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Título

On the relative stereochemistry of atomaric acid and related compounds

AutorDorta, Enrique CSIC; Díaz-Marrero, Ana R. CSIC ORCID; Cueto, Mercedes CSIC ORCID ; Darias, José CSIC
Palabras claveAtomaric acid
Stypopodium zonale
Diterpenes of mixed biogenesis
Fecha de publicación26-feb-2003
EditorElsevier
CitaciónTetrahedron 59(12): 2059-2062 (2003)
ResumenThe stereochemistry at C-3 of the known compounds atomaric acid 2a, 5'a-desmethyl-5'-acetylatomaric acid 4a, and stypoquinonic acid 5a is revised to 2, 4, and 5 on the basis of a careful study of 2D NOESY experiments and also from comparison of their 1H and 13C chemical shifts with those of the related metabolites 6 and 7 isolated from Stypopodium zonale. Compound 7 is a novel unusually functionalized 1-keto-5'a-desmethyl atomaric acid derivative whose structure and stereochemistry were determined by spectroscopic means.
Descripción4 pages, 1 figure, 1 table, 1 scheme.-- Printed version published Mar 17, 2003.
Versión del editorhttp://dx.doi.org/10.1016/S0040-4020(03)00215-1
URIhttp://hdl.handle.net/10261/13272
DOI10.1016/S0040-4020(03)00215-1
ISSN0040-4020
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