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董春娥
中文, 英语
湖北省
武汉大学
Medical School
  • 2000年 - 有机化学博士,中国科学院成都有机化学研究所
  • 在维也纳大学、渥太华大学和伊利诺伊大学香槟分校做博士后研究
  • 2000-2001 - 维也纳大学,博士后研究员
  • 2002-2004 - 渥太华大学,博士后研究员
  • 2004-2006 - 伊利诺伊大学香槟分校,博士后研究员
具有潜在药物活性小分子的新法合成研究
有机化学新方法研究,特别是碳-杂键的构键以及不对称催化研究
生物模拟离子通道的设计合成和活性研究
  • An Expedient Approach to Highly Enantioenriched Cyclic Nitrones Mediated by Robust and Recoverable C3-Symmetric Cinchonine-Squaramide Catalyst, 董春娥*, 2012
  • A New Pathway for Phthalazine Derivatives via Metal-free Cyclization of ortho-Alkynylphenyl ketones and Hydrazine, 董春娥*, 2013
  • A simple and straightforward approach toward selective C=C bond reduction by hydrazine, 董春娥*, 2012
  • Enhanced efficiency of recyclable C3-symmetric cinchonine-squaramides in the asymmetric Friedel-Crafts reaction of indole with alkyl trifluoro pyruvate, 董春娥*, 2012
  • Chiral Squaramide as Multiple H-Bonds Donor Organocatalyst for Asymmetric Michael addition of 1, 3-Dicarbonyl Compounds to Nitroolefins, 董春娥*, 2012
  • Identification and structure-Activity relationships of a novel series of estrogen receptor ligands based on 7-thiabicyclo[2,2,1]hept-2-ene-7-oxide, 董春娥, 2012
  • C3-symmetric cinchonine-squaramide as new highly efficient and recyclable organocatalyst for enantioselective michael addition, 董春娥*, 2011
  • A Novel C3-Symmetric Prolinol-Squaramide Catalyst for the Asymmetric Reduction of Ketones by Borane, 董春娥*, 2011
  • Novel bifunctional chiral squaramide-amine catalysts for highly enantioselective addition of mono diketones to nitroalkenes, 董春娥*, 2011
  • Facile synthesis of 1,3,4-benzotriazepines and 1-arylamide-1H-indazoles via palladium catalyzed cyclization of aryl isocyanates and aryl hydrazones under microwave irradiation, 董春娥*, 2010
  • Discovery of novel SERMs with a ferrocenyl entity based on the oxabicyclo [2.2.1]hepte-ne scaffold and evaluation of their antiproliferative effects, 董春娥, 2012
  • Biocyclic core estrogens as full antagonists: synthesis, biological evaluation and structure-activity relationships of estrogen receptor ligands based on bridged oxabicyclic core arylsulfon-amides, 董春娥, 2012
  • Development of selective estrogen receptor modulator SERM-like activity through an indirect mechanism of estrogen receptor antagonism defining the binding mode of 7-oxabicyclo[2.2.1] hept-5-ene scaffold core ligands, 董春娥, 2012
  • Progress in small molecular inhibitors of protein protein interactions, 董春娥*, 2010
药物化学 合成 有机化学 碳-杂键 不对称催化 仿生学 离子通道 化学合成 研究 药品

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