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.

Visible-Light-Driven Competitive Stereo- and Regioisomerization of (E)-β-Nitroenones / Raviola, C.; Carrera, C.; Serra, M.; Palmieri, A.; Lupidi, G.; Maestri, G.; Protti, S.. - In: CHEMPHOTOCHEM. - ISSN 2367-0932. - (2021). [10.1002/cptc.202100081]

Visible-Light-Driven Competitive Stereo- and Regioisomerization of (E)-β-Nitroenones

Maestri G.
;
Protti S.
2021-01-01

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.
2021
Visible-Light-Driven Competitive Stereo- and Regioisomerization of (E)-β-Nitroenones / Raviola, C.; Carrera, C.; Serra, M.; Palmieri, A.; Lupidi, G.; Maestri, G.; Protti, S.. - In: CHEMPHOTOCHEM. - ISSN 2367-0932. - (2021). [10.1002/cptc.202100081]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11381/2896262
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