RESUMEN
Cyathenosin A, a spiropyranosyl derivative of protocatechuic acid was isolated from the stem pith of Cyathea phalerata Mart. Its structure was determined by MS, 1D and 2D NMR spectroscopic analyses and confirmed by single crystal X-ray analysis. Cyathenosin A is the first example of a naturally occurring compound containing a spirocyclic orthoester pyranosidic structure.
Asunto(s)
Helechos/química , Hidroxibenzoatos/química , Hidroxibenzoatos/aislamiento & purificación , Modelos Moleculares , Estructura Molecular , Monosacáridos , Tallos de la Planta/química , Compuestos de EspiroRESUMEN
NMR and GC-MS analysis of fractions of the CHCl3 extract of Trichilia catigua bark led to the identification of a mixture of three omega-phenyl alkanes, three omega-phenyl alkanoic acids, five omega-phenyl-gamma-lactones, two alkyl-gamma-lactones, one alkenyl-gamma-lactone and a mixture of fatty acids ranging from C-14 to C-26. Beta-sitosterol, stigmasterol and campesterol as free alcohols were also identified.