An Asymmetric Synthesis of PPAR-? Agonist Navaglitazar from (+)-Methyl (2S,3R)-3-(4-methoxyphenyl)glycidate
DOI:
https://doi.org/10.2533/chimia.2006.580Keywords:
Asymmetric synthesis, Navaglitazar, Noninsulin dependent diabetes mellitus (niddm), Peroxisome proliferator activated receptor (ppar) gamma agonistAbstract
An asymmetric synthesis of navaglitazar, a peroxisome proliferator activated receptor (PPAR) ? agonist, from commercially available (+)-methyl (2S,3R)-3-(4-methoxyphenyl)glycidate, is described. The new synthesis features high overall yield, low solvent usage, crystalline intermediates and operational simplicity.Downloads
Published
2006-09-01
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Scientific Articles
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Copyright (c) 2006 Swiss Chemical Society
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
[1]
Chimia 2006, 60, 580, DOI: 10.2533/chimia.2006.580.