This method shows effective hydrogen atom transfer in β-nitroacrylates, highlighting good yields and chemoselectivity.
A photocatalyzed reduction of the CC double bond in β‐nitroacrylates under flow conditions is developed. The reaction takes place upon irradiation at 390 nm in the presence of tetrabutylammonium decatungstate and requires γ‐terpinene as a hydrogen source. Products are obtained in good yields, and various functional groups are tolerated, such as unconjugated double bonds, benzyl groups and carbonyls, thus demonstrating a substantial chemoselectivity.
No takes yet. Share an insight, caveat, or question.
Lupidi et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: