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1 high catalytic activity towards reduction of 4-nitrophenol.
2 een demonstrated with catalytic reduction of 4-nitrophenol.
3 gh catalytic activities for the reduction of 4-nitrophenol.
4 ensitivity to the inhibition by 2,6-dichloro-4-nitrophenol.
5  Pd(atz,ur) complex at 457nm by the 2-chloro-4-nitrophenol (2-CNP) which produced from the reaction o
6                            The separation of 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol
7 ducts: 2-methoxy-5-nitrophenol (2), 2-chloro-4-nitrophenol (3), and 3-chloro-4-methoxyphenol (4), in
8 atechol are good substrates whereas 3-methyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol,
9 f 4-nitrophenol, 2,4-dinitrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol
10 hyl-4-nitrophenol, 3-methyl-4-nitrocatechol, 4-nitrophenol, 3-nitrophenol, and 4-chlorocatechol were
11 trophenol (3M2NP), (22.8 +/- 1.8) % 3-methyl-4-nitrophenol (3M4NP), (23.5 +/- 1.8) % 5-methyl-2-nitro
12 ity was tested using methylene blue (MB) and 4-nitrophenol (4-NP) as model pollutants under visible l
13 rticles (AuNPs) for the reduction process of 4-nitrophenol (4-NP) in the presence of sodium borohydri
14 ZVI was investigated during the reduction of 4-nitrophenol (4-NP) in unbuffered pH systems.
15 ibrous web showed the enhancive reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) within 45 s
16  four probe molecules-chloramphenicol (CAP), 4-nitrophenol (4-NP), amoxicillin (AMX), and furazolidon
17 h phenylboronic acid and in the reduction of 4-nitrophenol (4-NP).
18  co-complexed with reduced FAD (FADH(-)) and 4-nitrophenol (4NP) (HadA(WT)-FADH(-)-4NP) was solved at
19 ate), pesticides (metolachlor metabolite and 4-nitrophenol), a UV filter (benzophenone-1), and an ind
20  the effective photocatalytic destruction of 4-nitrophenol, a dangerous organic pollutant, are synthe
21 In addition, both enzymes were active toward 4-nitrophenol, a preferred substrate for CYP2E1.
22 enoxy)propionic acid, 3-phenoxybenozic acid, 4-nitrophenol, alachlor, atrazine, azoxystrobin, chlorpy
23 d to bind neutral guests, such as phenol and 4-nitrophenol, albeit weakly.
24 c acid methyl thioester, and the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic ele
25 ion rates of nitrite and HONO (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could signific
26 oxygen species (ROS) generation in degrading 4-nitrophenol and 2-nitrophenol.
27                                 Oxidation of 4-nitrophenol and 4-nitrocatechol was observed for both
28                    Besides carboxylic acids, 4-nitrophenol and 4-nitrocatechol were identified as fur
29 clohexylimidazole), toward different proton (4-nitrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl
30                                     Rates of 4-nitrophenol and formaldehyde production from the O-dem
31 ing H-bond base-pairing interactions between 4-nitrophenol and phosphine oxide side chains.
32 ydroxylation of 4-nitrophenylboronic acid to 4-nitrophenol and the following hydride reduction with N
33 ontrolled by applying TFM (3-trifluoromethyl-4-nitrophenol) and niclosamide to streams infested with
34  viscous films (10(-5)-10(-4) in the case of 4-nitrophenol) and overall reaction yields up to 0.3 in
35 itrophenol, 2-methyl-4-nitrophenol, 3-methyl-4-nitrophenol, and 2-nitrophenol (these are the dominant
36 ol (PFP), hexafluoroisopropyl alcohol (HFP), 4-nitrophenol, and N-hydroxyphthalimide.
37  polar compounds, phenol, 4-chlorophenol and 4-nitrophenol are extracted under headspace SPME conditi
38  when exposed to benzene, phenol, xylene and 4-nitrophenol as negative controls, thereby demonstratin
39 ax values for 4-methyl-7-hydroxycoumarin and 4-nitrophenol between on-line and off-line glucuronidati
40 on of estradiol, estrone, 4-aminophenol, and 4-nitrophenol by 103, 187, 162, and 92%, respectively (a
41 EPC [(2S,3S)-trans-3-phenyl-2-oxiranylmethyl 4-nitrophenol carbonate], suggesting that Cif may be red
42 NO (most notably, 4-nitrophenol and 2-methyl-4-nitrophenol) could significantly contribute to the occ
43 ors pentachlorophenol (PCP) and 2,6-dichloro-4-nitrophenol (DCNP) were used to modulate DNA adduct an
44 -containing polymers extracted up to >99% of 4-nitrophenol from aqueous solution, and the solvent-ext
45 ation is readily monitored by the release of 4-nitrophenol from the polymer using UV-vis spectrophoto
46                        A template with three 4-nitrophenol H-bond donor recognition units was used wi
47 ion of 5-nitro-benzisoxazole forming 2-cyano-4-nitrophenol has long served as a design platform of en
48 dient avobenzone and the industrial chemical 4-nitrophenol in follicular and seminal fluids suggests
49                                 2,6-Dichloro-4-nitrophenol inhibits phenolsulfotransferases, but not
50 to be catalytically active for conversion of 4-nitrophenol into 4-aminophenol, providing an example o
51  pH optimum for the standard assay substrate 4-nitrophenol is at pH 5.5; upon oxidation, the optimum
52 d lipophilicity of 2-nitrophenol over 3- and 4-nitrophenol is the lack of hydrogen bond acidity of 2-
53 d 4-6 ppm upfield from the aglycone 2-fluoro-4-nitrophenol (OFPNP).
54 ailed to catalyze the sulfate conjugation of 4-nitrophenol or 17beta-estradiol, prototypic substrates
55 s with either three phosphine oxide or three 4-nitrophenol recognition units to form the noncovalent
56 demonstrated in a recyclable manner by using 4-nitrophenol reduction as a probe reaction.
57 ssibility of Au25 (SG)18 is evaluated by the 4-nitrophenol reduction reaction.
58  palladium- or silver-nanoparticle-catalyzed 4-nitrophenol reduction, and 3) gold-nanoparticle-cataly
59            The lampricides 3-trifluoromethyl-4-nitrophenol (TFM) and 2',5-dichloro-4'-nitrosalicylani
60 s further used to quantify 3-trifluoromethyl-4-nitrophenol (TFM) reductive metabolism.
61 olerant native species, to 3-trifluoromethyl-4-nitrophenol (TFM), a pesticide commonly used in sea la
62            The lampricide, 3-trifluoromethyl-4-nitrophenol (TFM), is a primary component to sea lampr
63 control with the pesticide 3-trifluoromethyl-4-nitrophenol (TFM).
64 (11) shows high activity in the reduction of 4-nitrophenol to 4-aminophenol, while Cu(12) displays ve
65 rome P450s CYP3A1 and CYP2B1/2, testosterone/4-nitrophenol uridine diphosphate glucuronosyltransferas
66 time, the investigation of both pyridine and 4-nitrophenol vapor adsorption isotherms at very low con
67  (within 1 s of exposure) and ultrasensitive 4-nitrophenol vapor detection (at a sub-ppb level) were
68                                    Only when 4-nitrophenol was biodegraded by Pseudomonas sp. 1A did
69 onidation of 4-methyl-7-hydroxy coumarin and 4-nitrophenol were determined using the CE method and by
70 naphthalene, 2,4-dichloronicotinic acid, and 4-nitrophenol were similar to or higher than those of ur
71 d the more acidic 4-nitrophenol and 2-chloro-4-nitrophenol which mimic electronically excited cofacto
72 junction achieved an 86% degradation rate of 4-nitrophenol, while the MoS(2)/Bi(2)O(3)/CdS composite
73 s evaluated with respect to the reduction of 4-nitrophenol with NaBH4.