ライフサイエンスコーパス: molecular oxygen

1 cur before an irreversible reductive step at molecular oxygen.

2 ility to oxidize methane into methanol using molecular oxygen.

3 of superoxide anion to hydrogen peroxide and molecular oxygen.

4 case can catalyze electrooxidation of H2O to molecular oxygen.

5 l product, is reported from (-)-myrtenal and molecular oxygen.

6 ), is actively dissipated in the presence of molecular oxygen.

7 fer from one or more light-excited donors to molecular oxygen.

8 lowed by the strongly favorable reduction of molecular oxygen.

9 nteraction between neutral gold clusters and molecular oxygen.

10 single-site catalysts for the activation of molecular oxygen.

11 radical reactions of organic compounds with molecular oxygen.

12 mely, the ability to convert superoxide into molecular oxygen.

13 y transferring aldehyde-derived electrons to molecular oxygen.

14 achieve selective four-electron reduction of molecular oxygen.

15 ates and upon reduction can be reoxidized by molecular oxygen.

16 plays very little role in the reaction with molecular oxygen.

17 trates using NADPH as the electron donor and molecular oxygen.

18 oxidation when irradiated in the presence of molecular oxygen.

19 lfide isomerase (PDI) and passing them on to molecular oxygen.

20 trolled factors immediately upon exposure to molecular oxygen.

21 on oxidation of ubiquinol in the presence of molecular oxygen.

22 ur cluster, and a low potential heme b(L) or molecular oxygen.

23 true dehydrogenase that does not react with molecular oxygen.

24 face TiO(2)(110) in reactions with water and molecular oxygen.

25 flavin ring and, finally, to cytochrome c or molecular oxygen.

26 s also exhibit differential requirements for molecular oxygen.

27 ompeting with the primary electron acceptor: molecular oxygen.

28 a direct oxygenation of aryl C-H bonds with molecular oxygen.

29 reaction product is exclusively derived from molecular oxygen.

30 nverts superoxide into hydrogen peroxide and molecular oxygen.

31 e (CEES), in the presence of an aldehyde and molecular oxygen.

32 ransferring electrons from reduced flavin to molecular oxygen.

33 nt peroxo oxygen atoms in 3 are derived from molecular oxygen.

34 and NO2 the major product in the presence of molecular oxygen.

35 he catalytic oxidation of water that evolves molecular oxygen.

36 lective reaction of an amine/borane FLP with molecular oxygen.

37 ctions can be carried out in the presence of molecular oxygen.

38 photoexcited electrons in the perovskite and molecular oxygen.

39 dations, all involving stepwise reduction of molecular oxygen.

40 mediates light-induced oxidation of water to molecular oxygen.

41 The reactions of excited state singlet molecular oxygen ((1)Delta(g),(1)O(2)) continue to witne

42 The first singlet excited state of molecular oxygen ((1)O(2)) is an important oxidant in ch

43 mentation to generate high yields of singlet molecular oxygen ((1)O(2)).

44 ,22R-dihydroxycholesterol in the presence of molecular oxygen ((18)O2), and coupled assays were used

45 under anaerobic conditions in the absence of molecular oxygen abrogates Sup35 protein damage and supp

46 The mechanism of molecular oxygen activation is the subject of controvers

47 A unique mode of molecular oxygen activation, involving metal-ligand coop

48 Molecular oxygen acts as the terminal electron sink in t

49 lative energies of the transition states for molecular oxygen addition to C9, C5, and C14 (where spin

50 he experimental values for HO* reactions and molecular oxygen addition, and a factor of 5 for peroxyl

51 isretinoid photocleavage at sites of singlet molecular oxygen addition.

52 crystal structures also revealed "pre-bound" molecular oxygen adjacent to the active site.

53 bates at solid interfaces and the roles that molecular oxygen, adsorbed water, and relative humidity

54 Studies in the presence and absence of molecular oxygen allow us to conclude that the imidazoli

55 occurs by hydrogen-transfer from Fl(red) to molecular oxygen, allowing radical coupling of the forme

56 capabilities for phototrophy, scavenging of molecular oxygen, anaerobic respiration, and fermentatio

57 iver electrons from the cosubstrate NADPH to molecular oxygen, analogous to other P450s.

58 Molecular oxygen and 1,4-benzoquinone can serve as elect

59 ing dioxygenases requiring for activity both molecular oxygen and 2-oxoglutarate that, under normoxia

60 or nonchiral amines was realized simply with molecular oxygen and a carbonate base.

61 ysaccharides utilizing a mechanism involving molecular oxygen and an electron donor.

62 oxidative cleavage of glycosidic bonds using molecular oxygen and an external electron donor.

63 Molecular oxygen and carbon dioxide are the primary gase

64 alpha-MnO2 nanotubes easily accommodated the molecular oxygen and exhibited excellent catalytic activ

65 he cellular milieu through the assistance of molecular oxygen and glutathione.

66 The reduction of molecular oxygen and hydrophilic quinones leads to the p

67 phenyliodonium diacetate in the presence of molecular oxygen and N-hydroxyphthalimide or N-hydroxybe

68 r dry and humid conditions in the absence of molecular oxygen and NO2 the major product in the presen

69 om of the C2(1)-formyl group originates from molecular oxygen and not from H2O.

70 cytochrome c to CcO's catalytic site reduce molecular oxygen and produce a water molecule.

71 olol and honokiol radicals do not react with molecular oxygen and produce no superoxide radical under

72 cleavage step was tested using (18)O-labeled molecular oxygen and purified P450 11A1.

73 Release of molecular oxygen and regeneration of resting enzyme are

74 ltaneous resonant two-photon dissociation of molecular oxygen and resonant two-photon pumping of the

75 made, pointing to a mechanism in which both molecular oxygen and the olefinic substrate coordinate t

76 adventitious electron transfer from nNOS to molecular oxygen and thereby preventing accumulation of

77 he quantum yields were enhanced by excluding molecular oxygen and thermally activated delayed fluores

78 MalE-LacZ lethality requires molecular oxygen, and its expression induces ROS product

79 ational studies on the reactions with water, molecular oxygen, and the superoxide radical anion suppo

80 a capability to reduce Fe(III) minerals and molecular oxygen, and thereby generating Fenton chemistr

81 from three flavin-linked electron acceptors (molecular oxygen, APAD(+), and ferricyanide), in the pre

82 s originating from hydroxide ions instead of molecular oxygen are incorporated into the alcohol durin

83 phosphate-modified hydrotalcite support and molecular oxygen as a benign oxidant.

84 tive and require either hydrogen peroxide or molecular oxygen as a cosubstrate to generate a reactive

85 that have been characterized to date require molecular oxygen as a cosubstrate.

86 lymer to enable the controlled generation of molecular oxygen as a function of pH.

87 ve aromatization reaction sequence utilizing molecular oxygen as a green oxidant.

88 catalysts using the oxidation of methane by molecular oxygen as a model system.

89 y cryptochrome photoreceptors if paired with molecular oxygen as a reaction partner.

90 tertiary amines to tertiary amides by using molecular oxygen as a sole oxidant using a Pd/C catalyst

91 n the presence of an organic base and aerial molecular oxygen as a stoichiometric oxidant.

92 oxidation of (hetero)aryl acetimidates using molecular oxygen as a sustainable oxidant.

93 n and functionalization of styrene utilizing molecular oxygen as a terminal oxidant.

94 none oxidoreductase, Photosystem II produces molecular oxygen as an enzymatic product.

95 rimary alpha-ketoamides by using sustainable molecular oxygen as an oxidant.

96 t oxidative esterification of alcohols using molecular oxygen as benign oxidant.

97 c metabolism therefore makes use of reactive molecular oxygen as co-substrate of oxygenases to hydrox

98 nt formation of an aldehyde intermediate and molecular oxygen as final electron acceptor.

99 dehyde as enzyme-associated intermediate and molecular oxygen as final electron acceptor.

100 which lacks an integral heme cofactor, uses molecular oxygen as its electron acceptor.

101 lized in the blue bottle experiment, deplete molecular oxygen as long as a sacrificial reduction comp

102 rational bands of nitric oxide, hydroxyl and molecular oxygen as signatures of nitrogen, oxygen, and

103 site and one catalytic residue, and utilizes molecular oxygen as source for the hydroxyl group oxygen

104 drastic reduction in oxidase activity using molecular oxygen as the electron acceptor and a small in

105 rbon bonds of the six-membered ring and uses molecular oxygen as the hydrogen acceptor.

106 ther than its molybdenum center and utilizes molecular oxygen as the physiological oxidant.

107 of two C-H bonds under mild conditions using molecular oxygen as the sole oxidant.

108 In the presence of molecular oxygen as the terminal oxidant the reaction is

109 the catalyst, a cocatalyst capable of using molecular oxygen as the terminal oxidant, and ligands th

110 inates position C4 in a reaction implicating molecular oxygen, as demonstrated with labeling experime

111 The production of molecular oxygen at a high potential is verified by meas

112 the title compound involves the splitting of molecular oxygen by carbene-stabilized diphosphorus.

113 The oxidation of water to molecular oxygen by photosystem II (PSII) is inhibited i

114 l gold clusters (Au(n); 4 </= n </= 21) with molecular oxygen by probing the highly characteristic O-

115 rate how light-triggered SiNc reactions with molecular oxygen can be potentially sensed and discuss t

116 oteins and immunoglobulins demonstrates that molecular oxygen can diffuse through the polypeptide mat

117 Molecular oxygen can replace sacrificial olefins as the

118 genous or xenobiotic small molecules such as molecular oxygen, cellular metabolites, or polyaromatic

119 ions investigated, both coadsorbed water and molecular oxygen change the gas-phase product distributi

120 The presence of molecular oxygen changes product distribution, and only

121 the enzyme are unaffected by the presence of molecular oxygen commonly present in electrolyte.

122 o-hydroxylation of L-tyrosine to L-DOPA by a molecular oxygen dependent pathway in the presence of di

123 The subsequent molecular oxygen-dependent oxidation of the multicenter

124 roxylation is catalyzed by a membrane-bound, molecular oxygen-dependent, and ferredoxin-dependent act

125 -phenylindeno[2,1-alpha]phenalene (ipp) with molecular oxygen derived from air, yielding 12-hydroxy-7

126 They reduce molecular oxygen (dioxygen) to water, avoiding the produ

127 It is shown that molecular oxygen dissociates easily on the supported Pd(

128 hanges in proportion to the concentration of molecular oxygen dissolved in plasma or interstitial tis

129 e surface are a significant redox partner to molecular oxygen due to the strong hybridization between

130 oxygen atom is incorporated from atmospheric molecular oxygen during the present process.

131 the biofuel and the biooxidant, glucose and molecular oxygen, each readily available in human lachry

132 In this mechanism, molecular oxygen first reacts with NSMOA(FAD(red)) to yi

133 nization after soft x-ray photoionization of molecular oxygen follows a complex multistep process.

134 wo classes both require an iron cofactor and molecular oxygen for activity and are inhibited by azide

135 at requires SAM, a thiol reducing agent, and molecular oxygen for activity.

136 In contrast to GFP, which requires only molecular oxygen for chromophore maturation, phytochrome

137 s inherently aerobic due to a requirement of molecular oxygen for one of the key enzymes.

138 Nature often utilizes molecular oxygen for oxidation reactions through monoxyg

139 es P450 must be reduced to bind and activate molecular oxygen for substrate oxidation.

140 to effect the challenging task of utilizing molecular oxygen for the selective epoxidation of cycloo

141 ploys the reaction of iodoalkyl radical with molecular oxygen: for instance, CH2I + O2 --> CH2OO + I.

142 tertiary C25 atom of the side chain without molecular oxygen forming a tertiary alcohol.

143 ts semiquinone, which then is re-oxidized by molecular oxygen, forming superoxide that induces cell d

144 As steroid biosynthesis requires molecular oxygen, fossil steranes have been used to draw

145 water oxidation, but catalysts that produce molecular oxygen from water are needed to avoid excessiv

146 lkyl-substituted diazenes in the presence of molecular oxygen generates an unexpectedly complex produ

147 toactivatable dye, which upon encounter with molecular oxygen generates the reactive oxygen species t

148 er drug with light, which in the presence of molecular oxygen, generates cytotoxic reactive oxygen sp

149 ic amines through a metal-free activation of molecular oxygen has been developed.

150 urfaces with direct propylene epoxidation by molecular oxygen have not resolved these problems becaus

151 on of a bare palladium cluster Pd(6)(+) with molecular oxygen in an octopole ion trap under multicoll

152 this review article, we consider the use of molecular oxygen in reactions mediated by polyoxometalat

153 ations, we investigate here the migration of molecular oxygen in the bc1 complex in order to identify

154 both confirmed the requirements for DHP and molecular oxygen in the catalytic generation of 5,5'-Br2

155 ing of singlet oxygen, but do not react with molecular oxygen in the ground state, i.e., triplet stat

156 mutation known to affect the disposition of molecular oxygen in the LOX active site.

157 tied to the first widespread availability of molecular oxygen in the ocean-atmosphere system.

158 , and the reduced flavin is then oxidized by molecular oxygen in the oxidative half-reaction.

159 single-walled carbon nanotubes (C-SWCNT) to molecular oxygen in water in the dark.

160 ive low-temperature oxidation catalysts with molecular oxygen, in stark contrast to the nobility of t

161 n and the incorporation of (18)O at C-4 from molecular oxygen indicate otherwise.

162 ) is not reduced by Mn(II) in the absence of molecular oxygen, indicating that substrate oxidation re

163 a sustained electron flow is maintained with molecular oxygen instead of carbon dioxide serving as th

164 nge of biological reactions by incorporating molecular oxygen into organic substrates.

165 in varying yields with the incorporation of molecular oxygen into the structures.

166 ogen peroxide by radical chain reductions of molecular oxygen into water in buffers leads to hinge de

167 Activation of molecular oxygen is a key step in converting fuels into

168 The oxidation of water to molecular oxygen is a kinetically demanding reaction tha

169 Although HNO reactivity with molecular oxygen is described in the literature, the pro

170 Molecular oxygen is essential for the development, growt

171 Molecular oxygen is evolved after four sequential light-

172 This reactive state of molecular oxygen is generated locally by the optical tra

173 n atmospheric oxygen levels, suggesting that molecular oxygen is indeed the key regulator of this pat

174 Hypoxia reduced ARSB activity, since molecular oxygen is needed for post-translational modifi

175 ating group and require that the O-O bond of molecular oxygen is not cleaved prior to substrate activ

176 ctive oxidation of methane to methanol using molecular oxygen is possible.

177 Molecular oxygen is produced from water via the followin

178 Molecular oxygen is proposed to participate in the catal

179 In this way molecular oxygen is released, maintaining an aerobic atm

180 ng to these results and due to the fact that molecular oxygen is the only known physiological electro

181 In organisms that live aerobically, molecular oxygen is used enzymatically to oxidize cystei

182 When molecular oxygen is used, the structure of the CsPbI3 QD

183 Singlet oxygen, the lowest excited state of molecular oxygen, is an intermediate often involved in n

184 interaction between the neutral polymer and molecular oxygen leading to a reduction in electron mobi

185 In the late Archean, molecular oxygen likely cycled as a biogenic trace gas,

186 and that electron shuttling through CNTs to molecular oxygen may be a potential mechanism for DNA da

187 ring, and end-game manipulations featuring a molecular oxygen mediated gamma-CH oxidation, a Stetter

188 pe II photosensitization reactions, in which molecular oxygen mediates the radicalization of proteins

189 hown to oxidize an alcohol using a metal and molecular oxygen, not NAD(P)(+).

190 Molecular oxygen (O(2)) and trace metals [e.g., copper(I

191 Molecular oxygen (O(2)) began to accumulate in the atmos

192 The concentration of molecular oxygen (O(2)) began to increase in the Earth's

193 Singlet molecular oxygen, O(2)(a(1)Delta(g)), can be created in

194 Singlet molecular oxygen, O(2)(a(1)Delta(g)), can influence many

195 lmalonate), which was used to detect singlet molecular oxygen O2((1)Deltag) production in water.

196 so results in direct enzymatic conversion of molecular oxygen (O2 ) to reactive oxygen species (ROS)

197 f biological detection by optical sensing of molecular oxygen (O2) are reviewed, with particular emph

198 ears to be mediated during the activation of molecular oxygen (O2) by reduced flavoenzymes, forming s

199 Molecular oxygen (O2) is a key substrate for mitochondri

200 rbon monoxide (CO) and the infrared inactive molecular oxygen (O2) products are readily detected from

201 y reactive species formed by the addition of molecular oxygen (O2) to organic radicals.

202 Molecular oxygen (O2), however, despite its detection on

203 w widely appreciated that nutrients, such as molecular oxygen (O2), modulate skeletal muscle formatio

204 n rich terrestrial-type exoplanets including molecular oxygen (O2), ozone (O3), water vapor (H2O), ca

205 ing reactions, we investigated the role that molecular oxygen (O2), solvent and light-source (CF lamp

206 The eighth key metabolite is molecular oxygen (O2), thermodynamically activated for r

207 3), is irreversibly damaged upon exposure to molecular oxygen (O2).

208 s for use as a fluorescent probe for singlet molecular oxygen, O2(a(1)Deltag).

209 s of the partial oxidation of isobutane with molecular oxygen on Rh(111) single-crystal surfaces were

210 s responsible for adsorption and reaction of molecular oxygen on the surface of sp(2)-hybridized carb

211 ime frame of the accumulation of atmospheric molecular oxygen on this planet.

212 To assess effects of molecular oxygen on TNFR2 expression, we subjected cultu

213 e phosphorescence is effectively quenched by molecular oxygen, optical sensors operating in a wide ra

214 mental evidence indicates DosS senses either molecular oxygen or a redox change.

215 ditions but could be enhanced by exposure to molecular oxygen or by the addition of alternative elect

216 Upon reaction with either molecular oxygen or di-tert-butylperoxide in the presenc

217 at rates competitive to sulfide oxidation by molecular oxygen or iron oxides.

218 proposed enzymatic activity of AcsF requires molecular oxygen, our studies suggest that the roles of

219 high activities for the electroreduction of molecular oxygen (oxygen reduction reaction, ORR), which

220 after this expansion show increasing use of molecular oxygen (P = 3.4 x 10(-8)) and redox-sensitive

221 nese speciation appeared to be controlled by molecular oxygen (pe(-) = 15.90).

222 It was shown that molecular oxygen plays the key role in this process.

223 gger critical metabolic pathways to detoxify molecular oxygen produced by photosynthesis, thereby per

224 ubsequent quenching of the triplet states by molecular oxygen produces singlet oxygen ((1)O2), which

225 n site initiate redox cycling reactions with molecular oxygen, producing superoxide radicals and hydr

226 lysts that promote the oxidation of water to molecular oxygen, protons, and "energized" electrons, an

227 The molecular oxygen quenching of the solid-state emission f

228 such as hydrogen peroxide (H2O2) or singlet molecular oxygen, rather than free-radical species, perf

229 in the presence of (18)O(2) establishes that molecular oxygen, rather than oxygen from water, is inco

230 , we regulate proton transport to a Cu-based molecular oxygen reduction reaction catalyst.

231 Interactions between biological pathways and molecular oxygen require robust mechanisms for detecting

232 Subsequent reaction of Fl(red) with molecular oxygen restores the postulated Fl(N5[O]) via a

233 g substrate turnover by a side reaction with molecular oxygen, resulting in the continuous production

234 py)PdMe(2) (1) (bipy = 2,2'-bipyridine) with molecular oxygen results in the formation of the palladi

235 360 mV (vs. Ag/AgClsat) in the presence of a molecular oxygen saturated electrolyte with current dens

236 PHD1 to PHD3 are molecular oxygen sensors and increasingly considered as

237 PHD1 to PHD3 are molecular oxygen sensors and increasingly considered as

238 Prolyl hydroxylase enzymes (PHD1-3) are molecular oxygen sensors that regulate hypoxia-inducible

239 ase domain (PHD) enzymes are regarded as the molecular oxygen sensors.

240 pper-catalyzed alkene aminooxygenation where molecular oxygen serves as both oxidant and oxygen sourc

241 e combustion reactor between water vapor and molecular oxygen so that only hydrogen isotope compositi

242 ns to an atmosphere which became enriched in molecular oxygen spurred the development of a layered sy

243 T1 Cu species only formed in the presence of molecular oxygen, suggesting the T1 Cu intermediate is a

244 , which is different from isolated atomic or molecular oxygen surface structures, was observed with i

245 PR spectroscopy using NO as a spin probe and molecular oxygen surrogate reveals that Ps-HppE's metal

246 ited state ensembles against deactivation by molecular oxygen though quenching and photooxidation mec

247 tes methane, which subsequently incorporates molecular oxygen through a radical process.

248 cal processes, including the biosynthesis of molecular oxygen (through the photosystem II complex) an

249 emperature without the rigorous exclusion of molecular oxygen, thus making this newly developed Ir-ph

250 on to 15 aromatic compounds; (2) addition of molecular oxygen to 65 carbon-centered aliphatic and cyc

251 or a dominant delivery channel that shuttles molecular oxygen to a specific region of the active site

252 intermediates may be trapped via exposure to molecular oxygen to afford oxygen-containing adducts.

253 avin species that transfers a single atom of molecular oxygen to an organic substrate.

254 the active site, thereby creating space for molecular oxygen to bind to Fe2.

255 The power of molecular oxygen to drive many crucial biogeochemical pr

256 (P(Ar)(tBu)2)2] (1, Ar=naphthyl) reacts with molecular oxygen to form Pd(II) hydroxide dimers in whic

257 ates the transfer of electrons from NADPH to molecular oxygen to generate superoxide for host defense

258 rhenium(V), (ONO(Cat))ReO(PPh3), reacts with molecular oxygen to give triphenylphosphine oxide and th

259 asm; instead, the four-electron reduction of molecular oxygen to harmless water ensures that the acti

260 uced TPQ is reoxidized with the reduction of molecular oxygen to hydrogen peroxide.

261 ycle pathway involving reversible binding of molecular oxygen to iridium, which contributes to the ai

262 prene reacts with hydroxyl radicals (OH) and molecular oxygen to produce isoprene peroxy radicals (IS

263 ectron transport chain, which is captured by molecular oxygen to produce reactive oxygen species (ROS

264 copper oxidases that couple the reduction of molecular oxygen to proton translocation across the bact

265 We then added molecular oxygen to the system and modeled the oxidation

266 s the stereospecific addition of one atom of molecular oxygen to the vinyl side chain of styrene in t

267 ine oxidase enzyme superfamily which utilize molecular oxygen to transform amines to imines that are

268 The addition of triplet molecular oxygen to two types of conjugatively stabilize

269 dase (CcO), which catalyzes the reduction of molecular oxygen to water in the mitochondrial and bacte

270 chondria and bacteria catalyzes reduction of molecular oxygen to water, and conserves much of the lib

271 erobic organisms, catalyzes the reduction of molecular oxygen to water.

272 ffects the calculated OA mass, mass spectra, molecular oxygen-to-carbon ratio (O/C), and f44.

273 h more versatile redox chemistry, biospheric molecular oxygen triggered the selective fixation of the

274 can be directly converted to methanol using molecular oxygen under mild conditions in the gas phase,

275 The reduction chemistry of molecular oxygen underpins the energy metabolism of mult

276 A material capable of rapid, reversible molecular oxygen uptake at room temperature is desirable

277 bunit enzyme which generates superoxide from molecular oxygen using NADPH as the electron donor.

278 as a photoredox catalyst in the presence of molecular oxygen using visible light and, when it was us

279 tly split carbonate into carbon monoxide and molecular oxygen via a low-energy pathway needing no sac

280 oposals have been made for the activation of molecular oxygen via both a Cu(II)-aminoquinol catalytic

281 Abundant molecular oxygen was discovered in the coma of comet 67P

282 e anion generated by dithionite reduction of molecular oxygen was not a factor in the reaction kineti

283 ithium intercalated into Li(x)V(2)O(5) while molecular oxygen was reduced to form lithium peroxide on

284 Its quenching by molecular oxygen was studied at 25 and 60 degrees C and

285 Cyanide, a mimic of molecular oxygen, was found to bind to the metal ion onl

286 uperoxide radical into hydrogen peroxide and molecular oxygen, whereas the catalase and peroxidases c

287 ding py and pz orbitals are degenerate as in molecular oxygen, which has singly occupied orbitals.

288 tal observations regarding the activation of molecular oxygen, which is a crucial issue in Au catalyz

289 The reaction requires molecular oxygen, which is activated by a di-iron centre

290 of a small organic molecule, luciferin, with molecular oxygen, which is catalysed by the enzyme lucif

291 cotinamide adenine dinucleotide phosphate to molecular oxygen, which leads to the production of super

292 s become active sites for oxidizing water to molecular oxygen, which was investigated with the photoc

293 of BzOH from 1 followed by rapid reaction of molecular oxygen with (IMes) 2Pd(0) and protonolysis of

294 ransfer from the Breslow intermediate to the molecular oxygen with formation of a radical couple that

295 elucidate the mechanism for the reaction of molecular oxygen with palladium-hydride complexes, (pyri

296 Triplet carbenes react with molecular oxygen with rates that approach diffusion cont

297 the reactivity by following the reaction of molecular oxygen with surface hydroxyl formed by water d

298 mitochondria could occur by the reaction of molecular oxygen with the ferrous CL:cyt c complex in ad

299 NadB turnover depends upon its oxidation by molecular oxygen, with H(2)O(2) as a product.

300 intramitochondrial [NAD(+) ]/[NADH] pool to molecular oxygen, with irreversible reduction of oxygen

301 r results support a model in which access to molecular oxygen within the active site directs the outc

302 We reasoned that availability of molecular oxygen within the LOX active site favors oxyge