6533b856fe1ef96bd12b261a

RESEARCH PRODUCT

Secondary metabolites from the aerial parts of Cytisus villosus Pourr

Fadila BenayacheDorota WieczorekSamira BenyahiaStephen J. CutlerFrancisco LeónAnna PoliwodaFarida LaritMohamed M. RadwanSamir BenayacheIzabela Jasicka-misiakPiotr WieczorekManal A. Nael

subject

Circular dichroism010405 organic chemistryStereochemistryMonoterpeneCytisus villosusPlant Science010402 general chemistryCytisus villosus01 natural sciencesBiochemistryisoflavonoidsArticle0104 chemical scienceschemistry.chemical_compoundchemistryPhytochemicalECDChrysinmonoterpenoidsAgronomy and Crop ScienceTwo-dimensional nuclear magnetic resonance spectroscopyBiotechnology

description

Phytochemical investigation of the aerial parts of Cytisus villosus Pourr. resulted in the isolation and characterization of a new isoflavan, (3S, 4S)-2′,4′-dihydroxy-3′-methoxy-6,7-methylenedioxyisoflavan- 4-ol (1), and a new monoterpene, (4R,6S)-4-hydroxy-2,2,6-trimethyl-9-oxabicyclo [4.2.1] non-1(8)-en-7-one (2), together with four known flavonoids: geinstein (3), chrysin (4), chrysin -7-O-β-D-glucopyranoside (5) and 2″-O-α-L-rhamnosylorientin (6). The structures of the new compounds were elucidated on the basis of extensive spectroscopic analysis, including 1D, 2D NMR ((1)H, (13)C, COSY, TOCSY, HMBC and HSQC) and HRESIMS. The absolute configurations of 1 and 2 were established by the comparison of experimental and calculated electronic circular dichroism (ECD) spectra.

10.1016/j.phytol.2017.12.012https://www.sciencedirect.com/journal/phytochemistry-letters/vol/24/suppl/C