Title of article
Semisynthesis of (+)-angeloyl-gutierrezianolic acid methyl ester diterpenoid
Author/Authors
I.S. Marcos، نويسنده , , A. Benéitez، نويسنده , , R.F Moro، نويسنده , , P. Basabe، نويسنده , , D. D?ez، نويسنده , , J.G Urones، نويسنده ,
Issue Information
هفته نامه با شماره پیاپی سال 2010
Pages
10
From page
8605
To page
8614
Abstract
This paper describes the use of zamoranic acid in the first semisynthesis of the furolabdane (+)-angeloyl-gutierrezianolic acid methyl ester diterpenoid, which also establishes the absolute configuration of the natural product. Direct deconjugation of Δ7 in zamoranic acid and Bestmann methodology for the furan ring synthesis are the key steps.
Keywords
labdanes , diterpenes , Furolabdanes , zamoranic acid , Angeloyl-gutierrezianolic acid
Journal title
Tetrahedron
Serial Year
2010
Journal title
Tetrahedron
Record number
1102616
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