Effect of Natural Deep Eutectic Solvents on trans-Resveratrol Photo-Chemical Induced Isomerization and 2,4,6-Trihydroxyphenanthrene Electro-Cyclic Formation

Effect of Natural Deep Eutectic Solvents on trans-Resveratrol Photo-Chemical Induced Isomerization and 2,4,6-Trihydroxyphenanthrene Electro-Cyclic Formation

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trans-Resveratrol is a natural bioactive compound with well-recognized health promoting effects. When exposed to UV light, this compound can undergo a photochemically induced trans/cis isomerization and a 6π electrochemical cyclization with the subsequent formation of 2,4,6-trihydroxyphenanthrene (T...

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Bibliographic Details
Main Authors: Ciogli, A. (Author), d'Erme, M. (Author), Di Risola, D. (Author), Federico, R. (Author), Fontana, M. (Author), Francioso, A. (Author), Gasparrini, F. (Author), Maggiore, A. (Author), Mattioli, R. (Author), Mosca, L. (Author), Villani, C. (Author)
Format: Article
Language:English
Published: NLM (Medline) 2022
Subjects:
2,4,6-trihydroxyphenanthrene
chemistry
chromatographic separation
Deep Eutectic Solvents
glycerol
Glycerol
isomerism
Isomerism
isomerization and 6π photochemical electrocyclization
natural deep eutectic solvents
pentafluorophenyl stationary phase
phenanthrene derivative
Phenanthrenes
photochemistry
photo-stability
resveratrol
Resveratrol
solvent
Solvents
trans/cis-resveratrol
UV light
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