ライフサイエンスコーパス: oxidation

1 ically have a low yield due to inhomogeneous oxidation.

2 ss for heterogeneous catalysis and materials oxidation.

3 hat the imidazolium salts is crucial for the oxidation.

4 cule therefore indicate the extent of starch oxidation.

5 tive oxidant species produced through Fe(II) oxidation.

6 ee centuries, accompanied by signs of lignin oxidation.

7 stine titania nanotubes fabricated by anodic oxidation.

8 from coordinated ammonia, a key step in NH3 oxidation.

9 PDH-E1alpha Ser(300) phosphorylation and FA oxidation.

10 in Controls, suggesting an increase in lipid oxidation.

11 lve back into the underlying perovskite upon oxidation.

12 pendent switch from glycolysis to fatty acid oxidation.

13 ted electron-transfer reaction initiates the oxidation.

14 ity (2.4 +/- 0.24 mA cm(-2) mM(-1)) for H2O2 oxidation.

15 c epithelial cells (colonocytes) toward beta-oxidation.

16 ct their respective contributions to ammonia oxidation.

17 pression of the genes involved in fatty acid oxidation.

18 lipase 3 and enzymes for mitochondrial beta-oxidation.

19 the phenomena occurring during the olive oil oxidation.

20 rmediates that are important in nucleic acid oxidation.

21 orus is stable against long-term (> 30 days) oxidation.

22 te electron injection and light-driven Br(-) oxidation.

23 e pathways are at work in copper-based water oxidation.

24 for the different parameters indicating fat oxidation.

25 tron O2 reduction and two-electron substrate oxidation.

26 reactive oxygen species, preventing membrane oxidation.

27 ategies known to enable remote aliphatic C-H oxidations.

28 learly different LambdaC-H values: 28 +/- 4 (oxidation), 0.7 +/- 0.1 and 0.9 +/- 0.1 (hydrolytic deha

29 Despite increased FA oxidation, Acot1 knockdown reduced the expression of per

30 kinetics of CO rebinding to carbon monoxide oxidation activator protein (ChCooA) are measured over a

31 To address the challenges of low carbon oxidation activity and low carbon utilization, a highly

32 ration and restructuring at the nanoscale on oxidation activity is demonstrated.

33 possible relevance to reductive elimination/oxidation addition reaction chemistry of transition meta

34 91), no correlation was observed between DTT oxidation and (*)OH formation.

35 Faradaic efficiencies of 71 +/- 5% for Br(-) oxidation and 94 +/- 2% for H2 production were measured.

36 nt of the two borylation reactions involving oxidation and acetal formation.

37 e post-translational modifications including oxidation and acetylation were detected.

38 estigated the impact of six protein diets on oxidation and anti-oxidation status in the muscle of you

39 FRU increased postprandial net carbohydrate oxidation and decreased net carbohydrate storage (estima

40 s been shown to recapitulate the reduced fat oxidation and elevated atrial natriuretic peptide messag

41 ased the redox potential, promoted the lipid oxidation and elevating the hue color of the mortadellas

42 rs of this spiro molecule through controlled oxidation and epimerization of the C13 spirocenter under

43 hence, their contributions to Earth surface oxidation and Fe deposition remain unknown.

44 Flux balance analysis showed H2 oxidation and formate production using FHL became an alt

45 hods have been utilized to assign glycation, oxidation and glycoxidation protein targets in diverse h

46 the detection of hybridization both guanine oxidation and indicator reduction signal changes at the

47 Apoplastic events such as monolignol oxidation and lignin polymerization are difficult to stu

48 As the major coenzyme in fuel oxidation and oxidative phosphorylation and a substrate

49 This work identifies bacterial formate oxidation and oxygen respiration as metabolic signatures

50 we have developed a systematic study on the oxidation and passivation of mechanically exfoliated bla

51 flexibility with restored preprandial lipid oxidation and postprandial glucose flux in ZDF rats.

52 As a consequence of increased FA oxidation and reduced PPARalpha activity, Acot1 knockdow

53 -doped fuels are effective in promoting soot oxidation and reducing the DPM mass emissions, but lead

54 ein tyrosine phosphatases (PTPs) through the oxidation and reduction of their active site cysteine.

55 The kinetics of the oxidation and reduction process are examined through tim

56 hich demonstrates hot-electron activation of oxidation and reduction reactions in the junctions, indu

57 light on the structural changes accompanying oxidation and reduction.

58 LDs away from the mitochondrial pathways for oxidation and ROS generation, thereby sustaining cancer

59 balance in post-mortem muscle, early protein oxidation and the onset of pale, soft and exudative (PSE

60 hearts have increased glucose and palmitate oxidation and UCP3.

61 e protein S-mycothiolation, reversible thiol-oxidations and their impact on gene expression in Mycoba

62 selective in vitro cytochrome P450-mediated oxidation, and chemical oxidation was used to complete t

63 acetylation target; improved fatty acid beta-oxidation; and ameliorated liver steatosis and glucose i

64 y metabolic pathways such as fatty acid beta-oxidation are unclear.

65 ess than 1, suggesting that enhanced sulfide oxidation as a result of glaciation may act as a source

66 ration has to be equal or below that of NADH oxidation, as further increases in [NADH] elevate ubiqui

67 to be similar to those reported for nitrite oxidation, as well as for anaerobic dissimilatory nitrat

68 stent with the reaction sequence for sulfide oxidation being: H2S --> glutathione persulfide --> sulf

69 a were not directly involved in full methane oxidation, but their crucial participation, likely being

70 ethane as the principal hydrocarbon, methane oxidation by abundant members of ANME-1 was likely the p

71 Our present study implies that aerobic NH3 oxidation by AOB occurs via two obligate intermediates,

72 y focused at the mechanistic features of the oxidation by Fe(V)O of hydrocarbons including cyclohexan

73 findings reveal the catalytic process of TMA oxidation by marine bacterial Tmm and first show that NA

74 ere we investigate the potential for Cr(III) oxidation by Mn oxides within fixed solid matrices commo

75 oxides, suggesting Cr(VI) generation through oxidation by Mn-oxides.

76 nt with previous studies that ozonolysis and oxidation by NO3 are sources of nighttime HO2.

77 Abiotic Fe(II) oxidation by O2 commonly occurs in the presence of miner

78 Similar products were formed by the CPA oxidation by OH in the gas-phase, at the air-water inter

79 ects, particularly an increase in fatty acid oxidation, cannot be explained by decarboxylated osteoca

80 urther explain previously observed prolonged oxidation capability of TiO2 powder without light irradi

81 teins involved in SCN(-) degradation, sulfur oxidation, carbon fixation, and nitrogen removal.

82 oxidation catalysts.Improving platinum as an oxidation catalyst requires understanding its structure

83 of their oxidized forms to activate a water oxidation catalyst, or the absence of a sufficiently red

84 irst generation MOF-based, selective methane oxidation catalyst.

85 ily heterogeneous Co, Ni, and Mn based water oxidation catalysts are reviewed.

86 -carbon-supported IrPdRu nanoparticles-as H2 oxidation catalysts in alkaline media.

87 the presence of active O atoms, crucial for oxidation catalysts.Improving platinum as an oxidation c

88 on (Lactobacillales), and syntrophic acetate oxidation (Clostridiaceae).

89 nsaturated chains, and a lower generation of oxidation compounds (conjugated dienes in chains having

90 The rapid agglomeration of Pd atoms under CO oxidation conditions even at 6 degrees C leads to the pr

91 easurements of energy expenditure, substrate oxidation, core temperature, cold and hunger scores, and

92 ET may also have a role in anaerobic methane oxidation coupled to sulfate reduction, an important con

93 revealed that denitrifying anaerobic methane oxidation (DAMO) archaea, Anammox bacteria and DAMO bact

94 We examined dihydrorhodamine 123 (DHR) oxidation data for percentage of X-chromosome inactivati

95 itis hearts showed a significant increase in oxidation-dependent calcium and calmodulin-dependent pro

96 M1 macrophage response, revealing reduction-oxidation-dependent mechanisms of signal transducer and

97 compounds and acetaldehyde, as well as lipid oxidation derived odorants to the overall odor of rice p

98 t markedly increases rates of whole-body fat oxidation during exercise in race walkers over a range o

99 units (Fe(V)O), wherein the iron atom is two oxidation equivalents above the Fe(III) resting state.

100 ant buildup in atmospheric oxygen, the Great Oxidation Event (GOE), began in the early Paleoproterozo

101 he palaeontological record between the Great Oxidation Event 2.4 billion years ago (Ga) and the last

102 n atmospheric oxygen on the Earth (the Great Oxidation Event).

103 Subsequent self-oxidation eventually causes deactivation.

104 of magnitude greater than the rate of pyrite oxidation expected under similar conditions.

105 9 steady-state, single precursor hydrocarbon oxidation experiments after passing through a temperatur

106 particles along with single atoms during CO oxidation experiments.

107 egradation, reactive oxidative species (ROS) oxidation, extracellular oxidative metabolism (EXOMET),

108 duction of SOA from a diesel engine using an oxidation flow reactor (OFR).

109 C-H hydroxylation is strongly favored over N-oxidation for numerous amine derivatives.

110 mmatory cytokines, and end products of lipid oxidation had a synergistic effect on TLR2 activation.

111 A late-stage TEMPO-mediated regioselective oxidation has been performed to achieve the required uro

112 the yields of two major products of benzene oxidation, i.e., phenol and aldehyde, were positively co

113 res necessary for successfully driving water oxidation in a light-driven system are explored along wi

114 plored due to their higher susceptibility to oxidation in air.

115 found to be the most effective at retarding oxidation in air.

116 nes involved in thermogenesis and fatty acid oxidation in brown fat.

117 Reduced mitochondrial protein oxidation in FABP4/aP2(-/-) macrophages attenuates the m

118 attributes well-suited to the study of lipid oxidation in heterogeneous samples.

119 otene/linoleic acid system, and reduction of oxidation in lipid system.

120 s, previously validated for monitoring lipid oxidation in plant oils, was extended to follow lipid ox

121 information regarding the role of substrate oxidation in the development of obesity and insulin resi

122 OxyHb promoted lipid oxidation in washed muscle more effectively compared to

123 vities, and are thus promising for pollutant oxidation in wastewater treatment.

124 in plant oils, was extended to follow lipid oxidation in water-in-oil emulsions.

125 ic regulation (i.e. incorporation, flux, and oxidation, in a tissue-specific and whole-body fashion)

126 ) phosphorylation was decreased, and glucose oxidation increased.

127 or oxygen storage due to its easy reversible oxidation into LuFe(3+)2O4.5.

128 trate that silver nanoparticle collision and oxidation is highly dynamic and likely controlled by a s

129 ynamic process of nanoparticle collision and oxidation is imaged by single-particle fluorescence micr

130 cially in polyhaline estuaries where ammonia-oxidation is largely driven by AOB.

131 We also provide evidence that fatty acid oxidation is negatively regulated by miR-29 overexpressi

132 cally, our understanding of ROS-mediated PTP oxidation is not yet sufficient to predict the molecular

133 at the fringe of the methane plume show that oxidation is primarily mediated by the reduction of iron

134 and the critical parameters governing lipid oxidation is required prior to the industrial adoption o

135 Persulfate (S2O8(2-))-based in situ chemical oxidation (ISCO) has gained more attention in recent yea

136 G2 enhanced LD breakdown and fatty acid (FA) oxidation, leading to increased ROS production and apopt

137 S detection was used to determine the sample oxidation level.

138 t can cycle through a series of ground-state oxidation levels to achieve a series of discrete yet fun

139 different molecular weight distributions and oxidation levels, lead to an increase in the expression

140 ction of the D1-Asn(87) residue in the water-oxidation mechanism.

141 hese issues are addressed by electrochemical oxidation methods, but such approaches typically have a

142 mponents from wild-type and peroxisomal beta-oxidation mutants including (omega - 1)-linked acyl, eno

143 The chemical changes (oxidation/nitrosation) of meat proteins during digestion

144 ociated with a new Fe species with a reduced oxidation number (from Fe(3+) to Fe(2+)) likely bonded w

145 Ammonium oxidation occurred solely by the activity of anammox bac

146 nations are discussed to the extent that net oxidation occurs by loss of H2.

147 s in good yields when R = alkyl or aryl, but oxidation of 2H-pyrans also gives alkyl cleavage product

148 The oxidation of 4 with AgBF4 affords [(Cp(Bn)Fe)2(mu,eta(5:

149 ated in a metal-free heterogeneous selective oxidation of 5-hydroxymethyl-furfural (HMF) to 2,5-furan

150 ncides with the nitrotyrosine formation, the oxidation of [4Fe-4S] clusters of dehydratases, and DNA

151 quiv) of aqueous hydrogen peroxide, from the oxidation of a broad range of olefins.

152 a Friedel-Crafts triflation and a late-stage oxidation of a furan ring.

153 yst with a unique efficacy for the selective oxidation of a single hydroxyl group among many in unpro

154 mily members, catalyzes the NAD(+)-dependent oxidation of aldehydes to their respective carboxylic ac

155 O nanohybrid in detail via the H2O2-mediated oxidation of Amplex Red (AR) to form fluorescent resoruf

156 The mechanism of the oxidation of arylsilanes to phenols has been investigate

157 h sub-nanometer thickness formed through the oxidation of atomically thin two-dimensional boron nitri

158 report a novel and efficient method for the oxidation of benzylic carbons (amines and cyanides) into

159 ic activity of (249)Bk (t1/2 = 320 d) causes oxidation of Bk(III) and only Bk(IV) is present after a

160 Subsequent N-oxidation of calothrixin B delivered calothrixin A.

161 clable medium for the environmentally benign oxidation of conjugated alkenes with H2O2.

162 reducing agents post-ATRP which prevent the oxidation of Cu(I) catalyst required by the Glaser coupl

163 s anoxic in the uppermost aquifer due to the oxidation of dissolved organic carbon.

164 ctivated to generate O(MeAN) and perform the oxidation of external substrates by two complementary st

165 Relative to oxidation of Fe(II)(aq) alone, both goethite and gamma-A

166 Chromium(VI) produced from the oxidation of indigenous Cr(III) minerals is increasingly

167 The inability to switch between the oxidation of lipid and carbohydrate appears to be an imp

168 two compartment mitochondrial model of beta-oxidation of long-chain fatty acids and main energy-redo

169 MAO, the potential source is the atmospheric oxidation of marine derived trimethylarsine.

170 ns spp. archaea thought to perform anaerobic oxidation of methane linked to iron reduction were abund

171 se 4 (NOX4), an enzyme known to catalyse the oxidation of NAD(P)H, is upregulated when p16 is inactiv

172 mitoNEET is a redox enzyme that may promote oxidation of NADH to facilitate enhanced glycolysis in t

173 to both overlapping oxygen evolution and the oxidation of Ni(OH)2 to NiOOH.

174 hanced electrocatalytic response towards the oxidation of NO as compared to other control electrodes.

175 toproducts can be attributed to photoinduced oxidation of oil.

176 iacy of Co(IV)-O species in cobalt-catalysed oxidation of organic substrates as well as in the cataly

177 ndustrial significance such as reduction and oxidation of organics, inorganics, and CO2 transformatio

178 hydroxylase flavoprotein family catalyze the oxidation of para-substituted phenols.

179 Here, we investigate if the oxidation of PCB 51 and PCB 102 by different microsomal

180 om the fungus Penicillium simplicissimum For oxidation of phenols by VAO to occur, they must first be

181 ly conserved C-terminal domain catalyzes the oxidation of polyunsaturated fatty acids, generating an

182 organic aerosol (SOA) formation during photo-oxidation of primary emissions from cookstoves used in d

183 utilization A (PutA) catalyzes the two-step oxidation of proline to glutamate using separate proline

184 ss spectrometry (HDX-MS), fast photochemical oxidation of proteins (FPOP), alanine shave mutagenesis,

185 he dynamic collision behavior of the electro-oxidation of single Ag nanoparticles is observed at Au m

186 The proposed explanation is oxidation of sorbed Fe(II) and reductive Fe(II) release

187 catalyze metal-oxo-mediated anti-Markovnikov oxidation of styrenes with high efficiency.

188 sensing mechanism is based upon ROS-induced oxidation of the ascorbic acid units within the hydrogel

189 ation of SDs, whereas a new pathway yielding oxidation of the benzene ring after the cleavage of the

190 ctivation step characterized by one-electron oxidation of the CTA.

191 Hence, oxidation of the enantioenriched dihydrofuran precursors

192 semble into metal oxide films during thermal oxidation of the sacrificial graphene template.

193 vity patterns parallel those observed in the oxidation of the same substrates with H2O2 catalyzed by

194 intercalation of the capping agent promotes oxidation of the silver core, occurring at 0.50 V (vs. A

195 icals are generated from the single-electron oxidation of the trifluoroborates, and these radicals ar

196 protective effect of TPO against the primary oxidation of these refined oils was significantly correl

197 ganic substrates as well as in the catalytic oxidation of water that evolves molecular oxygen.

198 telet-derived growth factor evokes transient oxidation on or close to RAB5+/ early endosome antigen 1

199 s important for understanding the effects of oxidation on starch properties, and this information may

200 rates that have biased affinities for either oxidation or reduction by PDI.

201 nanocatalysis the nanoparticles can undergo oxidation or reduction in situ, and thus the redox speci

202 nsporters and consider how the role of sugar oxidation, or oxidative fermentation, operates with mult

203 substances, effective inhibition of protein oxidation (P<0.01) and less colour loss during frozen st

204 redox transformation via catalytic or direct oxidation pathways.

205 mental studies on the origin of the backward oxidation peak of MOR coincide well with DFT predictions

206 s by screening for inefficient seedling beta-oxidation phenotypes.

207 e and pyrimidine metabolism, fatty acid beta-oxidation, phospholipid catabolism, arachidonic acid and

208 rs was used to initiate reactions (NOx photo-oxidation, photolysis of H2O2, ozonolysis, or thermal de

209 key life processes including fatty acid beta-oxidation, photorespiration, synthesis of hormones, and

210 The oxidation potential for aggregated 4 and 15 nm diameter

211 7 folds higher catalytic activity with lower oxidation potential towards CC than SPCE modified with G

212 This oxidation potential-gated technology is amenable to endo

213 egrees C form a volcano plot versus relative oxidation potential.

214 cture of HOMO that leads to length-invariant oxidation potentials and cation radical excitation energ

215 rm to selectivity wherein the discrepancy in oxidation potentials between internal versus C-terminal

216 In this work, an oxidation predictive model was proposed, following a met

217 nanoparticles typically undergo only partial oxidation prior to diffusing away from the Au electrode

218 UV) and free chlorine (UV-chlorine) advanced oxidation process that produces highly reactive hydroxyl

219 o merge soft enolization with a Pd-catalyzed oxidation process.

220 ) photolysis, and the corresponding advanced oxidation processes (AOPs) (i.e., O3/H2O2 and UV/H2O2) w

221 e probes for use in electrochemical advanced oxidation processes (EAOPs), due to the neglect of alter

222 eatures for these species in interchange and oxidation processes are also reviewed.

223 We isothermally dilute the oxidation products from the limonene+NO3 reaction at 25

224 , oxidative stress and chlorophyll allomers (oxidation products).

225 essential cofactor of this cycle, and other oxidation-prone folate derivatives kills human, mouse an

226 activity issues, and the origin of competing oxidation/protodeboronation side reactions.

227 Here, we quantify BPA oxidation rates and the formation of its predominant pro

228 te and gamma-Al2O3 surfaces increased Fe(II) oxidation rates regardless of pO2 levels, with goethite

229 cidic and basic solution toward the methanol oxidation reaction (MOR) compared to larger PtZn iNPs sy

230 During charging, the oxidation reaction at significantly reduced charge poten

231 tion involves decarboxylation followed by an oxidation reaction enabled just by using DMSO as the sol

232 A possible mechanism of the oxidation reaction was proposed and the reaction product

233 rophotometry and the heat flux dissipated by oxidation reactions and measured directly in water-in-oi

234 cts as tools to implement selectivity in C-H oxidation reactions are briefly discussed.

235 Palladium(II)-catalyzed oxidation reactions exhibit broad utility in organic syn

236 od type pathways that have been proposed for oxidation reactions on single supported atom.

237 lications for other Pd-catalyzed aerobic C-H oxidation reactions.

238 a promising route for enhancing the rates of oxidation reactions.

239 g of Pt(111) electrodes upon electrochemical oxidation/reduction in 0.1 M HClO4 was studied by in sit

240 We first examined redox (oxidation/reduction) properties and stability of 3-NT in

241 ons in terms of anion adsorption and surface oxidation/reduction.

242 ty affects metabolism well beyond fatty acid oxidation, regulating biochemical pathways associated wi

243 crystals, enabling materials with a greater oxidation resistance and hence a higher temperature capa

244 uality-related characteristics (HDL particle oxidation, resistance against oxidative modification, ma

245 Conventional chemical oxidation routes for the production of graphene oxide (G

246 cellular energy and mitochondria their major oxidation site.

247 ectly predicting the experimentally observed oxidation sites in various complex diketopiperazine case

248 bilised by Quillaja saponin showed decreased oxidation stability due to naturally occurring metals bu

249 ate (80 pi electrons) and aromatic in its 6+ oxidation state (78 pi electrons).

250 of 2.4 nanometres, is antiaromatic in its 4+ oxidation state (80 pi electrons) and aromatic in its 6+

251 iscrete methyl intermediate where the formal oxidation state (FOS) on the carbon remains unchanged at

252 ggregation state (single vs. few layers) and oxidation state (unmodified graphene vs. oxidized graphe

253 ields bearing the Ge2(2+) ion with Ge in the oxidation state +1.

254 nverse-trans-influence may occur beyond high oxidation state 5f metals and hence could encompass mid-

255 attributed to differences in aerosol carbon oxidation state [Formula: see text].

256 f metals and hence could encompass mid-range oxidation state actinides and lanthanides.

257 lony and its microenvironment and the copper oxidation state and succession of copper coordinating li

258 Depending on its oxidation state and the environmental conditions, it can

259 on of tetrahedral S(-I) sites, with the same oxidation state as in arsenopyrite (FeAsS), although rar

260 hanical properties, morphology evolution and oxidation state changes during electrochemical processes

261 ction of the surface arsenic (30-60%) has an oxidation state consistent with As(0).

262 We report that the oxidation state of PEG-thiol is key to anisotropic silic

263 he plasticized poly(vinyl chloride) ISM, the oxidation state of the electrodeposited PPy-PFOS was adj

264 monitor of toxicity of uranium (in the U(VI) oxidation state) in a plant cell model of Brassica napus

265 ric field, can significantly increase the Ni oxidation state.

266 te, elemental composition, iron content, and oxidation state.

267 nd condition-dependent changes in metabolite oxidation states and elucidation of the mechanisms where

268 ing a redox-active ligand in three different oxidation states has been synthesized, including the imi

269 potential, and resulting alterations in the oxidation states of intracellular metabolites and enzyme

270 These complexes have formal Co(-I) oxidation states, representing the only coordination com

271 H, and S in the solid Earth depends on their oxidation states, which are related to oxygen fugacity (

272 ysteines are reported to occupy these higher oxidation states, which effectively inactivate the corre

273 t of six protein diets on oxidation and anti-oxidation status in the muscle of young rats.

274 lectron transfer to lower the potentials for oxidation steps and catalysis.

275 Met oxidation studies (pH 7, D2O, 0.01 M phosphate, 25 degre

276 After oxidation, the adsorption of ammonium increased while ph

277 During oxidation, the hydroxyl groups of starch molecules are f

278 PTEN down-regulation may promote beta-oxidation through beta-catenin, whereas hypertrophy was

279 es encoding the upper branch of methyl group oxidation to CO2 as well as membrane-bound heterodisulfi

280 ixture, at neutral pH, electrochemical water oxidation to hydrogen peroxide was observed, albeit with

281 cepted model for AOB metabolism involves NH3 oxidation to nitrite (NO2(-)) via a single obligate inte

282 om nitrogen (N) in three steps: (1) ammonium oxidation to nitrite; (2) denitrification of nitrite to

283 al results agree that ZnCu undergoes surface oxidation under the reaction conditions so that surface

284 ubilization of HC components and their photo-oxidation up to O4-5 of mainly high double bond equivale

285 ystem of irreversible 2-nitro-5-thiobenzoate oxidation used in the detection of reduced glutathione (

286 N2O production by hydroxylamine oxidation was further stimulated by NH4(+), whereas nitr

287 n urban site were analyzed, and although DTT oxidation was significantly correlated with H2O2 generat

288 Lipid oxidation was tracked by measuring the peroxide value, a

289 chrome P450-mediated oxidation, and chemical oxidation was used to complete the scalable construction

290 apolipoprotein B-containing lipoproteins to oxidation, was significantly increased in e-cigarette us

291 thermodynamic objections to such an unlikely oxidation, we present several observations that show tha

292 In this study, the alkaline CuO oxidation, which liberates a set of lignin-derived pheno

293 hell electrodes undergoes light-driven water oxidation with an incident photon to current efficiency

294 condensations with a tripyrrane, followed by oxidation with DDQ in refluxing toluene, gave carbaporph

295 A subsequent oxidation with Dess-Martin periodinane provides the targ

296 ce also exhibited increased rates of glucose oxidation with increased energy expenditure, despite red

297 Oxidation with potassium permanganate gave good yields o

298 converted into their endoperoxides 1-O2 upon oxidation with singlet oxygen.

299 f limonene, linalool and citral occurs by co-oxidation with the substrate, due to very fast self-term

300 ate spatially and temporally limited protein oxidation within cells, and suggest that platelet-derive

301 Most likely, KIO3 caused glutenin oxidation within each individual dough layer to such ext