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李祥乾

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助理研究员

性别：男

在职信息：在职

所在单位：微生物技术研究院

入职时间：2019-09-23

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[21] 虞燕燕. Self-developed NF-κB inhibitor 270 protects against LPS-induced acute kidney injury and lung injury. Biomedicine & Pharmacotherapy, 147, 112615, 2022.
[22] 李超. Highly Selective Protein Tyrosine Phosphatase Inhibitor, 2,2 ',3,3 '-Tetrabromo-4,4 ',5,5 '-tetrahyd. Molecular Pharmaceutics, 1839, 2019.
[23] 李祥乾. Rational Multitargeted Drug Design Strategy from the Perspective of a Medicinal Chemist. Journal of Medicinal Chemistry, 10581, 2021.
[24] 史晓琳. Palladium-Catalyzed Remote C-H Phosphonylation of Indoles at the C4 and C6 Positions by a Radical Ap. Angew. Chem. Int. Ed, 13871, 2021.
[25] 戴佳佳. Toward a Treatment of Cancer: Design and In Vitro/In Vivo Evaluation of Uncharged Pyrazoline Derivat. INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES , 23, 2022.
[26] 李宇修. Highly E-Selective Synthesis of alpha-Fluoro-beta-arylalkenyl Sulfones from gem-Difluoroalkenes with. The Journal of Organic Chemistry, 6983, 2021.
[27] 史大永. Palladium-Catalyzed Remote C-H Phosphonylation of Indoles at the C4 and C6 Positions by a Radical Ap. Angew. Chem. Int. Ed, 60, 13871, 2021.
[28] 史婷. Nitrogenous Compounds from the Antarctic Fungus Pseudogymnoascus sp. HSX2#-11. Molecules, 26, 2021.
[29] 李宇修. Highly E-Selective Synthesis of alpha-Fluoro-beta-arylalkenyl Sulfones from gem-Difluoroalkenes with. The Journal of Organic Chemistry, 86, 6983, 2021.
[30] 史婷. Sesquiterpenoids From the Antarctic Fungus Pseudogymnoascus sp. HSX2#-11. Frontiers in Microbiology, 12, 2021.
[31] 李祥乾. Rational Multitargeted Drug Design Strategy from the Perspective of a Medicinal Chemist. 《Journal of Medicinal Chemistry》, 64, 10581, 2021.
[32] 李晓伟. Nickel-Catalyzed Arylation of C(sp(3))-O Bonds in Allylic Alkyl Ethers with Organoboron Compounds. Organic Letters, 23, 6612, 2021.
[33] 陈平. A Unified Approach for Divergent Synthesis of Heterocycles via TMSOTf-Catalyzed Formal [3+2] Cycload. Advanced Synthesis & Catalysis, 2021.
[34] 李祥乾. Rational Multitargeted Drug Design Strategy from the Perspective of a Medicinal Chemist. Journal of Medicinal Chemistry, 10581, 2021.
[35] Luo, Jiao. Antidiabetic activity in vitro and in vivo of BDB, a selective inhibitor of protein tyrosine phospha. BRITISH JOURNAL OF PHARMACOLOGY, 177, 4464, 2020.
[36] 李晓伟. AcOH-mediated aerobic oxidative synthesis of 2-thioalkylbenzothiazoles via a three-component reactio. Tetrahedron Letters, 61, 2020.
[37] Zhang, Liang. 16S rRNA Sequencing and Metagenomics Study of Gut Microbiota: Implications of BDB on Type 2 Diabetes. MARINE DRUGS, 18, 2020.
[38] 李宇修. Visible-Light-Promoted E-selective Synthesis of α-fluoro-β-arylalkenyl Sulfides via Deoxygenation . 化学通讯, 2152, 2021.
[39] 李宇修. Visible-light-promoted E-selective synthesis of alpha-fluoro-beta-arylalkenyl sulfides via the deoxy. chemical communications, 57, 2152, 2021.
[40] 史大永 , 李祥乾 and Shi, Xiaolin. Ligand- and Additive-Free 2-Position-Selective Trifluoromethylation of Heteroarenes Under Ambient Co. FRONTIERS IN CHEMISTRY, 7, 2019.

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