Title of article
Stereoselective synthesis of the C94–C104 fragment of symbiodinolide
Author/Authors
Takamura، نويسنده , , Hiroyoshi and Tsuda، نويسنده , , Kosuke and Kawakubo، نويسنده , , Yohei and Kadota، نويسنده , , Isao and Uemura، نويسنده , , Daisuke، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2012
Pages
3
From page
4317
To page
4319
Abstract
Stereoselective synthesis of the C94–C104 fragment of symbiodinolide which is a polyol marine natural product with a molecular weight of 2860 has been accomplished. The synthetic route features Achmatowicz rearrangement and RuO4-catalyzed dihydroxylation for the construction of the tetrahydropyran moiety and the dithiane addition to the aldehyde for the introduction of the side chain.
Keywords
Polyol marine natural product , Symbiodinolide , Achmatowicz rearrangement , Dithiane addition
Journal title
Tetrahedron Letters
Serial Year
2012
Journal title
Tetrahedron Letters
Record number
1881507
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