| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5275007 | Tetrahedron Letters | 2011 | 4 Pages |
Abstract
A novel biocatalytic method for the enantioselective synthesis of (R)-bromo-3-[4-(2-methoxy-ethyl) phenoxy]-2-propanol [(R)-BMEPP], a precursor for the synthesis of (S)-metoprolol, an anti hypertensive drug is described. We have developed kinetic resolution of rac-BMEPP by transesterification using Candida rugosa lipase and vinyl acetate as the acyl donor affording the product with excellent conversion (49%) and ee (>99%). Various reaction parameters (source of enzyme, reaction media, and concentration of substrate and acylating agent) for the enzymatic kinetic resolution have been reported.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Abhishek Kaler, Vachan Singh Meena, Manpreet Singh, Brahmam Pujala, Asit K. Chakraborti, Uttam Chand Banerjee,
![First Page Preview: Lipase-mediated kinetic resolution of (RS)-1-bromo-3-[4-(2-methoxy-ethyl)-phenoxy]-propan-2-ol to (R)-1-bromo-3-(4-(2-methoxyethyl) phenoxy) propan-2-yl acetate Lipase-mediated kinetic resolution of (RS)-1-bromo-3-[4-(2-methoxy-ethyl)-phenoxy]-propan-2-ol to (R)-1-bromo-3-(4-(2-methoxyethyl) phenoxy) propan-2-yl acetate](/preview/png/5275007.png)