Asymmetric Synthesis of (S)-metoprolol via Sharpless Asymmetric Dihydroxylation Induced by A Recoverable Polymer Ligand QN-AQNOPEG- OMe

Author(s): Sikun Cheng, Xueying Liu, Pingan Wang, Xiaoye Li, Wei He, Shengyong Zhang

Journal Name: Letters in Organic Chemistry

Volume 9 , Issue 7 , 2012

Become EABM
Become Reviewer
Call for Editor


The catalytic asymmetric dihydroxylation (AD) discovered by Sharpless, a Nobel Prize winner in 2001, has rapidly become an invaluable synthetic tool in the possibility of converting prochiral olefins to chiral vicinal diols. After our long-running investigation of optimized methodology for the production of stereo-defined diols based on the AD reaction, an efficient and environmentally friendly approach for the synthesis of (S)-metoprolol via AD reaction was reported. The synthetic route proceeded in four-step reactions of nucleophilic substitution, AD reaction, cyclization, and nucleophilic ring opening. The key step, AD reaction, proceeded effectively in homogeneous catalysis by using a soluble polymer chiral ligand QN-AQN-OPEG-OMe, which can be easily separated from the reaction system and reused at least four times while maintaining its high catalytic activity and enantioselectivity. This protocol has been demonstrated to produce kilogram quantities of (S)-metoprolol on scale.

Keywords: Asymmetric dihydroxylation, asymmetric synthesis, polymer ligand, recoverable, (S)-metoprolol, biocatalysis, migraine, headaches, anxiety, beta-blocker

Rights & PermissionsPrintExport Cite as

Article Details

Year: 2012
Page: [516 - 519]
Pages: 4
DOI: 10.2174/157017812802139645
Price: $65

Article Metrics

PDF: 17