ライフサイエンスコーパス: oxy

1 with triplet O2, forming diamagnetic (S = 0) oxy-Hb.

2 -dihydro-4,4,5,5-tetramethyl-1H-imidazolyl-1-oxy-3-oxide (carboxy-PTIO, an NO scavenger), 1H-[1,2,4]-

3 nging; (ii) 2,2,6,6-tetramethylpiperidinyl-1-oxy (TEMPO) scavenging; (iii) ferric ions (Fe(3+)) reduc

4 ak area reproducibility were obtained for 14 oxy-compounds present in trace amount in the complex bio

5 -tert-butyl-1,2-quinone-(3,5-di-tert-butyl-2-oxy-1-phenyl)imine) to give five-coordinate (X)(Y)Si(ON[

6 terest because of its formation from Fe(3+) (oxy)hydroxides via dissimilatory iron reduction.

7 a series of catecholic and non-catecholic 3-oxy- (and deoxy)-anthocyanidins.

8 vity relationship (SAR) for the compound's 3-oxy site.

9 ther, these results indicate that both the 3-oxy and 4'-benzylamide positions in (R)-1 can accommodat

10 ied introduction of larger moieties at the 3-oxy site in (R)-1 was offset, in part, by including unsa

11 all nonpolar, nonbulky substituents at the 3-oxy site provided compounds with pronounced seizure prot

12 roups tethered by a 1,4-phenylenebis(butyl-4-oxy) unit (the strap) and carrying a methylbenzoic ester

13 s shown that the polarizing agent 1-(TEMPO-4-oxy)-3-(TEMPO-4-amino)propan-2-ol (TOTAPOL) has a strong

14 In the Y257F-4NC-oxy complex, the O(2) is bound side-on to the Fe(II), wh

15 lylations to afford the desired 1,3-dienyl-6-oxy motif and enable complex polyketide synthesis in a r

16 is of the privileged polyketide 1,3-dienyl-6-oxy motif.

17 acetoxybenzyl-based, 4-(5-(((4-acetoxybenzyl)oxy)amino)-2-carboxy-5-oxopentyl)benzoic acid, 12, provi

18 itrate and ferric ammonium citrate), against oxy- and met-hemoglobin erythrocytes used as controls.

19 nd adsorbed by iron (Fe) and aluminium (Al) (oxy) hydroxide minerals.

20 The ester 4-((tosyl-l-alanyl)oxy)phenyl tosyl-l-alaninate (TAPTA) was synthesized and

21 ular anionic cyclization of (2-alkynylbenzyl)oxy nitriles has been developed for the preparation of s

22 (20 mol %) to a solution of (2-alkynylbenzyl)oxy nitriles in tetrahydrofuran at room temperature in a

23 ed base (BB) catalysis and the use of alpha'-oxy enones as enabling Michael acceptors with ambivalent

24 Experiments show that the alpha'-oxy ketone moiety plays a key role in the above realizat

25 ones, thiazolones, and azlactones) to alpha'-oxy enones can afford the corresponding tetrasubstituted

26 ubstituted aliphatic, alpha-amino, and alpha-oxy acids as well as a variety of electron-deficient alk

27 ectively functionalize alpha-amino and alpha-oxy sp(3) C-H bonds in both cyclic and acyclic systems.

28 n successfully applied to a variety of alpha-oxy and alpha-amino acids, as well as simple hydrocarbon

29 y on the enantioselective synthesis of alpha-oxy carboxylic acids.

30 ds, including hydrocarbon-substituted, alpha-oxy, and alpha-amino acids, provides a versatile CO2-ext

31 nd the chlorine radical source for the alpha-oxy C(sp(3))-H arylation of cyclic and acyclic ethers.

32 way is the cleavage of peroxide to the alpha-oxy radical (likely catalyzed by Cu), which is computati

33 Overall, this approach to alpha-oxy amides provides an innovative complement to alternat

34 We describe an alternative oxy-hemoglobin assay that eliminates dithionite and sugg

35 ated by thermal transformation of aluminium (oxy)hydroxides, structural differences between them aris

36 he aqueous AlAl12(7+) ion to solid aluminum (oxy)-hydroxide phases, we found that this ion lies close

37 cotinamide core structure, 5-((3-amidobenzyl)oxy)nicotinamides offered excellent activity against SIR

38 Therefore, 5-((3-amidobenzyl)oxy)nicotinamides represent a new class of SIRT2 inhibit

39 d for the first time as means to evaluate an oxy-fuel power plant with CO(2) capture.

40 It was found that in an oxy-combustion atmosphere (mostly CO2), the re-emission

41 rries obtained from two limestones, under an oxy-combustion atmosphere.

42 tituted pyrimidine derivatives armed with an oxy-functionalized acetate chain at the ring is describe

43 imaging of a targeted fluorescent agent and oxy- and deoxyhemoglobin gave functional information abo

44 of the Fe-O(2) center in oxy-hemoglobin and oxy-myoglobin is a long-standing issue in the field of b

45 odocyclohexenone followed by methylation and oxy-Cope rearrangement delivered enantiomerically enrich

46 s (PAHs), PAH derivatives (nitro- (NPAH) and oxy-(OPAH)), organic carbon (OC), and particulate matter

47 OOD), and a coke oven (COKE), and to PAH and oxy-PAH containing fractions of these.

48 Naphthenic (CnH2n+zO2) and oxy-naphthenic (CnH2n+zOx) acids represented the largest

49 Cobalt oxides and (oxy)hydroxides have been widely studied as electrocataly

50 amura's chiral allylzinc reagent, an anionic oxy-Cope rearrangement, and the Lewis acid-promoted cycl

51 lation of a cyclic enone followed by anionic oxy-Cope rearrangement delivered the ketone as a mixture

52 that relies on a diastereoselective anionic oxy-Cope rearrangement to set the relative configuration

53 Extended N(4)-(3-arylpropyl)oxy derivatives of uridine-5'-triphosphate were synthesi

54 Thus, an extended N(4)-(3-arylpropyl)oxy group accessed a structurally permissive region on t

55 ato-oxy lowered AHI by 63% (34-86%), from 28.5 (10.9-51.6) e

56 lacebo to 6.3 (3.0 to 18.3)%/cm H(2)O on ato-oxy (P < 0.001).

57 80 mg atomoxetine plus 5 mg oxybutynin (ato-oxy) to placebo administered before sleep.

58 iple functional groups, the chemistry of BCP-oxy and other alkoxy radicals in the system is diverse.

59 e corresponding bicyclic alkoxy radical (BCP-oxy).

60 (6S)-2-nitro-6-{[4-(trifluoromethoxy)benzyl]oxy}-6,7-dihydro-5H-imidazo[2,1-b][1, 3]oxazine (PA-824)

61 -[(Guanine-9H-yl)methyl]propane-1,3-diyl)bis(oxy)]bis(methylene)}diphosphonic acid (compound 17) exhi

62 hyrinato zinc(II) 1 and 5-(2,5-phenylene-bis(oxy)diacetamide)-10,15,20-tris(triphenylamino)porphyrina

63 on prompts reaction with H2 to give a borane-oxy-borate derivative, the product of C-O bond cleavage.

64 ut on an alert macaque demonstrate that both oxy- and deoxyhemoglobin concentrations in the frontal l

65 eoxy), CO-inhibited (carboxy), and O2-bound (oxy) hemes in myoglobin (MB) and hemoglobin (HB) solutio

66 ethyl 6-bromo-8-(4-((tert-butyldimethylsilyl)oxy)benzamido)-4-oxo-4H-chromene-2-carboxy late (19) wit

67 pyl)-4-(((4-methoxyphenyl)(methyl) carbamoyl)oxy)indolin-1-ium hydrochloride) with IC50s of 0.4 and 1

68 d analog of [4-[[N-(3-chlorophenyl)carbamoyl]oxy]-2-butynyl]trimethylammonium chloride (McN-A-343).

69 erivatives: (3beta)-3-((thiophene-2-carbonyl)oxy)-olean-12-en-28-oic acid (1a) (IZ=22mm) and (2alpha,

70 (2alpha,3beta-2,3-bis((thiophene-2-carbonyl)oxy)olean-12-en-28-oic acid (2a) (IZ=24mm).

71 cal to the double bond of 3-[(1-carboxyvinyl)oxy]benzoic acid.

72 Employing a copper-catalyzed oxy-alkenylation strategy, a range of readily available,

73 icient strategy involving a copper-catalyzed oxy-alkynylation of diazo compounds with ethynylbenziodo

74 ein, we report the first palladium-catalyzed oxy- and aminoalkynylation using aliphatic bromoalkynes,

75 Hg(2+) is similar regardless of whether CO2 (oxy-fuel combustion) or N2 (air combustion) are the main

76 In this context, oxy- and aminoalkynylation are especially important reac

77 substrate and H(2)O(2) are needed to convert oxy-DHP to the catalytically active ferric state.

78 the absence of TCP, H(2)O(2) alone converts oxy-DHP to an inactive state (compound RH) instead of ox

79 Most notably, changes in cortical oxy-haemoglobin during a Japanese phonetic fluency task

80 2 catalyst indicate the presence of a crotyl-oxy surface intermediate.

81 ort EPR spectroscopic studies of cryoreduced oxy-F33Y-CuBMb, a functional model of HCOs engineered in

82 o EPR signal, in contrast to the cryoreduced oxy-wild-type (WT) Mb, which is unable to deliver a prot

83 pectroscopy data on solution and crystalline oxy-Hb indicate both geometric and electronic structure

84 concentrations of deoxy-hemoglobin (ctHHb), oxy-hemoglobin (ctHbO2), water (ctH2O), lipid, and TOI (

85 f the synthesis include a diastereoselective oxy-Cope rearrangement/oxidation sequence to install the

86 The usage of a diastereoselective oxy-Michael addition/benzylidene acetal formation couple

87 onitrile (5a) and (Z)-6-((2,6-dichlorobenzyl)oxy)-2-(pyridin-4-ylmethylene)benzofuran-3(2H)-one (5b)

88 wart rearrangement of (dimethylcarbamothioyl)oxy (oxa)helicenes in a flow reactor or nucleophilic sub

89 including (2S,2'S)-1,1'-(butane-1,4-diylbis(oxy))bis(N-isopropylpropan-2-amine) 7, (2S,2'S)-1,1'-(pe

90 lithiated (2S,2'S)-1,1'-(pentane-1,5-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 10 is a mono

91 amine) 7, (2S,2'S)-1,1'-(pentane-1,5-diylbis(oxy))bis(N-isopropylpropan-2-amine) 8, and (2S,2'S)-1,1'

92 e) 8, and (2S,2'S)-1,1'-(heptane-1,7-diylbis(oxy))bis(N-isopropyl-3-methylbutan-2-amine) 9 are dimers

93 ies, Hf(OTf)4 was used to convert the double oxy-Michael product 28 into C1-C19 building block 10.

94 SO(2) and SO(3), is considerably high during oxy-fuel combustion even though the sulfur content in Mo

95 erefore, for Morwell coal utilization during oxy-fuel combustion, additional sulfur removal, or polis

96 tonation step to form an enantiodiscriminant oxy-allyl cation prior to the stereodefining nucleophili

97 bis{[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}-1,5-dihydroxycyclohexane-1-carboxylic methyl ester

98 LC-MS(3) analysis of intact esterified oxy-lipids and LC-MS(2) analysis of the hydrolysis produ

99 electron-donating (4-methoxy-1-(2-ethylhexyl)oxy)benzene (MEH) and electron-accepting benzothiadiazol

100 SHSAMs: ITO/IFL/poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl][ 2-[[(2-eth

101 conducting PTB7 (poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl][3-fluor o-2

102 ar-cell material poly[[4,8-bis[(2-ethylhexyl)oxy]benzo[1,2-b:4,5-b']dithiophene-2,6-diyl][3-fluoro -2

103 -b']dithiophene-2,6-diyl][ 2-[[(2-ethylhexyl)oxy]carbonyl]-3-fluorothieno[3,4-b]thiophenediyl]]:pheny

104 pecies, ZnS, Zn3(PO4)2, and Zn associated Fe oxy/hydroxides, also regardless of the form of Zn added.

105 adsorption capacity for As(V) of a single Fe oxy-hydroxide combined with enhanced As(III) removal bas

106 t the ratio of ZnS and Zn associated with Fe oxy/hydroxide depended on the redox state and water cont

107 organically complexed Fe, and colloidal Fe (oxy)hydroxides, stabilized by surface interactions with

108 critical component of record-activity Ni/Fe (oxy)hydroxide (Ni(Fe)OxHy) oxygen evolution reaction (OE

109 Moreover, we found selective removal of Fe (oxy)hydroxides by aggregation at increasing salinity, wh

110 arosite and other minerals (e.g., clays, Fe-(oxy)hydroxides).

111 Ferric-oxy multimers, tetramers, and/or larger mineral nuclei f

112 inct steps: 1) initial oxidation of ferrous (oxy) to ferryl Hb; 2) autoreduction of the ferryl interm

113 multiple conformations of the binary ferrous-oxy species of the IDOs.

114 ize the active-site structure of the ferrous-oxy complexes of human (hIDO) and Shewanella oneidensis

115 accelerates the rate of decay of the ferrous-oxy/ferric-superoxo species in substrate turnover.

116 T. cruzi and N-(3-chloro-4-((3-fluorobenzyl)oxy)phenyl)-7-(4-((4-methyl-1,4-diazepan-1-yl)sulf onyl)

117 gen, such as 4-((3-chloro-4-((3-fluorobenzyl)oxy)phenyl)amino)-6-(4-((4-methyl-1,4-diazepan-1- yl)sul

118 rophenyl) piperazin-1-yl)-2-((4-fluorobenzyl)oxy)-ethanone, or DPFE, demonstrates improved solubility

119 For oxy, two unpaired Fe(d) spins and, thus by definition, a

120 eal that: (i) the lipid binding affinity for oxy-Mb increases as the chain length increases (i.e. C12

121 t prediction of similar binding energies for oxy- and carbonmonoxymyoglobin.

122 sly for PAHs but here for the first time for oxy-PAHs and N-PACs.

123 nvolving H2O molecules, which is absent from oxy-WTMb.

124 ab-scale in a relevant environment) and full oxy-fuel combustion (TRL 4 being the component and syste

125 This 1,3,2-diazaborole functionalized oxy ligand has been used to stabilize the first acyclic

126 ational spectroscopy reveals that a furfuryl-oxy intermediate forms on TiO(2) as a result of a charge

127 rface activate the formation of the furfuryl-oxy intermediate via an electron transfer to furfuraldeh

128 This furfuryl-oxy intermediate is a highly active and selective precur

129 rities--typical of flue gas from natural gas oxy-fuel combustion processes--the measured dew point pr

130 DA by VMAT2 increase levels of DA-generated oxy radicals ultimately resulting in degeneration of DAe

131 -beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy]-20-[(6-O-beta-d-xylopyra nosyl-beta-d-glucopyranosy

132 -beta-d-xylopyra nosyl-beta-d-glucopyranosyl)oxy]-dammar-24-en-19-al; (3beta)-28-oxo-28-(phenylmethox

133 -beta-d-glucopyranosyl-beta-d-glucopyranosyl)oxy]-ent-kaur-16-en-19-oic acid beta-d-glucopyranosyl es

134 eta-d-glucopy ranosyl)-beta-d-glucopyranosyl]oxy]-(3beta)-lanost-9(11)-en-24-one; 4-(2Z)-2-decen-1-yl

135 the concentration of oxygenated hemoglobin ([oxy-Hb]) in the cerebral cortex.

136 Here, using 3d-M hydr(oxy)oxides, with distinct stoichiometries and morphologi

137 hydroxybenzoate (1), 2-2-[(4-hydroxybenzoyl)-oxy]-ethyl-4-methoxy-4-2-[(4-methylpentyl)oxy]-3,4-dihyd

138 s TCE by Fe(II) associated with the Fe(III) (oxy)hydroxide coating is substantially slower than that

139 also lead to transformation of the Fe(III) (oxy)hydroxide coating to more crystalline phases, the ra

140 to the abundance of precipitated iron(III) (oxy)hydroxides, are hot spots for the removal and rediss

141 and reactivity of floc amorphous Fe((III))-(oxy)hydroxide (FeOOH) phases under ice ([FeOOH](summer)

142 ental ligands on the dissolution of Cr(III)-(oxy)hydroxide solids and associated Cr isotope fractiona

143 vestigated the stability of Cr(III)-Fe(III)-(oxy)hydroxides, common Cr(VI) remediation products, with

144 a non-natural substrate, benzaldehyde imino-oxy acetic acid (BIAA).

145 riptions are correct for the Fe-O2 center in oxy-Hb.

146 lectronic structure of the Fe-O(2) center in oxy-hemoglobin and oxy-myoglobin is a long-standing issu

147 Patients with MDD had smaller changes in oxy-haemoglobin in the frontal and temporal cortices tha

148 ed using a 52-channel system, and changes in oxy-haemoglobin in the frontal and temporal regions were

149 on submicrometer fly ash at higher levels in oxy-firing than in air-blown combustion.

150 In both regions of interest, oxy-haemoglobin was not associated with any of the clini

151 lude an acid-catalyzed tandem intermolecular oxy-Michael/intramolecular trans-ketalization reaction a

152 An intramolecular oxy-Michael reaction under basic conditions was used to

153 A room-temperature intramolecular oxy- and aminoarylation of alkenes with aryldiazonium sa

154 tion was carried out on the N1-(p-iodobenzyl)oxy]methyl derivative of compound 5 using propagyl alcoh

155 d is employed to fabricate well-defined iron oxy-hydroxides and transitional metal doped iron oxy-hyd

156 Specifically, the Co-doped iron oxy-hydroxides (Co0.54Fe0.46OOH) show the excellent elec

157 hydroxides and transitional metal doped iron oxy-hydroxides nanomaterials, which show good catalytic

158 r performance in comparison to the pure iron oxy-hydroxide (FeOOH) catalysts, originate from the bran

159 Iron (oxy)hydroxide solids in the shallowest sediments likely

160 rce of orthophosphate to WEOM-adsorbed iron (oxy)hydroxide AFM tips suggesting that the molecular mas

161 he phase transformation from amorphous iron (oxy)hydroxide to goethite, resulting in pyrite surface p

162 d a reference peat soil material to an iron (oxy)hydroxide mineral surface.

163 nding force between orthophosphate and iron (oxy)hydroxide that was coated onto atomic force microsco

164 be induced by biological reduction of iron (oxy)hydroxide solids.

165 se data set for chromate adsorption on iron (oxy)hydroxides (ferrihydrite and goethite).

166 ral organic matter (NOM) and suspended iron (oxy)hydroxides.

167 han structural differences between the iron (oxy)hydroxides.

168 rganic matter (WEOM) for adsorption to iron (oxy)hydroxide mineral surfaces is an important factor in

169 rted over longer distances compared to iron (oxy)hydroxides.

170 f calcium phosphate, calcium carbonate, iron(oxy)(hydr)oxide, silica, and also amino acids as an exam

171 xes and precipitated as nanoparticulate iron(oxy)hydroxides which aggregated as the pH increased, wit

172 thus became more coupled to that of the iron(oxy)hydroxides downstream in the circumneutral streams.

173 M but at pH >4.5 became associated with iron(oxy)hydroxides, and its transport thus became more coupl

174 og, we developed the bis((isopropoxycarbonyl)oxy)methyl ester prodrug (ACT-281959, 45).

175 high-spin Mn(V)-oxo complex and not a Mn(IV)-oxy radical as the most oxidized species.

176 Layered (oxy) hydroxide minerals often possess out-of-plane hydro

177 biosolids with iron, aluminum, and manganese oxy/hydroxides has been advocated as a key mechanism lim

178 hat is, the growth of a self-assembled metal oxy(hydroxide) active layer.

179 of dissolved organic matter (DOM) to metal (oxy)hydroxide mineral surfaces is a critical step for C

180 n of a family of thin-film transition metal (oxy)hydroxides as OER catalysts.

181 (3), BiVO(4), Si) paired with various metal-(oxy)hydroxide overlayers (e.g., Ni(Fe)O (x)H (y) and CoO

182 oxocyclohexa-1,4-dien-1-yl)methylene]-N-meth oxy-undecanamide (E3330-amide), a novel uncharged deriva

183 l)-oxy]-ethyl-4-methoxy-4-2-[(4-methylpentyl)oxy]-3,4-dihydr o-2H-6-pyranylbutanoic acid (2) and 3-((

184 d (3S)-(15-methyl-3-((13-methyltetradecanoyl)oxy)hexadecanoyl)glycyl-l-serine, abbreviated as l-serin

185 The development of a single-phase Fe/Mn oxy-hydroxide (delta-Fe0.76Mn0.24OOH), highly efficient

186 indicated the contribution of reductive Mn (oxy)hydoxide dissolution with Mn eventually becoming a t

187 waters due to reductive dissolution of Fe/Mn(oxy)hydroxides below the SWI.

188 ypes of regio- and enantioselective multiple oxy- and amino-functionalizations of terminal alkenes vi

189 s are important as Fe-containing Co- and Ni-(oxy)hydroxides are the fastest OER catalysts known.

190 vior of the anodic peak for amorphous nickel oxy/hydroxide (a-NiOx) films in basic media was investig

191 cluding 97 different parent, alkyl-, nitro-, oxy-, thio-, chloro-, bromo-, and high molecular weight

192 Notably, [oxy-Hb] change in the left dorsolateral prefrontal corte

193 (eta(1)-ONO(2)) demonstrating the ability of oxy coboglobin models to promote the nitric oxide dioxyg

194 Phylogenetic analysis of oxy-tryptophan dimerization gene homologs found within a

195 urther, although the rate of autoxidation of oxy-DHP is somewhat enhanced by the presence of TCP, the

196 tion that the cryoreduced ternary complex of oxy-P450scc-CH is catalytically competent and hydroxylat

197 Crystallography of oxy-F33Y-CuBMb reveals an extensive H-bond network invol

198 ioselective, with preferential deposition of oxy-Zn(II) species within the small pores of NU-1000.

199 ies, the electronic structure description of oxy-Hb remains elusive, with at least three different de

200 The effects of oxy-PAHs are, however, poorly known.

201 ic reactions of PAH lead to the formation of oxy and nitro derivatives, reviewed here, too.

202 , and oxalic acids confirms the potential of oxy aromatics to produce light-absorbing aqueous seconda

203 ped using the long-established principles of oxy-allyl cation chemistry.

204 scribed in detail the magnetic properties of oxy- and deoxyhemoglobin, as well as those of closely re

205 ossible contributions to the ground state of oxy-pfp.

206 henol (TCP) brings about facile switching of oxy-DHP to the enzymatically active ferric state via a p

207 n of spectral features identical to those of oxy-tyrosinase indicates that oxy-NspF contains a Cu(2)O

208 res with H2O vapor concentrations typical of oxy-combustion conditions.

209 ature survey showed surface complexation of (oxy)anions (As, B, and PO4) is consistently exothermic,

210 s desulfurization (WFGD) plants, focusing on oxy-coal combustion processes and differences when compa

211 ormation following binding to either met- or oxy(Fe(2+))-alpha.

212 oxygenation reactions: anthracene oxidation, oxy-functionalization of citronellol through the Schenck

213 ed performance when coated with metal-oxide/(oxy)hydroxide overlayers that are catalytic for the wate

214 9i (LMK235) (N-((6-(hydroxyamino)-6-oxohexyl)oxy)-3,5-dimethylbenzamide) showed similar effects compa

215 f more polar PACs including oxygenated PAHs (oxy-PAHs).

216 e included in such a study, oxygenated-PAHs (oxy-PAHs) and nitrogen containing heterocyclic PACs (N-P

217 reveals that the distal pocket of the parent oxy-P450scc-cholesterol complex exhibits an efficient pr

218 For application at cement plants, partial oxy-fuel combustion, amine scrubbing, and calcium loopin

219 4- methyl-1-oxo-2-[(1-oxopropyl)amino]pentyl]oxy]-L-leucyl-N,O-dimethyl-,(7-->1)-lac tone (9CI)}, a n

220 uantify SOx and NOx emissions from gas-phase oxy-combustion systems.

221 potent P2Y4R-selective N(4)-(3-phenylpropyl)oxy agonist was phenyl ring-substituted or replaced with

222 The potent N(4)-(3-(4-methoxyphenyl)-propyl)oxy analogue 19 (EC50: P2Y2R, 47 nM; P2Y4R, 23 nM) was f

223 AZ12799734 [4-({4-[(2,6-dimethyl-3-pyridinyl)oxy]-2-pyridinyl}amino)benzenesulfonamide] (IC(50) = 18

224 nder three different atmospheres: pyrolysis, oxy-fuel combustion, and carbon dioxide gasification con

225 S(2) are the major species during pyrolysis, oxy-fuel, and gasification.

226 formation, [2,3]-sigmatropic rearrangement, oxy-Cope rearrangement, enol-keto tautomerization and fi

227 the oxidized met form but not in the reduced oxy form.

228 classified using frontal and temporal region oxy-haemoglobin, respectively.

229 the catalytically inactive oxyferrous state (oxy-DHP), we find that the combination of H(2)O(2) and t

230 ort the use of bis(((difluoromethyl)sulfinyl)oxy)zinc (DFMS) as a source of CF2H radical for a rapid

231 tor 2-hydroxy-4-[[[[(4-methylphenyl)sulfonyl]oxy]acetyl]amino]-benzoic acid (NSC74859).

232 tion and subsequent annealing of the ternary oxy-cytochrome P450scc-cholesterol complex.

233 from N-methylpyridone to a tetrahydropyranyl oxy-pyridine derivative.

234 Our results indicate that oxy-PAH containing mixtures can be as potent Ahr activat

235 al to those of oxy-tyrosinase indicates that oxy-NspF contains a Cu(2)O(2) core where peroxide is coo

236 This suggests that oxy-Mb may play an important role in fuel delivery in Mb

237 Our results suggest that [oxy-Hb] change in the prefrontal cortex during the susta

238 The oxy-cobolglobin models of the general formula (NH(3))Co(

239 The oxy-combustion mechanisms available in the literature ca

240 The oxy-hemoglobin concentration change and the beta band po

241 In addition, the oxy intermediate of the reaction cycle of Y257F-4NC + O(

242 spF, we have generated and characterized the oxy form of its active site.

243 e boiler and CO2 separation units during the oxy-fuel fluidized-bed combustion using this coal.

244 ing the same oxidation state as found in the oxy-bridged MOF, the triply oxidized HITP(3-) found in C

245 nd higher N2O formation were observed in the oxy-fuel atmosphere.

246 Most significantly, in the oxy-P450cam complex Gly248 adopts a position midway betw

247 Another important intermediate is the oxy-P450cam complex when bound to Pdx.

248 otonation and hence further reduction of the oxy complex to the hydroperoxy intermediate resulting in

249 nd applied it to study the properties of the oxy-ferrous complex of a human membrane bound P450, CYP1

250 A sharp increase of the oxy-hemoglobin concentration change, together with a dra

251 Probing the oxy-complexes of CYP19A1 poised for hydroxylase and lyas

252 According to this structuration, the oxy-hydroxide maintains the high adsorption capacity for

253 FM-300(V(IV)) shows CO2 bound side-on to the oxy group and sandwiched between two phenyl groups invol

254 AH fraction of the WOOD extract and with the oxy-PAH fraction of the COKE extract.

255 The [oxy-Hb] change during the sustained attention task (SAT)

256 We found that the [oxy-Hb] change during the verbal fluency task (VFT) was

257 f a three-step sequence comprising a thermal oxy-Cope rearrangement, an iridium-catalyzed hydrogenati

258 This oxy form is found to react with monophenols, indicating

259 te these results with measurements of tissue oxy- and deoxyhemoglobin concentration during oxygen dep

260 both fatty acids and acylcarnitines bind to oxy-Mb in 1:1 stoichiometry.

261 ox active form of the protein in contrast to oxy-NGB.

262 30, provide direct and sustainable routes to oxy-functionalized derivatives of these building block m

263 xide dioxygenation (NOD) reaction similar to oxy-hemes.

264 S)-N-isobutyl-3-methyl-1-((triisopropylsilyl)oxy)butan-2-amide forms both a 2:2 mixed aggregate and a

265 S)-N-isobutyl-3-methyl-1-((triisopropylsilyl)oxy)butan-2-amine and n-butyllithium are characterized b

266 ithium (S)-N-isopropyl-1-((triisopropylsilyl)oxy)propan-2-amide forms mostly a 2:2 ladder-type mixed

267 d from (S)-N-isopropyl-1-((triisopropylsilyl)oxy)propan-2-amine, (R)-N-(1-phenyl-2-((triisopropylsily

268 ithium (R)-N-(1-phenyl-2-((triisopropylsilyl)oxy)ethyl)propan-2-amide.

269 amine, (R)-N-(1-phenyl-2-((triisopropylsilyl)oxy)ethyl)propan-2-amine, or (S)-N-isobutyl-3-methyl-1-(

270 iyama-Michael reaction of 2-[(trimethylsilyl)oxy]furan with diverse alpha,beta-unsaturated ketones is

271 the effect of the gases present in a typical oxy-coal combustion atmosphere on mercury speciation and

272 fur was found to be converted to SO(3) under oxy-fuel combustion, whereas SO(3) was undetectable duri

273 ion of those species was also assessed under oxy-fuel condition.

274 oncentrations were considerably higher under oxy-fuel combustion compared to that in the air combusti

275 n coal in a 10 kWth fluidized bed unit under oxy-fuel combustion conditions.

276 gether, our results support a model in which oxy-Mb is a novel regulator of long-chain acylcarnitine

277 of both fatty acids and acylcarnitines with oxy-Mb using molecular dynamic simulations and isotherma

278 of either fatty acids or acylcarnitines with oxy-Mb.

279 ) fail to achieve a stable conformation with oxy-Mb.

280 developed leading to selective [2,3]-Wittig-oxy-Cope and isomerization-Claisen rearrangements.

281 table catalyst for the selective, high yield oxy-functionalization of methane.

282 ble 2',2''-(10-(2-((2,5-dioxopyrrolidin-1-yl)oxy)-2-oxoethyl)-1,4,7,10-tetraazacyclod odecane-1,4,7-t

283 with the [(2,2,6,6-tetramethylpiperidin-1-yl)oxy] (TEMPO) stable free radical.

284 nyl]-4-yl)-6-chloro-1H-benzo[d]imidazol-2-yl)oxy)-2-methylbenzo ic acid, 42 (MK-3903).

285 aminomethyl)-6-(trifluoromethyl)pyridin-2-yl)oxy)phenyl)(3- fluoro-4-hydroxypyrrolidin-1-yl)methanone

286 N-{trans-3-[(5-Cyano-6-methylpyridin-2-yl)oxy]-2,2,4,4-tetramethylcyclobutyl}imid azo[1,2-a]pyrimi

287 (2-(5-bromofuran-2-yl)-4-oxo-4H-chromen-3-yl)oxy)acetamide (CB7993113), was further tested for its ab

288 dimethyl-1-(3-((2,4,5-trimethylthiophen-3-yl)oxy)propyl)piperazin-1-ium bromide] conjugated polyelect

289 inhibitor, N-(4-((6,7-dimethoxyquinolin-4-yl)oxy)-3-fluorophenyl)-1,5-dimethyl-3-oxo-2-pheny l-2,3-di

290 omatic)-N'-{4-[(6,7-dimethoxyquinazolin-4-yl)oxy]phenyl}urea were identified as potent and selective

291 nol, 2, 4-[(4-fluoro-2-methyl-1 H-indol-5-yl)oxy]-6-methoxyquinazolin-7-ol, by chloropyrrolidine, 3,

292 )methylene)-3-oxo-2,3-dihydrobenzofuran-6-yl)oxy)acetonitrile (5a) and (Z)-6-((2,6-dichlorobenzyl)oxy

293 methylamino)-N-(3-{2-[(4-oxo-4H-chromen-7-yl)oxy]acetamido}phenyl) (12j).

294 nthren-3-yl]o xy]-6-(hydroxymethyl)oxan-3-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol], an alkaloid iso

295 l-N-phenyl-2-{[2-(pyridin-2-yl)quinolin-4-yl]oxy}propanamide (22a; rat Ki=0.10 nM; human TSPO genotyp

296 6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin- 4-yl}oxy)-1-piperidinecarboxylate (GSK1104252A) (3), a potent

297 xy-pyridin-3-yl)-benzyl]-5-(pyridin-2-ylmeth oxy)-1H-indol-2-yl]-2,2-dimethyl-propionic acid (11j) is

298 Zr(25) is a pentagonal assembly of 25 Zr-oxy/peroxo/hydroxyl polyhedra and is the largest Zr/Hf c

299 -4-(trifluoromethyl-3H-diazirin-3-yl)ben zyl]oxy]carbonyl]nonanoyl]-sn-glycero-3-phosphocholine to th

300 -4-(trifluoromethyl-3H-diazirin-3-yl)ben zyl]oxy]carbonyl]nonanoyl]-sn-glycero-3-phosphocholine, the