| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 70338 | Journal of Molecular Catalysis B: Enzymatic | 2012 | 5 Pages |
Highly enantioselective and enantiospecific resolution processes were developed for 2-(3-methoxy-4-methyl-phenyl)-propan-1-ol (VI), 2-(2-methoxy-5-methyl-phenyl)-propan-1-ol (VII), 2-(3,4,5-trimethoxy-phenyl)-propan-1-ol (VIII) and 2-(3-hydroxy-4-methyl-phenyl)-propan-1-ol (XII) via lipase-catalyzed transesterification and hydrolysis using vinyl propionate as acylating agent. The general procedure for synthesis and kinetic resolution of 2-phenylpropan-1-ol derivatives would be beneficial for getting chiral building block of bisabolane types of natural and unnatural sesquiterpenes. Gallic acid moiety was diversified with a chiral center at the benzylic position and subsequent resolution process gave resolved isomers with higher enantiopurity. Both isomers were separated with ee of at least 95%. Enantioselectivity, E was even higher up to 316 during the process. These resolved chiral intermediates will facilitate the commercial synthesis of bio-active natural and unnatural xanthorrhizol, elvirol and gallate derivatives.
Graphical abstractFigure optionsDownload full-size imageDownload as PowerPoint slideHighlights► The study covers the synthesis and resolution process of phenolic esters and alcohols containing a chiral center at the benzylic position. ► The resolved alcohols are essential building block of natural and unnatural synthetic sesquiterpenes and sesquiterpenoides. ► Among several lipases, CAL-B showed higher enantioselectivity up to (E = 316). ► The diversified chiral gallic acid moiety will open the opportunity to get optimized biological active compounds for food and pharmaceutical industry.
