Producción Científica Profesorado

The absoluteconfiguration of cuauhtemone and related compounds



Suárez Castillo, Oscar Rodolfo

2003

The absolute configuration of cuauhtemone and related compounds. Torres-Valencia J. M., Quintero-Mogica D. L., León G. I., Suárez-Castillo O. R., Villagómez-Ibarra J. R., Maldonado E., Cerda-García-Rojas C. M., Joseph-Nathan P. DOI: http://dx.doi.org/10.1016/S0957-4166(03)00042-9


Abstract


The absoluteconfiguration of cuauhtemone, a eudesmane-type sesquiterpene isolated from Pluchea species (Asteraceae), has been revised from 1 to 2 by chemical correlation with (R)-(+)-2-methyl-1,2-butanediol 3 through the naturally occurring 2,3-epoxy-2-methylbutanoate derivative 4. The relative stereochemistry of 4 was confirmed by X-ray diffraction analysis. The obtained data are also useful for reconsideration of the absoluteconfigurations of a relevant group of natural products, which were elucidated according to the stereochemistry of cuauhtemone.



Producto de Investigación




Artículos relacionados

Conformational studies on indole alkaloids from Flustra foliacea by NMR and molecular modeling

Absolute configuration determination of 2-(2-oxo-3-indolyl)acetamide derivatives

Cleavage of alkoxycarbonyl protecting groups from carbamates by t-BuNH2

Aromatic Bromination versus Oxidation of Indolylmalonates by Bromine

Synthesis of Bromoindole Alkaloids from Laurencia brongniartii

One-potsynthesis of conformationallyrestrictedspirooxindoles

Role of lipid peroxidation in biliary obstruction in the rat

Regioselective Synthesis of 3-Indolyl(alkoxy)acetates

Preparation of 3-hydroxyoxindoles with dimethyldioxirane and their use for the synthesis of natural ...

Cascade [1,3]-Sigmatropic Rearrangements of Ketene O,O-Acetals: Kinetic and DFT Level Mechanistic St...