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Improved plasmalogen synthesis using organobarium intermediates.
Van den Bossche, Jeroen; Shin, Junhwa; Thompson, David H.
Affiliation
  • Van den Bossche J; Department of Chemistry, 560 Oval Drive, Purdue University, West Lafayette, Indiana 47907, USA.
J Org Chem ; 72(13): 5005-7, 2007 Jun 22.
Article in En | MEDLINE | ID: mdl-17539687
ABSTRACT
An improved synthesis of plasmalogen type lipids is described. Transmetalation of lithioalkoxy allyl intermediates with BaI(2) and subsequent alkylation with 1-iodoalkanes enables the stereoselective formation of O-(Z)-alkenyl ether as precursors for the synthesis of plasmenyl- and bisplasmenylcholines. This method provides a simple and adaptable approach for the stereocontrolled synthesis of plasmenyl derivatives with variations at the sn-1, sn-2, and sn-3 positions of the glycerol backbone.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Organic Chemicals / Plasmalogens / Barium Compounds Language: En Journal: J Org Chem Year: 2007 Document type: Article Affiliation country:
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Organic Chemicals / Plasmalogens / Barium Compounds Language: En Journal: J Org Chem Year: 2007 Document type: Article Affiliation country: