Design and synthesis of novel phthalazine and benzofuran scaffolds using CoFe2O4@CNSCu nanocatalyst: evaluation of PARP-1 inhibitory activity
10.1016/j.jorganchem.2025.123997 · doi-reference
An efficient one-pot synthesis of pyridazinones and phthalazinones using HY-zeolite
10.1002/jhet.649 · doi-reference
Green one-pot synthesis of thiazole scaffolds catalyzed by reusable NiFe 2 O 4 nanoparticles: In silico binding affinity and in vitro anticancer activity studies
10.1021/acsomega.4c05587 · doi-reference
Novel green synthesis of polyfunctionally substituted phthalazines promoted by visible light, DFT studies and molecular docking with antimicrobial and antibiofilm potency
10.1038/s41598-026-47154-w · doi-reference
Controlled microwave-assisted reactions: a facile synthesis of polyfunctionally substituted phthalazines as dual EGFR and PI3K inhibitors in CNS SNB-75 cell line
10.1016/j.bioorg.2022.105740 · doi-reference
A convenient metal-free one-pot synthesis of some phthalazine derivatives mediated by 3-picolinic acid
10.1007/s11164-025-05682-6 · doi-reference
Reaction of 1-nitroso-2-naphthols with α-functionalized ketones and related compounds: the unexpected formation of decarbonylated 2-substituted naphtho[1,2-d][1,3]oxazoles
10.1021/jo3022956 · doi-reference
Palladium-catalyzed synthesis of 4-aminophthalazin-1(2H)-ones by isocyanide insertion
10.1021/ol202784d · doi-reference
Multicomponent synthesis of 4-aminophthalazin-1(2H)-ones by palladium-catalyzed isocyanide insertion
10.1021/jo401131p · doi-reference
Microwave assisted palladium-catalyzed synthesis of phthalazinones and pyridopyridazinones
10.1016/j.tetlet.2013.05.006 · doi-reference
Synthesis of tetrahydrophthalazine and phthalamide (phthalimide) derivatives via palladium-catalysed carbonylation of iodoarenes
10.1016/j.tet.2011.09.095 · doi-reference
Palladium-catalyzed synthesis of phthalazinones: efficient carbonylative coupling of 2-bromobenzaldehydes and hydrazines
10.1002/chem.201200267 · doi-reference
Palladium-catalyzed phthalazinone synthesis using paraformaldehyde as carbon source
10.1021/ol502498y · doi-reference
Palladium-catalyzed acylation reactions: a one-pot diversified synthesis of phthalazines, phthalazinones and benzoxazinones
10.1002/ejoc.201800159 · doi-reference
Multicomponent reactions with Meldrum’s acid and isocyanides as a valuable synthetic approach: an update
10.1007/s11030-026-11469-7 · doi-reference
Highlighting multicomponent reactions as an efficient and facile alternative route in the chemical synthesis of organic-based molecules: a tremendous growth in the past 5 years
10.3389/fchem.2024.1469677 · doi-reference
Visible light amination/smiles cascade: access to phthalazine derivatives
10.1039/c6sc01095d · doi-reference
Synthesis of the possible carcinogenic dihydrodiol and diol epoxide of phthalazine
10.1016/j.tet.2004.11.071 · doi-reference
The mechanism of the triple aryne–tetrazine reaction cascade: theory and experiment
10.1039/c8sc01796d · doi-reference
Triple aryne-tetrazine reaction enabling rapid access to a new class of polyaromatic heterocycles
10.1039/c5sc01726b · doi-reference
Phthalazine derivatives from aromatic aldazines
10.1016/0040-4039(81)80093-7 · doi-reference
A convenient access to benzo-substituted phthalazines as potential precursors to DNA intercalators
10.1016/s0040-4039(01)01302-8 · doi-reference
Iptycene-derived pyridazines and phthalazines
10.1021/jo702000d · doi-reference
Phthalazines and phthalazine hybrids as antimicrobial agents: synthesis and biological evaluation
10.1177/1747519819883840 · doi-reference
Benzo[4,5]imidazo[2,1-a]phthalazines: I. substituted o-nitrophenylhydrazines in the synthesis of phthalazin-1(2H)-ones
10.1134/s1070428008050175 · doi-reference
Synthesis of benzo[4,5]imidazo[2,1- a] phthalazines
10.1016/j.tetlet.2003.12.070 · doi-reference
Synthesis of 4-substituted chlorophthalazines, dihydrobenzoazepinediones, 2-pyrazolylbenzoic acid, and 2-pyrazolylbenzohydrazide via 3-substituted 3-hydroxyisoindolin-1-ones
10.1021/jo3000628 · doi-reference
New convenient one-step synthesis of 4-arylphthalaz-1 -ones
10.1016/s0040-4020(01)91312-2 · doi-reference
Synthesis and antitumor activities of novel 1,4-disubstituted phthalazine derivatives
10.1016/j.ejmech.2010.05.016 · doi-reference
Design and synthesis of phthalazine-based compounds as potent anticancer agents with potential antiangiogenic activity via VEGFR-2 inhibition
10.1080/14756366.2019.1642883 · doi-reference
Rational design, synthesis, in vitro, and in-silico studies of pyrazole-phthalazine hybrids as new α-glucosidase inhibitors
10.1038/s41598-025-87258-3 · doi-reference
Phthalazine PDE4 inhibitors. Part 2: the synthesis and biological evaluation of 6-methoxy-1,4-disubstituted derivatives
10.1016/s0960-894x(00)00587-4 · doi-reference
An overview of different synthetic routes for the synthesis of phthalazine derivatives
10.9734/jpri/2019/v27i630189 · doi-reference
Anti-HIV activity of stilbene-related heterocyclic compounds
10.1016/j.bmcl.2006.04.087 · doi-reference
Recent advances in the synthesis of phthalazin-1(2H)-one core as a relevant pharmacophore in medicinal chemistry
10.1016/j.ejmech.2018.10.047 · doi-reference
One-pot synthesis of phthalazines and pyridazino-aromatics: a novel strategy for substituted naphthalenes
10.1021/ol301167q · doi-reference
Synthesis, biological evaluation and in silico studies of novel N-substituted phthalazine sulfonamide compounds as potent carbonic anhydrase and acetylcholinesterase inhibitors
10.1016/j.bioorg.2019.103004 · doi-reference
N-substituted phthalazine sulfonamide derivatives as non-classical aldose reductase inhibitors
10.1002/jmr.2991 · doi-reference
Prodromal dysfunction of α5GABA-A receptor modulated hippocampal ripples occurs prior to neurodegeneration in the TgF344-AD rat model of Alzheimer’s disease
10.1016/j.heliyon.2021.e07895 · doi-reference
The plasma–occupancy relationship of the novel GABAA receptor benzodiazepine site ligand, α5IA, is similar in rats and primates
10.1111/j.1476-5381.2009.00216.x · doi-reference
