Title of article
Synthetic studies on altohyrtins (spongistatins): synthesis of the C15–C28 (CD) spiroacetal portion
Author/Authors
Terauchi، نويسنده , , Takeshi and Terauchi، نويسنده , , Taro and Sato، نويسنده , , Ippei and Tsukada، نويسنده , , Tomoharu and Kanoh، نويسنده , , Naoki and Nakata، نويسنده , , Masaya، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2000
Pages
5
From page
2649
To page
2653
Abstract
The C15–C28 portion of altohyrtins (spongistatins) was prepared in a convergent manner from methyl (S)-3-hydroxy-2-methylpropionate, d-arabitol, and diacetone-d-glucose via dithiane couplings with epoxides as the key segment coupling process.
Keywords
altohyrtins , dithianes , epoxides , spiro compounds
Journal title
Tetrahedron Letters
Serial Year
2000
Journal title
Tetrahedron Letters
Record number
1636948
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