Herein, we reported an efficient and facile visible-light-induced 3-alkyl chromone synthesis from easily accessible o -hydroxyaryl enaminones and α-diazo esters. In this protocol, excellent yields were obtained with a broad substrate scope at room temperature, tolerating various functional groups. Of note is that this eco-friendly methodology features catalyst- and additive-free, mild reaction conditions, simple operation procedure, and easy scale-up, which affords a convenient pathway for the preparation of 3-alkyl chromones. Experimental results and density functional theory (DFT) computation analyses confirm the participation of carbene species and active cyclopropane intermediate.
Keyphrases
- visible light
- density functional theory
- room temperature
- ionic liquid
- molecular dynamics
- physical activity
- high glucose
- diabetic rats
- randomized controlled trial
- minimally invasive
- oxidative stress
- drug induced
- low cost
- genetic diversity
- mass spectrometry
- highly efficient
- quantum dots
- stress induced
- molecular dynamics simulations
- crystal structure
- metal organic framework