Synthesis of γ-hydroxy-γ-perfluoroalkyl butenolides and exocyclic double bond butanolides via regioselective allylic alkylations of MBH carbonates with 2-perfluoroalkyl-oxazol-5(2H)-ones

Bo Zhu, Tao Zhang, Yongmei Yu, Dandan Pan, Haichen Mao, Gongming Zhu and Junbiao Chang

Org. Chem. Front., 2022, 9, 2955
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Synthesis and in vitro evaluation of pyrimidine-fused 3-alkenyloxindoles as potential anticancer agents

Xiong-Li Liu, Ting-Ting Feng, Dan-Dan Wang, Huan-Huan Liu, Chao Yang, Xiao-Nian Li, Bing Lin, Zhi Zhao and Ying Zhou

Tetrahedron Letters, 2016, 57, 4113
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Stereoselective Synthesis of 3,3-Disubstituted Oxindoles and Spirooxindoles via Allylic Alkylation of Morita–Baylis–Hillman Carbonates of Isatins with Cyclic Sulfamidate Imines Catalyzed by DABCO

Sanjeeva K. Arupula, Soumitra Guin, Anubha Yadav, Shaikh M. Mobin and Sampak Samanta

J. Org. Chem., 2018, 83, 2660
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Molecular diversity of the reactions of MBH carbonates of isatins and various nucleophiles

Zi-Ying Xiao, Jing Sun and Chao-Guo Yan

Beilstein J. Org. Chem., 2025, 21, 286
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Molecular Hybridization‐Guided Construction of Convolutamydine A‐fused β‐Ionone Scaffolds and their Biological Evaluation for Anticancer Activities

Xiong‐Wei Liu, Jun Yang, Guan‐Lian Wang, Yi Gong, Ting‐Ting Feng, Xiong‐Li Liu, Yu Cao, Ying Zhou and Wei‐Cheng Yuan

Journal of Heterocyclic Chem, 2018, 55, 351
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Rapid, microwave-accelerated synthesis and anti-osteoporosis activities evaluation of Morusin scaffolds and Morusignin L scaffolds

Bing Lin, Jun-Fei Huang, Xiong-Wei Liu, Xi-Tao Ma, Xiong-Li Liu, Yi Lu, Ying Zhou, Feng-Min Guo and Ting-Ting Feng

Bioorganic & Medicinal Chemistry Letters, 2017, 27, 2389
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3-Methyl-4-nitro-5-isatylidenyl-isoxazoles as 1,3-dipolarophiles for synthesis of polycyclic 3,3′-pyrrolidinyl-dispirooxindoles and their biological evaluation for anticancer activities

Bing Lin, Wen-Hui Zhang, Dan-Dan Wang, Yi Gong, Qi-Di Wei, Xiong-Li Liu, Ting-Ting Feng, Ying Zhou and Wei-Cheng Yuan

Tetrahedron, 2017, 73, 5176
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Part I: Diastereoselective Reactions Involving β‐Mono‐ and β,β′‐Disubstituted Alkylidene Oxindoles: Pondering Alkene Geometry

Madhu Ganesh, Madhuri P. Rao and Shruti J. Mirajakar

Asian J Org Chem, 2018, 7, 250
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Highly enantioselective allylic alkylation of 5 H -oxazol-4-ones with Morita-Baylis-Hillman carbonates

Han Xu, Feng Sha and Xin-Yan Wu

Tetrahedron, 2018, 74, 4331
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Convenient synthesis of chromene-fused spirocyclopentane-1,2-dioxindoles via base promoted annulation reaction

Kun Huang, Ting Tang, Ying Han, Jing Sun and Chao-Guo Yan

Tetrahedron Letters, 2025, 156, 155455
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Diversity‐oriented Construction of Chromanone‐fused Polycyclic Pyrrolidinyl‐dispirooxindoles

Ting‐Ting Feng, Yi Gong, Qi‐Di Wei, Guan‐Lian Wang, Huan‐Huan Liu, Min‐Yi Tian, Xiong‐Li Liu, Zhi‐Yong Chen and Ying Zhou

Journal of Heterocyclic Chem, 2018, 55, 1136
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A Double Deprotonation Strategy for Cascade Annulations of Palladium–Trimethylenemethanes and Morita–Baylis–Hillman Carbonates to Construct Bicyclo[3.1.0]hexane Frameworks

Zhen‐Hong Yang, Peng Chen, Zhi‐Chao Chen, Zhi Chen, Wei Du and Ying‐Chun Chen

Angewandte Chemie, 2021, 133, 14032
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Asymmetric synthesis of chiral 3,3-disubstituted oxindoles using isatin as starting material

Ghodsi Mohammadi Ziarani, Razieh Moradi and Negar Lashgari

Tetrahedron: Asymmetry, 2015, 26, 517
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A Double Deprotonation Strategy for Cascade Annulations of Palladium–Trimethylenemethanes and Morita–Baylis–Hillman Carbonates to Construct Bicyclo[3.1.0]hexane Frameworks

Zhen‐Hong Yang, Peng Chen, Zhi‐Chao Chen, Zhi Chen, Wei Du and Ying‐Chun Chen

Angew Chem Int Ed, 2021, 60, 13913
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Catalyst-Controlled Divergent Intramolecular Cyclizations of Morita–Baylis–Hillman Carbonates

Wei Cai, Yanlin He, Yiming Zhou and You Huang

J. Org. Chem., 2021, 86, 12267
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A facile and efficient synthesis of polycyclic spiropyrrolidine oxindoles bearing mesityl oxide unit via a three-component 1,3-dipolar cycloaddition reaction

Hui-Juan Wang, Bo-Wen Pan, Wen-Hui Zhang, Chao Yang, Xiong-Li Liu, Zhi Zhao, Ting-Ting Feng, Ying Zhou and Wei-Cheng Yuan

Tetrahedron, 2015, 71, 8131
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Construction of turmerone motif-fused spiropyrrolidine oxindoles and their biological evaluation for anticancer activities

Xiong-Li Liu, Chao Yang, Wen-Hui Zhang, Gen Zhou, Xi-Tao Ma, Bing Lin, Min Zhang, Ying Zhou and Ting-Ting Feng

Tetrahedron Letters, 2016, 57, 1385
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A facile and efficient synthesis of hexahydro-1H-pyrido[2,3-b]indol-2-one scaffolds via a sequential Michael addition/amidation/reductive cyclization process

Xiong-Li Liu, Wen-Hui Zhang, Zhen Yao, Xiong-Wei Liu, Li-Jun Peng, Zhi Zhao, Yi Lu, Ying Zhou and Wei-Cheng Yuan

Tetrahedron, 2015, 71, 9483
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1,3-Dipolar cycloaddition enabled isoxazole-fused spiropyrrolidine oxindoles syntheses from 3-methyl-4-nitro-5-alkenyl-isoxazoles and azomethine ylides

Xiong-Wei Liu, Zhen Yao, Jun Yang, Zhi-Yong Chen, Xiong-Li Liu, Zhi Zhao, Yi Lu, Ying Zhou and Yu Cao

Tetrahedron, 2016, 72, 1364
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DABCO-catalyzed sp3 C–H activation: rapid access to isoxazole or coumarin-fused 3-quaternary carbon oxindoles and isoxazole-fused pyrrolidinones

Xiong-Li Liu, De-Hong Jing, Zhen Yao, Wen-Hui Zhang, Xiong-Wei Liu, Zhou-Jie Yang, Zhi Zhao, Ying Zhou and Xiao-Nian Li

Tetrahedron Letters, 2015, 56, 5637
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Diversity-oriented one-pot multicomponent synthesis of spirooxindole derivatives and their biological evaluation for anticancer activities

Jun Yang, Xiong-Wei Liu, Dan-Dan Wang, Min-Yi Tian, Shuo-Nan Han, Ting-Ting Feng, Xiong-Li Liu, Ren-Qiang Mei and Ying Zhou

Tetrahedron, 2016, 72, 8523
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Transformations of Modified Morita‐Baylis‐Hillman Adducts from Isatins Catalyzed by Lewis Bases

Zhi‐Chao Chen, Zhi Chen, Wei Du and Ying‐Chun Chen

The Chemical Record, 2020, 20, 541
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Molecular hybridization-guided 1,3-dipolar cycloaddition reaction enabled pyrimidine-fused spiropyrrolidine oxindoles synthesis as potential anticancer agents

Xiong-Li Liu, Ting-Ting Feng, Wei-Dong Jiang, Chao Yang, Min-Yi Tian, Yan Jiang, Bing Lin, Zhi Zhao and Ying Zhou

Tetrahedron Letters, 2016, 57, 4411
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Catalyst-free synthesis of 3-alkenyloxindoles from isatin-derived Morita–Baylis–Hillman carbonates

Lin Jiang, Yong-Gen Li, Hang Li, Ming-Wei Yuan, Yong-Ming Chuan, Hong-Li Li and Ming-Long Yuan

Journal of Chemical Research, 2017, 41, 160
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