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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] 史婷. Nitrogenous Compounds from the Antarctic Fungus Pseudogymnoascus sp. HSX2#-11. Molecules, 26, 2021.
[22] 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.
[23] 史婷. Sesquiterpenoids From the Antarctic Fungus Pseudogymnoascus sp. HSX2#-11. Frontiers in Microbiology, 12, 2021.
[24] 李祥乾. Rational Multitargeted Drug Design Strategy from the Perspective of a Medicinal Chemist. 《Journal of Medicinal Chemistry》, 64, 10581, 2021.
[25] 李晓伟. Nickel-Catalyzed Arylation of C(sp(3))-O Bonds in Allylic Alkyl Ethers with Organoboron Compounds. Organic Letters, 23, 6612, 2021.
[26] 陈平. A Unified Approach for Divergent Synthesis of Heterocycles via TMSOTf-Catalyzed Formal [3+2] Cycload. Advanced Synthesis & Catalysis, 2021.
[27] 李祥乾. Rational Multitargeted Drug Design Strategy from the Perspective of a Medicinal Chemist. Journal of Medicinal Chemistry, 10581, 2021.
[28] 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.
[29] 李晓伟. AcOH-mediated aerobic oxidative synthesis of 2-thioalkylbenzothiazoles via a three-component reactio. Tetrahedron Letters, 61, 2020.
[30] Zhang, Liang. 16S rRNA Sequencing and Metagenomics Study of Gut Microbiota: Implications of BDB on Type 2 Diabetes. MARINE DRUGS, 18, 2020.
[31] 李宇修. Visible-Light-Promoted E-selective Synthesis of α-fluoro-β-arylalkenyl Sulfides via Deoxygenation . 化学通讯, 2152, 2021.
[32] 李宇修. Visible-light-promoted E-selective synthesis of alpha-fluoro-beta-arylalkenyl sulfides via the deoxy. chemical communications, 57, 2152, 2021.
[33] 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.
[34] 史大永 , 李祥乾 and Li, Xiaowei. Recent advances in transition-metal-catalyzed incorporation of fluorine-containing groups. Beilstein Journal of Organic Chemistry, 15, 2213, 2019.
[35] 史大永 and 李祥乾. Highly Selective Protein Tyrosine Phosphatase Inhibitor, 2,2′,3,3′- Tetrabromo-4,4′,5,5′-tetrahy. Molecular Pharmaceutics , 16, 1839, 2019.
[36] 史大永 and 李祥乾. Design, synthesis and biological evaluation of bromophenol-thiazolylhydrazone hybrids inhibiting the. European Journal of Medicinal Chemistry, 177, 153, 2019.
[37] 史大永 and 李祥乾. Inhibition of PTP1B blocks pancreatic cancer progression by targeting the PKM2/AMPK/mTOC1 pathway. Cell Death & Disease, 10, 2019.
[38] 李祥乾 and 史大永. Toward a treatment of diabesity: In vitro and in vivo evaluation of uncharged bromophenol derivative. EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY, 166, 178, 2019.

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