Title of article
Enantio- and stereocontrolled formation of the bisspiroacetal core of spirolide B
Author/Authors
Ishihara، نويسنده , , Jun and Ishizaka، نويسنده , , Tomoko and Suzuki، نويسنده , , Takanori and Hatakeyama، نويسنده , , Susumi، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2004
Pages
4
From page
7855
To page
7858
Abstract
The bisspiroacetal core of spirolide B, a marine natural toxin, was synthesized from triketone 10 via one-step bisspiroacetalization, methylation, and silylation accompanied by isomerization of the C-15 spirocenter. The equilibrium of two isomers under acidic conditions was also examined.
Keywords
Bisspiroacetal , Spirolide
Journal title
Tetrahedron Letters
Serial Year
2004
Journal title
Tetrahedron Letters
Record number
1843568
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