Abstract
A combined experimental and computational investigation of the photoreactivity of (E)-β-nitroenones pointed out the occurrence of competitive pathways namely stereoisomerisation to (E)-β-nitroenones and deconjugation to β-nitro-β,γ-enones. Both processes are generated from the triplet excited state of the starting substrates.
Cite
CITATION STYLE
APA
Raviola, C., Carrera, C., Serra, M., Palmieri, A., Lupidi, G., Maestri, G., & Protti, S. (2021). Visible-Light-Driven Competitive Stereo- and Regioisomerization of (E)-β-Nitroenones. ChemPhotoChem, 5(9), 871–875. https://doi.org/10.1002/cptc.202100081
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.
Already have an account? Sign in
Sign up for free