张士磊

 

 

  名:张士磊

职称职务:教授

联系电话:0512-65880959

电子邮箱:zhangshilei@suda.eud.cn

办公地址:苏州市工业园区仁爱路199号药学院云轩楼

 

个人简介:

一、学习工作经历

1998.9-2002.7:中国海洋大学化学化工学院海洋化学专业,大学本科

2002.9-2007.7:中国科学院上海药物研究所,药物化学,博士学位

2007.7-2008.9:华东理工大学药学院药物化学系,讲师

2008.10-2012.1:美国新墨西哥大学(University of New Mexico),有机化学,博士后

2012.2-至今:苏州大学医学部药学院,教授

 

二、研究方向

1)化学方法学、手性药物研究

2)制药工艺过程研究及杂质研究

3)抗癌药物和抗菌药物研究

 

三、发表论文

(*表示为通讯作者)

 

1)      Mao, Y.; Liu, Y.; Hu, Y.; Wang, L.; Zhang, S.;* Wang, W. “Pd-Catalyzed Debenzylation and Deallylation of Ethers and Esters with Sodium HydrideACS catal., 2018, 8, 3016-3020. (IF=10.614)

2)      Jiang, J.; Hu, Y.; Cai, X.; Wang, L.; Hu, Y.; Chen, S.; Zhang, S.; Zhang, Y. “Bis(phenylsulfonyl)methane mediated synthesis of olefins via a halogen elimination and double bond migrationOrg. Biomol. Chem., 2018, 16, accepted.(IF=3.564)

3)      Yang, J.; Qiu, G.; Jiang, J.; Hu, Y.;* Chen, S.; Zhang, S.;* Zhang Y.Asymmetric Organocatalytic Synthesis of Benzopyran- and Benzofuran-Fused Polycyclic AcetalsAdv. Synth. Catal., 2017, 359, 2184-2190. (IF=5.646)

4)      Qian, P; Wan, H; Jiang, J; Hu, Y; Chen, X;* Zhang S.-L.;* Discovery of a Special Intramolecular Aldol-Like Reaction in the Synthesis of Related Substance E of TadalafilChin. J. Org. Chem. 2016, 36, 1878-1882. (IF=1.010)

5)      Xie, R.; Hu, Y.; Wan, H.; Hu, Y.; Chen, S.; Zhang, S.;* Zhang, Y. An efficient synthesis of 4,6-substituted pyrrolo[3,2-d]pyrimidines by silver-catalyzed cyclization of acyetylene amineTetrahedron Lett. 2016, 57, 2418-2421. (IF=2.193)

6)      Chen, X.; Zhang, Y.; Wan, H.; Wang, W.; Zhang, S.* “Stereoselective organocatalytic oxidation of alcohols to enals: a homologation method to prepare polyenes” Chem. Commun., 2016, 3532-3535. (IF=6.319)

7)      Wang, J.; Qian, P.; Hu, Y.; Yang, J.; Jiang, J.; Chen, S.; Zhang, Y.; Zhang, S.*Organocatalytic aldol addition reaction of cyclic hemiacetals to aldehydesTetrahedron Lett. 2015, 56, 2875-2877. (IF=2.193)

8)      Liu, S.; Hu, Y.; Qian, P.; Hu, Y.; Ao, G.; Chen, S.; Zhang, S.;* Zhang, Y. An efficient cascade approach to dibenzoxazepinones via nucleophilic aromatic substitution and Smiles rearrangementTetrahedron Lett. 2015, 56, 2211-2213. (IF=2.193)

9)      Liu, S.; Zhu, S.; Wu, Y.; Gao, J.; Qian, P.; Hu, Y.; Shi, L.; Chen, S.; Zhang, S.;* Zhang, Y. One-pot synthesis of N-aryl-nicotinamides and diaryl-amines based on a tunable Smiles rearrangementEur. J. Org. Chem., 2015, 3048-3052. (IF=2.834)

10)  Zhu, Y.; Qian, P.; Yang, J.; Chen,S.; Hu, Y.; Wu, P.; Wang, W.; Zhang, W.; Zhang, S.*Organocatalytic Enantioselective Michael Addition of Cyclic Hemiacetals to Nitroolefins: A Facile Access to Chiral Substituted 5- and 6-Membered Cyclic EthersOrg. Biomol. Chem., 2015, 13, 4769-4775. (IF=3.564)

11)  Liu, S.; Chen, X.; Hu, Y.; Yuan, L.; Chen, S.; Wu, P.; Wang, W.; Zhang, S.;* Zhang W.An Efficient Method for the Production of Terminal Alkynes from 1,1-Dibromo-1-alkenes and its Application in the Total Synthesis of Natural Product DihydroxerulinAdv. Synth. Catal., 2015, 357, 553-560. (IF=5.646)