宋淳
山东大学药学院教授,博士生导师
宋淳 ,男,1967年1月出生,现为山东大学药学院教授,博士生导师美国化学学会
研究领域
1. 药物化学:基于计算机靶标模拟的小分子和大分子药物的设计合成与修饰
2. 药理学研究:药物效应动力学,研究药物对机体的作用,包括药物的作用和效应、作用机制及临床应用等。
药物代谢动力学,研究药物在机体的作用下所发生的变化及其规律,包括药物在体内的吸收、分布、代谢和排泄过程,特别是血药浓度随时间变化的规律、影响药物疗效的因素等。
3. 生物分析学研究:用来测定临床前/临床药物动力学参数的生物分析技术研究、方法验证及标准实验室管理系统。
4. 新药开发:开展针对妇科肿瘤、消化道肿瘤的抗肿瘤原创药物(一类新药)的研发。
经历
1990.9-1993.7 理学硕士 山东大学 化学系
1998.2-2001.11哲学博士 Brigham Young University 有机化学
2009.9-2012.7 哲学博士 天津大学 药学院
1993.7-1995.12 工程师 山东华鲁科技公司
1996.1-1997.9 工程师 山东省科学院
2001.11-2007.5 高级科学家 辉瑞制药
2008.3-2010.5 首席科学家 日东电工
2010.8-2011.4 资深科学家 诺华制药
2011.5-至今教授 山东大学药物制剂与释药系统研究中心
年度招生
研究生2名,博士生2名
论文著作
论文
1.Enantioselectiveβ-Boration of Acyclic Enones by a [2.2] Paracyclophane -Based N-HeterocyclicCarbene Copper(I) Catalyst. J. Org. Chem. 2013, 78, 1677−1681.
2.Synthesis of planar chiral[2.2]paracyclophane-based amino thioureas andtheir application in asymmetric aldol reactions of ketones with isatins.Tetrahedron: Asymmetry. 2013,24:1082–1088.
3.Synthesis of novel planar chiral Ag and RhN-heterocyclic carbene complexes derived from [2.2]paracyclophane and theirapplication in ultrasound assisted asymmetric addition reactions oforganoboronic acids to aldehydes. Tetrahedron: Asymmetry .24 (2013) 241–248.
4.Synthesis of newalkoxy/sulfonate-substituted carbene precursors derived from[2.2]paracyclophane and their application in the asymmetric arylation ofaldehydes. Tetrahedron: Asymmetry.2012,23 :1369–1375.
5.Planar Chirality Change in DediazoniationReactions of Paracyclophanes and Mechanistic Implication. Organicletters.2012,14:5436–5439.
6.Asymmetric β-Boration ofr,β-UnsaturatedN-Acyloxazolidinones by [2.2]Paracyclophane-Based Bifunctional Catalys .Organicletters. 2012,14:5780–5783.
7.Benzophenone imine paracyclophane amination.Tetrahedron Lett. 2012, (submitted).
8.Novel effecinet NCH ligands ascross-coupling catalyst and in chiral organocatalysis. Acc.Chem.Res2012,(submitted).
9.Synthesis of cyclophanes with planarandhelical chirelity. J. Org. Chem. 2011, 76, 1953–1956.
10.Synthesis of planar chiral imidazo [1,5-α]pyridinium salts based on [2.2] paracyclophane for asymmetric β-borylation ofenones. Tetrahedron: Asymmetry. 22 (2011) 1055–1062.
11.A new chapter: hematopoietic stem cells aredirect players in immunity. Cell &Bioscience. 2011, 1: 33-37.
12.Synthesis of planar chiral imidazo [1,5-α]pyridinium salts based on [2.2] paracyclophane for asymmetric β-borylation ofenones. Tetrahedron: Asymmetry 2011, 22. 1055.
13.Synthesis of cyclophanes with planarandhelical chirelity. J. Org. Chem. 2011, 76(6), 1953.
14.Planar chiral imidazolium salts based on[2.2]paracyclophane in the asymmetric rhodium-catalyzed 1,2-addition ofarylboronic acids aldehydes. Tetrahedron: Asymmetry. 2010, 21(3), 292.
15.An efficient catalyst system forPd-catalyzed amination of [2.2]paracyclophanyl bromides. J. Org. Chem. 2009,74(17), 6867.
16.Asymmetric allylation of aldehydes withalltrichlorosilane using aza-paracyclophane -oxazoline-N-oxide catalysts.Tetrahedron. Lett. 2006, 47, 8611- 861.
17.Rapid homogeneous-phase sonogashiracoupling reaction using controlled microwave heating in water (invited paper).Green Chemistry, 2005.
18.Palladium catalyzed Suzuki-Miyaura couplingwith aryl chlorides using a bulky phenanthryl N-heterocyclic carbeneligand.Tetrahedron. 2005, 61(31), 7438-7446.
19.Bis-paracyclophane N-heterocycliccarbene-ruthenium catalyzed asymmetric ketone hydrosilylation. TetrahedronLett. 2005, 46(18), 3241-3244.
20.Asymmetric imidazolium catalyzed conjugateaddition. Angew. Chem. Inter. Eng.2003, 42, 5871-5874.
专利
1.PCT/CN2013/077729:Lanthanide labeled peptide and use thereof
2.US2013/882,797 :PEGYLATED CYCLOPAMINEANALOGUE, PREPARATION METHOD AND USES THEREOF
3.PCT/CN2011/000303: PEGYLATED CYCLOPAMINEANALOGUE, PREPARATION METHOD AND USES THEREOF
4.扩增造血干细胞的化合物及其应用
科研项目
1.21310004011267防治放化疗造成的白细胞减少症的一类新药KEM0977023 临床前研究 山东省科技厅
2.23110371611014新型妇科肿瘤化学治疗体系及其评价系统的建立 教育部创新基金
3.21310005081323新型热休克蛋白90抑制剂的设计合成及抗癌检测 济南市科技局
4.21310005201301 新型大取代基的N-杂环卡宾配体(NHC)配体设计,合成及应用的研究 山东省自然科
获奖项目
2011 泰山学者海外特聘专家
参考资料
最新修订时间:2023-10-27 21:01
目录
概述
研究领域
经历
参考资料