ライフサイエンスコーパス: nitrobenzene

1 ce of a major contaminant (4-methylphenol or nitrobenzene).

2 ion in four steps and 24% overall yield from nitrobenzene.

3 ane, the long elusive phosphorus analogue of nitrobenzene.

4 nm), the nitroso oxide rapidly rearranges to nitrobenzene.

5 bearing clay minerals on the bioreduction of nitrobenzene.

6 are excellent catalysts in the reduction of nitrobenzene.

7 ,4,6-trichlorophenol, pentafluorophenol, and nitrobenzene.

8 ion by microbial and/or abiotic reduction of nitrobenzene.

9 from 15 to 1.7% for the 1347 cm(-1) mode of nitrobenzene.

10 r ortho (if para is substituted) position of nitrobenzene.

11 ethoxy-2-nitroaniline and 1-iodo-4-methoxy-2-nitrobenzene.

12 ates, as well as the intersystem crossing of nitrobenzene.

13 f the ion trap and has been demonstrated for nitrobenzene.

14 of several cytotoxic antitumor quinones and nitrobenzenes.

15 in large positive shifts in potential of the nitrobenzene(0/)(-) cyclic voltammetry wave with little

16 explosives and explosives-related compounds nitrobenzene, 1,3-dinitrobenzene, o-nitrotoluene, 2,4-di

17 , 3-nitroaniline, 4-nitroaniline, 1-chloro-2-nitrobenzene, 1-chloro-3-nitrobenzene, and 1-chloro-4-ni

18 Reductive hydrodynamic voltammograms of nitrobenzene, 2,4,6-trinitrotoluene, and hexahydro-1,3,5

19 cluding an array of nitroaromatic compounds (nitrobenzene, 2-, 3-, and 4-nitrotoluene, 2,4- and 2,6-d

20 dimethoxy-5,5'-binaphthoquinone in refluxing nitrobenzene (210 degrees C) gives, in a single syntheti

21 imulant methyl salicylate (1.24 ppb) and for nitrobenzene (629 pptr) are achieved.

22 acy of 86-92% for nitromethane and 1-ethyl-2-nitrobenzene, 71% for different mixtures of nitromethane

23 1,3-diphenylpropane (6), benzyl alcohol (7), nitrobenzene (8), and cyanobenzene (9).

24 Allylic esters of nitrobenzene acetic acids undergo facile palladium-catal

25 The three-component reaction between a nitrobenzene, an aldehyde, and a dienophile in the prese

26 tinum disk electrode in a solution of 0.06 M nitrobenzene and 0.5 M tetra-n-butylammonium hexafluorop

27 66% p-nitrophenol and 34% m-nitrophenol from nitrobenzene and 100% p-methoxyphenol from methoxybenzen

28 The limits of detection for nitrobenzene and 2,4-dinitrotoluene using SPI were also

29 stem is tested using the explosive simulants nitrobenzene and 2,4-dinitrotoluene, and with the nitram

30 stable intermediate in the biodegradation of nitrobenzene and 2-aminophenol by Pseudomonas pseudoalca

31 ame enzyme that initiates the degradation of nitrobenzene and 2-nitrotoluene also oxidizes 4-nitrotol

32 responding catechols by two enzymes, namely, nitrobenzene and 2-nitrotoluene dioxygenase (NBDO and 2N

33 sponding (13)C-KIEs for the dioxygenation of nitrobenzene and 2-nitrotoluene were 1.025 +/- 0.001 and

34 ioxygenation of two nitroaromatic compounds (nitrobenzene and 2-nitrotoluene) by nitrobenzene dioxyge

35 . strain JS42, which is capable of growth on nitrobenzene and 2-nitrotoluene, in experiments to exami

36 Detection limits are 25 ng for nitrobenzene and 50 ng for 2,4-dinitrotoluene.

37 ar lack of positional selectivity is seen in nitrobenzene and benzonitrile.

38 nd energies of attraction in acetonitrile of nitrobenzene and its anion radical and dianion with a se

39 ractionation revealed a common mechanism for nitrobenzene and nitrotoluenes.

40 known Pd catalysts for the hydrogenation of nitrobenzene and styrene and the Suzuki coupling reactio

41 ion cascade reaction between 2-amino/hydroxy nitrobenzenes and activated methyl groups.

42 aniline, 1-chloro-2-nitrobenzene, 1-chloro-3-nitrobenzene, and 1-chloro-4-nitrobenzene, could not onl

43 ides into solutions of DC18C6 in chloroform, nitrobenzene, and 1-octanol was undetectable.

44 sociated with the transformation of toluene, nitrobenzene, and four substituted nitrotoluenes by perm

45 The classic nitrobenzene anion-radical (NB(-*) or nitrobenzenide) is

46 on/ion reactions between peptide cations and nitrobenzene anions have been examined at both room temp

47 yl ether, tetrahydrofuran, benzophenone, and nitrobenzene are involved, the coordination number of th

48 s and alkyl-/arylthioanilides using 1-iodo-4-nitrobenzene as catalyst and oxone as an inexpensive and

49 hione S-conjugate precursor, 1-chloro-2,4-di-nitrobenzene, as well as cadmium.

50 thoxy-substituted giant biaryl (e.g., 21) in nitrobenzene at 260 degrees C does not yield the corresp

51 with 6,6'-dimethoxy-5,5'-binaphthoquinone in nitrobenzene at higher temperatures (250-260 degrees C),

52 illonite SWy-2 and nontronite NAu-2 enhanced nitrobenzene bioreduction.

53 rnover of large substrates such as furan and nitrobenzene but caused no similar increase for the phys

54 tion from the O-demethylation of 1-methoxy-4-nitrobenzene by P450 1A2 isolated from rabbit liver prod

55 lso an intermediate in the biodegradation of nitrobenzene by Pseudomonas pseudoalcaligenes JS45.

56 reaction between hydroxyl radical (*OH) and nitrobenzene (C(6)H(5)NO(2)) were measured in subcritica

57 DNT), 2,6-dinitrotoluene (2,6-DNT), 1-chloro-nitrobenzene (CNB), and nitrobenzene (NB), by their effe

58 ene, 1-chloro-3-nitrobenzene, and 1-chloro-4-nitrobenzene, could not only be detected but the electro

59 3) and CsCl from an aqueous D(2)O layer into nitrobenzene-d(5) as inferred from (1)H NMR spectroscopi

60 mination occurred upon themolysis of 1a,b in nitrobenzene-d(5).

61 d to 2-aminomuconic acid semialdehyde in the nitrobenzene-degrading strain Pseudomonas pseudoalcalige

62 4.6 for aqueous pyridine or 2.2-3.7 for neat nitrobenzene, depending on the analyzed vibrational mode

63 hydrogen bonding was studied for a series of nitrobenzene derivative radical anions, working as large

64 Highly fluorinated nitrobenzene derivatives are suitable substrates for pal

65 Reduction of nitrobenzene derivatives in the presence of arylureas in

66 via electrochemical reduction of 4-fluoro-3-nitrobenzene diazonium ion has been developed and utiliz

67 Molecular grafting of p-nitrobenzene diazonium salt at the surface of (Li)FePO4-

68 orts a genetic analysis of the expression of nitrobenzene dioxygenase (NBDO) in Comamonas sp. strain

69 mpounds (nitrobenzene and 2-nitrotoluene) by nitrobenzene dioxygenase (NBDO) to obtain insights into

70 cts from 3-nitrotoluene than those made from nitrobenzene dioxygenase.

71 di- and polyarylureas possessing pyrene and nitrobenzene end groups separated by a variable number o

72 all three redox active ferrocene, C(60), and nitrobenzene entities.

73 roM GS-Succ-BP is provided by dinitrophenol, nitrobenzene, ethacrynic acid, and S-hexylglutathione, a

74 found that chemically reduced NAu-2 reduced nitrobenzene faster as compared to chemically reduced SW

75 (14) and ethyl 2-chloropropionate (16) with nitrobenzene followed by subsequent addition of an alkyl

76 oxygen atom transfer from electron-deficient nitrobenzenes, followed by trapping of the resultant acy

77 nitrate analysis was developed by producing nitrobenzene from the nitrate in the samples and benzene

78 Attaching a 4-nitrobenzene group to the open end of the spiropyran uni

79 are observed during the 1-e(-) reduction of nitrobenzene in acetonitrile solutions.

80 These results are unexpected since nitrobenzene is a polar solvent that generally leads to

81 Arylation of nitrobenzene is also reported.

82 tions then show that thermal dissociation of nitrobenzene is dominated by 'roaming-mediated isomeriza

83 een 2,4-dinitrotoluene, ammonium nitrate and nitrobenzene is on a par with other state-of-the-art exp

84 Nitrobenzene is treated with the same computational prot

85 Additional exposure of the nitrobenzene layer to chloroform and water gives 3 in it

86 r from the pyrene donors in gel 2 to trapped nitrobenzene molecules.

87 thionite) iron-bearing clay minerals reduced nitrobenzene more rapidly than biologically reduced iron

88 this study are to demonstrate degradation of nitrobenzene (NB) as a probe compound for sequential ele

89 llected from several sites contaminated with nitrobenzene (NB) or chlorobenzene (CB) were tested for

90 generated electrons to catalyze reduction of nitrobenzene (NB) to aniline with a yield of 97.8% durin

91 cis-syn-cis-dicyclohexano-18-crown-6 (1) in nitrobenzene (NB) was correlated with the standard Gibbs

92 n aqueous solutions and benzonitrile (BN) or nitrobenzene (NB) was measured and used to evaluate the

93 etection of nitroaromatic molecules, such as nitrobenzene (NB), 2,4-dinitrotoluene (DNT), 2,4,6-trini

94 This was observed with nitrobenzene (NB), 7,7,8,8-tetracyanoquinodimethane (TCN

95 (2,6-DNT), 1-chloro-nitrobenzene (CNB), and nitrobenzene (NB), by their effective quenching of the n

96 unds [m-nitroaniline and p-nitroaniline] and nitrobenzenes [nitrobenzene, p-nitrotoluene, 2,4-dinitro

97 t (13)C- and (2)H-kinetic isotope effects of nitrobenzene, nitrotoluene isomers, 2,6-dinitrotoluene,

98 ly 5 ps to form QD(*-); electron transfer to nitrobenzene or the intermediates nitrosobenzene and phe

99 ificantly better aryl radical acceptors than nitrobenzenes or phenyl ethers.

100 pecificity for 4-nitroaniline and 1-chloro-2-nitrobenzene over other nitroaniline isomers and nitroch

101 could extract KF from an aqueous phase into nitrobenzene, overcoming the high hydration energies of

102 d by application of thioacidolysis, alkaline nitrobenzene oxidation and acetyl bromide analyses.

103 ramatically slowed, the regiospecificity for nitrobenzene oxidation is altered, and 10-fold more T111

104 te constant for p-nitrophenol resulting from nitrobenzene oxidation.

105 iline and p-nitroaniline] and nitrobenzenes [nitrobenzene, p-nitrotoluene, 2,4-dinitrotoluene, and 2,

106 (+) cation of the CsNO(3) extracted into the nitrobenzene phase by receptor 3 may be released into th

107 extracted from the water phase into the bulk nitrobenzene phase containing highly lipophilic ionophor

108 o the aqueous phase by contacting the loaded nitrobenzene phase with an aqueous KClO(4) solution.

109 The nitrobenzene produced was measured on a gas chromatograp

110 irectional transport of the electrogenerated nitrobenzene radical anion over macroscopic distances wi

111 ative of reversible hydrogen bonding between nitrobenzene radical anions and arylureas.

112 ucture-activity relationships when comparing nitrobenzene radical anions.

113 ologically driven, but at later time points, nitrobenzene reduction by biologically formed structural

114 On short time scales (<50 h), nitrobenzene reduction was primarily biologically driven

115 sulfenyl)phthalimide, and 4-azido-1-fluoro-2-nitrobenzene, respectively, and characterized as reversi

116 p-cresol and p-nitrophenol from toluene and nitrobenzene, respectively, as well as produced 2-naphth

117 The behavior of both the pyrene and nitrobenzene singlet states has been investigated by mea

118 or for cesium chloride and cesium bromide in nitrobenzene solution.

119 The cations form weak complexes with neutral nitrobenzene, stronger ion pairs with the monoanion, and

120 ure-dependent release of a model compound, 3-nitrobenzene sulfonate (3-NBS), from individual opticall

121 sol from toluene and 100% m-nitrophenol from nitrobenzene; thus, for the first time a true meta-hydro

122 d during initial steps in the degradation of nitrobenzene to a novel ring-fission lower pathway in Ps

123 le-light photocatalysts for the reduction of nitrobenzene to aniline through six sequential photoindu

124 Dioxygenation of nitrobenzene to catechol and 2-nitrotoluene to 3-methylc

125 elect) for the liquid-phase hydrogenation of nitrobenzene under standard operating conditions.

126 l conversion process for both the pyrene and nitrobenzene upper singlet states, as well as the inters

127 synthesis of derivatives of Indoprofen from nitrobenzene using readily available inexpensive startin

128 g the probe compounds tert-butyl alcohol and nitrobenzene verified the bubble-water interface as the

129 rent reactivity of SWy-2 versus NAu-2 toward nitrobenzene was caused by different forms of structural

130 on under extraction conditions from water to nitrobenzene was determined from plots of the cesium dis

131 When approximately 5% nitrobenzene was gelated together with benzene, fluoresc

132 of a synthetic heparin mimetic, Arixtra, at nitrobenzene/water microinterfaces was investigated to o

133 1-nitronaphthalene in the presence of excess nitrobenzene, where it was shown that the resulting SOA

134 roxylation with all substrates tested except nitrobenzene, which gives only m-nitrophenol.

135 ry also agreed well for the dioxygenation of nitrobenzene, which was associated with (2)H- and (13)C-

136 ical behavior of cyclooctatetraene (COT) and nitrobenzene with Density Functional Theory and the cond

137 The cyclocondensation reactions of nitrobenzene with hydrogen-terminated Si(100) and Si(111

138 larger substrates such as ethane, furan, and nitrobenzene with Q while decreasing the rate constant f

139 an imaging study of the photodissociation of nitrobenzene with state-specific detection of the result

140 ical anions from para- and ortho-substituted nitrobenzenes with 1,3-diethylurea in acetonitrile was p