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¡¡¡¡ºÎ¿Æå«Í¬Ñ§£¬2010Äê7Ô±ÏÒµÓÚÎ÷ºþѧԺ»¯Ñ§×¨Òµ£¬Í¬Ä꿼ÈëËÄ´¨Ê¦·¶´óѧ¹¥¶Á˶ʿѧλ¡£2015Äê9Ô½øÈëÎ÷°²½»Í¨´óѧ¹¥¶Á²©Ê¿Ñ§Î»¡£½üÄêÀ´ÔÚ¹ú¼ÊȨÍþ¿¯Îï·¢±í¶àƪÎÄÕ£¬2017ÄêÔÚAngew. Chem. Int. Ed¡¶µÂ¹úÓ¦Óû¯Ñ§¡··¢±í¡°Acceptorless Dehydrogenation of N-Heterocycles by Merging Visible-Light Photoredox Catalysis and Cobalt Catalysis"¡¶¿É¼û¹âºÍ½ðÊôîÜЭͬ´ß»¯µÄµªÔÓ»·ÍÑÇâ·´Ó¦¡·Ó°ÏìÒò×Ó´ïIF = 11.709

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¡¡¡¡1. He, K.-H.; Tan, F.-F.; Zhou, C.-Z.; Zhou, G.-J.; Yang, X.-L.; Li, Y.*£¬¡°Acceptorless Dehydrogenation of N-Heterocycles by Merging Visible-Light Photoredox Catalysis and Cobalt Catalysis"¡¶¿É¼û¹âºÍ½ðÊôîÜЭͬ´ß»¯µÄµªÔÓ»·ÍÑÇâ·´Ó¦¡· Angew. Chem. Int. Ed¡¶µÂ¹úÓ¦Óû¯Ñ§¡·, 2017, 56, 3080 (IF = 11.709).

¡¡¡¡2.He, K.-H^.; Zhang, W.-D^.; Yang, M.-Y.; Tang, K.-L.; Qu, M.; Ding, Y.-S.; Li, Y.* ,"Redox-Divergent Hydrogen-Retentive or Hydrogen-Releasing Synthesis of 3,4-Dihydroisoquinolines or Isoquinolines ¡¶Ñõ»¯»¹Ô­Çâ±£³ÖÐÔ»òÊÍ·ÅÇâÆøµÄ3,4-¶þÇâÒìà­ßø»òÒìà­ßøµÄºÏ³É¡·", Org. Lett. ¡¶Óлú»¯Ñ§Í¨Ñ¶¡· 2016, 18, 2840-2843 (IF = 6.324). (^ equal contribution).

¡¡¡¡3.He, K-H.; Li,Y.*, Oxidant-Free Dehydrogenative Coupling Reactions via Hydrogen Evolution¡¶ÎÞÑõ»¯¼ÁÌõ¼þµÄÇâÍÑżÁª·´Ó¦), ChemSusChem. ¡¶»¯Ñ§¿É³ÖÐø»¯Ñ§¡· 2014, 7, 2788-2790 (IF = 7.117).

¡¡¡¡4. Li, H.; He, K.-H.; Liu, J., Wang, B.-Q., Zhao, K.-Q. Shi, Z.-J., Straightforward synthesis of phenanthrenes from styrenes and arenes. ¡¶±½ÒÒÏ©ºÍ·¼ÌþÖ±½ÓºÏ³É·Æ¡· Chem. Commun. ¡¶»¯Ñ§Í¨Ñ¶¡·2012, 48, 7028-7030 (IF = 6.118).

¡¡¡¡5. Li, Y.; Wang, W.-H.; He, K.-H.; Shi, Z.-J. Mechanistic Insight into the Regioselective Palladation of Indole Derivatives: Tetranuclear Indolyl Palladacycles with High C2¨CPd or C3¨CPd Bond Selectivity.Organometallics ¡¶Óлú½ðÊô¡·2012, 31, 4397-4400 (IF = 4.253).

¡¡¡¡6. Li, Y.; Zhang, X.-S.; Chen, K.; He, K.-H.; Pan, F.; Li, B.-J.; Shi, Z.-J. N-Directing Group Assisted Rhodium-Catalyzed Aryl C-H Addition to Aryl Aldehydes. Org. Lett., ¡¶Óлú»¯Ñ§Í¨Ñ¶¡· 2012,14, 636 (IF = 6.324).

¡¡¡¡7. Li, H., Zhu, R.-Y., Shi, W. -J., He, K-H., Shi, Z.-J. Synthesis of Fluorenone Derivatives through Pd-Catalyzed Dehydrogenative Cyclization. Org. Lett. ¡¶Óлú»¯Ñ§Í¨Ñ¶¡·2012, 14, 4850¨C4853 (IF = 6.324).

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