Anticancer Activity, Antibacterial activity, Azo compounds, Heterocycles, Sulfones
Anticancer activity, CSIC reaction, cyclization, DFT calculations, Sulfonates, Tautomerism
Pd(II)/Pt(II) π-complexes, X-Ray diffraction study, anti-metastatic and pro-apoptotic effect, MCF-7 cell spheroids, GGT activity
CSIC reaction, DFT calculations, Medium-sized heterocycles, Molecular docking, Sulfonamides, Sultams
lanthanide, cationic heteroleptic complexes, carbacylamidophosphate, sulfonylamidophosphate, luminescence, crystal structure.
N-alkoxy-N-chloroureas, N-alkoxy-N-(dimethoxyphosphory)ureas, synthesis, structure.
N-alkoxy-N-dimethoxyphosphory-N'-arylureas, structure, single crystal X-ray diffraction study.
thiazolo[2, 3-b]pteridines, synthesis, spectral data, photophysical properties, X-ray
Anticancer activity, CSIC reaction, Cytotoxicity, Medium-sized heterocycles, Sulfonamides, Sultams
Diels-Alder reaction, (E)-1, 1, 1, 4, 4, 4-hexafluoro-2-butene, (Z)-1, 1, 1, 4, 4, 4-hexafluoro-2-butene, furan, 2, 3-dimethyl-buta-1, 3-diene, 2-methyl-buta-1, 3-diene, cyclohexane-1, 3-diene
1, 2, 3-triazole, iododi(per)fluoroalkylation, carboxamides, visible-light induced reactions, fluorescein
amino alcohols, hydroxyimines, oxazolidines, Schiff bases, 2D NMR
Ferrocene, hydrazines, heterocyclization, reaction optimisation, XRD analysis
Ethyl 3, 3-difluoro-2-phenylacrylate, gemi-Difluoroalkene, Fluoropyrimidine, 6‑Fluoropyrimidone, Heterocyclization
N, N-dialkyl-N′-sulfonyl amidines, hindered rotation, rotational barrier, variable-temperature NMR spectroscopy, quantum-chemical calculations