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1.Q. Hou, C. Cai, S.J. Liu, W. Huang, C. Peng, G. Zhan*, B. Han*, Catalyst-controlled regiodivergence and stereodivergence in formal cross [4+2] cycloadditions: the unique effect of bismuth(III), Science Advances, 2025, 11. (ÖпÆÔºÒ»Çø£¬IF:11.7)

2.K. Ma; T. Qi, L. Hu; C. Chen, W. Wang; J.L. Li, C. Peng, G. Zhan*, B. Han*, Atroposelective Synthesis of Biaryl N-Oxides via Cu-Catalyzed De Novo Heteroaromatic N-Oxide Ring Formation, Advanced Science, 2024, 11(40): 2405743. (ÖпÆÔºÒ»Çø£¬IF:14.3)

3.Q.Q. Yang, C. Chen, D.H. Yao, W. Liu, B. Liu*, J. Zhou, D. B. Pan, C. Peng, G. Zhan*, B. Han*, Catalytic Atroposelective Synthesis of Axially Chiral Azomethine Imines and Neuroprotective Activity Evaluation, Angew. Chem. Int. Ed., 2024, 63(5): e202312663. (ÖпÆÔºÒ»Çø£¬IF:16.6)

4.C. Chen, J. Zhou, J. Jiang, Y. Li, T. Mao, C. Peng, G. Zhan*, W. Huang*, Remote stereocontrol in the (4?+?2) cycloadditions of 1,7-zwitterions: Asymmetric synthesis of multifunctionalized tetrahydroquinoline derivatives, Chinese Chem. Lett., 35 (2024) 108295. (ÖпÆÔºÒ»Çø£¬IF:9.4)

5.H. Zhao, L. Yao, Y. Gu, Y. Niu, B. Han, W. Huang*, G. Zhan*, Cooperative Gold(I)/DMAP Catalysis Enabled (2+3) Cycloadditions of Yne-Enones with Oxindole-Derived MBH Carbonates, Org. Lett., 26 (2024), 3790¨C3795. (ÖпÆÔºÒ»Çø£¬IF:4.9)

6.L. Yao, Y. Gu, Y. Wu, C. Peng, B. Han*, G. Zhan*, Bifunctional Lewis Base-Catalyzed (3+2) Cycloadditions of Pyrazolone-Derived MBH Carbonates with Arynes, Org. Lett., 26 (2024) 9108-9113. (ÖпÆÔºÒ»Çø£¬IF:4.9)

7.Q.Q. Yang, Z. Zheng, M. Wang, J. Zhou, W. Du, C. Peng, G. Zhan*, B. Han*, Ag-Catalyzed Switchable Synthesis of Site-Specifically Functionalized Pyrroles via Azafulvenium Intermediates, Org. Lett., 26 (2024) 4684-4689. (ÖпÆÔºÒ»Çø£¬IF:4.9)

8.Peng, F., Liao, M., Jin, W. Wei Liu, Z. Li, Z. Fan, L. Zou, S. Chen, L. Zhu, Q. Zhao, G. Zhan, L. Ouyang, C. Peng, B. Han*, J. Zhang*, L.L. Fu*, 2-APQC, a small-molecule activator of Sirtuin-3 (SIRT3), alleviates myocardial hypertrophy and fibrosis by regulating mitochondrial homeostasis, Sig. Transduct. Target. Ther., 9 (2025) 133. (ÖпÆÔºÒ»Çø£¬IF:40.8)

9.Y.-L. Ji, H. Wang, X.-H. He*, J. Zhu, C. Peng, Q. Zhao, G. Zhan*, B. Han*, Visible-Light-Driven Synergistic Se/Fe Catalysis for the Synthesis of 2-Aminoquinoline Derivatives, Org. Lett., 27 (2025) 10.1021/acs.orglett.5c00129. (ÖпÆÔºÒ»Çø£¬IF:4.9)

10.K. Xu, H.P., Li, Y. Ji, C. Peng, G. Zhan*, Q.Q. Yang*, B. Han*, Sc-Catalyzed Asymmetric [2+2] Annulation of 2-Alkynylnaphthols with Dienes to Access Cyclobutene Frameworks, Org. Lett., 27 (2025) 1006-1011. (ÖпÆÔºÒ»Çø£¬IF:4.9)

11.K. Xie, G.Q. Zhang, B.R. Kong, Z.J. Jia, Z.C. Chen*, G. Zhan*, W. Du, Y.C. Chen*, Asymmetric construction of enantioenriched furo[2,3-b]pyridines through sequential gold, palladium/phosphoric acid catalysis, Org. Chem. Front., 11 (2024) 3900-3905. (ÖпÆÔºÒ»Çø£¬IF:4.6)

12.J. Wang, T. Qi, S.R. He, W. Huang, C. Peng, G. Zhan*, B. Han*, Catalyst-Controlled Switchable (5 + 4)/(3 + 4) Cycloadditions for the Divergent Synthesis of Pyrazole-Fused Seven- and Nine-Membered Heterocycles, ACS Catal., 13 (2023) 10694-10704. (ÖпÆÔºÒ»Çø£¬IF:12.9)

13.Y.D. Niu, L.P. Yao, H.L. Zhao, X. Tang, Q. Zhao*, Y.L. Wu, B. Han, W. Huang*, G. Zhan*, Construction of Cyclopentanes Consisting of Five Stereocenters via NHC-Catalyzed Cascade Reactions of Enals with Oxindole-Dienones, Org. Lett., 25 (2023) 8445-8450. (ÖпÆÔºÒ»Çø£¬IF:5.2)

14.Y.L. Wu, W.J. Zhou, L.P. Yao, Y.D. Niu, H.L. Zhao, C. Peng, B. Han, W. Huang*, G. Zhan*, Organocatalytic atroposelective synthesis of naphthoquinone thioglycosides from aryl-naphthoquinones and thiosugars, Chem. Commun., 59 (2023) 7279-7282. (ÖпÆÔº¶þÇø£¬IF:4.9)

15.H.P. Li, X.L. Wu, G. Zhan*, X.J. Fu, J.H. Chen, X.H. He*, B. Han*, Construction of cyclopenta[b]dihydronaphthofurans via TsOH-catalyzed consecutive biscyclization of dithioallylic alcohols and 1-styrylnaphthols, Chem. Commun., 59 (2023) 2275-2278. (ÖпÆÔº¶þÇø£¬IF:4.9)

16.H.Y. Fang, Y. Li, L. Zhang*, Z.H. Yan, K. Ma, C. Peng, W. Huang*, G. Zhan*, Chemo- and Diastereoselective Cycloisomerization/[2+3] Cycloaddition of Enynamides: Synthesis of Spiropyrazolines as Potential Anticancer Reagents, J. Org. Chem., (88) 2023 7311-7319. (ÖпÆÔº¶þÇø£¬IF:3.6)

17.M.L. Luo, Q. Zhao*, X.H. He, X. Xie, H.P. Zhu, F.M. You, C. Peng, G. Zhan*, W. Huang*, Research progress of indole-fused derivatives as allosteric modulators: Opportunities for drug development, Biomed. Pharmacother., 162 (2023) 114574. (ÖпÆÔº¶þÇø£¬IF:7.5)

18.J. Jiang, J. Zhou, Y. Li, C. Peng, G. He, W. Huang, G. Zhan*, B. Han*, Silver/chiral pyrrolidinopyridine relay catalytic cycloisomerization/(2?+?3) cycloadditions of enynamides to asymmetrically synthesize bispirocyclopentenes as PDE1B inhibitors, Commun. Chem., 6 (2023). (ÖпÆÔº¶þÇø£¬IF:5.9)

19.R. Qin, F.M. You, Q. Zhao, X. Xie, C. Peng, G. Zhan*, B. Han*, Naturally derived indole alkaloids targeting regulated cell death (RCD) for cancer therapy: from molecular mechanisms to potential therapeutic targets, J. Hematol Oncol., 15 (2022) 133. (ÖпÆÔºÒ»Çø£¬IF:28.3)

20.X.F. Cong, Q.D. Zhuo, N. Hao, Z.B. Mo, G. Zhan, M. Nishiura, Z.M. Hou*, Regio- and Diastereoselective [3+2] Annulation of Aliphatic Aldimines with Alkenes by Scandium-Catalyzed ¦Â-C(sp3)-H Activation, Angew. Chem. Int. Ed., 66 (2022). (ÖпÆÔºÒ»Çø£¬IF:16.6)

21.Q.Q. Luo, Z. Tian, J. Tang, J. Wang, Y. Tian*, C. Peng, G. Zhan*, B. Han*, Design and Application of Chiral Bifunctional 4-Pyrrolidinopyridines: Powerful Catalysts for Asymmetric Cycloaddition of Allylic N-Ylide, ACS Catal., 12 (2022) 7221-7232. (ÖпÆÔºÒ»Çø£¬IF:12.9)

22.J. Tang, Z.H. Yan, G. Zhan*, Q.Q. Yang, Y.Y. Cheng, X. Li*, W. Huang*, Visible-light-mediated sequential Wolff rearrangement and Staudinger cycloaddition enabling the assembly of spiro-pyrazolone-beta-lactams, Org. Chem. Front., 9 (2022) 4341-4346. (ÖпÆÔºÒ»Çø£¬IF:5.4) 

23.C.H. Li, W.F. Zuo, J. Zhou, W.J. Zhou, M. Wang, X. Li, G. Zhan*, W. Huang*, Catalytic asymmetric synthesis of 3,4'-indole-pyrazole derivatives featuring axially chiral bis-pentatomic heteroaryls, Org. Chem. Front., 9 (2022) 1808-1813. (ÖпÆÔºÒ»Çø£¬IF:5.4)

24.X.H. He, X.J. Fu, G. Zhan*, N. Zhang, X. Li, H.P. Zhu, C. Peng, G. He*, B. Han*, Organocatalytic asymmetric synthesis of multifunctionalized alpha-carboline-spirooxindole hybrids that suppressed proliferation in colorectal cancer cells, Org. Chem. Front., 9 (2022) 1048-1055. (ÖпÆÔºÒ»Çø£¬IF:5.4)

25.Q.W. Pang, J. Zhou, Y.L. Wu, W.J. Zhou, W.F. Zuo, G. Zhan*, B. Han*, Construction of Oxo-Bridged Diazocines via Rhodium-Catalyzed (4+3) Cycloaddition of Carbonyl Ylides with Azoalkenes, Org. Lett., 24 (2022) 1362-1366. (ÖпÆÔºÒ»Çø£¬IF:5.2)

26.M.L. Luo, Q.M. Hou, S.J. Liu, Q. Zhao, R. Qin, C. Peng, B. Han*, G. Zhan*, One-Step Synthesis of Hydropyrrolo[3,2-b]indoles via Cascade Reactions of Oxindole-Derived Nitrones with Allenoates, Org. Lett., 24 (2022) 8493-8497. (ÖпÆÔºÒ»Çø£¬IF:5.2)

27.D.A. Li, X.H. He, X. Tang, Y.L. Wu, H.L. Zhao, G. He, C. Peng, B. Han*, G. Zhan*, Organo/Silver Dual Catalytic (3+2)/Conia-Ene Type Cyclization: Asymmetric Synthesis of Indane-Fused Spirocyclopenteneoxindoles, Org. Lett., 24 (2022) 6197-6201. (ÖпÆÔºÒ»Çø£¬IF:5.2)

28.Z. Tian, J. Jiang, Z.H. Yan, Q.Q. Luo, G. Zhan*, W. Huang, X. Li*, B. Han*, Catalytic asymmetric [3+2] cycloaddition of pyrazolone-derived MBH carbonate: highly stereoselective construction of the bispiro-[pyrazolone-dihydropyrrole-oxindole] skeleton, Chem. Commun., 58 (2022) 5363-5366. (ÖпÆÔºÒ»Çø£¬IF:4.9)

29.R. Qin, Q. Zhao, B. Han, H.P. Zhu, C. Peng, G. Zhan*, W. Huang*, Indole-Based Small Molecules as Potential Therapeutic Agents for the Treatment of Fibrosis, Front. Pharmacol., 13 (2022). (ÖпÆÔº¶þÇø£¬IF:5.6)

30.H.J. Leng, Q. Zhao, Q. Mao, S.J. Liu, M.L. Luo, R. Qin, W. Huang*, G. Zhan*, NHC-catalysed retro-aldol/aldol cascade reaction enabling solvent-controlled stereodivergent synthesis of spirooxindoles, Chin. Chem. Lett., 32 (2021) 2567-2571. (ÖпÆÔºÒ»Çø£¬IF:9.1)

31.W.F. Zuo, J. Zhou, Y.L. Wu, H.Y. Fang, X.J. Lang, Y. Li, G. Zhan*, B. Han*, Synthesis of spiro(indoline-2,3 '-hydropyridazine) via an "on-water" [4+2] annulation reaction, Org. Chem. Front., 8 (2021) 922-927. (ÖпÆÔºÒ»Çø£¬IF:5.4)

32.Q. Zhao, C. Peng, Y.-T. Wang, G. Zhan*, B. Han*, Recent progress on the construction of axial chirality through transition-metal-catalyzed benzannulation, Org. Chem. Front., 9 (2021) 2772¨C2785. (ÖпÆÔºÒ»Çø£¬IF:5.4)

33.X. Tang, Y.L. Wu, J. Jiang, H.Y. Fang, W.J. Zhou, W. Huang*, G. Zhan*, Formal (3+1+1) Carboannulation of Morita-Baylis-Hillman Carbonates with Pyridinium Ylides: Access to Spiro-Cyclopentadiene Oxindoles, Org. Lett., 23 (2021) 8937-8941. (ÖпÆÔºÒ»Çø£¬IF:5.2)

34.X.F. Cong, G. Zhan, Z.B. Mo, M. Nishiura, Z.M. Hou*, Diastereodivergent [3+2] Annulation of Aromatic Aldimines with Alkenes via C-H Activation by Half-Sandwich Rare-Earth Catalysts, J. Am. Chem. Soc., 142 (2020) 5531-5537. (ÖпÆÔºÒ»Çø£¬IF:15.0)

35.X. Tang, N. Zhang, G. He, C.H. Li, W. Huang, X.Y. Wang, G. Zhan*, B. Han*, Unconventional [2+3] Cyclization Involving [1,4]-Sulfonyl Transfer to Construct Polysubstituted Fluorazones as Inhibitors of Indoleamine 2,3-Dioxygenase 1, Org. Lett., 22 (2020) 7909-7914. (ÖпÆÔºÒ»Çø£¬IF:5.2)

36.R. Zhou+, J.S. Li+, H.W. Cheo, R. Chua, G. Zhan, Z.M. Hou, J. Wu*, Visible-light-mediated deuteration of silanes with deuterium oxide, Chem. Sci., 10 (2019) 7340-7344. (ÖпÆÔºÒ»Çø£¬IF:8.4)

37.G. Zhan, H.L. Teng, Y. Luo, S.J. Lou, M. Nishiura, Z.M. Hou*, Enantioselective Construction of Silicon-Stereogenic Silanes by Scandium-Catalyzed Intermolecular Alkene Hydrosilylation, Angew. Chem. Int. Ed., 57 (2018) 12342-12346. (ÖпÆÔºÒ»Çø£¬IF:16.6)

38.Y.H. Ma, S.J. Lou, G. Luo, Y. Luo, G. Zhan, M. Nishiura, Y. Luo, Z.M. Hou*, B(C6F5)3/Amine-Catalyzed C(sp)-H Silylation of Terminal Alkynes with Hydrosilanes: Experimental and Theoretical Studies, Angew. Chem. Int. Ed., 57 (2018) 15222-15226. (ÖпÆÔºÒ»Çø£¬IF:16.6)

39.H.L. Teng, Y.H. Ma, G. Zhan, M. Nishiura, Z.M. Hou*, Asymmetric C(sp)-H Addition of Terminal Alkynes to Cyclopropenes by a Chiral Gadolinium Catalyst, ACS Catal., 8 (2018) 4705-4709. (ÖпÆÔºÒ»Çø£¬IF:12.9)

40.G. Zhan+, W. Du+, Y.C. Chen*, Switchable divergent asymmetric synthesis via organocatalysis, Chem. Soc. Rev., 46 (2017) 1675-1692. (ÖпÆÔºÒ»Çø£¬IF:42.6)

41.G. Zhan, M.L. Shi, W.J. Lin, Q. Ouyang, W. Du*, Y.C. Chen*, Direct Asymmetric Aza-Vinylogous-Type Michael Additions of Nitrones from Isatins to Nitroalkenes, Chem. Eur. J., 23 (2017) 6286-6289. (ÖпÆÔº¶þÇø£¬IF:4.3)

42.G. Zhan, M.L. Shi, Q. He, W.J. Lin, Q. Ouyang, W. Du, Y.C. Chen*, Catalyst-Controlled Switch in Chemo- and Diastereoselectivities: Annulations of Morita-Baylis-Hillman Carbonates from Isatins, Angew. Chem. Int. Ed., 55 (2016) 2147-2151. (ÖпÆÔºÒ»Çø£¬IF:16.6)

43.G. Zhan, M.L. Shi, Q. He, W. Du, Y.C. Chen*, [4+3] Cycloadditions with Bromo-Substituted Morita-Baylis-Hillman Adducts of Isatins and N-(ortho-Chloromethyl)aryl Amides, Org. Lett., 17 (2015) 4750-4753.IF: (ÖпÆÔºÒ»Çø£¬IF:5.2)

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