Published on November 2021 | Organic synthesis and spectrscopy
Variously substituted 2,6-diphenylpiperidin-4-one 4-fluorobenzhydrazides were synthesized by direct condensation of the corresponding 2,6-diphenylpiperdin-4-one with 4-fluorobenzhydrazide. All the compounds are characterized by IR, NMR spectra readings. NMR spectral assignments are made unambiguously by their one-dimensional (H1 NMR and C13 NMR) NMR spectra. All the compounds have screened for their in vitro anti-oxidant and anti-bacterial activity in contradiction of various free radicals, and various bacterial strains respectively. The current study discloses that these compounds could be used as an outline for future development through derivatization to design more potent anti-oxidant and anti-microbial agents.