张松林 照片

张松林

教授

所属大学: 苏州大学

所属学院: 材料与化学化工学部

邮箱:
zhangsl@suda.edu.cn

研究领域

镧系金属及其化合物用于有机合成的选择性反应;新型手性配体的设计合成及在不对称合成中的应用研究;铁/(铜)体系促进的偶联反应研究;光学纯度的ß-氨基酸及其衍生物的制备技术

近期论文

Efficient Synthetic Method of Allyl-Epoxides via Allylation of a-Haloketones or Esters with Allylmagnesium Bromid, Liyuan, Fan, Min, Zhang, Songlin Zhang*, Organic & Biomolecular Chemistry., 2012, DOI:10.1039/C2OB00051B

A Novel Ketone Olefination via Organozinc Reagents in the Presence of Diphenyl Phosphite, Hua, Cui, Ying, Li, Songlin Zhang*, Organic & Biomolecular Chemistry., 2012, DOI:10.1039/C2OB06821D

Efficient synthetic method for allyl- and propargyl-epoxide Preparation, Jie Pan, Min Zhang and Songlin Zhang*, Organic & Biomolecular Chemistry., 2012, 10, 1060

An Efficient Copper-Catalyzed Homocoupling of Terminal Songlin Zhang*, Xiaoyan Liu and Tongqiang Wang, Adv. Synth. Catal. 2011, 353, 1463 – 1466

Efficient Iron/Copper Cocatalyzed N-Arylation of Arylamines with Bromoarenes, Xiaoyan Liu and Songlin Zhang*, Synlett 2011, No. 8, 1137–1142

Efficient Iron/Copper-Cocatalyzed O-arylation of Phenols with Bromoarenes, Xiaoyan Liu and Songlin Zhang*, Synlett 2011, No. 2, 0268–0272

Di-Applications of Allylsamarium Bromide as Grignard Reagent and a Single Electron Transfer Reagent, Yuanyuan Hu, Tao Zhao, Songlin Zhang* Chem. Eur. J. 2010, 16, 1697-1705.

A Novel and Efficient Method for the Olefination of Carbonyl Compounds, Tongqiang Wang, Yuanyuan Hu, Songlin Zhang*., Organic & Biomolecular Chemistry., 2010, 8, 2312–2315

Multi-Product Classes Obtained from Allylation of a-Halo Ketones with Allylzinc Bromide, Min, Zhang, Yuanyuan Hu, Songlin, Zhang*, Chem. Eur. J. 2009, 15, 10732-10735.

Are ß-acyl amino acrylates hydrogenated in the same way as a-acyl amino, Hans-Joachim Drexler, Wolfgang Baumann, Thomas Schmidt, Songlon Zhang, Detlef Heller, Angew.Chem. Int. Ed., 2005, 44, 1184-1188.

Preparation and Asymmetric Hydrogenation of B- Aryl –Substituted B-Acylaminoacrylates, Jingsong You, Hans-Joachim Drexler, Songlin Zhang, Detlef Heller, Angew.Chem. Int. Ed., 2003, 42, 913-916.