using a chiral Lewis acid-bonded nucleophile to control stereochemistry. Angew. Chem. Int. Ed. 2010, 49, 5558-5562.
8) Guo, C.; Xue, M.-X.; Zhu, M.-K.; Gong, L.-Z.* Organocatalytic asymmetric formal [3+2] cycloaddition reaction of iocyanoesters to nitroolefinsleading to highly optically active dihydropyrroles. Angew. Chem. Int. Ed. 2008, 47, 3414-3417.