Title of article
Flexible synthesis of vulpinic acids from tetronic acid
Author/Authors
Willis، نويسنده , , Catherine and Bodio، نويسنده , , Ewen and Bourdreux، نويسنده , , Yann and Billaud، نويسنده , , Célia and Gall، نويسنده , , Thierry Le and Mioskowski، نويسنده , , Charles، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2007
Pages
4
From page
6421
To page
6424
Abstract
Several vulpinic acids were synthesized in a few steps from a single precursor, the tetronic acid. This commercial compound was converted in a few steps to an iodide. Suzuki–Miyaura cross-couplings involving this common intermediate and various arylboronates allowed to gain access to several vulpinic acids (or methyl pulvinates). Among them, two natural products, vulpinic acid and pinastric acid, were prepared.
Keywords
natural products , Pulvinic acid , Vulpinic acid , Suzuki–Miyaura cross-coupling , Tetronic acid
Journal title
Tetrahedron Letters
Serial Year
2007
Journal title
Tetrahedron Letters
Record number
1856365
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