[1] M.-Y. Li, X.-M. Nong, H. Xiao, A. Gu, S. Zhai, J. Li, G. Zhang, Z.-J. Xue, Y. Liu*, C. Li*, G.-Q. Lin, and C.-G. Feng*, Aggregation-enabled alkene insertion into carbon-halogen bonds. Aggregate 2023, 4, e346. (IF = 18.8, DOI: 10.1002/agt2.346)
[2] M.-Y. Li, J. Li, A. Gu, X.-M. Nong, S. Zhai, Z.-Y. Yue, C.-G. Feng*, Y. Liu*, and G.-Q. Lin, Solvent-free and catalyst-free direct alkylation of alkenes. Green Chem. 2023, 25, 7073–7078. (IF = 11.0, DOI: 10.1039/D3GC02685J)
[3] M.-Y. Li, S. Zhai, X.-M. Nong, A. Gu, J. Li, G.-Q. Lin*, and Y. Liu*, Trisubstituted alkenes featuring aryl groups: stereoselective synthetic strategies and applications. Sci. China Chem. 2023, 66, 1261–1287. (IF = 10.4, DOI: 10.1007/s11426-022-1515-5)
[4] M.-Y. Li, D. Wei*, C.-G. Feng, and G.-Q. Lin*, Tandem Reactions involving 1,4‐Palladium Migrations. Chem. Asian. J. 2022, 17, e202200456. (Top Cited Article in WILEY, Best Paper Awards, IF = 4.8, DOI: 10.1002/asia.202200456)
[5] M.-Y. Li, P. Han, T.-J. Hu, D. Wei, G. Zhang, A. Qin, C.-G. Feng*, B. Z. Tang, and G.-Q. Lin*, Suzuki-Miyaura Coupling Enabled by Aryl to Vinyl 1,4-Palladium Migration. iScience 2020, 23, 100966. (IF = 6.1, DOI: 10.1016/j.isci.2020.100966)
[6] M.-Y. Li*, A. Gu, J. Li, and Y. Liu*, Advanced green synthesis: Solvent-free and catalyst-free reaction. Green Synth. Catal. 2025, 6, 33-66. (IF = 8.3, DOI: 10.1016/j.gresc.2024.11.001)
[7] M.-Y. Li*, A. Gu, J. Li, N. Tang, M. Matin, G. Zhang*, A. G. Atanasov*, Food and Medicine Homology Substances in Cancer Treatment: A Focus on Resveratrol against Gastrointestinal Tumors. Food Med. Homol. (Just Accepted)
[8] M.-Y. Li*, A. Gu, J. Li, N. Tang, M. Matin, Y. Yang*, G. Zengin*, A. G. Atanasov*. Exploring food and medicine homology: potential implications for cancer treatment innovations. Acta Materia Medica 2025, 4, 200-206. DOI: 10.15212/AMM-2025-0003
[9] M.-Y. Li*, Q. Zhang, J. Li, G. Zengin*. Food and medicine homology in cancer treatment: traditional thoughts collide with scientific evidence. Food & Medicine Homology, 2025, 2(3), 9420120. https://doi.org/10.26599/FMH.2025.9420120
[10] G. Zhang,# M.-Y. Li,# W.-B. Ye, Z.-T. He, C.-G. Feng*, and G.-Q. Lin*, Borylation of Unactivated C(sp3)–H Bonds with Bromide as a Traceless Directing Group. Org. Lett. 2021, 23, 2948–2953. (co-first author, IF = 6.1, DOI: 10.1021/acs.orglett.1c00617)
[11] J. Li, A. Gu, X.-M. Nong, S. Zhai, Z.-Y. Yue, M.-Y. Li*, Y. Liu*, Six-Membered Aromatic Nitrogen Heterocyclic Anti-Tumor Agents: Synthesis and Applications. Chem. Rec. 2023, 23, e202300293. (corresponding author, Cover Paper, IF = 7.5, DOI: 10.1002/tcr.202300293)
[12] A. Gu,# J. Li,# J.-A. Wu, M.-Y. Li*, Y. Liu*, Exploration of Dan-Shen-Yin against pancreatic cancer based on network pharmacology combined with molecular docking and experimental validation. Curr. Res. Biotech. 2024, 7, 100228. (corresponding author, IF = 5.6, DOI: 10.1016/j.crbiot.2024.100228)
[13] X.-M. Nong, A. Gu, S. Zhai, J. Li, Z.-Y. Yue, M.-Y. Li*, Y. Liu*, 1,3-Diene-Based AIEgens: Stereoselective Synthesis and Applications. iScience 2024, 27, 109223. (corresponding author, IF = 6.1, DOI: 10.1016/j.isci.2024.109223)
[14] A. Gu, J. Li, S. Qiu, S. Hao, Z.-Y. Yue, S. Zhai, M.-Y. Li*, Y. Liu*, Pancreatic cancer environment: From patient-derived models to single-cell omics. Mol. Omics 2024, 20, 220–233. (corresponding author, Cover Paper, ESI Highly Cited Paper, IF = 3.0, DOI: 10.1039/D3MO00250K)
[15] J. Li, A. Gu, M.-Y. Li*, Heteroaryl Group Containing Trisubstituted Alkenes: Synthesis and Anti-tumor Activity. Chem. Biodivers. 2024, 21, e202401469. (corresponding author, Cover Paper, Excellent Author Award in WILEY, IF = 2.5, DOI: 10.1002/cbdv.202401469)
[16] J. Li, A. Gu, N. Tang, M.-Y. Li*, Y. Liu*, Efficacy and Mechanisms of Ci-Gu-Tang Against Pancreatic Cancer: A Study Using Patient-Derived Models. J. Future Foods. 2025, DOI: 10.1016/j.jfutfo.2024.10.009 (corresponding author, IF = 7.2)
[17] J. Li, A. Gu, N. Tang, Z. Sun, G. Zhang, M.-Y. Li*, Exploring anti-tumor potential of food and medicine homology substances: An in-silico evaluation of Citri Grandis Exocarpium against gallbladder cancer. Food Med. Homol. 2026, 3, 9420084. (corresponding author, DOI: 10.26599/FMH.2026.9420084)
[18] A. Gu#, J. Li#, M.-Y. Li*, Y. Liu*, Patient-derived xenograft model in cancer: establishment and applications. MedComm, 2025, 6, e70059. (IF = 10.7, corresponding author, DOI: 10.1002/mco2.70059)
[19] M. V. Cetiz, S. Ahmed, G. Zengin*, K. I. Sinan, G. Emre, K. Dolina, A. Kalyniukova, A. I. Uba, I. Koyuncu, O. Yuksekdag, M.-Y. Li*, Bioinformatic and experimental approaches to uncover the bio-potential of Mercurialis annua extracts based on chemical constituents. J. Mol. Liq. 2025, 427, 127390. DOI: 10.1016/j.molliq.2025.127390.
[20] A. Gu, J. Li, N. Tang, G. Zengin*, M.-Y. Li*, Food and Medicine Homology Substance in Cancer Treatment: Mechanism of Astragalus against Pancreatic Cancer. Mol. Model. Connect 2025, 1, 20250004 DOI: 10.69709/MolModC.2025.131915
[21] J. Li†, A. Gu†, N. Tang†, G. Zengin*, M.-Y. Li*, Y. Liu*, Patient-derived xenograft models in pan-cancer: From bench to clinic. Interdiscip. Med. 2025, 3, e20250016. (corresponding author, IF = 13.6, DOI: 10.1002/INMD.20250016)
[22] J. Li, A. Gu, N. Tang, J.-W. Zhou*, C. Li*, G. Zengin*, M.-Y. Li*, Unveiling Lysine Vitcylation as a Novel Mechanistic Bridge Between Immune Activation and Cancer Therapy. BIO Integration. 2025, 6, 10. DOI: 10.15212/bioi-2025-0057
[23] E. R. Boukhari, M. Matin, L. Bouissane, M. Ławiński, O. Lushchak, R. K. Singla, M.-E. Mickael, et al. Enhancing human gut health: Global innovations in dysbiosis management. iMeta. 2025, 4, e70028. DOI: 10.1002/imt2.70028. IF = 33.2
[24] G. Zhang, X.-J. Feng, M.-Y. Li, X.-M. Ji, C.-G. Feng, G.-Q. Lin, Synthesis of Tetrasubstituted Allenes via a 1,4-Palladium Migration/Carbene Insertion/β-H Elimination. Org. Bio. Chem. 2022, 20, 5383–5386. (IF = 3.2, DOI: 10.1039/D2OB00751G)
[25] Z.-J. Xue, M.-Y. Li, B.-B. Zhu, Z.-T. He, C.-G. Feng, G.-Q. Lin, A 1,4-Palladium Migration/Heck Sequence with Unactivated Alkenes: Stereoselective Synthesis of Trisubstituted 1,3-Dienes. Adv. Synth. Catal. 2021, 363, 2089–2092. (IF = 5.4, DOI: 10.1002/adsc.202001589)
[26] G. Zhang, Y.-K. Song, F. Zhang, Z.-J. Xue, M.-Y. Li, G.-S. Zhang, B.-B. Zhu, J. Wei, C. Li, C.-G. Feng, G.-Q. Lin, Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon. Nat. Commun. 2021, 12, 728. (IF = 16.6, DOI: 10.1038/s41467-020-20740-w)
[27] G. Zhang, J.-G. Fu, Q. Zhao, G.-S. Zhang, M.-Y. Li, C.-G. Feng, G.-Q. Lin, Silver-promoted synthesis of vinyl sulfones from vinyl bromides and sulfonyl hydrazides in water. Chem. Commun. 2020, 56, 4688–4691. (IF = 4.9, DOI: 10.1039/D0CC00784F)
[28] Z.-J. Xue, M.-Y. Li, B.-B. Zhu, Z.-T. He, C.-G. Feng, G.-Q. Lin, Stereoselective synthesis of conjugated trienes: Via 1,4-palladium migration/Heck sequence. Chem. Commun. 2020, 56, 14420–14422. (IF = 4.9, DOI: 10.1039/D0CC06452A)
[29] D. Wei, M.-Y. Li, B.-B. Zhu, F. Zhang, C.-G. Feng, G.-Q. Lin, Sequential Cross-Coupling/Annulation of ortho-Vinyl Bromobenzenes with Aromatic Bromides for the Synthesis of Polycyclic Aromatic Compounds. Angew. Chem. Int. Ed. 2019, 58, 16543–16547. (IF = 16.6, DOI: 10.1002/anie.201910792)
[30] S.-S. Zhang, T.-J. Hu, M.-Y. Li, C.-G. Feng, G.-Q. Lin, Asymmetric Alkenylation of Enones and Imines Enabled by A Highly Efficient Aryl to Vinyl 1,4-Rhodium Migration. Angew. Chem. Int. Ed. 2019, 58, 3387–3391. (IF = 16.6, DOI: 10.1002/anie.201813585)
[31] T.-J. Hu, M.-Y. Li, Q. Zhao, C.-G. Feng, G.-Q. Lin, Highly Stereoselective Synthesis of 1,3-Dienes via Aryl to Vinylic 1,4-Palladium Migration/Heck Sequence. Angew. Chem. Int. Ed. 2018, 57, 5871–5875. (IF = 16.6, DOI: 10.1002/anie.201801963)