Title of article
Highly functionalized trans-2,5-disubstituted tetrahydrofurans from ribofuranoside templates: precursors to linked polycyclic ethers
Author/Authors
Dabideen، نويسنده , , Darrin and Mootoo، نويسنده , , David R.، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2003
Pages
4
From page
8365
To page
8368
Abstract
Iodoetherification of C5 allylated ribo-furanosides leads to trans-2,5-disubstituted tetrahydrofurans with high selectivity. The application of this reaction to the synthesis of complex polycyclic ethers is illustrated in the preparation of a truncated, tricyclic analog of monensin A.
Keywords
polyethers , Iodoetherification , Tetrahydrofuran , Acetogenins
Journal title
Tetrahedron Letters
Serial Year
2003
Journal title
Tetrahedron Letters
Record number
1655465
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