Total Asymmetric Synthesis and Stereochemical Confirmation of (+)- and (-)-Lyoniresinol and Its Deuterated Analogues.
Tuan Minh LuongLisa Ivy PilkingtonDavid BarkerPublished in: The Journal of organic chemistry (2022)
Lyoniresinol and its derivatives are lignans which have been isolated from a plethora of plant species. In addition to exhibiting a range of interesting biological activities including anticancer, anti-inflammatory, antimicrobial, and others, these compounds have also been discovered in wines and spirits and shown to have gustatory effects in these alcoholic matrices. (+)-Lyoniresinol 1 is reported to impart a strong bitter taste while its enantiomer (-)-lyoniresnol 2 is tasteless. The first total asymmetric synthesis of both natural enantiomers (+)- 1 and (-)- 2 and their deuterated analogues ( D 4 )-(+)- 3 and ( D 4 )-(-)- 4 has been achieved, confirming the structure and stereochemistry of the natural products. The synthesized compounds can be utilized as internal standards in stable isotope dilution analysis for improving and optimizing the existing lyoniresinol quantitation methods in the future.
Keyphrases
- structure activity relationship
- anti inflammatory
- liquid chromatography tandem mass spectrometry
- molecular docking
- liquid chromatography
- ms ms
- staphylococcus aureus
- mass spectrometry
- liver injury
- current status
- solid state
- high performance liquid chromatography
- tandem mass spectrometry
- drug induced
- simultaneous determination
- oxide nanoparticles