ライフサイエンスコーパス: acetone

1 conventional solvents (methanol, ethanol and acetone).

2 layers of reagents (namely acetophenone and acetone).

3 bodies (acetoacetate, 3-hydroxybutyrate, and acetone).

4 e extracted using two solvents (methanol and acetone).

5 the reaction intermediates acetaldehyde and acetone.

6 hospholipids (ePL) produced by deoiling with acetone.

7 laser spectroscopic setup to measure breath acetone.

8 n methanol isotopomers, ethylene glycol, and acetone.

9 ine (TEA), thionyl chloride, chloroform, and acetone.

10 formation of the desired mono-alpha-arylated acetone.

11 hydrogen atom abstraction from methanol and acetone.

12 o the original material upon reabsorption of acetone.

13 2-butanone to 6-methoxy-2-naphthaldehyde and acetone.

14 nanoelectrospray plume entraining lipids and acetone.

15 s mainly attributed to methanol, ethanol and acetone.

16 her, trimethylamine, trimethylphosphine, and acetone.

17 e surfaces inactive for the hydrogenation of acetone.

18 e solvent for antioxidant extraction was 80% acetone.

19 ic compounds: benzaldehyde, propan-2-ol, and acetone.

20 ly formed alkyl radical (8b) to form dA* and acetone.

21 grape using 50% methanol, 70% methanol, 50% acetone, 0.01% pectinase, or petroleum ether were also e

22 The best results were obtained for the water-acetone (1/3-2/3) binary mixture, presenting TPC, DPPP a

23 The best ternary mixture was water-ethanol-acetone (1/6-1/6-2/3), with 60.96 mg GAE/g, 380.53 mumol

24 In addition, we found MeOH/ACN/Acetone (1:1:1, v/v/v) as extraction cocktail could achi

25 In these experiments, DMSO:acetone (1:40 v/v) solution of 17AAG (500 nmol) was appl

26 ia the Pechmann reaction of 2-naphthols with acetone-1,3-dicarboxylates, followed by an intramolecula

27 aximized antioxidants extraction were 63.48% acetone, 115.14 min, and 48.66 degrees C.

28 the-fly KMC model for the destruction of (1) acetone, (2) trichloroethylene (TCE), and (3) polyethyle

29 method, alternate winterization (0.1g/mL oil/acetone, 24h, -80 degrees C, precooled Buchner filtratio

30 obile phase consisted of chloroform:methanol:acetone:25% ammonium hydroxide (75:15:10:1.6 v/v/v/v), d

31 /ppbv CO), acetaldehyde (3.93 pptv/ppbv CO), acetone (3.59 pptv/ppbv CO), methyl ethyl ketone (1.42 p

32 cationic transition-metal complexes [(Cp*)M(acetone)3 ](OTf)2 (Cp*=pentamethylcyclopentadienyl and M

33 201.6 cm(3) g(-1) at 196 K, under 1 atm) and acetone (5 wt %), a sorption property that was attribute

34 of PEG-PBA-PEG, olive oil (0.5 and 0.88 mg), acetone (6 and 10.25 ml), and Tween 60 (3.0 and 4.25 mg)

35 The crude extract was prepared with acetone (60% v/v) and purified using chromatographic met

36 orm (7 stocks), thionyl chloride (3 stocks), acetone (7 stocks), and TEA (3 stocks), respectively, an

37 ic ratios when the reaction was conducted in acetone, a significant matched/mismatched effect was obs

38 While smaller organic compounds such as acetone, acetaldehyde, isoprene, or cysteamine can be de

39 fied eight metabolites (3-D-hydroxybutyrate, acetone, acetoacetate, citrate, lactate, creatine, creat

40 Along with the model reaction of acetone addition to propyne and allene, the addition of

41 the open-source code, CRITIC2, and tested on acetone, adipic and maleic acids molecular crystals, eac

42 Lack of acetone adsorption at Pt(111) and Pt(100) due to a weak

43 , such as diethyl ether, THF, ethyl acetate, acetone, alcohol, acetonitrile, DMF, and DMSO, identify

44 ing a tunable percentage of photoinitiators (acetone/alcohol) that drives the sample to the MS throug

45 as hypothesized following the observation of acetone among photolysis products.

46 slowest, producing sizable concentrations of acetone, an isomer of propionaldehyde.

47 Furfural acetone and 2-decanol functioned as "honey-traps" attrac

48 mechanism of the catalytic activation of the acetone and 4-nitrobenzaldehyde by the acidic surface si

49 atively catalyzed aldol condensation between acetone and 4-nitrobenzaldehyde on alkylamine (or alkyle

50 2 ng/mg cell protein for chlorophylls in the acetone and [C(4)mim]Cl extracts, respectively.

51 the chlorophylls were bioaccessible from the acetone and [C(4)mim]Cl extracts, respectively.

52 ifferent solvents (water, methanol, 1M NaCl, acetone and acetonitrile) and best binding was observed

53 ition to propyne and allene, the addition of acetone and acetophenone to methyl propargyl and methyl

54 ridium ljungdahlii was engineered to produce acetone and achieved a mass yield 138% of the previous t

55 The enzyme was extracted and purified using acetone and aqueous two-phase systems.

56 suggest that the interaction between excited acetone and aryl triflate is essential to these coupling

57 Photosensitization with acetone and chemical quenching with N, N, N, N-tetrameth

58 e isotropic and anisotropic Raman spectra of acetone and deuterated acetone isolated in an argon matr

59 that photoexcited aliphatic ketones, such as acetone and diacetyl, can be used as promising low-cost

60 ors can detect disease biomarkers, including acetone and ethanol for diabetes and H2S for cardiovascu

61 g performance was characterized by measuring acetone and ethanol vapors at their characteristic C-H a

62 a-valerolactone- (and some concentrations of acetone and ethanol) water cosolvents, a significant fra

63 and avocado oil (0.5-2.0 mg); solvent, using acetone and ethyl acetate (6-12 ml); and surfactant conc

64 (ACs) catalyze the conversion of substrates acetone and HCO3(-) to form the product acetoacetate.

65 with two strongly overlapping interferents, acetone and hexane.

66 -MS is demonstrated by the quantification of acetone and isoprene in exhaled breath.

67 Validation measurements of gas-phase acetone and nigrosin aerosol absorption cross sections a

68 ue or green-yellow light upon irradiation in acetone and showed Stokes shifts in the region of 70-96

69 52.14% and 13.02% conversion was achieved in acetone and tert-butanol solvent systems, respectively.

70 conversion increased to 60.74% and 65.73% in acetone and tert-butanol system, respectively.

71 ine intermediates, formed covalently between acetone and the catalytic lysine residue, was found to b

72 tal, which on deprotonation dissociates into acetone and tropone.

73 idation of 6 with Fremy's salt and KH2PO4 in acetone and water, followed by dehydrogenation using pal

74 were obtained by a conventional method using acetone and, an alternative method using ionic liquid (1

75 ated carbonyl compounds (e.g., formaldehyde, acetone) and alpha,beta-unsaturated aldehydes (e.g., acr

76 acid), QT (quercetin), LT (luteolin) in ACE (acetone) and RT (rutin) in EtOH (ethanol) solvent at 60

77 thin 10% with those measured previously (for acetone) and those predicted by Mie theory (for nigrosin

78 to mould; (b) y-nonalactone, y-hexalactone, acetone, and 1-nonanol that are decisive to classify OK

79 owed that a 10g/l liquid to solid ratio, 58% acetone, and 12h extraction time yielded the highest amo

80 and fusel alcohols (1-propanol, 2-propanol, acetone, and acetaldehyde) was found in the majority of

81 bolic emissions, such as isoprene, methanol, acetone, and acetic acid.

82 OAVs, cis-linalool oxide (furanoid), geranyl acetone, and cinnamyl acetate were identified as other p

83 on but are not as effective as acetonitrile, acetone, and ethyl acetate.

84 ...O hydrogen bonds in crystals, chloroform, acetone, and water have nearly identical lengths and ver

85 Extraction of hop samples with 70% acetone (aq) followed by a C-18 Solid Phase Extraction y

86 e - glycerol (1:3) as extraction solvent and acetone as aprotic solvent at pH 6.0 were used for the p

87 ogenative diol lactonization reactions using acetone as both the solvent and hydrogen acceptor.

88 after 96h of synthesis, at 45 degrees C and acetone as solvent.

89 conducted in environmentally benign water or acetone as solvents.

90 rtificial aldolase with high specificity for acetone as the aldol donor can be reengineered via singl

91 ghest production of esters was obtained with acetone as the reaction solvent.

92 s were generated by addition of H2O2/base in acetone at -90 degrees C.

93 -octanol as immobilized solvent; toluene and acetone at 1:5 ratio as extraction and disperser solvent

94 In dry, degassed acetone at 295 K, the radical 2 has a half-life, tau1/2

95 cle size less than 0.5mm when extracted with acetone at 50 degrees C.

96 ryl azide, ciprofloxacin, and an aldehyde in acetone at room temperature.

97 obtained with aqueous mixtures of ethanol or acetone at variable concentrations, and the condensed ta

98 ory calculations (M06/SDD-6-311G(d,p)-IEFPCM(acetone)//B3LYP/SDD-6-31G(d)) predict that the product d

99 haking and by adding 30% of ethyl acetate in acetone, being beta-carotene the major carotenoid (7.8 a

100 s demonstrated for regular and perdeuterated acetone, benzene, and toluene as well as toluene-(13)C7

101 course of malaria: carbon dioxide, isoprene, acetone, benzene, cyclohexanone, and 4 thioethers.

102 beling of NDM-1 with 1,1,1-trifluoro-3-bromo acetone (BFA), and its use to study binding events and c

103 er distillation of the extractant phase, the acetone, butanol and ethanol mixture is upgraded to long

104 h, producing in excess of 40 g of solvents (acetone, butanol and ethanol) between the completely imm

105 ents sugar to a mixture of organic solvents (acetone, butanol and ethanol).

106 onventional diluted solvent mixes containing acetone, butanol, and ethanol were superior or equally e

107 industrial producer of the organic solvents acetone, butanol, and ethanol.

108 resence of practically unreactive compounds (acetone, butanol, propionic, and butyric acids).

109 One canonical example of such processes is acetone-butanol-ethanol (ABE) fermentation by Clostridiu

110 anic solvents such as CH3OH, THF, CH3CN, and acetone by means of fluorescence emission intensity.

111 aggregated model for the explanations of the acetone C=O vibration NCE phenomenon and its concentrati

112 , 2-acetylpyrrole, farnesyl acetone, geranyl acetone, cadinol, cubenol and dihydroactinidiolide.

113 In this study, the release of acetone, carbon disulfide, dimethyl sulfide, nitromethan

114 and acnB in steady-state behavioural assays, acetone carboxylase subunit (acxC) mutant behaviour was

115 Acetone carboxylases (ACs) catalyze the conversion of su

116 The first structural rationale for acetone carboxylation is presented here, focusing on the

117 highest category of exposure to hexane with acetone coexposure.

118 In all cases (except acetone), complex 3 exhibits significantly faster overal

119 elected factors; solid/solvent ratio (g:mL), acetone concentration (%), time of extraction in acidifi

120 The acetone concentration exhaled in the breath of three typ

121 ng more studies with T1D minors, because the acetone concentration in the breath of the minors differ

122 ed TPC under the optimal MAE conditions (51% acetone concentration in water (v/v), 500 W microwave po

123 The effects of aqueous acetone concentration, microwave power, extraction time

124 nd rest and measured their individual breath acetone concentrations in good agreement with benchtop p

125 The hydrocyanation reaction employs acetone cyanohydrin as a practical alternative to HCN ga

126 catalysts also promote the dedeuteration of acetone-d(6) to afford a deuterated ammonium ion.

127 studies as well as FTIR analysis of adsorbed acetone-d6 and D2O unambiguously showed that a highly ac

128 ng ability up to approximately 1 kcal/mol in acetone-d6 correlated with a theoretical increase of H5

129 ifluoromethylphenyl) (1) at -78 degrees C in acetone-d6 or toluene-d8 yields HOOOH (16-20%) and trans

130 connects, printed gas sensor for ethanol and acetone detection, and printable supercapacitors and emb

131 The mixture design consisted of ethanol, acetone, dichloromethane and chloroform solvents and the

132 ts varying from polar to nonpolar (methanol, acetone, dichloromethane, and n-hexane) were selected to

133 The samples were dissolved in acetone-dichloromethane-methanol (3:2:1, v/v/v) and dilu

134 ed by addition of a stoichiometric amount of acetone during the oxidation step allowing for selective

135 Acetone, ethanol and hexane were used as direct or blend

136 The solvents used were acetone, ethanol and water and the responses analyzed we

137 r common water-organosolv cosolvent systems (acetone, ethanol, and gamma-valerolactone) exhibit phase

138 (ssDNA) and double-stranded DNA (dsDNA) with acetone, ethanol, H2S and HCl.

139 ange of polar and non-polar organic liquids (acetone, ethanol, methanol, N-methyl-2-pyrrolidone (NMP)

140 were extracted simultaneously with n-hexane/acetone/ethanol (50/25/25, v/v/v).

141 ectiveness of some solvents (water, ethanol, acetone, ethyl acetate), used as pure or in binary and t

142 In this study, N,N'-bis (acetyl acetone) ethylenediimine (Fe3O4@SiO2-EDN) was synthesize

143 ectrometric and ion mobility measurements of acetone, eucalyptol, and diisopropyl methanephosphonate.

144 e) compared to a calculated 87% ee in "neat" acetone (exptl 85% ee).

145 ntioxidant activity was found for the powder-acetone extract followed by the liquid methanol and liqu

146 An aqueous acetone extract from coffee pulp was purified using Seph

147 thanol extract of Laminaria digitata and the acetone extract of Undaria pinnatifida showed inhibitory

148 1.05mM of AOT at pH 4 for precipitation, and acetone extraction (with 1mM NaCl), which resulted in an

149 Direct acetone extraction of vegetable powders allowed for sati

150 We further integrated the MeOH/ACN/Acetone extraction with the HILIC-FTMS method for metabo

151 t followed by the liquid methanol and liquid acetone extracts (p < 0.05).

152 Calculation of Fe balance (summing Fe in acetone extracts and Fe in the residue after haem Fe ext

153 nd determined quantitatively in methanol and acetone extracts from quince peel and pulp, namely 3-O-c

154 Crude chloroform, ethanol and acetone extracts of nineteen seaweed species were screen

155 A 5 mg/mL solution of water, methanol and acetone extracts of seaweeds were used for alpha-glucosi

156 Flavonol glycosides were identified from acetone extracts of seed coats of black beans, pinto bea

157 The results showed acetone extracts of Undaria pinnatifida has the stronges

158 th results obtained for the hydrogenation of acetone featuring an isolated carbonyl functional group

159 n extraction and protein precipitation using acetone followed by pellet digestion with trypsin.

160 nd haem Fe was extracted using acidified 80% acetone for 60 min.

161 Better results were obtained using 500muL of acetone for Cd and 700muL of acetonitrile for Pb as disp

162 ion are proposed and the origin of selective acetone formation on Cu-SA/NPC is clarified.

163 s (aqueous, ethanolic and acetonic) and only acetone fraction showed a high concentration of procyani

164 Acetone fractionation on two types of HOHS sunflower oil

165 Data are presented on elevated breath acetone from two individuals following an overnight fast

166 6-methyl 5-hepten-2-one (6-MHO) and geranyl acetone (GA) with average yields of 0.22 and 0.16, respe

167 e product of isopropanol electrooxidation is acetone, generated with a Faradaic efficiency of 94 +/-

168 lool, (Z)-jasmone, 2-acetylpyrrole, farnesyl acetone, geranyl acetone, cadinol, cubenol and dihydroac

169 Hexane: methanol: acetone: glacial acetic acid (8:2:0.5:0.1, by volume) is

170 eversed-phase chromatography with a methanol-acetone gradient and coupling to the ICP-sfMS via a dedi

171 the cosolvent systems in the order of THF > acetone > ethanol > gamma-valerolactone.

172 only) and also of cyclopropanecarbaldehyde > acetone >/= t-Bu-CH horizontal lineO.

173 al absorbance at 280 nm was also observed in acetone:H2O extracts, if the acetone had not completely

174 lso observed in acetone:H2O extracts, if the acetone had not completely evaporated before the extract

175 Extraction using DMSO and acetone has shown to be appropriate for voltammetric ana

176 the Michael acceptor bis(2-hydoxybenzylidene)acetone (HBB2), a dual activator of NRF2 and HSF1, prote

177 improvement with the three solvents assayed (acetone, hexane, ethanol).

178 emperature, is triggered by the injection of acetone in a mixture of precursors that would remain unr

179 compact device is demonstrated for measuring acetone in breath samples.

180 zed studies to better understand the role of acetone in diabetes.

181 simultaneously to study their relation with acetone in exhaled breath.

182 A robust method is demonstrated to measure acetone in human breath at sub parts-per-million by volu

183 0 degrees C), time (1-60 min), percentage of acetone in n-hexane (25-75%, v/v) and solvent volume (10

184 C, time 40 min, a solvent composition of 25% acetone in n-hexane (v/v) and solvent volume 40 ml.

185 d that 60% potassium hydroxide solution with acetone in the ratio of 0.1 (ml/ml) was the ideal binary

186 ng primers (5, 10, 15, 20 or 30 wt% PENTA in acetone) in improving resin-Y-TZP bond strength.

187 determine the best solvent to use (hexane or acetone) in terms of the operational parameters and prop

188 Topical application of an acetone insecticide formulation to circumvent lipid-base

189 re found to be the in situ generation of the acetone intermediate and the cross-aldol condensation be

190 nd alcohols, an unambiguous determination of acetone is demonstrated with a precision of 13 ppbv that

191 Acetone is identified as the major product with a Farada

192 t as acids but as their conjugate bases, and acetone is neither an acid nor a base.

193 d peak formed from regular and perdeuterated acetone is observed, which can most likely be attributed

194 of the new insights, the usage of cosolvent acetone is shown to enable control of product selectivit

195 Acetone is trapped out of breath and released into the o

196 opic Raman spectra of acetone and deuterated acetone isolated in an argon matrix have been recorded f

197 after 5 min averaging at typical breath mean acetone levels in synthetic gas samples mimicking human

198 e onset and progression of increasing breath acetone levels that indicate intensified body fat metabo

199 de nucleophiles, such as thiols, to yield an acetone-linked bridge (ACE).

200 The scope of the acetone-linked peptides was further explored through the

201 Together, these studies suggest that acetone linking is generally applicable to peptide macro

202 ds of Rosmarinus officinalis extract (powder-acetone, liquid-methanol, liquid-acetone) were used to e

203 Acetone may potentiate the neurotoxicity of n-hexane.

204 der: chloroform, ethyl acetate acetonitrile, acetone, methanol, and acetic acid.

205 eptor, the association in deuterated benzene/acetone/methanol 70:30:1 at 283 K reaches Ka =(2.11+/-0.

206 mutagenesis (ISM) has been applied to phenyl acetone monooxygenase (PAMO), a thermally robust Baeyer-

207 adsorption of the studied VOCs (2-propanol, acetone, n-butanol, toluene, 1,2,4-trimethylbenzene) at

208 A mixture of acetone/n-hexane (1:1, v/v) was selected for accelerated

209 ature of 30 degrees C and solvent mixture of acetone/n-hexane 1:3 (v/v) provided optimal conditions f

210 Samples were extracted using acetone/n-hexane mixtures at different ratios (1:3, 2:2

211 solvents were tested to isolate proteins, an acetone:n-hexane combination being the best protein prec

212 secondary reaction of the key intermediate, acetone, namely the acetone-to-isobutene reaction.

213 thods, the extraction step in buffer or acid acetone often becomes limiting if muscle is oxidised and

214 Cell lysis solvent and PB reagent (acetone or benzophenone) are delivered into the micropip

215 ed to produce high-melting point stearins by acetone or hexane fractionation.

216 rsions were stable at high concentrations in acetone or, with some exceptions, in water and produced

217 ebound pathway, which gives tert-butanol and acetone, or a separated radical pair.

218 face that is active for the hydrogenation of acetone over a wide range of reaction conditions.

219 riegee intermediates, formaldehyde oxide and acetone oxide, decrease with increasing temperature in t

220 s well as different oximes (formaldehyde and acetone oxime) were considered.

221 e the experimental data over a wide range of acetone partial pressures.

222 atile contaminants (methyl-tert-butyl ether, acetone, pentanone, butanol, and hexanol) accumulated in

223 Acetone peroxides are attractive for their inexpensive a

224 Carotenoids were isolated using acetone-petroleum ether extraction followed by spectroph

225 The acetone-phenol method was found to produce good protein

226 erned with a photoresist and lifted off with acetone, photodetectors that outperform more standard Au

227 sed method compared to the conventional cold acetone precipitation method.

228 with concomitant decarboxylation and loss of acetone, proceeds in high yields and excellent enantiose

229 ecies, and four compounds-methyl isocyanate, acetone, propionaldehyde, and acetamide-that had not pre

230 ess the protein present in quinoa seeds, TCA/Acetone protein extraction was performed using four diff

231 The aqueous mixtures of acetone provided the highest extraction yields in total

232 The 3-->1 transformation through acetone reabsorption is also demonstrated.

233 Repeat extractions with 80% acetone recovered additional haem Fe, suggesting that pr

234 In agreement with previous results for acetone reduction, the Pt(100) surface is specifically a

235 treatments, the solventogenesis method with acetone resulted in maximum extraction of naringin and l

236 boiling-point, low-polarity solvent, such as acetone, results in catalysts with an atomic dispersion

237 d 23%, rhodoxanthin (E/Z)-isomer mixtures in acetone revealed color hues (CIE-h degrees ) ranging fro

238 e in humid environment as well, suitable for acetone sensing in exhaled breath that clearly distingui

239 ioxide (RGO/SnO(2)) binary nanocomposite for acetone sensing performance was successfully studied and

240 e introduce a compact and inexpensive breath acetone sensor based on Si-doped WO3 nanoparticles that

241 As a result, this simple breath acetone sensor enables easily applicable and hand-held b

242 but not the ketones beta-hydroxybutryate or acetone, shows antiseizure activity in two acute ex vivo

243 Using the acetone signature between 1150 and 1250 cm(-1) and a mul

244 bones were found to oxidize chloride ions in acetone solution.

245 of the insoluble cell wall material in water/acetone solutions and the high amounts of polyphenols th

246 Most of the experiments with acetone solutions extracted more bioactive compounds, an

247 bipyridine; bpz = 2,2'-bipyrazine), in Br(-) acetone solutions, led to the formation of Br-Br bonds i

248 p-G(2) BDS is obtained from its acetone solvate, AcMe@G(2) BDS, by single-crystal-to-sin

249 creases to 90% in simulations in an implicit acetone solvent (SMD) because the oxygen rebound becomes

250 e identification of halogenated methanes and acetones suggested that those compounds were formed as u

251 ased to 62.9% in tert-butanol system, unlike acetone system.

252 ffects of solvent concentration (methanol or acetone), temperature and time on the extraction of tota

253 plantar, cold-plate (5 and 10 degrees C), or acetone tests.

254 reater sensitivity to evaporative cooling by acetone than control animals.

255 lylic halide, reacts 30 times faster with KI/acetone than does benzyl chloride at room temperature.

256 In the case of acetone the oxo-vinyl complex results in two rotational

257 30 cm(-1) at 3.38 mum allows, in addition to acetone, the simultaneous measurement of isoprene, ethan

258 P4O12] with trifluoroacetic anhydride in wet acetone; this simple procedure affords the oxoacid salt

259 ng a homologous series of seven ketones from acetone to 2-dodecanone.

260 ion limit increased from 1.1 x 10(3) ppm for acetone to 5.7 x 10(3) ppm for 2-dodecanone.

261 f fluorescence from pigment extracted in 90% acetone to assess the variability in phytoplankton class

262 n the aldolization and self-deoxygenation of acetone to isobutene.

263 type reactions: enamine-mediated addition of acetone to nitrostyrenes, and nitroalkane addition to co

264 (raw) hazelnut was extracted with 80% (v/v) acetone to obtain crude phenolic extract that was then f

265 ted acidity could catalyze the rate-limiting acetone-to-isobutene reaction, the presence of Bronsted

266 of the key intermediate, acetone, namely the acetone-to-isobutene reaction.

267 linear and branched alcohols, acetonitrile, acetone, toluene, and ethyl acetate.

268 Acetone treatment of cocoa powder prior to SDS-PAGE led

269 The acetone treatment was further optimized by RSM for the m

270 ns were efficient under inert atmosphere and acetone triplet-sensitized conditions indicating that th

271 ldol condensation of aromatic aldehydes with acetone under mild reaction conditions with near quantit

272 ion of trifluoroethanol (TFE), DMSO, DMF and acetone, uniform fiber-like nanoparticles from PLLA dibl

273 The sample was extracted with 10mL acetone using a tissue homogenizer, followed by derivati

274 An acetone vapor bath was used to smooth acrylonitrile-buta

275 precipitation efficiency of both ethanol and acetone was achieved when stirred into the starting mate

276 olkin based on precipitation with ethanol or acetone was developed.

277 The acidified 70% acetone was identified as the ideal solvent for the maxi

278 of pyrrole with pentafluorobenzaldehyde and acetone was investigated to determine the potential for

279 Acetone was more suitable than hexane as a solvent for H

280 ion in the (1)H NMR spectrum was used, where acetone was observed as the suitable solvent in terms of

281 A third ketone body, acetone, was significantly lower in the 30 mg/kg alpha-H

282 d in binary and ternary mixtures composed of acetone, water, carbon dioxide or nitrogen at elevated p

283 The Acetone/Water (70:30 v/v) was the most effective solvoly

284 ynes using tetrabutylammonium fluoride in an acetone/water mixture and the investigation of the 10-me

285 aliphatic carboxylic acids by Selectfluor in acetone/water provides access to fluorinated compounds u

286 (three with methanol followed by three with acetone/water solution).

287 ion of rhodoxanthin (E/Z)-isomer mixtures in acetone/water yielded red (CIE-h degrees = 29 degrees )

288 butyric, pentanoic, and hexanoic acids) and acetone were elevated in ex vivo experiments in the head

289 ction with hexane/isopropanol or with hexane/acetone were investigated, as was the effect of previous

290 The aqueous mixtures of acetone were more effective than the corresponding aqueo

291 acetic acid, formic acid, acetaldehyde, and acetone were observed during photodegradation, and their

292 ectly quantified in the extracts when SO2 or acetone were removed by solid-phase extraction with a C1

293 act (powder-acetone, liquid-methanol, liquid-acetone) were used to examine the effects of format-solv

294 ple, acetonitrile, N,N-dimethylformamide, or acetone, which indicated the exceptional nucleophilicity

295 potential E(Br(*)/Br(-)) = 1.22 V vs SCE in acetone, which is about 460 mV less positive than the ac

296 ing nickel-catalyzed mono-alpha-arylation of acetone with aryl chlorides, pivalates, and carbamates h

297 us quantification of methanol with H(3)O(+), acetone with NO(+), and dimethyl sulfide with O(2)(+*) r

298 en extended to the unprecedented coupling of acetone with phenol derivatives.

299 It was also found that 2 reacts with acetone with the formation of 3,3-dimethyl-6-phenyl-2,3-

300 r, and 0.14 to 7.5 L m(-2) h(-1) bar(-1) for acetone, with an unchanged low molecular weight cut off