Titanium complexes of chiral amino alcohol derived Schiff bases as efficient catalysts in asymmetric oxidation of prochiral sulfides with hydrogen peroxide as an oxidant
- 作者：Prasanta Kumar Bera ; Debashis Ghosh ; Sayed Hasan Razi Abdi ; shrabdi@csmcri.org ; Noor-ul Hasan Khan ; Rukhsana Ilays Kureshy ; Hari Chandra Bajaj
- 关键词：Asymmetric oxidation ; Sulfoxidation ; Schiff base ; Chiral titanium complex ; Hydrogen peroxide
- 刊名：Journal of Molecular Catalysis A ; Chemical
- 出版年：2012
- 期刊代码：57_13811169
- 类别：ch
- 出版时间：September, 2012
- 卷：361-362
- 期：Complete
- 页码：36-44
- 文件大小：930 K
摘要
An efficient asymmetric oxidation of prochiral sulfides catalyzed by a series of simple in situ generated complexes based on chiral amino alcohol derived Schiff bases with Ti(Oi-Pr)4 was carried out in presence of cheap and environmentally benign oxidant H2O2 at 0 掳C. Prochiral sulfides were converted to respective chiral sulfoxides efficiently (conversion, 93%; up to ee, 98%) with this system in 10 h at 0 掳C. The present study demonstrated a significant role of steric influence of the substituent attached on both aryl and alkyl moiety on the enantioselectivity. Kinetic studies of the catalytic reaction showed first order dependence on substrate and catalyst whereas it is zero for the oxidant. Kinetic studies in combination with UV-vis. spectral studies were used to propose a catalytic cycle for the sulfoxidation reaction.