FeO(OH)@C-Catalyzed Selective Hydrazine Substitution of p-Nitro-Aryl Fluorides and their Application for the Synthesis of Phthalazinones.

ChemistryOpen

State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Chemistry and Chemical Engineering, Hunan University, Changsha, 410082, P. R. China.

Published: May 2022

An efficient hydrazine substitution of p-nitro-aryl fluorides with hydrazine hydrates catalyzed by FeO(OH)@C nanoparticles is described. This hydrazine substitutions of p-nitro-aryl fluorides bearing electron-withdrawing groups proceeded efficiently with high yield and selectivity. Similarly, hydrogenations of p-nitro-aryl fluorides containing electron-donating groups also smoothly proceeded under mild conditions. Furthermore, with these prepared aryl hydrazines, some phthalazinones, interesting as potential structures for pharmaceuticals, have successfully been synthesized in high yields.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9117154PMC
http://dx.doi.org/10.1002/open.202200023DOI Listing

Publication Analysis

Top Keywords

p-nitro-aryl fluorides
16
hydrazine substitution
8
substitution p-nitro-aryl
8
feooh@c-catalyzed selective
4
hydrazine
4
selective hydrazine
4
p-nitro-aryl
4
fluorides
4
fluorides application
4
application synthesis
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!