Synthesis of a Peroxime Proliferator Activated Receptor (PPAR) α/γ Agonist via Stereocontrolled Williamson Ether Synthesis and Stereospecific SN2 Reaction of S-2-Chloro Propionic Acid with Phenoxides-Reference-Cited by-同舟云学术

Synthesis of a Peroxime Proliferator Activated Receptor (PPAR) α/γ Agonist via Stereocontrolled Williamson Ether Synthesis and Stereospecific SN2 Reaction of S-2-Chloro Propionic Acid with Phenoxides

Published:2005-05-05 Issue:12 Volume:70 Page:4695-4705
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Aikins James A.¹,Haurez Michael¹,Rizzo John R.¹,Van Hoeck Jean-Pierre¹,Brione Willy¹,Kestemont Jean-Paul¹,Stevens Christophe¹,Lemair Xavier¹,Stephenson Gregory A.¹,Marlot Eric¹,Forst Mindy¹,Houpis Ioannis N.¹

Affiliation:

1. Chemical Product Research and Development, Lilly Development Centre, rue Granbonpre 11, B-1348 Mont-St-Guibert, Belgium, and Lilly Technology Center, B-110, Indianapolis, Indiana 46285

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo050268e

Reference25 articles.

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2. Diabetic Dyslipidemia: Causes and Consequences

3. An Antidiabetic Thiazolidinedione Is a High Affinity Ligand for Peroxisome Proliferator-activated Receptor γ (PPARγ)

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