化学与分子工程学院??????
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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： jzhou@chem.ecnu.edu.cn
办公地址： 化学馆C-302
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-302
教育经历
2008.11 -至今：华东师范大学化学系?教授、博导。
2005.10 - 2008.9：德国马普煤炭研究所Benjamin List教授小组进行博士后研究；
2004. 9 - 2005. 8：日本东京大学药学院Shu Kobayashi教授小组进行博士后研究；
1999. 9－2004. 7：上海有机化学研究所?在唐勇研究员指导下进行硕博连读?研究生会主席；
1997. 7 - 1999. 8：四川教育学院组织人事处?助教；
1993. 9 - 1997. 7：四川师范大学化学系?校学生会主席。
工作经历
个人简介
社会兼职
(2012.8-)Member of Advisory Board ofofOrganic & Biomolecular Chemistry(IF = 3.69)
(2014.2- )Member of Advisory Board ofOrganic Chemistry: Current Research
(2014.5- )Member of Advisory Board ofCurrent Organocatalysis
(2015.8- )Member of Advisory Board of化学学报
(2016.4- )Member of Advisory Board ofMini-Reviews in Organic Chemistry
(2013.12) 上海市第十一届青年联合会委员
小组成员
小组目前成员
2014级：廖奎
2015级：朱仁义、丁佩刚、武文彪、王才、胡小思
2016级：高小童、谢石良
2017级：陈小月、穆博帅、陈晨
2018级：何俊雄、张志豪
2019级：崔效源、巩艺、张正
助理研究员：张学鑫、高杨、田俊菘
小组已毕业成员
2019年：徐鹏巍（博士毕业）
2018年：王雨卉、尹小平、廖富民（博士毕业）
2016年：陈龙、余金生、曾兴平（博士毕业）
2015年：刘运林、曹中艳（博士毕业）、高卫明（硕士毕业）
2014年：周锋（博士毕业），朱锋（硕士毕业）
2013年：计丛斌（博士毕业）
2012年：丁苗（硕士毕业）、王超、张永学（本科毕业）
2010年：曹俊杰（本科毕业）
2009年：钱自清（本科毕业）
诚恳欢迎对有机化学（特别是不对称催化合成）感兴趣的本科生和硕士生加盟。为保证研究工作的连续性，本小组只招收愿意攻读博士学位的研究生。
小组成员获奖情况
学生获奖情况：
恭喜获奖同学，也藉此感谢所有成员为课题组的健康发展所付出的努力和艰辛。
2018年度：
博士研究生国家奖：徐鹏巍
校长奖学金： 徐鹏巍
2017年度：
日本JSPS奖学金： 余金生
上海市优秀毕业生： 曾兴平
2016年度：
玛丽-居里奖学金：曹中艳
上海市优秀毕业生： 余金生
上海市优秀博士论文： 周锋
博士研究生国家奖： 曾兴平
2015年度：
洪堡奖学金：刘运林
博士研究生国家奖： 余金生
华东师范大学校长奖学金： 余金生
华东师范大学优博培育： 尹小平
上海市优秀毕业生： 高卫明
2014年度：
博士研究生国家奖： 刘运林、陈龙
硕士研究生国家奖： 尹小平、高卫明
华东师范大学宝钢优秀奖：曹中艳
上海市优秀硕士论文： 丁苗
上海市优秀毕业生：周锋
2013年度：
博士研究生国家奖： 周锋、曹中艳
教育部学术新人奖： 曹中艳
华东师范大学宝钢特别奖：刘运林（全校唯一）
华东师范大学研究生校长奖学金：周锋（全校共七人）
华东师范大学优秀研究生奖学金：陈龙
2012年度：
博士研究生国家奖： 刘运林
教育部学术新人奖： 刘运林
硕士研究生国家奖： 余金生、朱锋
华东师范大学校长特别奖：刘运林（全校共六名）
华东师范大学校长奖学金一等奖：周锋
华东师范大学智慧奖学金：曹中艳
华东师范大学校长奖学金二等奖：陈龙、余金生、朱锋
研究方向
课题组目前致力于“具有四取代碳手性中心的不对称催化构建”。
四取代碳手性中心广泛存在于天然产物和药物分子中,包括季碳、杂原子取代、螺环等多种类型。发展高效构建方法可以促进相关活性分子的合成与修饰，以及构效关系研究，对于有机合成化学和药物合成与研发等具有重要意义。利用不对称催化的方法构建四取代碳手性中心，特别是季碳手性中心，是有机合成化学一个重要前沿研究课题，因为反应过渡态较拥挤，反应活性往往较低，而且潜手性中心的取代基的位阻差异性较小，选择性识别很困难。
我们课题组运用“协同活化”的理念，采用“双功能催化”和“多种催化剂协同催化”这两种实现协同效应的策略，来提高反应速度和加强选择性控制，从而发展构建全取代碳手性中心的不对称催化新反应。通过几年的探索，我们形成了以下的特色研究成果：
第一、发展了一种新的实现“协同催化”的策略：“副产物作为（助）催化剂”的串联反应，被同行认为是一个概念性的突破；开发了胺-膦酰胺新型手性双功能催化剂；利用手性双金络合物实现了首例金催化的烯烃与重氮化合物的不对称环丙烷化反应。
第二、围绕具有四取代碳手性中心的药物核心骨架如3,3-双取代氧化吲哚、螺环氧化吲哚、Cα-四取代氨基酸和叔醇等，发展了一系列不对称催化的新反应。例如，首次利用不对称催化的炔烃和叠氮的环加成反应，6π电环化反应和Morita-Baylis-Hillman（MBH）反应来构建四取代碳手性中心。
共发表通讯作者论文92篇，包括J. Am. Chem. Soc.(5篇);Angew. Chem. Int. Ed.(7篇);Nat. Commun(1篇).Chem. Sci.(2篇) ,Acc. Chem. Res(1篇).Chem. Rev.(1篇)。通讯作者论文SCI他引3700多次。此外申请9项中国专利（6项获授权）。多篇论文被Synfacts（9篇次），Chemistryviews,Organic Chemistry Portal和《有机化学》作为亮点评述。
应Wiley出版社邀请撰写并出版专著《Multicatalyst System in Asymmetric Catalysis》。
开授课程
科研项目
学术成果
独立工作以来发表文章（自2008年11月加入华东师大）：
106) X.-S. Hu, J.-X. He, S.-Z. Dong, Q.-H. Zhao, J.-S. Yu and J. Zhou*. Regioselective Markovnikov hydrodifluoroalkylation of alkenes using difluoroenoxysilanes.Nature Communications, 2020, doi.org/10.1038/s41467-020-19387-4.
105) P.-G. Ding,X.-S. Hu,J.-S. Yu*and J. Zhou*. Diastereodivergent Synthesis of α-Chiral Tertiary Azides through Catalytic Asymmetric Michael Addition.Org. Lett.2020,doi/10.1021/acs.orglett.0c03178.
104) Y. Shi, B.‐W. Pan, J.‐S. Yu. Y. Zhou, J. Zhou*.Recent Advances in Applying Carbonyl‐stabilized Phosphorus Ylides for Catalysis.ChemCatChem, 2020, 12, doi.org/10.1002/cctc..
103) F. Zhou*, L. Zhu, B.-W. Pan, Y. Shi, Y.-L. Liu, J. Zhou*. Catalytic enantioselective construction of vicinal quaternary carbon stereocenters.Chem. Sci.2020,11, 9341–9365.
102) W.-B. Wu, J.-S. Yu, J. Zhou*. Catalytic Enantioselective Cyanation: Recent Advances and Perspectives.ACS Catal. 2020, 10, 7668?7690.
101) Q. Xiao, J.-S. Yu, Y.-F. Wang, D.-J. Ma, J. Zhou*, and X. Lou*. 3-Difluoroalkyl Quaternary Oxindoles Inhibit Macrophage Pyroptosis by Blocking Inflammasome Recruitment of Caspase-1.ACS Med. Chem. Lett.2020, 11, 1392?1401.
100) C. Wang, F. Zhou, J. Zhou*.Recent Advances in the Enantioselective Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Reaction.Chin. J. Org. Chem. 2020,40, DOI: 10.6023/cjoc.
99) F. Zhou*, J. Zhou*.Ni-Catalyzed Desymmetrization of Malononitriles to Cycloenones with a Nitrile-Containing All-Carbon Quaternary Center. Chin. J. Org. Chem.2020, 40, 2180-2181.
98)P.-G. Ding, F. Zhou, X. Wang, Q.-H. Zhao, J.-S. Yu and J. Zhou*.H-Bond donor-directed switch of diastereoselectivity in the Michael addition of α-azido ketones to nitroolefins.Chem. Sci.2020,DOI: 10.1039/D0SC00475H.
97) C. Chen, W.-B. Wu, Y.-H. Li, Q.-H. Zhao, J.-S. Yu, J. Zhou*.Activation of Chiral (Salen)TiCl2Complex by Phosphorane for the Highly Enantioselective Cyanation of Nitroolefins.Org. Lett.2020,22, 2099?2104.
96)W.-B. Wu, X.-P. Zeng, J. Zhou*Carbonyl-Stabilized Phosphorus Ylide as an Organocatalyst for Cyanosilylation Reactions Using TMSCN.J. Org. Chem.2020, DOI: 10.1021/acs.joc.9b03347
95）朱仁义、廖奎、余金生、周剑*P-手性膦氧化物的不对称催化合成研究进展.《化学学报》，2020，DOI: 10.6023/A**.
94)C. Wang, R.-Y. Zhu, K. Liao, F. Zhou, J. Zhou* .Enantioselective Cu(I)-Catalyzed Cycloaddition of Prochiral Diazides with Terminal or 1-Iodoalkynes.Org. Lett.2020?22, 1270-1274.
93) Y.-H. Wang, Z.-Y. Cao, Q.-H. Li, G.-Q. Lin,J. Zhou*, and P. Tian*.Activating Pronucleophiles with High pKa Values: Chiral Organo-Superbases.Angew. Chem. Int. Ed.2020, DOI:10.1002/anie.
92）Y.-H. Wang, J.-S. Tian, P.-W. Tan, Q. Cao, X.-X. Zhang, Z.-Y. Cao, F. Zhou, X. Wang, andJ. Zhou*.Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles.Angew. Chem. Int. Ed.2020,59, 1634 –1643.
91）R.-Y. Zhu, L. Chen, X.-S. Hu, F. Zhou andJ. Zhou*.Enantioselective synthesis of P-chiral tertiaryphosphine oxides with an ethynyl group via Cu(I)-catalyzed azide–alkyne cycloaddition.Chem. Sci.2020,11, 97–106.
90）S.-L. Xie, X.-T Gao, F. Zhou, H.-H. Wu,J. Zhou*.Enantioselective carboxylative cyclization of propargylic alcohol with carbondioxide under mild conditions.Chin. Chem. Lett.2020,31, 324–328.
89）Y. Gong, Z.-Y. Cao, Y.-B. Shi, F. Zhou, Y. Zhou andJ. Zhou*.A highly efficient Hg(OTf)2-mediated Sakurai–Hosomiallylation of N-tert butyloxycarbonylamino sulfones, aldehydes, fluoroalkylketones and α,β-unsaturated enones usingallyltrimethylsilane.Org. Chem. Front.2019,6, 3989–3995.
88)Y.-P. Tian, Y. Gong, X.-S. Hu, J.-S. Yu, Y. Zhou andJ. Zhou*.HClO4 catalysedaldol-type reaction of fluorinated silyl enol ethers with acetals or ketalstoward fluoroalkyl ethers.Org. Biomol. Chem.2019,17, 9430–9434.
87）X.-S. Hu, J.-S. Yu andJ. Zhou*.Catalytic selective mono- and difluoroalkylation using fluorinated silyl enol ethers.Chem.Commun.2019,55, 13638-13648.
86）X.-T. Gao, S.-L. Xie, F. Zhou, H.-H. Wu andJ. Zhou*.Multifunctional 1,3-diphenylguanidine for the carboxylativecyclization of homopropargyl amines with CO2 under ambient temperature and pressure.Chem. Commun.2019,55, 14303-14306.
85）S.-L. Xie, X.-Y. Cui, X.-T. Gao, F. Zhou, H.-H. Wu andJ. Zhou*.Stereoselective defluorinative carboxylation of gem-difluoroalkenes with carbon dioxide.Org. Chem. Front.2019,6, 3678-3682.
84)P.-W.Xu, J.-S.Yu,*C.Chen, Z.-Y.Cao,F.ZhouandJ.Zhou*.Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters.ACS Catalysis2019,9, 1820-1882.
83)K. Liao, X.-S. Hu, R.-Y. Zhu, R.-H. Rao, J.-S. Yu, F. Zhou, andJ. Zhou*.Catalytic Enantioselective Protonation of Monofluorinated Silyl Enol Ethers towards Chiral α-Fluoroketones.Chin. J.Chem.2019,37, 799-806.
82)Y.-J.Hao, Y. Gong, Z.-Y Cao, Y. Zhou, J. Zhou*.A highly efficient In(OTf)3-catalyzed[3+3] annulation of spirocyclopropyl oxindoles with 1,4-di-thiane-2,5-diol.Chin.Chem. Lett.doi.org/10.1016/j.cclet.2019.08.018
81)X.-S Hu, P.-G. Ding, J.-S. Yu andJ. Zhou*.A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivatedketimines.Org. Chem. Front.2019,6, 2500-2505.
80)Y. Gong, J.-S. Yu, Y.-J. Hao, Y. Zhou,J. Zhou*Catalytic Enantioselective Aldol-Type Reaction Using α-Fluorinated Enolates.AsianJ. Org. Chem.2019, 8, 610–626.
79) X.-S. Hu, J.-S. Yu,* Y. Gong, J. Zhou*Internally reuse by-product as promoter: A catalyst-free imine formation/Mukaiyama-Mannich sequence of α-amido sulfones with fluorinated silyl enol ethersJ. Fluorine Chem.2019,219, 106-114.
78) Y.-J. Hao, J.-S. Yu, Y. Zhou, W. Wang, J. Zhou*C―F…H―X相互作用在有机反应中的影响(Influence of C—F…H—X Interactions on Organic Reactions)Acta Chim. Sinica2018,76, 925—939
77) Y.-J. Hao, X.-S. Hu, J.-S. Yu, Y. Zhou*, F. Zhou, J. Zhou*An efficient Fe(III)-catalyzed 1,6-conjugate addition ofpara-quinone methides with fluorinated silyl enol ethers toward β,β-diaryl α-fluorinated ketones.Tetrahedron2018, 74, 7395-7398.
76)F.-M. Liao, Y. Du, F. Zhou, J. Zhou*Au(I)/手性双功能叔胺催化实现的一锅法串联成烯/不对称环化反应构建螺环季碳氧化吲哚(Au(I)/Chiral Tertiary Amine Catalyzed Tandem Olefination/Asymmetric Cyclization Reaction to Quaternary Spirocyclic Oxindoles) Acta Chim. Sinica 2018, 76, 862—868
75）Z.-Y. Cao,W. Wang,K. Liao,X. Wang,J. Zhou*and J. Ma*Catalytic enantioselective synthesis of cyclopropanes featuring vicinal all-carbon quaternary stereocenters with a CH2F group; study of the influence of C–F?H–N interactions on reactivityOrg. Chem. Front.2018,5, 2960-2968.
74) P.-W. Xu,C. Chen,J.-K. Liu,Y.-T. Song,F. Zhou,J. YanandJ. Zhou*One-Pot Sequential [3 + 3] Dipolar Cycloaddition of Aldehyde or Ketone and Hydroxylamine with Spirocyclopropyl Oxindole.J. Org. Chem.2018,83, 12763-12774
73)Z.-Y. Cao,F. Zhou, andJ. Zhou*Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles.Acc. Chem. Res.2018,51, 1443-1454.
72)P.-G. Ding,?X.-S. Hu,?F. Zhouand J. Zhou*Catalytic enantioselective synthesis of α-chiral azidesOrg. Chem. Front.2018, 5, 1542.
71)Y.-L. Liu, X.-P. Yin, J. Zhou*Internally Reuse Waste: Catalytic Asymmetric One-Pot Strecker Reaction of Fluoroalkyl Ketones, Anilines and TMSCN by Sequential CatalysisChin. J. Chem.2018,36, 321-328.
70) X.‐P. Yin, L. Zhu, J. Zhou*Metal‐Free Azidation of α‐Hydroxy Esters and α‐Hydroxy Ketones Using Azidotrimethylsilane.Adv. Synth. Catal.2018, 360, 1116-1122.
69) X.-T. Gao, C.-C. Gan, S.-Y. Liu, F. Zhou, *H.-H. Wu,*J. Zhou*Utilization of CO2 as a C1 Building Block in a Tandem Asymmetric A3 Coupling-Carboxylative Cyclization Sequence to 2-Oxazolidinones.ACS Catal.2017,7, 8588-8593
68)F.-M. Liao,X.-T. Gao,X.-S. Hu, S.-L. Xie, J. Zhou*A general and efficient Lewis acid catalysed Mukaiyama-aldol reaction of difluoroenoxysilanes and ketones. Sci. Bull.2017,62, 1504-1509.
67) P.-W. Xu,J.-K. Liu,L. Shen, Z.-Y. Cao,X.-L. Zhao,J. Yan,* J. Zhou*Diastereo- and enantioselective [3?+?3] cycloaddition of spirocyclopropyl oxindoles using both aldonitrones and ketonitrones.Nature Communications, 2017, 8,1619
66)F.Zhou
65)廖富民, 余金生, 周剑*三或四取代单氟烯烃的高立体选择性合成研究进展《有机化学》，2017，37, 2175-2186
64) X.-S. Hu, Y. Du, J.-S. Yu,* F.-M. Liao, P.-G. Ding,J. Zhou*A Highly Efficient Gold(I)-Catalyzed Mukaiyama–Mannich Reaction of α-Amino Sulfones with Fluorinated Silyl Enol Ethers To Give β-Amino α-Fluorinated KetonesSynlett2017, 16, 2194-2198.
63)F.-M. Liao, Z-Y. Cao,J.-S. Yu,J. Zhou*Highly Stereoselective Gold-Catalyzed Coupling of Diazo Reagents and Fluorinated Enol Silyl Ethers to Tetrasubstituted AlkenesAngew. Chem. Int. Ed.2017?56,2459-2463.
62) X. Ye, X.-P. Zeng, J. Zhou*Me2(CH2Cl)SiCN和Me3SiCN在醛的不对称氰化反应中的比较研究, Acta Chim. Sinica2016, 74, 984-989
61) Y.-H. Wang, Z.-Y. Cao,J. Zhou*Nucleophilic Difluoromethylenation of Ketones Using Diethyl Difluoro(trimethylsilyl)methylphosphonate Mediated by 18-Crown-6 Ether/KOAcJ. Org. Chem.2016,81, 7807-7816.
60) X.-P. Zeng,J. Zhou* Me2(CH2Cl)SiCN: Bifunctional Cyanating Reagent for the Synthesis of Tertiary Alcohols with a Chloromethyl Ketone Moiety via Ketone CyanosilylationJ. Am. Chem. Soc. 2016, 138, 8730-8733. Highlighted byhttp://www.x-mol.com/news/3137,双功能硅氰化试剂的设计、合成及在(S)-CPB pheromone全合成中的应用
59) 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, 5139-5144.
58) 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.
57)Y.-L. Zhao, Z.-Y. Cao, X.-P. Zeng, J.-M. Shi, Y.-H. Yu andJ. Zhou*Asymmetric sequential Au(I)/chiral tertiary amine catalysis: an enone-formation/cyanosilylation sequence to optically active 3-alkenyloxindoles from diazooxindolesChem. Commun.2016, 52, 3643-3646.
56)J.-S. Yu, J. Zhou*Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclicN-sulfonyl ketiminesOrg. Chem. Front. 2016, 3, 298-303.
55)Z.-Y. Cao, Y.-L. Zhao, J. Zhou*Sequential Au(I)/chiral tertiary amine catalysis: a tandem C–H functionalization of anisoles or a thiophene/asymmetric Michael addition sequence to quaternary oxindolesChem. Commun. 2016, 52, 2537
54)Z.-Y. Cao, J.-S. Jiang, J. Zhou*A highly enantioselective Hg(II)-catalyzed Sakurai–Hosomi reaction of isatins with allyltrimethylsilanesOrg. Biomol. Chem.2016,14,5500-5504 (invited for New Talent Issue).
53)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.
52)J.-S. Yu, J. Zhou*A highly efficient Mukaiyama–Mannich reaction ofN-Boc isatin ketimines and other active cyclic ketimines using difluoroenol silyl ethers catalyzed by Ph3PAuOTfOrg. Biomol. Chem.2015,13,10968(Feature article).
51) 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. (invited account)
50)Z.-Y. Cao, J. Zhou*Catalytic asymmetric synthesis of polysubstituted spirocyclopropyl oxindoles: organocatalysisversustransition metal catalysisOrg. Chem. Front.2015, 2, 849-858.
49)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.
48) 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.
47) J.-S. Yu, F.-M. Liao, W.-M. Gao, K. Liao,R.-L. Zuoand J. Zhou*Michael Addition Catalyzed by Chiral Secondary Amine Phosphoramide Using Fluorinated Silyl Enol Ethers: Formation of Quaternary Carbon Stereocenters.Angew. Chem. Int. Ed. 2015?54,7381.
46) L. Chen, Y. Du, X.-P. Zeng, T.-D. Shi, F. Zhou and 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. (Highlighted by Organic Chemistry Portalhttp://www.organic-chemistry.org/abstracts/lit4/873.shtm)
45) 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 Sulfones.Org. Lett.2015? 17, 972.
44) Y.-L. Liu, J. Zhou*Catalytic Asymmetric Strecker Reaction: Bifunctional Chiral Tertiary Amine/Hydrogen-Bond Donor Catalysis Joins the Field Synthesis, 2015,1210-1226 (invited mini-review)
43) 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, 15719.
42) 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.
41) F. Zhou, F.-M. Liao, J.-S. Yu, J. Zhou*Catalytic Asymmetric Electrophilic Amination Reactions To Form Nitrogen-Bearing Tetrasubstituted Carbon StereocentersSynthesis, 2014, 46, 2983-3003.(Invited focus review).
40) J.-S. Yu, Y.-L. Liu, J. Tang, X. Wang,* J. Zhou*Highly Efficient “On Water” Catalyst-Free Nucleophilic Addition Reactions Using Difluoroenoxysilanes: Dramatic Fluorine EffectsAngew. Chem. Int. Ed.2014?53, 9512-9516.
39)Y.-L. Liu, F.-M. Liao, Y.-F. Niu, X.-L. Zhao, J. Zhou*Highly stereoselective construction of adjacent tetrasubstituted carbon stereogenic centres via organocatalytic Mukaiyama-aldol reaction of monofluorinated silyl enol ethers to isatinsOrg. Chem. Front.2014, 1, 742-747.
38)L. Chen,X.-P. Yin, C.-H. Wang, J. Zhou*Catalytic functionalization of tertiary alcohols to fully substituted carbon centres.Org. Biomol. Chem.2014?12, 6033-6048(Invited review)
37)Y.-H. Wang,Z.-Y. Cao,Y.-F. Niu, X.-L. Zhao,J. Zhou*高对映选择性的有机催化的硝基烷烃对N-Boc靛红亚胺的不对称aza-Henry反应Acta Chim. Sinica.,2014, 72, 867-872. (Invited for special issue on organocatalysis)
36）Z.-Y. Cao, Y.-H. Wang,X.-P. Zeng,J. Zhou*Catalytic asymmetric synthesis of 3,3-disubstituted oxindoles: diazooxindole joins the fieldTetrahedron Lett. 2014, 55,2571-2584(InvitedDigest Paper).
35) Y.-H. Wang,Y.-L. Liu, Z.-Y. Cao,J. Zhou*An Organocatalytic Addition of Nitromethane to Activated KetiminesAsian J. Org. Chem.2014, 3, 429-432. (Invited for special issue on organocatalysis)
34)Y.-L. Liu, X. Wang, Y.-L. Zhao, F. Zhu, X.-P. Zeng,L. Chen, C.-H. Wang,X.-L. Zhao,J. Zhou*One-Pot Tandem Approach to Spirocyclic Oxindoles Featuring Adjacent Spiro-Stereocenters.Angew. Chem. Int. Ed.2013? 52?13735-13739. （Highlighted by Synfacts2014? 10, 204）
33) L. Chen, F. Zhu, H.-C. Wang,* J. Zhou*A highly efficient thiourea catalyzed dehydrative nucleophilic substitution reaction of 3-substituted oxindoles with xanthydrols.RSC Adv. 2013,3, 19880-19884.
32) 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）刘运林、朱锋、王翠红、周剑* 3-羟基氧化吲哚的不对称合成:金属催化vs有机催化《有机化学》,2013，33, 1595-1615(邀请综述）。
30) Z.-Y. Cao, X. Wang, C. Tan, X.-L. Zhao, J. Zhou*and K. DingHighly Stereoselective Olefin Cyclopropanation of Diazooxindoles Catalyzed by a C2-Symmetric Spiroketal Bisphosphine/Au(I) ComplexJ. Am. Chem. Soc. 2013? 135?8197-8200.
29) C.-B. Ji, Z.-Y. Cao,X. Wang,* D.-Y. WuandJ. Zhou*
A Catalyst-Free, One-Pot Three-Component Aminomethylation of α-Substituted Nitroacetates: Theoretical and Experimental Studies into the Rate-Accelerating Effects of the Solvent Methanol.Chem. Asian. J.2013,8, 877.
28) F. Zhou, X.-P. Zeng, C. Wang, X.-L. Zhao andJ. Zhou*Organocatalytic asymmetric synthesis of 3,3-disubstituted oxindoles featuring two heteroatoms at C3 positionChem. Commun.2013, 49, 2022-2024.
27) Y.-L. Liu, J.-S. Yu,J Zhou*Catalytic Asymmetric Construction of Stereogenic Carbon Centers that Feature a gem-Difluoroalkyl GroupAsian J. Org. Chem. 2013,2, 194-206. (Invited focus review)
26)L. Chen, T.-D. Shi, J, Zhou*Waste as Catalyst: Tandem Wittig/Conjugate Reduction Sequence to α-CF3γ-Keto Esters That Uses Ph3PO as Catalyst for the Chemoselective Conjugate Reduction.Chem. Asian. J.2013, 8, 556-559.(Highlited by Synfacts2013? 9? 559)
25) 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. (Highlited by Synfacts2013? 9? 415).
24) X.-P. Zeng, Y.-L. Liu, C.-B. Ji, J. Zhou*The First Catalytic Asymmetric Morita-Baylis-Hillman Reaction of Acrolein with Aromatic Aldehydes Chin. J. Chem. 2012, 30, 2631-2635 (邀请封面文章)
23) Y.-L. Liu, J. Zhou*Organocatalytic asymmetric cyanation of isatin derived N-Boc ketoimines.Chem. Commun.2013?49, 4421. (Invited for themed issue for 2013 Emerging Investigator).(Highlited by Synfacts2013? 9? 96).
22) L. Chen,J. Zhou*A Highly Efficient Friedel–Crafts Reaction of Tertiary α-Hydroxyesters or α-Hydroxyketones to α-Quaternary Esters or Ketones.Chem. Asian J.2012? 7?2510-2515. (VIP paper).Highlighted by ChemViews Magzine http://www.chemistryviews.org/details/ezine/**/Catalytic_FriedelCrafts_for_Quaternary_Carbonyl_Compounds.html
21) 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, 3129-3144. (invited feature article).
20) 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. (invited paper fora Thematic Series entitled “Organocatalysis”)
19)Y.-L. Liu?X.-P. Zeng?J. Zhou*高对映选择性的有机催化的二氟烯醇硅醚与β?γ-不饱和-α-酮酸酯的不对称Mukaiyama-aldol 反应《化学学报》?2012? 70? 1451-1456。
We report the first example of catalytic asymmetric reaction of difluoroenoxysilanes 1and β?γ-unsaturated α-ketoesters 2. In the presence of tertiary amine or tertiary amine-H-bonding donor bifunctional catalysts? it was found that the reaction selectively took place at the ketone moiety of ketoesters 2? and no conjugate reaction happened.Quinine derived urea catalyst 11was identified as a powerful catalyst for this Mukaiyama-aldol reaction to furnishα-difluoroalkyl substituted tertiary alcohols in good to high yield (44-81%)?with moderate to excellent enantioselectivity (72-96%).
18) Y.-L. Liu?X.-P. Zeng?J. Zhou*Ethylene Glycol: A Powerful Catalyst-Free Medium for C-C Bond-Forming ReactionsEthylene Glycol: A Powerful Catalyst-Free Medium for C-C Bond-Forming Reactions.Chem. Asian J.2012? 7?1759-1763.
We report the use of ethylene glycol as a remarkable catalyst-free medium to accomplish ahighly efficient Strecker reaction of α-CF2H or CF3ketoimines and TMSCN? and the activation potency of ethylene glycol could be utilized for several reactions? including the first example of catalyst-free Morita-Baylis-Hillman reaction.
17) L. Chen? F. Zhou? T.-D. Shi? J. Zhou*Metal-Free Tandem Friedel–Crafts/Lactonization Reaction to Benzofuranones Bearing a Quaternary Center at C3 PositionJ. Org. Chem.2012? 77? 4354-4362. (Highlighted by Organic Chemistry Portal:www.organic-chemistry.org/abstracts/lit3/623.shtm)
A metal-free tandem Friedel-Crafts/Lactonization reaction to 3?3-diaryl or 3-alkyl-3-aryl benzofuranones catalyzed by HClO4 was reported. A variety of tertiary α-hydroxy acid esters could readily react with substituted phenols to afford the desired products in rich diversity.The synthetic utility of the products was demonstrated by the synthesis of polycyclic compounds. 1H NMR studies supported that this tandem reaction proceeded via tandem Friedel-Crafts/lactonization sequence.
16) F. Zhou? M. Ding? J. Zhou*A Catalytic Metal-free Ritter Reaction to 3-Substituted 3-AminooxindolesOrg. Biomol. Chem.2012? 10? 3178-3183.
15) Y.-L. Liu? J. Zhou*Organocatalytic asymmetric synthesis of 3-difluoroalkyl 3-hydroxyoxindoles. Chem. Commun.2012? 48? 1919-1921. (Highlited by Synfacts2012? 8? 332).
14) C.-B. Ji? Y.-L. Liu? X.-L. Zhao? Y.-L. Guo? H.-Y. Wang? J. Zhou*Direct amination of α-substituted nitroacetates using di-tert-butyl azodicarboxylate catalyzed by Hatakeyama’s catalyst β-ICD.Org. Biomol. Chem.2012? 10? 1158-1161.(Invited for themed issue for Organocatalysis)
13) 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.
12) Z.-Y. Cao? Y. Zhang? C.-B. Ji? J. Zhou*A Hg(ClO4)2·3H2O Catalyzed Sakurai–Hosomi Allylation of Isatins and Isatin Ketoimines Using Allyltrimethylsilane. Org. Lett.2011? 13? 6398-6401.
11) C.-B. Ji? Y.-L. Liu? Z.-Y. Cao? Y.-Y. Zhang? J. Zhou* Hydroxymethylation of α-substituted nitroacetates. Tetrahedron Lett. 2011? 52? 6118-6121.
10）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 (pages 2945–2952)Adv. Syn. Catal. 2011? 353? 2945-2952.
9) 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 nitroolefins. Chem. Sci.2011? 2? 2035-2039. (Highlighted by Synfact2011? 1245）
8) 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. (Highlighted by Synfact 2011? 1015）
7）Y.-L. Liu? B.-L. Wang? J.-J. Cao? L. Chen? Y.-X. Zhang? C. Wang? J. Zhou* Organocatalytic Asymmetric Synthesis of Substituted 3-Hydroxy-2-oxindoles via Morita?Baylis?Hillman Reaction. J. Am. Chem. Soc. 2010? 132? 15176-15178.（Highlighted by Synfact 2010? 1422）
6) 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 reaction.Org. Biomol. Chem.2010? 8? 3847-3850. (本文为封面文章)
5）J.-J. Cao? F. Zhou? J. Zhou* Improving the Atom Efficiency of the Wittig Reaction by a “Waste as Catalyst/Co-catalyst” Strategy (pages 4976–4980). Angew. Chem. Int. Ed.2010? 49? 4976-4980.
4）F. Zhou? Y.-L. Liu? J. Zhou* Catalytic Asymmetric Synthesis of Oxindoles Bearing a Tetrasubstituted Stereocenter at the C-3 Position (pages 1381–1407). Adv. Syn. Catal. 2010? 352? 1381-1407.
3）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.
2) J. Zhou* Recent Advances in Multicatalyst Promoted Asymmetric Tandem Reactions Chem. Asian J.2010? 5?422-434.
1) 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 oxindoles.Chem. Commun.2009? 6753-6755.
独立工作以前发表的文章
1) J. Zhou?V. Wakchaure? P. Krafft? B. List? Primary Amine-Catalyzed Enantioselective Intramolecular Adolizations. Angew. Chem. Int. Ed.2008? 47? 7656-7658. (本文为封面文章?VIP文章）。
2) J. Zhou?B. List? Organocatalytic Asymmetric Reaction Cascade to Substituted Cyclohexylamines. J. Am. Chem. Soc. 2007? 129? 7498-7499.(本文入选2007年JACS第二季度“most accessed articles”）
3)J. Zhou?Y. Tang? Sidearm Effect: Improvement of the Enantiomeric Excess in the Asymmetric Michael Addition of Indoles to Alkylidene Malonates. J. Am. Chem. Soc.2002? 124? 9030-9031.
4) J. Zhou?Y. Tang? The development and application of chiral trisoxazolines in asymmetric catalysis and molecular recognition. Chem. Soc. Rev. 2005? 34? 664-676. (本文为封面文章).
5) L.-W. Ye? J. Zhou?Y. Tang? Phosphine-triggered synthesis of functionalized cyclic compounds. Chem. Soc. Rev. 2008? 37? 1140-1152.
6）S. C. Pan? J. Zhou?B. List? Catalytic Asymmetric Acylcyanation of Imines. Angew. Chem. Int. Ed. 2007? 45? 612-614.
7）W. Schrader? P. P. Handayani? J. Zhou? B. List? Characterization of Key Intermediates in a Complex Organocatalytic Cascade Reaction Using Mass Spectrometry. Angew. Chem. Int. Ed.2009? 48? 1463-1466.
8) V. Wakchaure? J. Zhou?S. Hoffmann? B. List? Catalytic Asymmetric Reductive Amination of a-Branched Ketones. Angew. Chem. Int. Ed.2010? 49? 4612-4614.
9) J.Zhou?Y. Tang? Enantioselective Friedel–Crafts reaction of indoles with arylidene malonates catalyzed by iPr-bisoxazoline–Cu(OTf)2.Chem. Commun.2004? 432-433.
10) J. Zhou?M.-C. Ye? Z.-Z. Huang? Y. Tang? Controllable Enantioselective Friedel-Crafts Reaction between Indoles and Alkylidene Malonates Catalyzed by Pseudo-C3-Symmetric Trisoxazoline Copper (II) Complexes. J. Org. Chem.2004? 69? 1309-1320.
11)J. Zhou?M.-C. Ye? Y. Tang? Sidearm Approach: A Promising Strategy for Construction of Bisoxazoline-Based Ligand Library. J. Comb. Chem.2004? 6? 301-304.
12) J. Zhou?Y. Tang? Pseudo-C3-symmetric trisoxazolines as ligands in copper catalyzed enantioselective Diels–Alder reaction. Org. Biomol. Chem.2004? 2? 429-433.
13) J. Zhou?B. List? Synthesis of trans-3-Substituted Cyclohexylamines via Br?nsted Acid Catalyzed and Substrate-Mediated Triple Organocatalytic Cascade Reaction. Synlett2007? 2037-2040.
14) M.-C. Ye? J. Zhou?Z.-Z. Huang? Y. Tang? Chiral tris(oxazoline)/Cu(II) catalyzed coupling of terminal alkynes and nitrones. Chem. Commun.2003? 2554-2555. [被Angew. Chem. Int. Ed. 的Highlights 栏目评述(Angew. Chem. Int. Ed.2004? 43? 2198.)].
15) M.-C. Ye? J. Zhou?Y. Tang? Trisoxazoline/Cu(II)-Promoted Kinugasa Reaction Enantioselective Synthesis of Lactams. J. Org. Chem.2006? 71? 3576-3582.
16) S. C. Pan? J. Zhou?B. List? Catalytic Acylcyanation of Imines with Acetylcyanide. Synlett2006? 3275-3276.
17) Z.-Z. Huang? Y. B. Kang? J. Zhou?M.-C. Ye? Y. Tang? Diastereoselectivity-Switchable and Highly Enantioselective 1?3-Dipolar Cycloaddition of Nitrones to Alkylidene Malonate. Org. Lett.2004? 6? 1677-1679?
18) M.-C. Ye? B. Li? J. Zhou?X.-L. Sun? Y. Tang? Modular Synthesis of Chiral Homo- and Heterotrisoxazolines.Improving the Enantioselectivity in the Asymmetric Michael Addition of Indole to Benzylidene Malonate. J. Org. Chem. 2005? 70? 6108-6110. (本文被Synfact收录? Synfacts? 2005? 203）.
19) J.-P. Qiu? Z.-H. Xu? J. Zhou?C.-L. Cao? X.-L. Sun? L.-X. Dai? Y. Tang? Ligand-Accelerated Asymmetric [1?2]-Stevens Rearrangment of Sulfur Ylides via Decomposition oof Diazomalonates Catalyzed by Chiral Bisoxazoline/Copper Complex. Adv. Syn. Catal. 2009, 351, 308-312.
20)C.-L. Cao, Y.-Y. Zhou, J. Zhou,X.-L. Sun, Y. Tang, Y.-X. Li, G.-Y. Li, J. Sun, An orgaonocatlaytic tandem reaction for the construction of bicyclic skeletons. Chem. Eur. J.2009, 15, 11384-11389.
21)J.-P. Qiu, C. Deng, J. Zhou,X.-L. Sun, Y. Tang, Switchable Reactions of Cyclopropanes with Enol Silyl Ethers. Controllable Synthesis of Cyclopentanes and 1,6-Dicarbonyl Compounds. J. Org. Chem. 2009, 74, 7684-7689.
荣誉及奖励
(14)2018年 入选科技部“中青年科技创新领军人才 ”
(13)2017年获国家自然科学基金委****基金资助
(12)2015年 The CSJ Asian International Symposium Distinguished Lectureship Award
Awarded byChemistry Society of Japan (CSJ)
(11)2014年 英国皇家化学会会士 （Fellow of Royal Society of Chemistry)
(10)2013年 上海市优秀学术带头人
(9)2012年 获国家自然科学基金委优秀青年基金资助
（8）2012年国家自然科学奖二等奖 完成人：唐勇、孙秀丽、叶松、周剑、康彦彪
（7）2011年“Thieme Chemistry Journal Award”
（6）2011年教育部“新世纪优秀人才支持计划”
（5）2011年上海市自然科学奖一等奖完成人：唐勇、孙秀丽、叶松、周剑、叶龙武
（4）2006年全国百篇优秀博士论文提名奖
（3）2006年上海市研究生优秀成果奖
（2）2005年中国科学院50篇优秀博士论文奖
（1）1996年四川省十佳大学生
招生信息
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