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[1]Han B.#, He X.-H.#, Liu Y.-Q., He G., Peng C.*; Li J.-L.*, Asymmetric organocatalysis: an enabling technology for medicinal chemistry. Chemical Society Reviews, 2021, 50, 1522.
[2]He X.-H., Fu X.-J., Zhan G., Zhang N., Li X., Zhu H.-P., Peng C., He G.*, Han B.* Organocatalytic asymmetric synthesis of multifunctionalized ¦Á-carboline spirooxindole hybrids that suppressed proliferation in colorectal cancer cells. Organic Chemistry Frontiers, 2022, 9, 1048.
[3]Ji Y.-L., Wang H., He X.-H.*, Zhu J., Peng C., Zhao Q., Zhan G.*, Han B.* Visible-Light-Driven Synergistic Se/Fe Catalysis for the Synthesis of 2-Aminoquinoline Derivatives. Organic Letters, 2025£¬accepted£¬10.1021/acs.orglett.5c00129.
[4]Li H.-P., Wu X.-L., Zhan G.*, Fu X.-J., Chen J.-H., He X.-H.*, Han B.* Construction of cyclopenta[b]dihydronaphthofurans via TsOH-catalyzed consecutive biscyclization of dithioallylic alcohols and 1-styrylnaphthols. Chemical Communications, 2023, 59, 2275.
[5]Li H.-P.#, He X.-H.#, Peng C., Li J.-L.*, Han B.* A straightforward access to trifluoromethylated natural products through late-stage functionalization. Natural Product Reports, 2023, 40, 988.
[6]Ji Y.-L.#, He X.-H.#, Li G., Ai Y.-Y., Li H.-P., Peng C.*, Han B.* Substrate-directed chemo- and regioselective synthesis of polyfunctionalized trifluoromethylarenes via organocatalytic benzannulation. Organic Chemistry Frontiers, 2020, 7, 563.
[7]Li G.#, He X.-H.#, Li H.-P., Zhao Q., Li D.-A., Zhu H.-P., Zhang Y.-H., Zhan G.*, Huang W.* Design, Synthesis, and Biological Evaluation of Tetrahydro-¦Á-carbolines as Akt1 Inhibitors That Inhibit Colorectal Cancer Cell Proliferation. ChemMedChem, 2022, e202200104.
[8]ÕÅÏöäì#£¬ºÎÏíºè#£¬·½×Óº®£¬ÓàÊï¹â£¬ÓÈÁ¼Õð£¬ÖìÈü±ò£¬³Â¿ÏÈ*£¬ÕŲ®Àñ*¡£»ùÓÚ¡°2020¡«2023Äê¶ÈÖÐÒ½Ò©Ê®´óѧÊõ½øÕ¹¡±·ÖÎöÖÐҽҩѧÊõ·¢Õ¹µÄÁÁµãÓëÇ÷ÊÆ. Öйú¿Æѧ£ºÉúÃü¿Æѧ, 2025, 55, 267.
[9]ºÎÏíºè, ÀîºÍƽ, ÕÔÙ», Åí³É*£¬»Æά*. ÖÐÒ©ÓÐЧ³É·ÖµÄÈý·ú¼×»ù»¯ºóÐÞÊÎÑо¿½øÕ¹ [J]. ÖлªÖÐҽҩѧ¿¯, 2022, 40 (11): 175-179+294-295.