常州大学制药与生命科学学院导师介绍:徐华栋
CONTACT: School of Pharmaceutical and Life Sciences Changzhou University (常州大学制
CONTACT:
School of Pharmaceutical and Life Sciences
Changzhou University (常州大学制药与生命科学学院)
Changzhou, Jiangsu 213164, China
Cell: ***********
Email Address:huadongxu@gmail.com
xuhd@cczu.edu.cn
RESEARCH INTERESTS:
Organic methodology research by Organometallic Chemistry and Sugar Chemistry.
(有机方法学研究,重点运用金属有机化学方法和糖化学方法)
Drug research and development for treating cancers.
(新型抗癌药物的研究)
FUNDINGS:
2013国家自然科学基金面上项目(项目批准号:21272077)
2011国家自然科学青年基金(项目批准号:21002032)
2011浦江人才基金 (11PJ1403100)
PROFESSIONAL EXPERIENCE:
2012-presentProfessor
School of Pharmaceutical and Life Sciences, Changzhou University, China.
2010-2012Associate Professor
East China Normal University, Shanghai. (华东师范大学)
2009-2010Senior Research Scientist
PharmaResources Shanghai CO. LTD.(上海鸿博智源医药研究有限公司)
2007-2009Postdoctoral Research Associate
Chemistry Department, University of Wisconsin-Madison, USA. (威斯康星大学-麦迪逊分校)
2003-2007Teaching Assistant and Research Assistant
Chemistry Department, University of Illinois at Chicago, USA.(伊利诺依大学-芝加哥分校)
2000-2003Assistant Researcher
Daiwei Ma’ s Research Group, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences (中国科学院上海有机化学研究所)
EDUCATIONAL BACKGROUND:
2007Ph.D in Organic Chemitry, Chemistry Department, University of Illinois at Chicago, USA. (伊利诺依大学-芝加哥分校)
2000 Master in Organic Chemistry, East China University of Science and Technology (Shanghai, P. R. China) (华东理工大学)
1998 Bachelor in Chemistry, Lanzhou University ( 兰州大学)
SELECTED PUBLICATIONS:
1.Synthesis of β-diazo-α-ketoamide and their cyclopropanation reaction with alkenes. Chen, X.; Hu, W.; Li, X.*; Xu, H-D.*Chin. J. Syn. Chem. 2012, 20, 1.
2.3-Diazo-N-[(2S)-1-hydroxypropan-2-yl]-2-oxopropanamide. Chen, X.; Hu, W.; Li, X.*; Xu, H-D.* Acta Cryst. 2011, E67, o1192.
3.Diastereoselectively Switchable Enantioselective Trapping of Carbamate Ammonium Ylides with Imines, Jiang, J.; Xu, H-D.; Xi, J.; Hu, W.* J. Am. Chem. Soc. 2011, 133, 8428.
4.Thermodynamic Control of the Electrocyclic Ring Opening of Cyclobutenes: C=X Substituents at C-3 Mask the Kinetic Torquoselectivity Um, J. M.; Xu, H-D.; Houk, K. N. *; Tang, W. * J. Am. Chem. Soc. 2009, 131, 6664.
5.DABCO-Catalyzed 1,4-Bromolactonization of Conjugated Enynes: Highly Stereoselective Formation of a Stereogenic Center and an Axially Chiral Allene, Zhang, W.; Xu, H-D.; Tang, W. * J. Am. Chem. Soc. 2009, 131, 3832.
6.Highly Selective Synthesis of Cyclobutenes via Transition Metal Catalyzed Rearrangement of Cyclopropyl Metal Carbenes. Xu, H-D., Zhang, W., Shu, D., Werness, J. B. and Tang, W. * Angew. Chem. 2008,47,8933.
7.Direct stereocontrolled synthesis of 3-amino-3-deoxy-β-mannopyranosides: importance of the nitrogen protecting group on stereoselectivity. Crich, D. *; Xu, H-D. J. Org. Chem. 2007, 72, 5183
8.Total synthesis and structural verification of some novel branched alkanes with quaternary carbons isolated from diverse geological sources. Crich, D. *; Xu, H-D.; Kenig, F. J. Org. Chem. 2006, 71, 5016.
9.Chiral 1,2,3,4-tetrahydroquinolinyl-oxazoline ligands for Ru-catalyzed asymmetric transfer hydrogenation of ketones. Zhou, Y.; Tang, F.; Xu, H-D.; Wu, X.; Ma, J.; Zhou Q. * Tetrahedron: Asymmetry 2002, 13, 469.
10.Remote substituent effect in palladium/pyridinyl-oxazolines catalyzed asymmetric allylic alkylation. Li, Z.; Tang, F.; Xu, H-D.; Wu, X.; Zhou, Q. *; Chan, A. S. C. J. Mol. Catal. A. 2002, 1-7, 3756.
11.A short synthesis of the HIV-protease inhibitor nelfinavir via a distereoselective addition of ammonia to the α-β-unsaturated sulfoxide derived from (R)-glyceraldehyde acetonide. Ma, D. *; Zou, B.; Zhu, W.; Xu, H-D. Tetrahedron Lett. 2002, 43, 8511.
12.Asymmetric hydroarylation of norbornene derivatives catalyzed by palladium complexes of chiral quinolinyl-oxazolines. Wu, X.; Xu, H-D.; Tang, F.; Zhou, Q.* Tetrahedron Asymmetry 2001, 12, 2565.
13.Enantioselecive Heck-type hydroarylation of norbornene with phenyl iodide catalyzed by palladium/quinolinyloxazolines. Wu, X.; Xu, H-D.; Zhou, Q. *; Chan, A. S. C. Tetrahedron: Asymmetry 2000, 11, 1255.
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