Scientific Production Faculty

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.



Research Product




Related articles

Role of lipid peroxidation in biliary obstruction in the rat.

Reactivity of TpMe2Ir(C2H4)(DMAD) with carboxylic acids. A DFT study on geometrical isomers and stru...

Firsttotalsyntheses of dihydroflustramine C and flustramine E, alkaloids from the marine bryozoan Fl...

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

Conformationalstudies of N-carbomethoxy-2-alkoxyindolenines by dynamic NMR, crystallography, and mol...

The absoluteconfiguration of cuauhtemone and related compounds

Synthesis of Indolylindolines Mediated by tert-BuNH2

13C NMR and crystallographic evidence of push-pull effects in furoindolic ?-enamino esters

One-potsynthesis of conformationallyrestrictedspirooxindoles

Total Syntheses of Five Indole Alkaloids from the Marine Bryozoan Flustra foliacea