Stereoselective Synthesis of Isomers of the Naturally Occurring 13-Hydroxy-2,4,9-tetradecatrienoic Acid. Part II [1]期刊界 All Journals 搜尽天下杂志传播学术成果专业期刊搜索期刊信息化学术搜索

Stereoselective Synthesis of Isomers of the Naturally Occurring 13-Hydroxy-2,4,9-tetradecatrienoic Acid. Part II [1]

Authors:	Antje?Huefner author-information" > author-information__contact u-icon-before" > mailto:antje.huefner@uni-graz.at" title=" antje.huefner@uni-graz.at" itemprop=" email" data-track=" click" data-track-action=" Email author" data-track-label=" " >Email author,Christa?Hoeller,Gottfried?Reznicek

Affiliation:	(1) Institute of Pharmaceutical Chemistry and Pharmaceutical Technology, University of Graz, A-8010 Graz, Austria;(2) Institute of Pharmacognosy, University of Vienna, PharmaCenter Vienna, A-1090 Wien, Austria

Abstract:	Summary. The stereoselective syntheses of four unsaturated hydroxy fatty acids 13S,2E,4E,9E)- 13-hydroxy-2,4,9-tetradecatrienoic acid, (13S,9Z,11E)-13-hydroxy-9,11-tetradecadienoic acid, (13S,9E, 11E)-13-hydroxy-9,11-tetradecadienoic acid, and (13S,2E,4E,9E)-13-hydroxy-2,4,9,11-tetradecatrienoic acid, are described. Wittig reactions, regioselective oxidation of dialcohol 3, and diastereomerization were used.

Keywords:	. Fatty acid Aldehydes Wittig Reaction (Z,E)-Isomerization.
本文献已被 SpringerLink 等数据库收录！