Title of article
Synthesis of maresin 1 and (7S)-isomer
Author/Authors
Ogawa، نويسنده , , Narihito and Tojo، نويسنده , , Toshifumi and Kobayashi، نويسنده , , Yuichi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2014
Pages
4
From page
2738
To page
2741
Abstract
Maresin 1 (with the 7R carbon) and (7S)-maresin 1 were synthesized stereoselectively. The conjugated triene system was constructed by Pd-catalyzed coupling of the trans cis-dienylborane (the C10–C22 part) with the trans vinyl iodide corresponding to the C1–C9 part. The stereogenic centers at C7 and C14 were created by Ru-catalyzed asymmetric reduction of ketone and asymmetric epoxidation/kinetic resolution of the racemic alcohol, respectively.
Keywords
Suzuki–Miyaura coupling , lipid mediator , Docosahexaenoic acid , Maresin 1 , stereoselective synthesis
Journal title
Tetrahedron Letters
Serial Year
2014
Journal title
Tetrahedron Letters
Record number
1889210
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