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
Link To Document :
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