ChemistrySelect (2026) 11(35): e74508. https://doi.org/10.1002/slct.74508
Green Synthesis, Antibacterial Activity, and Molecular Docking Study of γ-Phosphonyloxime Derivatives Wahbi, A.; Mhamdi, A.; Tahri, W.; Dridi, I.; Dridi, M. A.; Kamisky, W.; Kaabi, K.; Chatti, A.; Nasr, C. B.; Cavalier, J.-F.; Touil, S. Herein, we report an efficient, fast, and green approach to synthesize γ-phosphonyloximes (2) via microwave-assisted oximation of γ-phosphonylketones under solvent-free conditions. This method achieved high yields (up to 95%) in just 5 min. Su


Febs J (2022) 290: 1563-1582, https://doi.org/10.1111/febs.16645
Direct capture, inhibition and crystal structure of HsaD (Rv3569c) from M. tuberculosis Barelier, S.; Avellan, R.; Gnawali, G. R.;...


Bioorg. Med. Chem. Lett. 64 (2022) 128692
Design, synthesis and antibacterial activity against pathogenic mycobacteria of conjugated hydroxamic acids, hydrazides and...


J Mol Struct. (2021) 1229: 129634
Experimental and computational investigation of Z/E isomerism, X-ray crystal structure and molecular docking study of ...


FEBS Lett. (2020) 594: 79-93
Methyl arachidonyl fluorophosphonate inhibits Mycobacterium tuberculosis thioesterase TesA and globally affects vancomycin susceptibility...


Scientific Reports (2017) 7: 11751
Cyclipostins and Cyclophostin analogs as promising compounds in the fight against tuberculosis Nguyen, P. C.; Delorme, V.; Bénarouche,...






