張士磊,男,蘇州大學藥學院教授,已發表SCI論文30多篇,著作章節1篇,專利2項。
基本介紹
- 中文名:張士磊
- 畢業院校:中國海洋大學
- 職業:教師
- 性別:男
- 職稱:蘇州大學教授
人物經歷,研究方向,主要貢獻,
人物經歷
1998.9-2002.7:中國海洋大學化學化工學院海洋化學專業,大學本科
2002.9-2007.7:中國科學院上海藥物研究所,藥物化學,博士學位
2007.7-2008.8:華東理工大學藥學院藥物化學系,講師
2008.10-2012.1:美國新墨西哥大學(University of New Mexico),有機化學,博士後
2012.2-:蘇州大學醫學部藥學院,教授
研究方向
(1)抗癌藥物和抗菌藥物研究
(2)發展高效的催化方法構建藥物優勢結構
主要貢獻
(1) Xie, H.; Zhang, S.;* Li, H.; Zhang, X.; Zhao, S.; Xu, Z.; Song, X.; Yu, X.;* Wang, W.*“Total Synthesis of Polyene Natural Product Dihydroxerulin by Mild Organocatalyzed Dehydrogenation of Alcohols” Chem. Eur. J. 2012, 18, 2230-2234.
(2) Zhang, S.-L.; Xie, H.-X.; Zhu, J.; Li, H.; Zhang, X.-S.; Li, J.;* Wang, W.* “Organocatalytic enantioselective β-functionalization of aldehydes via oxidation of enamines and their application in cascade reactions” Nature Communications. 2011, 2, 211.
(3) Zhang, S.-L.; Xie, H.-X.; Song, A.-G.; Wu, D.-Y.; Zhu, J.; Zhao, S.-H.; Li, J.; Yu, X.-H.;* Wang, W.* “Efficient preparation of trans α-,β-unsaturated aldehydes from saturated aldehydes by oxidative enamine catalysis” Sci. China. Chem. 2011, 54, 1932-1936.
(4) Xie, H.; Zhang Y.; Zhang, S.; Chen, X.; Wang, W.* “Bifunctional Cinchona Alkaloid Thiourea Catalyzed Highly Efficient, Enantioselective Aza-Henry Reaction of Cyclic Trifluoromethyl Ketimines: Synthesis of Anti-HIV Drug DPC 083” Angew. Chem. Int. Ed. 2011, 50, 11773-11776.
(5) Liu, G.; Zhang, S.; Li, H.; Zhang, T.; Wang W.* “Organocatalytic Enantioselective Friedel-Crafts Reactions of 1-Naphthols with Aldimines” Org. Lett., 2011, 13, 828-831.
(6) Deng, J.; Zhang, S.; Ding, P.; Jiang, H.; Wang, W.;* Li, J.* “Facile Creation of Privileged 3-Indolyl-3-hydroxy-2-oxindoles by an Organocatalytic Enantioselective Friedel-Crafts Reaction of Indoles with Isatins” Adv. Synth. Catal., 2010, 352, 833-838.
(7) Zhang, S.; Li, J;* Zhao, S.; Wang, W.* “1,3-Benzodithiole-1,1,3,3-tetraoxide (BDT) as a versatile methylation reagent in catalytic enantioselective Michael addition reaction with enals” Tetrahedron Lett. 2010, 51, 1766-1769.
(8) Zhang, H.; Zhang, S.; Liu, L.; Luo, G.; Duan, W.-H.;* Wang, W.* “Synthesis of Chiral 3-Substituted Phthalides by a Sequential Organocatalytic Enantioselective Aldol-Lactonization Reaction. Three-Step Synthesis of (S)-(−)-3-Butylphthalide” J. Org. Chem. 2010, 75, 368–374.
(9) Xue, F.; Zhang, S.; Liu, L.; Duan, W.;* Wang, W.* “Organocatalytic Enantioselective Cross-Aldol Reactions of Aldehydes with Isatins: Formation of Two Contiguous Quaternary Centered 3-Substituted 3-Hydroxyindol-2-ones” Chem. Asian J., 2009, 4, 1664-1667.
(10) Zhang,S.; Zhang, Y.; Ji, Y.; Li, H.; Wang, W.* “Catalytic enantioselective conjugate addition of fluorobis(phenylsulfonyl)methane to enals: synthesis of chiral monofluoromethyl compounds” Chem. Commun., 2009, 4886-4888.
(11) Li, H.; Zhang, S.-L.; Yu, C. G.; Song, X.-X.; Wang, W.* “Synthesis of Chiral Fluorinated Quaternary Carbon Containing -Ketoesters by Direct Organocatalytic Asymmetric Conjugate Addition Reactions of Fluoroketoesters with Nitroolefins” Chem. Commun., 2009, 2136-2138.
(12) Zu, L.-S.; Zhang, S.-L.; Xie, H.-X.; Wang, W.* “Catalytic Asymmetric oxa-Michael-Michael Cascade for Facile Construction of Chiral Chromans via an Aminal Intermediate” Org. Lett., 2009, 11, 1627-1630.
(13) Ma, S.; Zhang,S.; Duan, W.;* Wang, W.*“An efficient enantioselective synthesis of (+)-(S)-[n]-gingerol via the L-proline-catalyzed aldol reaction” Bioorg. Med. Chem. Lett., 2009, 19, 3909-3911.
(14) Xue, F.; Zhang, S.-L.;* Duan, W.-H.;* Wang, W.* “A Novel Bifunctional Sulfonamide Primary Amine-Catalyzed Enantioselective Conjugate Addition of Ketones to Nitroolefins” Adv. Synth. Catal., 2008, 350, 2194-2198.
(15) Song, L.; Chen, X.; Zhang, S* Zhang, H.; Li, P.; Luo, G.; Liu, W.; Duan, W.;* Wang, W.* “An Organocatalytic Approach to the Construction of Chiral Oxazolidinone Rings and Application in the Synthesis of Antibiotic Linezolid and Its Analogues”Org. Lett. 2008, 10, 5489-5492.
(16) Mei, K.; Zhang, S.;* He, S.; Li, P.; Jin, M.; Xue, F.; Luo, G.; Zhang, H.; Song.; L.; Duan, W.;* Wang, W. “(S) Pyrrolidine sulfonamide catalyzed asymmetric direct aldol reactions of aryl methyl ketones with aryl aldehydes” Tetrahedron Lett., 2008, 49, 2681-2684.
(17) Zhang, S.; Chen, X.; Zhang, J.; Wang, W.; Duan, W.* “An Enantioselective Formal Synthesis of (R)-(+)--Lipoic Acid by L-Proline-catalyzed Aldol Reaction” Synthesis, 2008, 383-386.
(18) Xu, Y; Zhang S.-L.;* Duan, W.-H.* “A New Radical Way to N,N-Dimethylaniline Hydroperoxide (DMAHP) and Its Application in Organic Synthesis” Chin.Chem.Lett. 2007, 18, 807–810.
(19) Zhao X; Zhang S.-L.;* Duan, W.-H.* “A New Synthetic Method of Natural Product Trichostatin A” Chin. J. Org. Chem. 2007, 27, 1509-1515.
(20) Zhang, S.-L.; Duan, W.-H.;* Wang, W.* “Efficient, Enantioselective Organocatalytic Synthesis of Trichostatin A” Adv. Synth. Catal., 2006, 348, 1228-1234.