个人简历

Prof. Shu-Li You (游书力) was born in 1975 in Luohe, Henan province, China, and received his BSc in chemistry from Nankai University in 1996. He obtained his PhD from the Shanghai Institute of Organic Chemistry (SIOC) in 2001 under the supervision of Prof. Li-Xin Dai before doing postdoctoral studies with Prof. Jeffery W. Kelly at The Scripps Research Institute. From 2004, he worked at the Genomics Institute of the Novartis Research Foundation as a Principal Investigator before returning to SIOC in 2006. Since January 2017, He has been appointed as the Director of the State Key Laboratory of Organometallic Chemistry. His current research interests include asymmetric catalysis, synthetic methodology, natural product synthesis, as well as medicinal chemistry. Prof. Shu-Li You has published over 300 peer-reviewed papers and edited two books, and applied over 30 Chinese patents as a co-inventor. Dr. You’s papers have received total citations over 23000 and his h-index is 86 (until June 2022). He is the recipient of AstraZeneca Excellence in Chemistry Award (2011), RSC Merck Award (2015), Ho Leung Ho Lee Foundation Prize for Scientific and Technological Innovation (2016), Novartis Chemistry Lectureship (2017/2018), State Natural Science Award (2nd class) (2017), and Xplorer Prize (2019).\r
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Education and Working Experience\r
Jan. 2017-Present: Director, State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, China\r
Apr. 2006-Present: Professor, State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Shanghai, China\r
Feb. 2004-Apr. 2006: Principal Investigator, Genomics Institute of the Novartis Research Foundation, San Diego, CA USA\r
Sept. 2001-Feb. 2004: Postdoctoral fellow, Professor Jeffery W. Kelly, Department of Chemistry, The Scripps Research Institute, La Jolla, CA USA\r
Sept. 1996-July 2001: Graduate student (advisor: Professor Li-Xin Dai), Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai, China\r
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Professional service\r
Associate Editor, Journal of the American Chemical Society, 2021.1.1-\r
Associate Editor, Chemical Science, 2020.7.1-\r
Associate Editor, Organometallics, 2014.12.1-2019.12.31\r
Associate Editor, Chinese Journal of Organic Chemistry, 2017.1.1-\r
Associate Editor, Beilstein Journal of Organic Chemistry, 2013.1.1-2014.12.30\r
Editorial Board, Asian Journal of Organic Chemistry, 2012.7-\r
Advisory Board, Chemical Society Reviews, 2011.1.1-\r
Advisory Board, Organic & Biomolecular Chemistry, 2011.1.1-\r
Advisory Board, Chemical Communications, 2012.9-\r
Advisory Board, ACS Catalysis, 2013.11-\r
Advisory Board, Advanced Synthesis & Catalysis, 2014.1-\r
Advisory Board, Chinese Chemical Letters, 2015.10-\r
Advisory Board, Acta Chimica Sinica, 2015.7-\r
Series Editor, Topics in Current Chemistry, 2015.4-\r
Regional Editor, Current Organocatalysis, 2014.6.1-\r
Deputy Director, The Chinese Youth Chemical Society, 2014.1-\r
Fellow of the Royal Society of Chemistry, 2014.3-\r
International Advisory Board (IAB), International Symposium on Homogeneous Catalysis, 2016.3-

研究领域

"""""Catalytic Asymmeric Dearomatization\r
Catalytic Asymmeric C-H Functionalization\r
Development of New Chiral Ligand and Catalysts\r
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近期论文

Kinetic resolution of planar chiral metallocenes using Rh-catalysed enantioselective C–H arylation Liu, C.-X.; Zhao, F.; Feng, Z.; Wang, Q.; Gu, Q.; You, S.-L.* Nat. Synth. 2022, DOI: 10.1038/s44160-022-00177-3.\r
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Palladium(0)-Catalyzed Intermolecular Asymmetric Allylic Dearomatization of Substituted β-Naphthols with Morita–Baylis–Hillman (MBH) Adducts Zhang, Q.-X.; Gu, Q.; You, S.-L.* Org. Lett. 2022, 24, 43, 8031-8035.\r
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Iridium-Catalyzed Asymmetric Allylic Benzylation with Photogenerated Hydroxy-o-Quinodimethanes Yang, P.; Wang, R.-X.; Cheng, Y.-Z.; Zheng, C.; You, S.-L.* Angew. Chem., Int. Ed. 2022, e202213520.\r
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Enantioselective C-H Functionalization Reactions Enabled by Cobalt Catalysis. Zheng, Y.; Zheng, C.; Gu, Q.; You, S.-L.* Chem Catal. 2022, DOI: 10.1016/j.checat.2022.08.020.\r
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Enantioselective Dearomative Cyclization Enabled by Asymmetric Cooperative Gold Catalysis Zhao, K.; Kohnke, P.; Yang, Z.; Cheng, X.; You, S.-L.*; Zhang, L.* Angew. Chem., Int. Ed. 2022, 61, e202207518.\r
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Rh(III)-Catalyzed Enantioselective Intermolecular Aryl C-H Bond Addition to Aldehydes Wu, Z.-J.; Wu, Z.; Zhang, W.-W.; Gu, Q.*; You, S.-L.* Chin. J. Chem. 2022, 40, 2780-2784.\r
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Condensed Matter Chemistry in Asymmetric Catalysis and Synthesis Jiang, R.; Liu, C.-X.; Yang, P.; You, S.-L.* Prog. Chem. 2022, 34, 1537-1547.\r
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Visible-light enabled synthesis of cyclopropanefused indolines via dearomatization of indoles Haung, X.-L.; Cheng, Y.-Z.*; You, S.-L.* Org. Chem. Front., 2022, 9, 5463-5468.\r
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Energy-Transfer-Enabled Dearomative Cycloaddition Reactions of Indoles/Pyrroles via Excited-State Aromatics Zhu, M.; Zhang, X.; Zheng, C.; You, S.-L. Acc. Chem. Res. 2022, 55, 2510-2525.\r
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Ag2O/squaramide cocatalyzed asymmetric interrupted Barton-Zard reaction of 8-nitroimidazo[1,2-a]pyridines Wan, Q.; Zheng, C.; Yuan, Y.-F.; You, S.-L.* Sci. Bull. 2022, 67, 16, 1688-1695.\r
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Iridium-Catalyzed Intermolecular Asymmetric Allylic Amination with Pyridones Tu, H.-F.; Nie, Y.-H.; Zheng, C.; You, S.-L.* Adv. Synth. Catal. 2022, 364, 1-7.\r
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SCpRh(III)-catalyzed Enantioselective Synthesis of Atropisomers by C2-Arylation of Indoles with 1-Diazonaphthoquinones. Yin, S.-Y.; Pan, C.; Zhang, W.-W.; Liu, C.-X.; Zhao, F.; Gu, Q.; You, S.-L.* Org. Lett. 2022, 24, 3620-3625.\r
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Chiral Bronsted Acid Catalyzed Intramolecular Asymmetric Allylic Alkylation of Indoles with Primary Alcohols. Zou, L.-M.; Huang, X.-Y.; Zheng, C.; Cheng, Y.-Z.*; You, S.-L.* Org. Lett. 2022, 24, 3544-3548.\r
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Enantioselective Synthesis of Medium-sized-ring Lactones via Iridium-catalyzed Z-Retentive Asymmetric Allylic Substitution Reaction. Ding, L.; Song, H.; Zheng, C.; You, S.-L.* J. Am. Chem. Soc. 2022, 144, 4770-4775.\r
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Hyper-crosslinked Porous Chiral Phosphoric Acids: Robust Solid Organocatalysts for Asymmetric Dearomatization Reactions. Huang, X.-Y.; Zheng, Q.; Zou, L.-M.; Gu, Q.*; Tu, T.*; You, S.-L.* ACS Catal. 2022, 12, 4545-4553.\r
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Pd-Catalyzed Asymmetric Dearomative Arylation of Indoles via a Desymmetrization Strategy Nie, Y.-H.; Komatsuda, M.; Yang, P.; Zheng, C.; Yamaguchi, J.*; You, S.-L.* Org. Lett. 2022, 24, 1481-1485.\r
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Palladium-Catalyzed Dearomative Alkoxyallylation of 3-Nitroindoles with Allyl Carbonates. Liu, X.-J.; Zhang, W.-Y.; Zheng, C.; You, S.-L.* Angew. Chem. Int. Ed. 2022, 61, e2022001.\r
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Rhodium(III)-Catalyzed Enantioselective C–H Activation/Annulation of Ferrocenecarboxamides with Internal Alkynes. Wang, Q.; Nie, Y.-H.; Liu, C.-X.; Zhang, W.-W.; Wu, Z.-J.; Gu, Q.; Zheng, C.*; You, S.-L.* ACS Catal. 2022, 12, 3083-3093.\r
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Multicomponent Reactions and Photo/Electrochemistry Join Forces: Atom Economy Meets Energy Efficiency. Coppola, G. A.; Pillitteri, S.; Van der Eycken, E. V.*; You, S.-L.*; Sharma, U. K.* Chem. Soc. Rev. 2022, 51, 2313-2382.\r
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SmI2-mediated enantioselective reductive dearomatization of non-activated arenes. Wang, Y.; Zhang, W.-Y.; Yu, Z.-L.; Zheng, C.; You, S.-L.* Nature Synthesis 2022, 1, 401-406.\r