周正洪（Z.H. Zhou），教授，南開大學元素有機國家重點實驗室（SKLEOC）的教授
基本介紹
- 中文名：周正洪
- 外文名：Z.H.Zhou
- 國籍：中國
- 民族：漢族
- 出生地：四川綿陽江油
- 出生日期：1971-7
- 職業：教師
- 畢業院校：南開大學
教育及科研經歷：
學士， 1989–1993 四川師範學院化學系
博士， 1993-1998 南開大學元素有機所
教師， 1998–至今 南開大學元素有機所
博士， 1993-1998 南開大學元素有機所
教師， 1998–至今 南開大學元素有機所
榮譽和獎勵：
教育部新世紀優秀人才
研究領域：
不對稱催化；雜原子有機化學
科研成果與代表作：
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.
14.Yin Zheng, Lei Cui, Youming Wang, and Zhenghong Zhou*,Stereocontrolled Construction of Tetrahydropyrano[2,3‑c]pyrazoleScaffold via an Organocatalyzed Formal [3 + 3] Annulation,J. Org. Chem. 2016, 81, 4340−4346,DOI: 10.1021/acs.joc.6b00196.
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.
14.Yin Zheng, Lei Cui, Youming Wang, and Zhenghong Zhou*,Stereocontrolled Construction of Tetrahydropyrano[2,3‑c]pyrazoleScaffold via an Organocatalyzed Formal [3 + 3] Annulation,J. Org. Chem. 2016, 81, 4340−4346,DOI: 10.1021/acs.joc.6b00196.
