Name Zhou Zhenghong Gender Male Academic Background Doctor degree Graduate School Nankai University Professional Title professor Administrative Post Department/Institute Institute of Elemento-organic Chemistry Special Talent Address Telephone 23503891 Email z.h.zhou@nankai.edu.cn Research Group Website Research Interest Asymmetric catalysis Heteroatom Organic Chemistry History 1989–1993, Sichuan Normal Universtiy 1993–1998, Nankai Uiversity 1998–present, Institute of Elemento-Organic Chemistry, Nankai University Honors and Awards New Century Excellent Talents in University Scientific Achievements & Selected Publications 1. C. Wang, Z. Zhou*, C. Tang, Novel bifunctional chiral thiourea catalyzed highly enantioselective aza-Henry reaction, Org. Lett. 2008, 10, 1707. 2. T. Liu, Y. Wang, G. Wu, H. Song, Z. Zhou*, C. Tang, Organocatalyzed enantioselective Michael addition of 2-hydroxy-1,4-naphthoquinone to β,γ-unsaturated α-ketophosphonates, J. Org. Chem. 2011, 76, 4119. 3. R. Wu, X. Chang, A., Lu, Y. Wang, G. Wu, H. Song, Z. Zhou*, C. Tang, Chiral (thio)phosphorodiamides as excellent hydrogen bond donor catalysts in the asymmetric Michael addition of 2-hydroxy-1,4-naphthoquione to nitroolefins, Chem. Commun. 2011, 47, 5034. 4. A. Lu, T. Liu, R. Wu, Y. Wang, G. Wu, Z. Zhou*, J. Fang, C. Tang, A recyclable organocatalyst for asymmetric Michael addition of acetone to nitroolefins, J. Org. Chem. 2011, 76, 3872. 5. A. Lu, K. Hu, Y. Wang, H. Song, Z. Zhou*, J. Fang, C. Tang, Enantioselective Synthesis of trans-Dihydrobenzofurans via Primary Amine-Thiourea Organocatalyzed Intramolecular Michael Addition, J. Org. Chem. 2012, 77, 6208. 6. L. Wu, Y. Wang, H. Song, L. Tang, Z. Zhou*, C. Tang, Synthesis of optically active 2H-thiopyrano[2,3-b]quinolines with three contiguous stereocenters via an organocatalytic asymmetric tandem Michael-Henry reaction, Adv. Synth. Catal. 2013, 355, 1053. 7. L. Wu, Y. Wang, H. Song, L. Tang, Z. Zhou*, C. Tang, Enantioselective organocatalytic domino Michael-aldol reactions: An efficient protocol to stereocontrolled construction of 2H-thiopyrano[2,3-b]quinolone scaffolds, Chem. Asian J. 2013, 2204. 8. H. Yu, Q. Wang, Y. Wang, H. Song, Z. Zhou*, C. Tang, Stereoselective Synthesis of Highly Functionalized Nitrocyclopropanes via Organocatalyic Michael Addition initiated cyclization of bromonitromethane and β,γ-unsaturated α-ketoesters, Chem. Asian J. 2013, 8, 2859. 9. Y. Liu, Y. Wang, H. Song, Z. Zhou*, C. Tang, Asymmetric organocatalytic cascade Michael/hemiketalization/retro-aldol reaction of 2-((E)-2-nitrovinyl)phenols with 2,4-dioxo-4-arylbutanoates: A convenient access to chiral α-ketoesters, Adv. Synth. Catal. 2013, 355, 2544. 10. L. Wu, Y. Wang, H. Song, L. Tang, Z. Zhou*, C. Tang, Organocatalyzed highly diastereo- and enantioselective tandem sulfa-Michael-Mannich reaction of 2-mercaptoquinoline-3-carbaldimines with maleimides, ChemCatChem 2014, 6, 649. 11. Y. Liu, Q. Wang, Y. Wang, H. Song, Z. Zhou*, Chiral Bifunctional Squaramide-Catalyzed Highly Enantioselective Michael Addition of Allomaltol to β, γ-Unsaturated α-Ketoesters, ChemCatChem, 2014, 6, 2298. 12. Y. Zhen, Y. Wang, Z. Zhou*, Organocatalytic Multicomponent Synthesis of Polysubstituted Pyrroles from 1,2-diones, aldehydes and arylamines, Chem. Commun. 2015, 51, 11652. 13. Y. Wang, J. Pan, S. Chen, Y. Wang, Z. Zhou*, Sterercontrolled construction of 3,4-dihydrocoumarin scaffolds with a quaternary amino acid moiety via chiral squaramide catalyzed cascade Michael addition/lactonization reaction, Adv. Synth. Catal. 2015, 357, Doi: 10.1002/adsc.201500862. Professional Cultivation