Title of article
Regioselective opening of an oxirane system with trifluoroacetic anhydride. A general method for the synthesis of 2-monoacyl- and 1,3-symmetrical triacylglycerols
Author/Authors
Regioselective opening of an oxirane system with trifluoroacetic anhydride. A general method for the synthesis of 2-monoacyl- and 1، نويسنده , , 3-symmetrical triacylglycerols، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2005
Pages
11
From page
3659
To page
3669
Abstract
A trifluoroacetic anhydride-catalyzed opening of the oxirane system of glycidyl esters with a simultaneous migration of the acyl group provides a new, efficient entry to either 2-monoacylglycerols (2-MAG) or 1,3-symmetrical triglycerides (1,3-STG) as potential prodrug frameworks.
Keywords
2-Monoacylglycerols , 2-Arachidonoylglycerol , Glycidyl arachidonate , Acyl migration , 1 , 3-Symmetrical triacylglycerols , Prodrugs
Journal title
Tetrahedron
Serial Year
2005
Journal title
Tetrahedron
Record number
1088586
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