324059-79-2Relevant academic research and scientific papers
Synthesis, characterization and anion recognition studies of new fluorescent alkyl bis(naphthylureylbenzamide)-based receptors
Lopéz-Martínez, Luis Miguel,García-Elías, José,Ochoa-Terán, Adrián,Ortega, Hisila Santacruz,Ochoa-Lara, Karen,Monta?o-Medina, César Ulises,Yatsimirsky, Anatoli K.,Ramírez, José Z.,Labastida-Galván, Victoria,Ordo?ez, Mario
, (2020)
The synthesis of new alkyl (C3 to C8) bis(naphthylureylbenzamide)-based receptors and the study of their interaction with anions by UV–Vis, molecular fluorescence and 1H NMR were performed. The results suggest both ureylbe
Synthesis and anion recognition studies of new oligomethylene bis(nitrophenylureylbenzamide) receptors
García-Elías, José,Ochoa-Terán, Adrián,Yatsimirsky, Anatoli K.,Santacruz Ortega, Hisila,Ochoa-Lara, Karen,López-Martínez, Luis Miguel,Castro-Riquelme, Christian L.,García, ángel L.,Madrigal-Peralta, Domingo,Labastida-Galván, Victoria,Ordo?ez, Mario
, p. 39147 - 39162 (2019/12/15)
A new series of oligomethylene bis(nitrophenylureylbenzamide) receptors were synthesized varying the relative position of the urea and amide groups (ortho4 and meta8) and the length of the oligomethylene chain (C2 to C8). An anion re
Synthesis and cytotoxic effect of carbocyclic potential minor groove binders
Bartulewicz, Danuta,Anchim, Tomasz,Dabrowska, Milena,Midura-Nowaczek, Krystyna
, p. 211 - 214 (2007/10/03)
New carbocyclic potential minor groove binders were synthesised, using 3-nitrobenzoyl chloride and aliphatic α,ω-diamines with three, four and five methylene fragments. The half structures, compounds IV-VI can be compared to bis-amidines, compounds X-XII
