Title of article
Stereoselective synthesis of zooxanthellactone
Author/Authors
Jakobsen، نويسنده , , Martin Gjerde and Vik، نويسنده , , Anders and Hansen، نويسنده , , Trond Vidar، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
3
From page
2842
To page
2844
Abstract
The marine polyunsaturated natural product zooxanthellactone was synthesized in six steps and in 11% overall yield from eicosapentaenoic acid. The key synthetic steps were a Sonogashira cross-coupling reaction and a stereoselective semi-reduction. These efforts, together with NMR and optical rotation data, confirmed the reported structure of zooxanthellactone.
Keywords
Oxylipin , stereoselective synthesis , Polyunsaturated fatty acid , marine natural products , Zooxanthellactone
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1889290
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