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You, H., Rideau, E., Sidera, M. & Fletcher, S. P. Non-stabilized nucleophiles in Cu-catalysed dynamic kinetic asymmetric allylic alkylation. Nature. 517, 351–355 (2015).DOI: 10.1038/nature14089
Rideau, E., You, H., Sidera, M., Claridge, T. D. W. & Fletcher, S. P. Mechanistic studies on a Cu-catalyzed asymmetric allylic alkylation with cyclic racemic starting materials. J. Am. Chem. Soc. 139, 5614–5624 (2017).DOI: 10.1021/jacs.7b02440
Wang, J.,Li, J., Wang, Y., He, S., You, H. & Chen, F. Polymer-Supported Chiral Heterogeneous Copper Catalyst for Asymmetric Conjugate Addition of Ketones and Imines under Batch and Flow. ACS Catal. 9629–9637 (2022). DOI: 10.1021/acscatal.2c02056
Jun Li, Xiao Song, Yan Wang, Junrong Huang, Hengzhi You and Fen-Er Chen. Copper-Catalyzed Asymmetric Allylic Alkylation of Racemic Inert Cyclic Allylic Ethers under Batch and Flow. Chemical Science, 2023, 14, 4351 - 4356, DOI: 10.1039/D3SC00127J
Chao Wang, Yan Wang, Xuelei Jia, Junrong Huang, Hengzhi You, Fen-Er Chen. Recyclable Silica-Support Taniaphos/Copper(Ⅰ) complex for asymmetric allylic alkylation reactions, Journal of Catalysis, 2023, 425, 50-56, DOI: https://doi.org/10.1016/j.jcat.2023.05.025
Ana Xu; Chaoyi Li; Junrong Huang; Heng Pang; Chengyao Zhao; Lijuan Song; Hengzhi You; Xumu Zhang; Fen-Er Chen. Highly enantioselective synthesis of both tetrahydroquinoxalines and dihydroquinoxalinones via Rh–thiourea catalyzed asymmetric hydrogenation. Chemical Science, 2023, 14, 9024 - 9032, DOI: 10.1039/D3SC00803G
Ana Xu; Chaoyi Li; Junrong Huang; Heng Pang; Chengyao Zhao; Lijuan Song; Hengzhi You; Xumu Zhang; Fen-Er Chen. Highly enantioselective synthesis of both tetrahydroquinoxalines and dihydroquinoxalinones via Rh–thiourea catalyzed asymmetric hydrogenation. Chemical Science, 2023, 14, 9024 - 9032, DOI: 10.1039/D3SC00803G
Lei Xu, Gang Wang, Nianxin Rong, Yang Gu, Le’an Hu, Hengzhi You and Qin Yin. Enantioselective and Step-Economic Synthesis of the Chiral Amine Fragment in the Tyrosine Kinase Inhibitor Repotrectinib by Direct Asymmetric Reductive Amination under Batch and Flow, Org. Process Res. Dev., 2023, DOI: 10.1021/acs.oprd.3c00152
Xiao Song, Jing Qing, Jun Li, Xuelei Jia, Fusong Wu, Junrong Huang, Jian Jin, Hengzhi You. Copper-catalyzed asymmetric allyl alkylation using Grignard reagents under flow, Chinese Journal of Organic Chemistry, 2023, DOI: 10.6023/cjoc202303027.
Chao Wang, Yan Wang, Xuelei Jia, Junrong Huang, Hengzhi You, Fen-Er Chen. Recyclable Silica-Support Taniaphos/Copper(Ⅰ) complex for asymmetric allylic alkylation reactions, Journal of Catalysis, 2023, 425, 50-56, DOI: https://doi.org/10.1016/j.jcat.2023.05.025
卿晶，廖竞远，陈凯，代德胜，游恒志. 13C-尿素的合成工艺优化及连续流工艺研究 [J].当代化工研究，2023，（08）：146-148.
Jun Li, Xiao Song, Yan Wang, Junrong Huang, Hengzhi You and Fen-Er Chen. Copper-Catalyzed Asymmetric Allylic Alkylation of Racemic Inert Cyclic Allylic Ethers under Batch and Flow. Chemical Science, 2023, 14, 4351 - 4356, DOI: 10.1039/D3SC00127J
Jingyuan Liao; Xuelei Jia; Fusong Wu; Junrong Huang; Guifu Shen; Hengzhi You; Fen-Er Chen. Rapid mild macrocyclization of depsipeptides under continuous flow: total syntheses of five cyclodepsipeptides. Org. Chem. Front., 2022, Advance Article, DOI: 10.1039/D2QO01577C
Dongliang Zhang, Fusong Wu, Zhijian Wan, Yichun Wang, Xuan He, Bing Guo, Hengzhi You and Fen-Er Chen. Palladium Polyaniline Complex: A Simple and Efficient Catalyst for Batch and Flow Suzuki-Miyaura Cross-couplings. Chemical Communications, 2022, DOI: 10.1039/D2CC04051D
Jun Li, Xiao Song, Fusong Wu, Hengzhi You, and Fen-Er Chen. Cu-Catalyzed Asymmetric Allylic Alkylation of Racemic CyclicAllyl Bromides with Organolithium Compounds. Eur. J. Org. Chem.2022, e202200860；DOI: 10.1002/ejoc.202200860
Wang, J.,Li, J., Wang, Y., He, S., You, H. & Chen, F. Polymer-Supported Chiral Heterogeneous Copper Catalyst for Asymmetric Conjugate Addition of Ketones and Imines under Batch and Flow. ACS Catal. 9629–9637 (2022). DOI: 10.1021/acscatal.2c02056
Xiaofei Sun,Jingyuan Zhu,Bin Chen ,Hengzhi You ,Huiqing Xu;A feature transferring workflow between data-poor compounds in various tasks;Pols one; 202204；DOI: 10.1371/journal.pone.0266088
Sun Xiaofei, Zhu Jingyuan, Chen Bin, You Hengzhi;融合多模态数据的药物合成反应的虚拟筛选;计算机应用;2022；DOI: 10.11772/j.issn.1001-9081.2021122228
Yufeng Xie; Huaying Liu; Zhong-Liang Li; Xin Zhang; Lijuan Song; Kang Zhou; Feng Yuan; Hengzhi You; Engui Zhao; Zikai He; Construction of chiral through-space luminophores via symmetry breaking triggered by sequenced chlorination; Science China Chemistry; 202305 ;DOI: 10.21203/rs.3.rs-2258314/v1
Jingyuan Liao, Shilong Zhang, Zesheng Wang, Xiao Song, Dongliang Zhang, Ravi Kumar, Jian Jin, Peng Ren, Hengzhi You, Fen-Er Chen;Transition-metal catalyzed asymmetric reactions under continuous flow from 2015 to early 2020;Green Synthesis and Catalysis;202008；DOI: 10.1016/j.gresc.2020.08.001
Brij Mohan; Zhiyu Tao; Sandeep Kumar; Tiantian Xing; Shixuan Ma; Wenbin Huang; Xueping Yang; Hengzhi You; Peng Ren; Water- and pH-Stable Methylthio-Containing Metal–Organic Frameworks as Luminescent Sensors for Metal-Ion Detection; Crystal Growth & Design; 2022; DOI: 10.1021/acs.cgd.2c00493
Mohan, B.,Kumar, S.,Xi, H.,Ma, S.,Tao, Z.,Xing, T.,You, H.,Zhang, Y.,Ren, P; Fabricated Metal-Organic Frameworks (MOFs) as luminescent and electrochemical biosensors for cancer biomarkers detection; Biosensors and Bioelectronics; 2022; DOI: 10.1016/j.bios.2021.113738
Mohan, B.,Modi, K.,Parikh, J.,Ma, S.,Kumar, S.,Kumar Manar, K.,Sun, F.,You, H.,Ren, P; Efficacy of 2-nitrobenzylidene-hydrazine-based selective and rapid sensor for Cu2 ions, histidine, and tyrosine: Spectral and computational stud; Journal of Photochemistry and Photobiology A: Chemistry; 2022; DOI: 10.1016/j.jphotochem.2021.113557
Kumar, S.,Mohan, B.,Tao, Z.,You, H.,Ren, P; Incorporation of homogeneous organometallic catalysts into metal-organic frameworks for advanced heterogenization: A review; Catalysis Science and Technology; 2021; DOI: 10.1039/d1cy00663k
Wan, Z.,Tao, Y.,You, H.,Zhang, X.,Shao, J; Na-ZSM-5 Zeolite Nanocrystals Supported Nickel Nanoparticles for Efficient Hydrogen Production from Ammonia Decomposition; ChemCatChem; 2021; DOI: 10.1002/cctc.202100324
Wan, Z.,Tao, Y.,You, H.,Shao, J; Facile synthesis of a sintering-resistant zeolite confined Ni catalyst for efficient COx-free hydrogen generation from ammonia decomposition; Sustainable Energy and Fuels; 2021; DOI: 10.1039/d1se00417d
Kumar, S.,Liu, S.,Mohan, B.,Zhang, M.,Tao, Z.,Wan, Z.,You, H.,Sun, F.,Li, M.,Ren, P; Fluorine-Containing Triazole-Decorated Silver(I)-Based Cationic Metal-Organic Framework for Separating Organic Dyes and Removing Oxoanions from Water; Inorganic Chemistry; 2021; DOI: 10.1021/acs.inorgchem.0c03688
Mohan, B.,Kumar, S.,Ma, S.,You, H.,Ren, P; Mechanistic Insight into Charge and Energy Transfers of Luminescent Metal–Organic Frameworks Based Sensors for Toxic Chemicals; Advanced Sustainable Systems; 2021; DOI: 10.1002/adsu.202000293
Mohan, B.,Modi, K.,Patel, C.,Kumar, S.,Zhiyu, T.,You, H.,Ren, P; A new N-methylhydrazinecarbothioamide incorporated “naked-eye” and “turn-off” chemosensor for selective and low detection of Cu2 ions and computation study; Journal of Photochemistry and Photobiology A: Chemistry; 2021; DOI: 10.1016/j.jphotochem.2020.113097
Wan, Z.,Tao, Y.,Shao, J.,Zhang, Y.,You, H; Ammonia as an effective hydrogen carrier and a clean fuel for solid oxide fuel cells; Energy Conversion and Management; 2021;DOI: 10.1016/j.enconman.2020.113729
Liu, F.,Kumar, S.,Li, S.,You, H.,Ren, P.,Zhao, L; Bifunctional design of stable metal-organic framework bearing triazole–carboxylate mixed ligand: Highly efficient heterogeneous catalyst for knoevenagel condensation reaction under mild conditions; Catalysis Communications; 2020; DOI: 10.1016/j.catcom.2020.106032
Rideau, E., You, H., Sidera, M., Claridge, T. D. W. & Fletcher, S. P. Mechanistic studies on a Cu-catalyzed asymmetric allylic alkylation with cyclic racemic starting materials. J. Am. Chem. Soc. 139, 5614–5624 (2017).DOI: 10.1021/jacs.7b02440
You, H., Rideau, E., Sidera, M. & Fletcher, S. P. Non-stabilized nucleophiles in Cu-catalysed dynamic kinetic asymmetric allylic alkylation. Nature. 517, 351–355 (2015).DOI: 10.1038/nature14089
Dai, Y.,Wu, F.,Zang, Z.,You, H.,Gong, H.；Ni-catalyzed reductive allylation of unactivated alkyl halides with allylic carbonates；Chemistry - A European Journal；2012；DOI: 10.1002/chem.201102984
Yin, H.,Zhao, C.,You, H.,Lin, K.,Gong, H.; Mild ketone formation via Ni-catalyzed reductive coupling of unactivated alkyl halides with acid anhydrides; Chemical Communications; 2012;DOI: 10.1039/c2cc33232a
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