Title of article
Synthetic study of tautomycin. Part 2: Synthesis of Ichiharaʹs fragment based on regioselective enzymatic acetylation of complex molecule
Author/Authors
Yusuke Ishii، نويسنده , , Shinji Nagumo، نويسنده , , Takayuki Arai، نويسنده , , Masami Akuzawa، نويسنده , , Norio Kawahara، نويسنده , , Hiroyuki Akita، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2006
Pages
10
From page
716
To page
725
Abstract
Formal synthesis of tautomycin, which inhibits type 1 and type 2A protein phosphatases, was achieved. Spiroketal diol was synthesized from alcohol or . The regioselective enzymatic acetylation of with the lipase ‘Amano PS’ gave monoacetate in 90% yield, which was converted into Ichiharaʹs intermediate based on Julia coupling and Wittig homologation.
Keywords
tautomycin , Regioselective , Enzymatic acetylation
Journal title
Tetrahedron
Serial Year
2006
Journal title
Tetrahedron
Record number
1089538
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