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Z. Zhang, Y. Sun, Y. Gong, D.-L. Tang, H. Luo, Z.-P. Zhao, F. Zhou*, X. Wang* & J. Zhou* Enantioselective propargylic amination and related tandem sequences to α-tertiary ethynylamines and azacycles Nat. Chem. 2024, 10.1038/s41557-024-01479-z.
P.-W Xu, F. Zhou*, L. Zhu* & J. Zhou* Catalytic desymmetrization reactions to synthesize all-carbon quaternary stereocentres Nature Synthesis 2023, 2, 1020-1036.
Y. Gao, X.-X. Zhang, J.-S. Yu, J. Zhou* Recent Advances in Catalytic Enantioselective Synthesis of α -Chiral Tertiary Azides Acta Chim. Sinica 2023, 81, 1590-1608.
J.-S. Tian, Z. Tu, F. Zhou, J.-S. Yu and J. Zhou* Tandem imine generation/N-cyclization/C-alkylation sequence to access N-functionalized indoles featuring an aza-quaternary carbon Org. Chem. Front.2023, 10, 1759.
Y. Gong, C. Wang, F. Zhou,* K. Liao, X.-Y. Wang, Y. Sun, Y.-X. Zhang, Z. Tu, X. Wang,* and J. Zhou* Sulfonyl-PYBOX Ligands Enable Kinetic Resolution of α-Tertiary Azides by CuAAC Angew. Chem. Int. Ed. 2023, e202301470.
C.-W. Lei, X.-Y. Wang, B.-S. Mu, J.-S. Yu,* Y. Zhou,* and J. Zhou* Me2(CH2Cl)SiCF3 Facilitated Tandem Synthesis of Oxasilacycles Featuring a Trifluoromethyl Group Org. Lett. 2022, 24, 8364,8369.
B.-W. Pan, Y. Shi, S.-Z. Dong, J.-X. He, B.-S. Mu, W.-B. Wu, Y. Zhou,* F. Zhou * and J. Zhou* Highly stereoselective synthesis ofspirocyclopropylthiooxindoles and biological evaluation Org. Chem. Front.2022, 9, 2640.
X.-Y Cui, F. Zhou,* H.-H. Wu,* J. Zhou* Asymmetric Tandem Reactions Achieved by Chiral Amine & Gold(I) Cooperative Catalysis, Chin. J. Org. Chem. 2022, 42, 3033-3050.
W.-B. Wu,X. Yu, J.-S. Yu, X. Wang*, W.-G. Wang* & J. Zhou* Constructing Tertiary Alcohols with Vicinal Stereocenters: Highly Diastereo- and Enantioselective Cyanosilylation of α-Branched Acyclic Ketones and Their Kinetic Resolution, CCS Chem. 2022, 4, 2140–2152.
B.-S. Mu, Y. Gao, F.-M. Yang, W.-B. Wu, Y. Zhang, X. Wang,* J.-S. Yu,* and J. Zhou* The Bifunctional Silyl Reagent Me2(CH2Cl)SiCF3 Enables Highly Enantioselective Ketone Trifluoromethylation and Related Tandem Processes Angew. Chem. Int. Ed. 2022, e202208861.
B.-S. Mu, Z.-H. Zhang, W.-B. Wu*, J.-S. Yu, J. Zhou* Recent Advances in Synthesis of Chiral 1,2-Dihydropyridines Acta Chim. Sinica 2021, 79, 685-693.
P.-W. Xu, X.-Y. Cui, C. Chen, F. Zhou, J.-S. Yu, Y.-F. Ao,* and J. Zhou* Enantioselective Synthesis of Cα-Tetrasubstituted N-Hydroxyl-α-amino Nitriles via Cyanation of Ketonitrones Using Me2(CH2Cl)SiCN, Org. Lett. 2021, 23, 8471,8476.
K Liao, Y. Gong, R.-Y. Zhu, C Wang, F. Zhou,* and J. Zhou* Highly Enantioselective CuAAC of Functional Tertiary Alcohols Featuring an Ethynyl Group and Their Kinetic Resolution Angew. Chem. Int. Ed.2021, 60, 8488 –8493.
X.-Y. Cui, Y.-L. Zhao, Y.-M. Chen, S.-Z. Dong,* F. Zhou, H.-H. Wu,* and J. Zhou* Au-Catalyzed Formal Allylation of Diazo(thio)oxindoles: Application to Tandem Asymmetric Synthesis of Quaternary Stereocenters, Org. Lett. 2021, 23, 4864-4869.
B.-S. Mu, X.-Y. Cui, X.-P. Zeng, J.-S. Yu and J. Zhou*Modular synthesis of chiral 1,2-dihydropyridines via Mannich/Wittig/cycloisomerization sequence that internally reuses waste Nature Commun.2021, 12, 2219.
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 Commun. 2020, 11, 5500.
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, 22, 8578-8583.
Y. Shi, B.‐W. Pan, J.‐S. Yu. Y. Zhou, J. Zhou*Recent Advances in Applying Carbonyl‐stabilized Phosphorus Ylides for Catalysis.ChemCatChem, 2021, 13, 129-139.
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.
W.-B. Wu, J.-S. Yu, J. Zhou*Catalytic Enantioselective Cyanation: Recent Advances and Perspectives ACS Catal. 2020, 10, 7668,7690.
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.
C. Wang, F. Zhou, J. Zhou*Recent Advances in the Enantioselective Copper(I)-Catalyzed Azide-Alkyne Cycloaddition Reaction Chin. J. Org. Chem. 2020, 40, 3065-3077.
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.
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, 11, 3852-3861.
C. Chen, W.-B. Wu, Y.-H. Li, Q.-H. Zhao, J.-S. Yu, J. Zhou*Activation of Chiral (Salen)TiCl2 Complex by Phosphorane for the Highly Enantioselective Cyanation of Nitroolefins. Org. Lett. 2020, 22, 2099,2104.
W.-B. Wu, X.-P. Zeng, J. Zhou*Carbonyl-Stabilized Phosphorus Ylide as an Organocatalyst for Cyanosilylation Reactions Using TMSCN. J. Org. Chem. 2020, 85, 14342-14350.
R.-Y. Zhu, K. Liao, J.-S. Yu and J. Zhou* Recent Advances in Catalytic Asymmetric Synthesis of P-Chiral Phosphine Oxides Acta Chim. Sinica 2020, 78, 193-216.
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.
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, 59, 8004-8014.
Y.-H. Wang, J.-S. Tian, P.-W. Tan, Q. Cao, X.-X. Zhang, Z.-Y. Cao, F. Zhou, X. Wang, and J. Zhou* Regiodivergent Intramolecular Nucleophilic Addition of Ketimines for the Diverse Synthesis of Azacycles. Angew. Chem. Int. Ed. 2020, 59, 1634 –1643.
R.-Y. Zhu, L. Chen, X.-S. Hu, F. Zhou and J. 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.
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.
Y. Gong, Z.-Y. Cao, Y.-B. Shi, F. Zhou, Y. Zhou and J. 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.
Y.-P. Tian, Y. Gong, X.-S. Hu, J.-S. Yu, Y. Zhou and J. Zhou*HClO4 catalysed aldol-type reaction of fluorinated silyl enol ethers with acetals or ketalstoward fluoroalkyl ethers. Org. Biomol. Chem. 2019, 17, 9430–9434.
X.-S. Hu, J.-S. Yu and J. Zhou* Catalytic selective mono- and difluoroalkylation using fluorinated silyl enol ethers. Chem.Commun. 2019, 55, 13638-13648.
X.-T. Gao, S.-L. Xie, F. Zhou, H.-H. Wu and J. Zhou* Multifunctional 1,3-diphenylguanidine for the carboxylativecyclization of homopropargyl amines with CO2 under ambient temperature and pressure. Chem. Commun. 2019, 55, 14303-14306.
S.-L. Xie, X.-Y. Cui, X.-T. Gao, F. Zhou, H.-H. Wu and J. Zhou* Stereoselective defluorinative carboxylation of gem-difluoroalkenes with carbon dioxide. Org. Chem. Front. 2019, 6, 3678-3682.
P.-W. Xu, J.-S. Yu,* C. Chen, Z.-Y. Cao, F. Zhou and J. Zhou*. Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters. ACS Catalysis 2019, 9, 1820-1882.
K. Liao, X.-S. Hu, R.-Y. Zhu, R.-H. Rao, J.-S. Yu, F. Zhou and J. Zhou* Catalytic Enantioselective Protonation of Monofluorinated Silyl Enol Ethers towards Chiral α-Fluoroketones. Chin. J. Chem. 2019, 37, 799-806.
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.2020, 31, 681-684.
X.-S Hu, P.-G. Ding, J.-S. Yu and J. Zhou* A Sc(OTf)3 catalyzed Mukaiyama–Mannich reaction of difluoroenoxysilanes with unactivatedketimines. Org. Chem. Front. 2019, 6, 2500-2505.
Y. Gong, J.-S. Yu, Y.-J. Hao, Y. Zhou, J. Zhou* Catalytic Enantioselective Aldol-Type Reaction Using α-Fluorinated Enolates. Asian J. Org. Chem. 2019, 8, 610–626.
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 ethers. J. Fluorine Chem. 2019, 219, 106-114.
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. Sinica 2018, 76, 925—939
Y.-J. Hao, X.-S. Hu, J.-S. Yu, Y. Zhou*, F. 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 α-fluorinated ketones.Tetrahedron 2018, 74, 7395-7398.
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.
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 reactivity Org. Chem. Front. 2018, 5, 2960-2968.
P.-W. Xu, C. Chen, J.-K. Liu, Y.-T. Song, F. Zhou, J. Yan and 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
Z.-Y. Cao, F. Zhou and J. Zhou* Development of Synthetic Methodologies via Catalytic Enantioselective Synthesis of 3,3-Disubstituted Oxindoles Acc. Chem. Res. 2018, 51, 1443-1454.
P.-G. Ding, X.-S. Hu, F. Zhou and J. Zhou* Catalytic enantioselective synthesis of α-chiral azidesOrg. Chem. Front. 2018, 5, 1542-1559.
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 Catalysis Chin. J. Chem. 2018, 36, 321-328.
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.
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.
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.
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.
F.Zhou,* S.-L.Xie, X.-T.Gao, R. Zhang,* C.-H.Wang, G.-Q.Yin, J. Zhou* Activation of (salen)CoI complex by phosphorane for carbon dioxide transformation at ambient temperature and pressure. Green Chem. 2017, 19, 3908-3915.
F.-M. Liao, J.-S. Yu and J. Zhou* Recent Advances in the Highly Stereoselective Synthesis of Tri- or Tetra-substituted Monofluoroalkenes Chin. J. Org. Chem.2017, 37, 2175-2186.
X.-S. Hu, Y. Du, J.-S. Yu,* F.-M. Liao, P.-G. Ding and 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 Ketones Synlett 2017, 16, 2194-2198.
F.-M. Liao, Z-Y. Cao, J.-S. Yu and J. Zhou* Highly Stereoselective Gold-Catalyzed Coupling of Diazo Reagents and Fluorinated Enol Silyl Ethers to Tetrasubstituted Alkenes Angew. Chem. Int. Ed. 2017, 56,2459-2463.
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. Sinica 2016, 74, 984-989
Y.-H. Wang, Z.-Y. Cao, J. Zhou* Nucleophilic Difluoromethylenation of Ketones Using Diethyl Difluoro(trimethylsilyl)methylphosphonate Mediated by 18-Crown-6 Ether/KOAc. J. Org. Chem.2016, 81, 7807-7816.
X.-P. Zeng, J. Zhou* Me2(CH2Cl)SiCN: Bifunctional Cyanating Reagent for the Synthesis of Tertiary Alcohols with a Chloromethyl Ketone Moiety via Ketone Cyanosilylation. J. Am. Chem. Soc. 2016, 138, 8730-8733. Highlighted by http://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
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.
X.-P. Zeng, Z.-Y. Cao, Y.-H.Wang, F. Zhou, J. Zhou* Catalytic Enantioselective Desymmetrization Reactions to All-Carbon Quaternary Stereocenters. Chem. Rev. 2016. 116, 7330.
Y.-L. Zhao, Z.-Y. Cao, X.-P. Zeng, J.-M. Shi, Y.-H. Yu and J. Zhou* Asymmetric sequential Au(I)/chiral tertiary amine catalysis: an enone-formation/cyanosilylation sequence to optically active 3-alkenyloxindoles from diazooxindoles. Chem. Commun. 2016, 52, 3643-3646.
J.-S. Yu, J. Zhou* Organocatalytic enantioselective Mukaiyama–Mannich reaction of fluorinated enol silyl ethers and cyclicN-sulfonyl ketimines. Org. Chem. Front. 2016, 3, 298-303.
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 oxindoles. Chem. Commun. 2016, 52, 2537
Z.-Y. Cao, J.-S. Jiang, J. Zhou* A highly enantioselective Hg(II)-catalyzed Sakurai–Hosomi reaction of isatins with allyltrimethylsilanes. Org. Biomol. Chem. 2016, 14, 5500-5504 (invited for New Talent Issue).
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 Enones. J. Am. Chem. Soc. 2016, 138, 416-425.
J.-S. Yu, J. Zhou* A highly efficient Mukaiyama–Mannich reaction of N-Boc isatin ketimines and other active cyclic ketimines using difluoroenol silyl ethers catalyzed by Ph3PAuOTf. Org. Biomol. Chem. 2015, 13, 10968 (Feature article).
J.-S. Yu, F. Zhou, Y.-L. Liu, J. Zhou* A Journey in the Catalytic Synthesis of 3-Substituted 3-Aminooxindoles. Synlett 2015, 26, 2491-2504. (invited account)
Z.-Y. Cao, J. Zhou* Catalytic asymmetric synthesis of polysubstituted spirocyclopropyl oxindoles: organocatalysisversustransition metal catalysis. Org. Chem. Front. 2015, 2, 849-858.
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 tryptanthrin. Org. Biomol. Chem. 2015,13, 8906-8911.
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.
J.-S. Yu, F.-M. Liao, W.-M. Gao, K. Liao, R.-L. Zuo and 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.
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 Furans. Org. Lett. 2015, 17, 1557. (Highlighted by Organic Chemistry Portal http://www.organic-chemistry.org/abstracts/lit4/873.shtm)
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.
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)
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 phosphoramide. Chem. Commun.2014, 50, 15719.
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 Electrocyclization. Angew. Chem. Int. Ed. 2014, 53, 13740.
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.(Invited focus review).
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 Effects. Angew. Chem. Int. Ed. 2014, 53, 9512-9516.
.-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 isatins. Org. Chem. Front. 2014, 1, 742-747.
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)
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)
Z.-Y. Cao, Y.-H. Wang, X.-P. Zeng, J. Zhou* Catalytic asymmetric synthesis of 3,3-disubstituted oxindoles: diazooxindole joins the field. Tetrahedron Lett. 2014, 55, 2571-2584(Invited Digest Paper).
Y.-H. Wang, Y.-L. Liu, Z.-Y. Cao, J. Zhou*An Organocatalytic Addition of Nitromethane to Activated Ketimines. Asian J. Org. Chem. 2014, 3, 429-432. (Invited for special issue on organocatalysis)
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 Synfacts 2014, 10, 204）
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.
F. Zhou, C. Tan, J. Tang, Y.-Y. Zhang, W.-M. Gao, H.-H. Wu, Y.-H. Yu and J. Zhou* Asymmetric Copper(I)-Catalyzed Azide–Alkyne Cycloaddition to Quaternary Oxindoles. J. Am. Chem. Soc. 2013, 135, 10994-10997
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）。
Z.-Y. Cao, X. Wang, C. Tan, X.-L. Zhao, J. Zhou* and K. Ding Highly Stereoselective Olefin Cyclopropanation of Diazooxindoles Catalyzed by a C2-Symmetric Spiroketal Bisphosphine/Au(I) Complex. J. Am. Chem. Soc. 2013, 135, 8197-8200.
C.-B. Ji, Z.-Y. Cao, X. Wang,* D.-Y. Wu and J. 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.
F. Zhou, X.-P. Zeng, C. Wang, X.-L. Zhao and J. Zhou* Organocatalytic asymmetric synthesis of 3,3-disubstituted oxindoles featuring two heteroatoms at C3 position. Chem. Commun. 2013, 49, 2022-2024.
Y.-L. Liu, J.-S. Yu, J Zhou* Catalytic Asymmetric Construction of Stereogenic Carbon Centers that Feature a gem-Difluoroalkyl Group. Asian J. Org. Chem. 2013, 2, 194-206. (Invited focus review)
L. Chen, T.-D. Shi, J, Zhou* Waste as Catalyst: Tandem Wittig/Conjugate Reduction Sequence to α-CF3 γ-Keto Esters That Uses Ph3PO as Catalyst for the Chemoselective Conjugate Reduction. Chem. Asian. J.2013, 8, 556-559. (Highlited by Synfacts 2013, 9, 559)
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 Synfacts 2013, 9, 415).
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)
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 Synfacts 2013, 9, 96).
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/2656621/Catalytic_FriedelCrafts_for_Quaternary_Carbonyl_Compounds.html
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-Alkoxyoxindoles. Synthesis, 2012, 3129-3144. (invited feature article).
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 for a Thematic Series entitled “Organocatalysis”)
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。
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.
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. (Highlighted by Organic Chemistry Portal: www.organic-chemistry.org/abstracts/lit3/623.shtm )
F. Zhou, M. Ding, J. Zhou* A Catalytic Metal-free Ritter Reaction to 3-Substituted 3-Aminooxindoles. Org. Biomol. Chem.2012, 10, 3178-3183.
Y.-L. Liu, J. Zhou* Organocatalytic asymmetric synthesis of 3-difluoroalkyl 3-hydroxyoxindoles. Chem. Commun.2012, 48, 1919-1921. (Highlited by Synfacts2012, 8, 332).
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)
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)2,3H2O. Chem. Asian J.2012, 7, 233-241.
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.
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.
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.
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 Synfact 2011, 1245）
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）
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）
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 via the Strecker reaction. Org. Biomol. Chem.2010, 8, 3847-3850. (本文为封面文章)
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.
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.
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.
J. Zhou* Recent Advances in Multicatalyst Promoted Asymmetric Tandem Reactions Chem. Asian J. 2010, 5,422-434.
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
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）。
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”）
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.
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).
L.-W. Ye, J. Zhou, Y. Tang, Phosphine-triggered synthesis of functionalized cyclic compounds. Chem. Soc. Rev. 2008, 37, 1140-1152.
S. C. Pan, J. Zhou, B. List, Catalytic Asymmetric Acylcyanation of Imines. Angew. Chem. Int. Ed. 2007, 45, 612-614.
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.
V. Wakchaure, J. Zhou, S. Hoffmann, B. List, Catalytic Asymmetric Reductive Amination of a-Branched Ketones. Angew. Chem. Int. Ed. 2010, 49, 4612-4614.
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.
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.
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.
J. Zhou, Y. Tang, Pseudo-C3-symmetric trisoxazolines as ligands in copper catalyzed enantioselective Diels–Alder reaction. Org. Biomol. Chem.2004, 2, 429-433.
J. Zhou, B. List, Synthesis of trans-3-Substituted Cyclohexylamines via Br,nsted Acid Catalyzed and Substrate-Mediated Triple Organocatalytic Cascade Reaction. Synlett 2007, 2037-2040.
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.)].
M.-C. Ye, J. Zhou, Y. Tang, Trisoxazoline/Cu(II)-Promoted Kinugasa Reaction Enantioselective Synthesis of Lactams. J. Org. Chem.2006, 71, 3576-3582.
S. C. Pan, J. Zhou, B. List, Catalytic Acylcyanation of Imines with Acetylcyanide. Synlett 2006, 3275-3276.
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,
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）.
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 o of Diazomalonates Catalyzed by Chiral Bisoxazoline/Copper Complex. Adv. Syn. Catal. 2009, 351, 308-312.
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.
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.
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