基本介紹
- 中文名：宋淳
- 國籍：中國
- 出生日期：1967年1月
- 畢業院校：山東大學
- 學位/學歷：博士
- 職業：教師
- 專業方向：藥學
研究領域,經歷,年度招生,論文著作,科研項目,獲獎項目,
研究領域
1. 藥物化學：基於計算機靶標模擬的小分子和大分子藥物的設計合成與修飾
2. 藥理學研究：藥物效應動力學，研究藥物對機體的作用，包括藥物的作用和效應、作用機制及臨床套用等。
藥物代謝動力學，研究藥物在機體的作用下所發生的變化及其規律，包括藥物在體內的吸收、分布、代謝和排泄過程，特別是血藥濃度隨時間變化的規律、影響藥物療效的因素等。
3. 生物分析學研究：用來測定臨床前/臨床藥物動力學參數的生物分析技術研究、方法驗證及標準實驗室管理系統。
4. 新藥開發：開展針對婦科腫瘤、消化道腫瘤的抗腫瘤原創藥物（一類新藥）的研發。
經歷
1990.9-1993.7 理學碩士 山東大學 化學系
1998.2-2001.11哲學博士 Brigham Young University 有機化學
2009.9-2012.7 哲學博士 天津大學 藥學院
1993.7-1995.12 工程師 山東華魯科技公司
1996.1-1997.9 工程師 山東省科學院
2001.11-2007.5 高級科學家 輝瑞製藥
2008.3-2010.5 首席科學家 日東電工
2010.8-2011.4 資深科學家 諾華製藥
2011.5-至今教授 山東大學藥物製劑與釋藥系統研究中心
年度招生
研究生2名，博士生2名
論文著作
論文
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.
專利
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.擴增造血幹細胞的化合物及其套用
