PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
July 5, 2026The Journal of Organic Chemistry0 citations

Ru(II)-Catalyzed Hydrodefluorination of Monofluoroalkenes

View Full Paper
GSGao ShuJDJinpan DuanJWJuanjuan Wang

Key Points

  • The aim is to develop a selective method for the hydrodefluorination of monofluoroalkenes using a ruthenium(II) catalyst.
  • Utilized ruthenium(II) as a catalyst with sodium formate as a hydrogen source.
  • Demonstrated broad functional group tolerance and scalability to gram quantities.
  • Conducted experiments to minimize overhydrogenation byproducts.
  • Successfully cleaved C(sp2)–F bonds while preventing significant overhydrogenation, achieving efficient alkene production.
  • The method is practical and allows for varied functional groups without adverse effects.

Abstract

Despite significant advances in C–F bond functionalization, the selective hydrogenative defluorination of monofluoroalkenes remains a considerable challenge due to competing over-reduction issues. Here, we report a practical and selective protocol for the hydrodefluorination of monofluoroalkenes, employing an inexpensive ruthenium(II) catalyst with sodium formate as a safe and convenient hydrogen source. This method enables the selective cleavage of C(sp 2 )–F bonds while minimizing overhydrogenation byproducts, thus providing efficient access to the corresponding alkenes. The reaction demonstrates broad functional group tolerance and is scalable to gram quantities.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Shu et al. (2026) studied this question.

synapsesocial.com/papers/6a49f411f5d1d45b287ffd08https://doi.org/10.1021/acs.joc.6c00727
Ask AI
Helpful
Bookmark
Share
View Full Paper