Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1379220 | Bioorganic & Medicinal Chemistry Letters | 2006 | 4 Pages |
Abstract
Optically active (S)-2-ethylphenylpropanoic acid derivatives, dual agonists for human peroxisome proliferator-activated receptor (PPAR) α and δ, were efficiently prepared by using Evan’s chiral oxazolidinone technique and reductive amide N-alkylation as key steps.
Graphical abstractOptically active (S)-2-ethylphenylpropanoic acid derivatives, dual agonists for human peroxisome proliferator-activated receptor (PPAR) α and δ, were efficiently prepared.Figure optionsDownload full-size imageDownload as PowerPoint slide
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Jun-ichi Kasuga, Yuichi Hashimoto, Hiroyuki Miyachi,