周锋 副教授
化学与分子工程学院??????


导航
个人资料
研究方向
开授课程
科研项目
学术成果
荣誉及奖励







个人资料
部门： 化学与分子工程学院
毕业院校：
学位：
学历：
邮编：
联系电话：
传真：
电子邮箱： fzhou@chem.ecnu.edu.cn
办公地址： 化学馆C-201室
通讯地址： 上海市普陀区中山北路3663号华东师范大学化学馆C-201室

教育经历
(1) 2005.9–2009.6, 四川师范大学, 材料化学, 学士
(2) 2009.9–2014.6, 华东师范大学, 有机化学, 博士, 导师: 周剑
(3) 2014.7-2017.12, 华东师范大学, 化学与分子工程学院, 讲师
(4) 2017.12-至今, 华东师范大学, 化学与分子工程学院, 副教授

工作经历

个人简介

社会兼职


研究方向
主要围绕化学固定二氧化碳开展研究工作，探索二氧化碳参与的不对称催化新反应，通过开发更为高效的催化体系，基于电化学催化或不对称串联反应等策略，实现系列手性环碳酸酯或手性羧酸等系列化合物额高立体选择性合成。




开授课程
本科生教学
2016年至今 担任本科生《有机化学实验》教学工作
2018年至今 开设本科生选修课程《化学中的人类文明》
2019年9月 担任本科生基础必修课程《有机化学》教学工作
研究生教学
2016年至今 担任《实验室安全与法律法规》研究生必修课程教学工作
2018年至今 担任《不对称催化》研究生专业选修课程教学工作


科研项目
1. 国家自然科学基金面上项目，**，二氧化碳作为C1 合成子的不对称催化反应研究，2019/01-2022/12，主持
2. 国家自然科学基金青年基金项目，**，手性硫缩醛/酮的不对称催化合成研究，2016/01-2018/12，主持
3. 国家自然科学基金面上项目，**，铜催化的叠氮和炔烃的不对称环加成反应研究（主持人：周剑教授），2017/01-2020/12，参与（第二）
4. 国家自然科学基金****基金项目，**，不对称催化（主持人：周剑教授），2018/01-2022/12，参与（第二）


学术成果

1.C. Wang,R.-Y. Zhu,K. Liao,F. Zhou,*andJ. Zhou*, Enantioselective Cu(I)-Catalyzed Cycloaddition of Prochiral Diazides with Terminal or 1-Iodoalkynes, Org. Lett., 2020, 22, 1270-1274.
2.X.-T. Gao, S.-L. Xie, F. Zhou*, H.-H. Wu*, J. Zhou*, Multifunctional 1,3-diphenylguanidine for the carboxylative cyclization of homopropargyl amines with CO₂under ambient temperature and pressure.Chem. Commun.2019, 55, 14303-14306.
3.S.-L. Xie, X.-Y. Cui, X.-T. Gao, F. Zhou*, H.-H. Wu*, J. Zhou, Stereoselective defluorinative carboxylation of gem-difluoroalkenes with carbon dioxide. Org. Chem. Front.2019, 6, 3678-3682.
4.S. Xie, X. Gao, F. Zhou*, H. Wu*, J. Zhou*, Enantioselective carboxylative cyclization of propargylic alcohol with carbon dioxide under mild conditions. Chinese Chem. Lett.2019, DOI: 10.1016/j.cclet.2019.05.060.
5.P.-W. Xu,J.-S. Yu,*C. Chen,Z.-Y. Cao,F. Zhou, J. Zhou*, Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters. ACS Catal.2019, 9, 1820?1882.
6.Y.-H.Wang,J.-S.Tian,P.-W.Tan,Q.Cao,X.-X.Zhang,Z.-Y.Cao,F.Zhou,X.Wang,*Jian Zhou*, Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles. Angew.Chem.Int.Ed.2019, DOI:10.1002/anie.
7.K.Liao,X.-S.Hu,R.-Y.Zhu,R.-H.Rao,J.-S.Yu,*F.Zhou,J.Zhou*, Catalytic Enantioselective Protonation of Monofluorinated Silyl Enol Ethers towards Chiral α-Fluoroketones. Chin. J. Chem.2019, 37, 799-806.
8.Y.Gong,Z.-Y.Cao,Y.-B.Shi,F.Zhou,Y.Zhou*, J.Zhou*, A highly efficient Hg(OTf)₂-mediated Sakurai–Hosomi allylation of N-tert-butyloxycarbonylamino sulfones, aldehydes, fluoroalkyl ketones and α,β-unsaturated enones using allyltrimethylsilane. Org. Chem. Front.2019,DOI: 10.1039/c9qo01049a.
9.Z.-Y.Cao,F.Zhou, J.Zhou* Development of Synthetic Methodologies via CatalyticEnantioselective Synthesis of 3,3-Disubstituted Oxindoles. Acc. Chem. Res.2018, 51, 1443?1454.
10.F. Liao,Y. Du,F.Zhou,J.Zhou*,Au(I)/Chiral Tertiary Amine Catalyzed Tandem Olefination/Asymmetric Cyclization Reaction to Quaternary Spirocyclic Oxindoles. Acta Chim. Sinica2018, 76, 862-868.
11.P.-W.Xu,C.Chen,J.-K.Liu,Y.-T.Song,F.Zhou*,J.Yan*,J.Zhou*, One-Pot Sequential [3 + 3] Dipolar Cycloaddition of Aldehyde or Ketone and Hydroxylamine with Spirocyclopropyl Oxindole. J. Org. Chem.2018, 83, 12763?12774.
12.P.-G.Ding, X.-S. Hu,F.Zhou*, J.Zhou*, Catalytic enantioselective synthesis of α-chiral azides. Org. Chem. Front., 2018, 5, 1542-1559.
13.Y.-J.Hao,X.-S.Hu, J.-S.Yu, F.Zhou, Y.Zhou*, J.Zhou*, An efficient Fe(III)-catalyzed 1,6-conjugate addition of para-quinone methides with fluorinated silyl enol ethers toward β,β-diaryl afluorinated ketones. Tetrahedron 2018, 74, 7395-7398.
14.X.-T. Gao, C.-C. Gan, S.-Y. Liu,F. Zhou*, H.-H. Wu*, J. Zhou*, Utilization of CO₂as a C1 Building Block in a Tandem Asymmetric A³Coupling-Carboxylative Cyclization Sequence to 2?Oxazolidinones. ACS Catal.2017,7, 8588-8593.
15.F. Zhou*, S.-L. Xie, X.-T. Gao, R. Zhang,* C.-H. Wang, G.-Q. Yin, J. Zhou* Activation of (salen)CoI complex by phosphorene for carbon dioxide transformation at ambient temperature and pressure. Green Chem., 2017, 19, 3908-3915.
16.J.-S. Yu,H.-M. Huang,P.-G. Ding,X.-S. Hu,F. Zhou, J. Zhou,* Catalytic Enantioselective Construction of Sulfur-Containing Tetrasubstituted Carbon StereocentersACS Catal. 2016, 6, 5319-5344.
17.J.-S. Yu, W.-B. Wu, F. Zhou*, The first catalytic asymmetric thioacetalization by chiral phosphoric acid catalysis, Org. Biomol. Chem.2016, 14, 2205-2209.
18.X.-P. Zeng,Z.-Y. Cao,Y.-H. Wang,F. Zhou,J. Zhou,*Catalytic Enantioselective Desymmetrization Reactions to All-Carbon Quaternary StereocentersChem. Rev. 2016,116, 7330-7396.
19.X.-P. Zeng, Z.-Y. Cao, X. Wang, L. Chen, F. Zhou, F. Zhu, C.-H. Wang, J. Zhou,*Activation of Chiral (Salen)AlCl Complex by Phosphorane for Highly Enantioselective Cyanosilylation of Ketones and EnonesJ. Am. Chem. Soc.2016, 138, 416-425.
20.K. Liao, F. Zhou*, J.-S. Yu, W.-M. Gao, J. Zhou, Catalytic asymmetric sulfenylation to structurally diverse dithioketals, Chem. Commun.2015, 51, 16255-16258.
21.J.-S. Yu, F. Zhou, Y.-L. Liu, J. Zhou,*A Journey in the Catalytic Synthesis of 3-Substituted 3-Aminooxindoles Synlett2015, 26, 2491-2504.
22.F.-M. Liao, Y.-L. Liu, J.-S. Yu,F. Zhou, J. Zhou,*An efficient catalyst-free Mukaiyama-aldol reaction of fluorinated enol silyl ethers with tryptanthrinOrg. Biomol. Chem.,2015,13, 8906-8911.
23.Z.-Y. Cao, W. D. G. Brittain, J. S. Fossey,F. Zhou* Recent advances in the use of chiral metal complexes with achiral ligands for application in asymmetric catalysisCatal. Sci. Technol. 2015, 5, 3441-3451
24.X.-P. Yin,P.-W. Xu, K. Dong, K. Liao, F. Zhou, J. Zhou,*Ga(OTf)₃催化的3-羟基氧化吲哚与TMSN₃的取代反应研究Acta Chim. Sinica,2015, 73, 685-689.
25.L. Chen, Y. Du, X.-P. Zeng, T.-D. Shi, F. Zhou, J. Zhou,*Successively Recycle Waste as Catalyst: A One-Pot Wittig/1,4-Reduction/Paal–Knorr Sequence for Modular Synthesis of Substituted FuransOrg. Lett. 2015? 17,1557-1560.
26.F. Zhu, P.-W. Xu, F. Zhou, C.-H. Wang* and J. Zhou,*Recycle Waste Salt as Reagent: A One-Pot Substitution/Krapcho Reaction Sequence to α-Fluorinated Esters and SulfonesOrg. Lett.2015? 17, 972-975.
27.W.-M. Gao, J.-S. Yu, Y.-L. Zhao, Y.-L. Liu, F. Zhou, H.-H. Wu,* J. Zhou,*Highly enantioselective Michael addition of 3-arylthio- and 3-alkylthiooxindoles to nitroolefins catalyzed by a simple cinchona alkaloid derived phosphoramideChem. Commun.2014, 50, 15179-15182.
28.X.-P. Yin, X.-P. Zeng,Y.-L. Liu, F.-M. Liao, J.-S. Yu, F. Zhou, J. Zhou,*Asymmetric Triple Relay Catalysis: Enantioselective Synthesis of Spirocyclic Indolines through a One-Pot Process Featuring an Asymmetric6π ElectrocyclizationAngew. Chem. Int. Ed. 2014? 53,13740-13745.
29.F. Zhou, F.-M. Liao, J.-S. Yu, J. Zhou,*Catalytic Asymmetric Electrophilic Amination Reactions To Form Nitrogen-Bearing Tetrasubstituted Carbon Stereocenters Synthesis, 2014,46, 2983-3003.
30.F. Zhou, C. Tan, J. Tang, Y.-Y. Zhang, W.-M. Gao, H.-H. Wu, Y.-H. Yu andJ. Zhou,*Asymmetric Copper(I)-Catalyzed Azide–Alkyne Cycloaddition to Quaternary OxindolesJ. Am. Chem. Soc. 2013? 135?10994-10997
31.Z.-Y. Cao, F. Zhou, Y.-H. Yu, J. Zhou,*A Highly Diastereo- and Enantioselective Hg(II)-Catalyzed Cyclopropanation of Diazooxindoles and Alkenes Org. Lett.2013? 15, 42-45.
32.F. Zhu, F. Zhou, Z.-Y. Cao, C. Wang, Y.-X. Zhang, C.-H. Wang*,J. Zhou,*A Facile Method for the Synthesis of 3-Substituted 3-(Alkylthio)oxindoles or 3-AlkoxyoxindolesSynthesis, 2012, 44, 3129-3144.
33.J.-S. Yu, F. Zhou, Y.-L. Liu,J. Zhou*, Organocatalytic asymmetric Michael addition of unprotected 3-substituted oxindoles to 1,4-naphthoquinone. Beilstein. J. Org. Chem. 2012, 8, 1360-1365.
34.L. Chen?F. Zhou? T.-D. Shi? J. Zhou*,Metal-Free Tandem Friedel–Crafts/Lactonization Reaction to Benzofuranones Bearing a Quaternary Center at C3 Position J. Org. Chem. 2012? 77? 4354-4362.
35.F. Zhou? M. Ding? J. Zhou,*A Catalytic Metal-free Ritter Reaction to 3-Substituted 3-AminooxindolesOrg. Biomol. Chem.2012? 10? 3178-3183.
36.F. Zhou? Z.-Y. Cao? J. Zhang? H. B. Yang? J. Zhou,*A Highly Efficient Friedel–Crafts Reaction of 3-Hydroxyoxindoles and Aromatic Compounds to 3?3-Diaryl and 3-Alkyl-3-aryloxindoles Catalyzed by Hg(ClO₄)₂?3H₂OChem. Asian J. 2012? 7?233-241.
37.F. Zhou? M. Ding? Y.-L. Liu? C.-H. Wang? C.-B. Ji? Y.-Y. Zhang, J. Zhou,*Organocatalytic Asymmetric α-Amination of Unprotected 3-Aryl and 3-Aliphatic Substituted Oxindoles using Di-tert-butyl Azodicarboxylate Adv. Syn. Catal. 2011? 353? 2945-2952.
38.M. Ding?F. Zhou? Y.-L. Liu? C.-H. Wang? X.-L. Zhao? J. Zhou,* Cinchona alkaloid-based phosphoramide catalyzed highly enantioselective Michael addition of unprotected 3-substituted oxindoles to nitroolefinsChem. Sci. 2011? 2? 2035-2039.
39.Y.-L. Liu? T.-D. Shi? F. Zhou? X.-L. Zhao? X. Wang?* J. Zhou,*Organocatalytic Asymmetric Strecker Reaction of Di- and Trifluoromethyl Ketoimines. Remarkable Fluorine Effect Org. Lett. 2011? 13? 3826-3829.
40.Y.-L. Liu? F. Zhou? J.-J. Cao? C.-B. Ji? M. Ding? J. Zhou,*A facile method for the synthesis of oxindole based quaternary α-aminonitriles viathe Strecker reactionOrg. Biomol. Chem. 2010? 8? 3847-3850.
41.J.-J. Cao?F. Zhou?J. Zhou?*Improving the Atom Efficiency of the Wittig Reaction by a “Waste as Catalyst/Co-catalyst” Strategy Angew. Chem. Int. Ed. 2010? 49? 4976-4980.
42.F. Zhou? Y.-L. Liu? J. Zhou?*Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 PositionAdv. Syn. Catal. 2010? 352? 1381-1407.
43.M. Ding?F. Zhou? Z.-Q. Qian? J. Zhou?*Organocatalytic Michael addition of unprotected 3-substituted oxindoles to nitroolefins. Org. Biomol. Chem. 2010? 8? 2912-1914.
44.Z.-Q. Qian? F. Zhou? T.-P. Du? M. Ding? B.-L. Wang? X.-L. Zhao? J. Zhou?*Asymmetric construction of quaternary stereocenters by direct organocatalytic amination of 3-substituted oxindolesChem. Commun. 2009? 6753-6755.



荣誉及奖励
2016年6月，上海市优秀博士学位论文
2014年5月，上海市优秀毕业生
2013年12月，华东师范校长奖学金
2013年12月，博士研究生国家奖学金
2012年12月，华东师范大学校长奖学金一等奖


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