Title of article
Synthesis of the J ring segment of gambieric acid
Author/Authors
Kadota، نويسنده , , Isao and Takamura، نويسنده , , Hiroyoshi and Yamamoto، نويسنده , , Yoshinori، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2001
Pages
3
From page
3649
To page
3651
Abstract
The J ring segment 2 of gambieric acid was synthesized stereoselectively by the coupling between the cyclic ether component 3 and the alkenyl iodide 4. The tetrahydropyran 3 was stereoselectively synthesized by the 6-endo-cyclization of a hydroxyepoxide prepared from deoxy-d-ribose. The side chain moiety 4 was prepared by the stereoselective hydrostannation of an internal alkyne.
Journal title
Tetrahedron Letters
Serial Year
2001
Journal title
Tetrahedron Letters
Record number
1644914
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