Tetrahedron

Synthesis of trans-vaccenic acid and cis-9-trans-11-conjugated linoleic acid

PE Duffy, SM Quinn, HM Roche, P Evans

Index: Duffy, Patricia E.; Quinn, Sonia M.; Roche, Helen M.; Evans, Paul Tetrahedron, 2006 , vol. 62, # 20 p. 4838 - 4843

Full Text: HTML

Citation Number: 12

Abstract

The preparation of the monounsaturated fatty acid, trans-vaccenic acid (TVA), using both Wittig and one-pot Julia-Kocieński olefination protocol, was achieved in good yield. Similarly a Wittig approach was employed for the stereoselective synthesis of cis-9-trans-11- conjugated linoleic acid from trans-2-nonenal and (8-carboxyoctyl) triphenylphosphonium bromide.

Related Articles:

Efficient synthesis of unsaturated 1-monoacyl glycerols for in meso crystallization of membrane proteins

[Fu, Yu; Weng, Yue; Hong, Wen-Xu; Zhang, Qinghai Synlett, 2011 , # 6 p. 809 - 812]

Synthesis of trans-vaccenic acid and cis-9-trans-11-conjugated linoleic acid

[Tetrahedron, , vol. 62, # 20 p. 4838 - 4843]

Synthesis of trans-vaccenic acid and cis-9-trans-11-conjugated linoleic acid

[Tetrahedron, , vol. 62, # 20 p. 4838 - 4843]

Synthesis of trans-vaccenic acid and cis-9-trans-11-conjugated linoleic acid

[Tetrahedron, , vol. 62, # 20 p. 4838 - 4843]

The kinetics of thiyl radical-induced reactions of monounsaturated fatty acid esters

[Journal of the American Chemical Society, , vol. 124, # 43 p. 12816 - 12823]

More Articles...