| P2093 | author name string | Debabrata Maiti | |
| | Rajesh Kancherla | |
| | Togati Naveen | |
| P2860 | cites work | A farnesyltransferase inhibitor prevents both the onset and late progression of cardiovascular disease in a progeria mouse model | Q24657266 |
| | Fragment-based ligand design of novel potent inhibitors of tankyrases | Q27684619 |
| | Phase III trial of gemcitabine plus tipifarnib compared with gemcitabine plus placebo in advanced pancreatic cancer | Q33360410 |
| | Second generation analogues of the cancer drug clinical candidate tipifarnib for anti-Chagas disease drug discovery. | Q33879398 |
| | Cationic Pd(II)-catalyzed Fujiwara-Moritani reactions at room temperature in water | Q34108251 |
| | Aromatic substitution of olefins. VI. Arylation of olefins with palladium(II) acetate | Q34535495 |
| | Farnesyl protein transferase inhibitor ZARNESTRA R115777 - history of a discovery | Q35137612 |
| | A mild, palladium-catalyzed method for the dehydrohalogenation of alkyl bromides: synthetic and mechanistic studies | Q36206042 |
| | Ligand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst | Q36405081 |
| | Rational modification of a candidate cancer drug for use against Chagas disease | Q37274008 |
| | Palladium(II)-catalyzed C-H activation/C-C cross-coupling reactions: versatility and practicality | Q37294999 |
| | Towards mild metal-catalyzed C-H bond activation | Q37888484 |
| | Insights through AM1 calculations into the structural requirement of 3,4,6-substituted-2-quinolone analogs towards FMS kinase inhibitory activity | Q38431503 |
| | Palladium-catalyzed aerobic dehydrogenation of substituted cyclohexanones to phenols | Q38468279 |
| | The synthesis and structure-activity relationships of 4-aryl-3-aminoquinolin-2-ones: a new class of calcium-dependent, large conductance, potassium (maxi-K) channel openers targeted for post-stroke neuroprotection | Q38522580 |
| | Selective activation of apoptosis by a novel set of 4-aryl-3-(3-aryl-1-oxo-2-propenyl)-2(1H)-quinolinones through a Myc-dependent pathway | Q39917196 |
| | Synthesis and in vitro anti-hepatitis B virus activities of 4-aryl-6-chloro-quinolin-2-one and 5-aryl-7-chloro-1,4-benzodiazepine derivatives | Q39975359 |
| | Rh-Catalyzed decarbonylative coupling with alkynes via C-C activation of isatins | Q41558627 |
| | Allylic C-H acetoxylation with a 4,5-diazafluorenone-ligated palladium catalyst: a ligand-based strategy to achieve aerobic catalytic turnover | Q41970172 |
| | Pd-catalyzed aerobic oxidative coupling of arenes: evidence for transmetalation between two Pd(II)-aryl intermediates | Q42107834 |
| | Ligand-enabled triple C-H activation reactions: one-pot synthesis of diverse 4-aryl-2-quinolinones from propionamides | Q42753736 |
| | Design, synthesis, and activity of achiral analogs of 2-quinolones and indoles as non-thiol farnesyltransferase inhibitors | Q42816255 |
| | Ligand-controlled C(sp³)-H arylation and olefination in synthesis of unnatural chiral α-amino acids | Q42920887 |
| | Palladium-catalyzed intramolecular amidation of C(sp2)-H bonds: synthesis of 4-aryl-2-quinolinones | Q43072170 |
| | Synthesis and biological evaluation of new 1,2-dihydro-4-hydroxy-2-oxo-3-quinolinecarboxamides for treatment of autoimmune disorders: structure-activity relationship | Q44823676 |
| | Synthesis of 2-quinolones via palladium-catalyzed carbonylative annulation of internal alkynes by N-substituted o-iodoanilines | Q45074658 |
| | Iridium-catalyzed, intermolecular hydroamination of unactivated alkenes with indoles. | Q45975888 |
| | Mechanism of Pd(OAc)2/pyridine catalyst reoxidation by O2: influence of labile monodentate ligands and identification of a biomimetic mechanism for O2 activation. | Q46134647 |
| | On the interpretation of deuterium kinetic isotope effects in C-H bond functionalizations by transition-metal complexes | Q46145223 |
| | Synthesis of beta-, gamma-, and delta-lactams via Pd(II)-catalyzed C-H activation reactions | Q46333074 |
| | Towards ideal synthesis: alkenylation of aryl C-H bonds by a Fujiwara-Moritani reaction. | Q46472332 |
| | Regioselective Heck reaction of aliphatic olefins and aryl halides | Q46991296 |
| | 4-Aryl-3-(hydroxyalkyl)quinolin-2-ones: novel maxi-K channel opening relaxants of corporal smooth muscle targeted for erectile dysfunction | Q48826377 |
| | 3-Thio-quinolinone maxi-K openers for the treatment of erectile dysfunction. | Q50671069 |
| | 4-Aryl-3-(mercapto)quinolin-2-ones: novel maxi-K channel opening relaxants of corporal smooth muscle. | Q50671437 |
| | Indirect ortho functionalization of substituted toluenes through ortho olefination of N,N-dimethylbenzylamines tuned by the acidity of reaction conditions. | Q50682203 |
| | Practical route to 2-quinolinones via a Pd-catalyzed C-H bond activation/C-C bond formation/cyclization cascade reaction. | Q50988873 |
| | Selective arylation and vinylation at the α position of vinylarenes. | Q51274379 |
| | Intermolecular Mizoroki-Heck reaction of aliphatic olefins with high selectivity for substitution at the internal position. | Q51371956 |
| | Palladium-catalyzed C-S activation/aryne insertion/coupling sequence: synthesis of functionalized 2-quinolinones. | Q51745400 |
| | Copper-catalyzed domino cycloaddition/C-N coupling/cyclization/(C-H arylation): an efficient three-component synthesis of nitrogen polyheterocycles. | Q53091018 |
| | Aromatic substitution of styrene-palladium chloride complex | Q56482534 |
| | O2insertion into a palladium(ii)-hydride bond: Observation of mechanistic crossover between HX-reductive-elimination and hydrogen-atom-abstraction pathways | Q58482024 |
| P433 | issue | 23 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 8360-8364 | |
| P577 | publication date | 2015-04-21 | |
| P1433 | published in | Chemistry—A European Journal | Q898737 |
| P1476 | title | Palladium-Catalyzed [3+3] Annulation between Diarylamines and α,β-Unsaturated Acids through CH Activation: Direct Access to 4-Substituted 2-Quinolinones | |
| P478 | volume | 21 | |