¹Ù·½QQ
¹Ù·½Î¢ÐÅ
ÊÖ»ú°æ
ÄúµÄλÖãºÊ×Ò³ >˶ʿÉúµ¼Ê¦>ÖÐÒ©»¯Ñ§·½Ïò>ÏêϸÄÚÈÝ

ÖÐÒ©»¯Ñ§·½Ïò

ºÎÏíºè

d9d56045f7124e778f31e83144470543.Jpeg

 

     ºÎÏíºè£¬Öй²µ³Ô±£¬ÖÐҽѧ²©Ê¿ºó£¬ÖÐҩѧ²©Ê¿£¬Ë¶Ê¿Ñо¿Éúµ¼Ê¦£¨ÆƸñ£©£¬ÖйúÖÐÒ½Ò©±¨¡¶ÇàÄêר¿¯¡·ÇàÄê±àί¡£Ö÷Òª´ÓÊÂÖÐҩҩЧÎïÖÊ×÷ÓûúÖÆ¡¢Ò©Ð§ÎïÖʺóÐÞÊμ°ÊµÑé½Ìѧ¸Ä¸ïÑо¿£»Ö÷½²±¾¿ÆÉú¡¶Ò©Îﻯѧ¡·¡¢¡¶Ò©ÎﻯѧʵÑé¡·µÈ¿Î³Ì£»Ö÷³Ö¹ú¼Ò×ÔÈ»¿Æѧ»ù½ðÇàÄê»ù½ð¡¢Öйú²©Ê¿ºó¿Æѧ»ù½ðÃæÉÏÏîÄ¿¡¢ËÄ´¨Ê¡±¾¿Æ¸ßУ´´ÐÂÐÔʵÑéÏîÄ¿µÈ¸÷¼¶ÏîÄ¿6ÏÒÔµÚÒ»×÷Õß»òͨѶ×÷ÕßÔÚChem Soc Rev¡¢Nat Prod Rep¡¢Org Chem Front¡¢Org Lett¡¢Chem Commun¡¢Öйú¿Æѧ£ºÉúÃü¿ÆѧµÈ¹úÄÚÍâÆÚ¿¯·¢±íѧÊõÂÛÎÄ20Óàƪ£¬°üÀ¨¸ß±»ÒýÂÛÎÄһƪ£¬·âÃæÂÛÎÄ3ƪ¡£

    E-mail£ºhexianghong@cdutcm.edu.cn

 ¶þ¡¢´ú±íÐԳɹû£¨¿Éº¬³Ðµ£ÏîÄ¿¡¢·¢±íÂÛÎÄ¡¢ÂÛÖø¡¢»ñ½±µÈ£©

£¨Ò»£©³Ðµ£ÏîÄ¿

1.¹ú¼Ò×ÔÈ»¿Æѧ»ù½ðÇàÄê¿Æѧ»ù½ðÏîÄ¿£¨CÀࣩ£¬82304701£¬30Íò£¬Ö÷³Ö

2.Öйú²©Ê¿ºó¿Æѧ»ù½ðÃæÉÏÏîÄ¿£¬8Íò£¬2023M730379£¬Ö÷³Ö

3.ËÄ´¨Ê¡±¾¿Æ¸ßУ´´ÐÂÐÔʵÑéÏîÄ¿£¬Ö÷³Ö

4.mg老虎机游戏ÐÓÁÖѧÕß²©Ê¿ºóרÏBSH2023012£¬12Íò£¬Ö÷³Ö

£¨¶þ£©·¢±íÂÛÎÄ

[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 Reviews202150, 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 Frontiers20229, 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 Letters2025£¬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 Communications202359, 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 Reports202340, 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 Frontiers20207, 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. ChemMedChem2022, 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.


ÖÕÉó£ºÒ©Ñ§Ôº×ܹÜÀíÕ˺Å