ライフサイエンスコーパス: acetonitrile

1 a C18 column and gradient elution (water and acetonitrile).

2 x4.6mm) column and isocratic elution (68% of acetonitrile).

3 l range from 363 nm (cyclohexane) to 595 nm (acetonitrile).

4 yte is devised by dissolving H(3) PO(4) into acetonitrile.

5 oefficient of about 1 x 10(6) M(-1) s(-1) in acetonitrile.

6 e solvent from toluene to tetrahydrofuran to acetonitrile.

7 y of these thiaza[5]helicenes in toluene and acetonitrile.

8 ate [Yb(OTf)3], N-iodosuccinimide (NIS), and acetonitrile.

9 M p-toluenesulfonic acid (TsOH) in deaerated acetonitrile.

10 evealed robust helical folding propensity in acetonitrile.

11 inized with 0.5% sodium hydroxide) using 5mL acetonitrile.

12 4.0min of contact time, 0.3mL desorption by acetonitrile.

13 y mild potential (-0.16 V versus Fc(0/+)) in acetonitrile.

14 ent anions were studied in chloroform and in acetonitrile.

15 -2-en-1-yl]phenyl azide (1b)) was studied in acetonitrile.

16 obenzene, and ammonium cerium(IV) nitrate in acetonitrile.

17 applying a solvent gradient from 20% to 100% acetonitrile.

18 hesis from indole-3-pyruvic acid to indole-3-acetonitrile.

19 well as in other solvents, in particular, in acetonitrile.

20 nol, or DMF or in biphasic mixtures that use acetonitrile.

21 rolyte (BGE) contained higher percentages of acetonitrile.

22 hase composed of ammonium formate buffer and acetonitrile.

23 y immobilized Candida antarctica lipase B in acetonitrile.

24 or sequestration of small molecule guests in acetonitrile.

25 acted from fruit and vegetable matrices with acetonitrile.

26 of 25 mM borate buffer containing 5.0% (v/v) acetonitrile.

27 s of the dyes were soluble in chloroform and acetonitrile.

28 form from PPh(3) using the bromo reagent in acetonitrile.

29 r of 30 kJ mol(-1) in dimethyl sulfoxide and acetonitrile.

30 rrolidinium/pyrrolidine buffers in anhydrous acetonitrile.

31 in non-aqueous solvents dichloromethane and acetonitrile.

32 ous workup of organic reactions performed in acetonitrile.

33 aved from carboxyl with 2-3% (v/v) of TFA in acetonitrile (0-10 degrees C), without affecting TIPS pr

34 ibrium constant K(eq) = 1.8 x 10(5) M(-1) in acetonitrile (0.1% 1,2,2,6,6-pentamethylpiperidine) and

35 as water (0.1% acetic acid) as solvent A and acetonitrile (0.1% acetic acid) as solvent B.

36 d on a C18 column (250x4.6mm, 5microm) using acetonitrile/0.1% trifluoroacetic acid as the mobile pha

37 nd o(LA)16-PTX degraded substantially in 1:1 acetonitrile:10 mM PBS, pH 7.4, at 37 degrees C, generat

38 croL of water, 125mg of ZnSO4, 1175microL of acetonitrile, 1200microL of methyl alcohol and 740microL

39 1140uL of water, 125mg of ZnSO(4), 1175uL of acetonitrile, 1200uL of methyl alcohol and 740uL of prop

40 analytes from homogenized fish meat (5 g) in acetonitrile (15 mL, 1% acetic acid) after three-phase p

41 ng of 10mM aqueous ammonium acetate:methanol:acetonitrile (50:30:20; v/v/v) with detection at 288nm.

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

43 und to be a mixture of ammonium acetate 2 mM/acetonitrile (60/40 ; v/v).

44 refluxing with sodium hydrogen carbonate in acetonitrile, 7-chloro-5-(4-fluorophenyl)-1,3-dihydro-2,

45 sing mobile phase consisting of (A) methanol:acetonitrile (8:2) - (B) 0.1% formic acid in a gradient

46 comprising water (with 0.5% formic acid) and acetonitrile (90:10, v/v) on Phenomenex C18 column (5.0

47 nt organic framework, COF-701, directly from acetonitrile, a cheap commodity solvent, by combining/te

48 Under the promotion of NIS/AgOTf in acetonitrile, a series of Kdo glycosides was synthesized

49 em of ultrapure water (0.1% formic acid) and acetonitrile, a temperature of 35 degrees C and a flow r

50 igated: water, linear and branched alcohols, acetonitrile, acetone, toluene, and ethyl acetate.

51 s through the modified QuEChERS technique in acetonitrile acidified with acetic acid (1%, v/v) and ci

52 The extraction was performed using acetonitrile acidified with formic acid (1%, v/v).

53 c, electron-donating, polar solvents., e.g., acetonitrile (ACN) and tetrahydrofuran (THF), a lambda(3

54 n acidic extraction solution (ES) containing acetonitrile (ACN) inside a fused-silica capillary that

55 where the LiF layer provides mobile ions in acetonitrile (ACN) vapor.

56 Scandium triflate (Sc(OTf)(3)) in acetonitrile (ACN) was found to promote the construction

57 e different PMMA isomers in tetrahydrofuran, acetonitrile (ACN), and dioxane reveals that isomers wit

58 ng methanol (MeOH)-, isopropanol (IPA)-, and acetonitrile (ACN)-based PCMF at various concentrations.

59 ergi 4mu Hydro-RP 80A column using methanol: acetonitrile (ACN): 0.1% phosphoric acid (60:10:30) as m

60 used in combination with formic acid and/or acetonitrile addition.

61 Later dilution of the extract with acetonitrile allowed adequate separation in the HILIC sy

62 The addition of different amounts of acetonitrile allows for switching between distinct react

63 he plastic explosive composite Semtex 1A) in acetonitrile (AN) is reported.

64 oval of (5.8 +/- 1.3) x 10(8) M(-1) s(-1) in acetonitrile and (1.2 +/- 0.5) x 10(8) M(-1) s(-1) in CD

65 solvents (with ylide bands at 1625 cm(-1) in acetonitrile and 1586 and 1635 cm(-1) in tetrahydrofuran

66 The optimum conditions were 1840muL of acetonitrile and 160muL of dichloromethane and the re-su

67 tion within 10min by using a mobile phase of acetonitrile and acetate buffer of pH 6.3 (1:9, v/v).

68 Microjets of water, acetonitrile and alcohols have previously been studied;

69 ding trial, salmon fillets were extracted in acetonitrile and analyzed by liquid chromatography with

70 phase was evaporated, reconstituted in 25muL acetonitrile and analyzed by reversed-phase liquid chrom

71 (+)) and approximately 1.2 V (vs Ag/AgCl) in acetonitrile and artificial saliva, respectively, and th

72 is validated using QuEChERS extraction with acetonitrile and CG-MS and LC-MS analysis.

73 ounds were extracted from chili samples with acetonitrile and cleaned by freeze-out.

74 carbonylnitrene reacts with solvents such as acetonitrile and cyclohexane, while t-butyloxycarbonylni

75 hermic reactions of fluorine (F) atoms in d3-acetonitrile and d2-dichloromethane involve efficient en

76 s (1-5) of quinone units was investigated in acetonitrile and dichloromethane solutions.

77 amples were extracted with 1% formic acid in acetonitrile and directly analysed with HPLC-MS/MS.

78 sting of ultrasonic assisted extraction with acetonitrile and dispersion with salts, followed by disp

79 ted using 20 mL of ethyl acetate and 5 mL of acetonitrile and finally the extract was concentrated to

80 with that of biotin[6]uril, also studied in acetonitrile and in aqueous buffer at neutral pH.

81 thanol and water was used for rinsing, while acetonitrile and n-hexane were used as elution solvents.

82 On the other hand, in aqueous acetonitrile and neat water, other polar products are al

83 ted in the presence of nucleophiles, such as acetonitrile and phosphines, via a five-coordinate inter

84 e and the re-suspended mixture consisting in acetonitrile and sodium phosphate buffer 10mmolL(-1) pH

85 The juice samples were extracted with acetonitrile and subsequent cleanup was done by dispersi

86 ed for thionations in other solvents such as acetonitrile and sulfolane.

87 s method, we measure PCET thermochemistry in acetonitrile and tetrahydrofuran for substrates with O-H

88 ne, where the samples were only treated with acetonitrile and then diluted with the micellar diluent

89 original tetragonal phase reported by Lis in acetonitrile and toluene.

90 nt elution with a mobile phase consisting of acetonitrile and trifluoroacetic acid 0.025% (w/v).

91 chers ("Q"; electron donors) are reported in acetonitrile and two ionic liquids, 1-ethyl-3-methylimid

92 of a C18 column and an elution gradient with acetonitrile and water as mobile phases (both with formi

93 in mixture of acetonitrile and water followed by rigorous azeotropic d

94 cluding transient absorption spectroscopy in acetonitrile and with nanocrystals suspended in water, a

95 ffee, 100 muL of dichloromethane, 400 muL of acetonitrile and without sodium chloride addition.

96 milk and involved the addition of methanol, acetonitrile, and Carrez I and II reagents, after which

97 , or nonactivated substrates like toluene or acetonitrile, and constitute an exceptionally clean and

98 , extraction with acidified ethyl acetate or acetonitrile, and dilution of the final extract with aci

99 N(2) atmosphere in homogeneous (cyclohexane, acetonitrile, and methanol) and micellar (SDS) solution

100 her hand, in homogeneous media (cyclohexane, acetonitrile, and methanol) the observed product distrib

101 imal volumes of processed urine, formic acid/acetonitrile, and supernatant spotted onto the target pl

102 tion of dCyd/5mdCyd in three solvents-water, acetonitrile, and tetrahydrofuran-by combining femtoseco

103 litate recovery, tissues were homogenized in acetonitrile, and the homogenate was frozen.

104 ed to characterize the influence of ethanol, acetonitrile, and trifluoroacetic acid on the stability

105 ntate fashion in addition to two monodentate acetonitriles, and the dicationic complex is complemente

106 followed by addition of reaction mixture to acetonitrile (anti-solvent) to form a slurry and further

107 per(II) from Cu(I) in the less polar solvent acetonitrile are crucial to the selective mono-C-H funct

108 y and configurationally inert, while the two acetonitriles are labile and allow asymmetric transition

109 ely sodium acetate, benzophenone, water, and acetonitrile, are employed in a simple reaction protocol

110 Using acetonitrile as a dopant, an increased sensitivity was o

111 This reaction utilizes acetonitrile as a single nitrogen source and involves th

112 uL of chloroform as extraction solvent using acetonitrile as dispersant.

113 y(styrene-divinylbenzene) column using 1-10% acetonitrile as eluent and follows the reverse order of

114 .01% of trifluoroacetic acid as eluent A and acetonitrile as eluent B at a flow rate of 0.2 mL min(-1

115 ltrapure water as washing solvent, 150 uL of acetonitrile as eluent, 100 uL of sample at pH 2.5, five

116 sidues were extracted from the samples using acetonitrile as extracting solvent and the extracts were

117 imethylphosphine oxide (TMPO) and deuterated acetonitrile as probe molecules, reveal a homogeneous di

118 Reactions are performed under air, in acetonitrile as solvent, and in the absence of base or l

119 atment is based on the use of water-miscible acetonitrile as the extractant and acetonitrile phase se

120 ficient sample preparation protocol with 80% acetonitrile as the extraction solvent was first establi

121 valuated, and the best results were 1.5ml of acetonitrile as the extraction solvent, manual stirring

122 ting with an aqueous MF precondensate, using acetonitrile as the macroporogen and a variety of alipha

123 omethanesulfonic acid in dichloromethane and acetonitrile at -78 degrees C in the presence of primary

124 by isothermal titration calorimetry (ITC) in acetonitrile at 20 degrees C.

125 the benzamido functionality, in pyridine or acetonitrile at both ester groups.

126 ransformations were efficiently performed in acetonitrile at room temperature by employing pyridinium

127 g blue fluorescence with 2% quantum yield in acetonitrile at room temperature.

128 g varying solubility of the ester/alcohol in acetonitrile at room temperature.

129 the ultrafast dynamics of diphenylcarbene in acetonitrile at room temperature.

130 atalyst [Ru(bpy)(3)](2+) from a homogeneous, acetonitrile-based reaction mixture.

131 The sample (5 g) was deproteinized with acetonitrile before an aliquot (I) was withdrawn, and th

132 y exhibits stronger recognition of anions in acetonitrile, but weaker binding in water as compared to

133 -hydride 2 effects the reductive coupling of acetonitrile by hydride transfer to yield [K(2){[U(OSi(O

134 -sensitized catalysis, using Ir(ppy)3 in wet acetonitrile (CD3CN) solution, led to the observation of

135 otochemical reduction of CO(2) to formate in acetonitrile (CH(3)CN).

136 Acetonitrile (CH3 CN) is the simplest and one of the mos

137 thod was developed using acidified water and acetonitrile combined with high column temperature (55 d

138 n/thermal desorption cycle, can increase the acetonitrile concentration by up to a factor 93, thus, l

139 ng form (i.e. different oxidation states) in acetonitrile containing 0.01 M KTFAB, had a very stable

140 UV-LC-MS(2) features a gradient run of acetonitrile containing a tunable percentage of photoini

141 y (HILIC) under all possible combinations of acetonitrile content, salt concentration, and mobile-pha

142 hough general trends for BGEs with different acetonitrile contents could be simulated, these simulati

143 fused indeno-furanones, and use of tetrakis(acetonitrile)copper(I) provides indeno-furanones in the

144 With tetrakis(acetonitrile)copper(I) tetrafluoroborate as the catalyst

145 dition of H(2)O to the dioxonium cation 9 in acetonitrile- d(3) results in near-quantitative producti

146 rboxylation of cyclohexanecarboxylic acid in acetonitrile-d(3) over picosecond to millisecond timesca

147 In contrast, the content of indole-3-acetonitrile decreased rapidly during fermentation from

148 ) donating the proton to a gold electrode in acetonitrile demonstrate significantly different Tafel s

149 ly correlates with the induction of indole-3-acetonitrile-dependent auxin biosynthesis.

150 pared in one pot from adducts obtained using acetonitrile-derived carbanions.

151 re, the behavior and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl me

152 chloroform (extracting solvent), 1500 uL of acetonitrile (disperser solvent) and 1500 mg of NaCl (io

153 ether, THF, ethyl acetate, acetone, alcohol, acetonitrile, DMF, and DMSO, identify complex solvent sy

154 525 mV) are reversibly produced by localized acetonitrile doping under ambient conditions.

155 In acetonitrile electrolyte, triethylammonium (TEAH(+)) dis

156 are highly active for CO2 reduction to CO in acetonitrile electrolyte.

157 ogether with the use of 0.1% phosphoric acid/acetonitrile eluents in both dimensions.

158 /w was achieved by RP-HPLC-DAD using aqueous acetonitrile elution solvent (pH=2.8).

159 The increase in the content of indole-3-acetonitrile, especially considerable within the first 2

160 The acetonitrile extract was analyzed by GC-MS/MS.

161 gnesium sulfate and sodium chloride, 1 mL of acetonitrile extract was pipetted into a 2-mL centrifuge

162 rb fat and fatty acid residue present in the acetonitrile extract.

163 Acetate buffered acetonitrile extraction with Z-Sep+ and PSA dispersive-S

164 is based on liquid-liquid partitioning with acetonitrile followed by dispersive solid phase extracti

165 is based on liquid-liquid partitioning with acetonitrile followed by dispersive solid phase extracti

166 Extraction was performed with acidified acetonitrile, followed by a cleanup step with sodium ace

167 )-fold decrease in the HAT rate constants in acetonitrile following addition of 0.1 M HClO4.

168 on transfer (PCET) reactions were studied in acetonitrile for a Photosystem II (PSII)-inspired [Ru(bp

169 The method employed acetonitrile for extraction followed by clean-up with EM

170 using 500muL of acetone for Cd and 700muL of acetonitrile for Pb as dispersive solvents, 60muL of CCl

171 e tetraethylphosphonium tetrafluoroborate in acetonitrile; for positive polarization charging proceed

172 Ultrasonic extraction of binding gels in acetonitrile gave good and consistent recoveries for all

173 ptides under mild acidic conditions using an acetonitrile gradient.

174 e is a superbasic compound, with a pK(aH) in acetonitrile greater than that of 1,8-bis(dimethylaminon

175 CP derivatives with solubilities of >1 M in acetonitrile in all oxidation states.

176 Dilution of propionic anhydride 1:4 (v/v) in acetonitrile in combination with 50 muL of plasma result

177 chanism, are largely suppressed at 20-30% of acetonitrile in the eluent.

178 reviously unrecognized transformation in wet acetonitrile in the presence of air to yield a new Blatt

179 se in alcohol reduces the amount of residual acetonitrile in the solid.

180 d sieved to 250 mum, with 50 mL of 40% (v/v) acetonitrile in water at a temperature of 72 +/- 3 degre

181 us iron bromide in a mixture of pyridine and acetonitrile, in the presence of an organic amine, resul

182 NMR investigations in acetonitrile indicated the coexistence of both helix typ

183 d effect on GLS breakdown products (indole-3-acetonitrile, indole-3-carbinol, ascorbigen and 3,3'-dii

184 e the donor is bound too strongly or because acetonitrile inserts into a W horizontal lineC bond.

185 ometric incorporation of atmospheric N2 into acetonitrile is presented.

186 tions a rationale for the positive impact of acetonitrile is provided.

187 It shows that acetonitrile is the most effective solvent for obtaining

188 Acetonitrile is trimerized to generate protonated 2,4,6-

189 If acetonitrile is used as deposition solvent, TATP tends t

190 The acetonitrile layer (II) was recovered and the extracts c

191 An aliquot (1.5 mL) of the acetonitrile layer was aspirated and subjected to two-st

192 n transfer to pyridine in the order: water < acetonitrile < 1,4 - dioxane.

193 ON(CO) = 28 +/- 4 and Phi(CO) = 7 +/- 1%) in acetonitrile (MeCN) with 1,3-dimethyl-2-phenyl-2,3-dihyd

194 under a nitrogen atmosphere in cyclohexane, acetonitrile (MeCN), and methanol (MeOH) was investigate

195 f pH and background electrolyte, BGE (borax, acetonitrile, methanol and SDS concentrations), was stud

196 The extraction was accomplished using acetonitrile, methanol, water, ammonia, 50:40:9:1 (v/v/v

197 ge of 500-4000 cm(-1) for cyclohexane, DMSO, acetonitrile, methanol, water, benzene, and toluene usin

198 ane-methanol (3:2:1, v/v/v) and diluted with acetonitrile-methanol (v/v; 80:20) before the method was

199 HPLC method using a mobile phase containing acetonitrile:methanol:2-propanol in the ratio of 85:15:3

200 selection of quenching solvent (e.g., acidic acetonitrile:methanol:water) can mitigate such problems.

201 and TON of 54.4 has been obtained in a water/acetonitrile mixture.

202 n and samples eluted with a gradient acetate-acetonitrile mobile phase.

203 tes a six-coordinate Ni(IV) complex, with an acetonitrile molecule bound to Ni.

204 rescence lifetimes in polar solvents such as acetonitrile, MV(2+) has a short fluorescence lifetime i

205 cted in other organic solvents, for example, acetonitrile, N,N-dimethylformamide, or acetone, which i

206 4-nitrobenzenesulfenyl chloride in refluxing acetonitrile, N-propargylic beta-enaminones produced alp

207 A key finding is that the presence of acetonitrile obviates the need for using excess amounts

208 hiles) have been measured photometrically in acetonitrile or DMSO solution at 20 degrees C.

209 The acetonitrile or pivalonitrile Mo(NR)(CHR')(OR'')(Cl)(L)

210 ition metal hydrides have been determined in acetonitrile or water.

211 atment of a range of (het)aryl/unsubstituted acetonitriles or acetates with (het)aryl dithioesters in

212 The rhodium(III) catalyst tris(acetonitrile)pentamethylcyclopentadienylrhodium(III) hex

213 y thin film, which displays an unprecedented acetonitrile permeance of 339 L m(-2) h(-1) bar(-1).

214 -miscible acetonitrile as the extractant and acetonitrile phase separation under high-salt conditions

215 Samples were extracted with a mixture of acetonitrile-phosphoric acid and the extracts were defat

216 long-lived (1.3 ns in n-hexane and 3.4 ns in acetonitrile) polar S1.

217 olvents, including 2-propanol, methanol, and acetonitrile, pure or as mixture with dimethyl sulfoxide

218 The pKa values determined in acetonitrile range from 9.3 to 17.7 and show a linear co

219 The amount of acetonitrile required was found to have an optimal value

220 d turn-on response toward Mn(2+) in DMSO and acetonitrile, respectively.

221 Any amount of acetonitrile resulted in extremely slow transformations.

222 s titration experiments with eight anions in acetonitrile revealed high affinity for H(2)AsO(4)(-) (l

223 f the solvent used (e.g., dichloromethane vs acetonitrile) significantly affected the course of the r

224 gents, and reacts in the title reaction with acetonitrile, sodium chloride, and sodium methanesulfona

225 increase in the amounts of aqueous methanol-acetonitrile-soluble apiose but did not result in discer

226 hotolysis of phtaloyl peroxide (2) in liquid acetonitrile solution at room temperature has been inves

227 photocatalyst, and ascorbic acid in a water-acetonitrile solution debenzylates a variety of aryl N-h

228 In acetonitrile solution kinh varied with acylation: (0.9-2

229 Measurements carried out in acetonitrile solution revealed the formation of a transi

230 ons, have been determined photometrically in acetonitrile solution using CH acids as indicators.

231 , was found to be a potent photoreductant in acetonitrile solution with an estimated excited-state re

232 hat can act as a homogeneous ORR catalyst in acetonitrile solution.

233 = 7.3 compared to the molecular catalyst in acetonitrile solution.

234 nerated Ru(III)-tris-bipyridine oxidants, in acetonitrile solution.

235 etermined by resonance Raman spectroscopy in acetonitrile solutions are on average 9 cm(-1) red-shift

236 The titration of iodide into acetonitrile solutions of BiI3 resulted in the formation

237 tance, are able to fit the data collected in acetonitrile solutions reasonably well, but not the data

238 s have been performed in aqueous/ethanol (or acetonitrile) solutions by employing common graphite ele

239 lectronic conductivity of the desolvated and acetonitrile-solvated microporous framework Cu[Ni(pdt)(2

240 the coordination of the iridium atoms by the acetonitrile solvent and demonstrate the viability of us

241 condary, and benzylic alcohols by 1 and 5 in acetonitrile solvent at room temperature have been deter

242 copper(II) chloride and cesium carbonate in acetonitrile solvent is reported.

243 rements also indicate that several layers of acetonitrile solvent molecules are immobilized at the in

244 he reaction of Ar(F)-Bpin with Pd(OAc)(2) in acetonitrile solvent, with no homocoupling observed.

245 d selective detection of Fe(3+) and Cr(3+)in acetonitrile solvent.

246 od correlation between basicities in THF and acetonitrile spanning 25 orders of magnitude gives acces

247 The new cluster is made by a reaction of an acetonitrile suspension of K4Ge9 with (i)Pr3SnCl that ge

248 In acetonitrile, TEAH(+) also displays a much larger transf

249 cling at +1.33 V vs ferrocene/ferrocenium in acetonitrile/tetrabutylammonium hexafluorophosphate.

250 In acetonitrile, the hydricity of metal hydrides spans a ra

251 After drying and then redissolving in acetonitrile, the metabolite extract is labeled using a

252 After template retrieval with acetonitrile, these imprinted micelles were immobilized

253 with 1 mol % Cu/Au (3:1)-17 and 30% H2O2 in acetonitrile to afford chiral ketones in very good to ex

254 ormylphenylboronic acid, and chiral diols in acetonitrile to form fluorescent diastereomeric complexe

255 upon photoirradiation with visible light in acetonitrile to generate a thiolate-ligated, nonheme iro

256 are stabilized by [3 + 2] cycloaddition with acetonitrile to give 1,2,4-oxadiazoles.

257 d highly diastereoselective addition of aryl acetonitrile to N-protected isatin under mild conditions

258 e determining yet reversible ring opening by acetonitrile to the corresponding nitrilium cation 10 (c

259 reaction of dansyl chloride with aniline, in acetonitrile, to produce dansyl aniline.

260 ode and 1 M Mg(ClO(4))(2) electrolyte within acetonitrile, together with Mg (x)Mo(6)S(8) ( x ~ 2) as

261 The elution of rapeseed extracts with water/acetonitrile/trifluoroacetic acid (45/55/0.1% v/v) durin

262 uinoline N-oxides and aryldiazonium salts in acetonitrile under microwave irradiation is reported.

263 On average, glycosylation yields a 0.79% acetonitrile unit decrease in retention, compared with t

264 etonitrile units), and trisialylated (+1.94% acetonitrile units) glycans.

265 he hydrophobicity index, measured in percent acetonitrile units) used for modeling were measured for

266 7% acetonitrile units), disialylated (+0.61% acetonitrile units), and trisialylated (+1.94% acetonitr

267 acetonitrile units), monosialylated (-0.47% acetonitrile units), disialylated (+0.61% acetonitrile u

268 are drastically different for asialo (-1.37% acetonitrile units), monosialylated (-0.47% acetonitrile

269 e carbonyl stretching energy (1821 cm(-1) in acetonitrile vs 1777 cm(-1) for BTP) and bond length alt

270 substitution by visible light irradiation in acetonitrile was possible for three of the five complexe

271 asymmetrically substituted phenyl azides in acetonitrile was studied.

272 Solid-liquid extraction with acetonitrile was used for the analysis in fruits, the ex

273 d of NH(4)Ac, 1.0 mM, pH 4.0, in 70.0% (v/v) acetonitrile was used for the IEF of histidine.

274 overs of H2 upon photolysis of a solution of acetonitrile, water, triflic acid, and N,N-dimethylanili

275 d by extraction with LESA using a chloroform-acetonitrile-water (49:49:2) mixture and direct HRMS det

276 In an acetonitrile-water mixture, at neutral pH, electrochemic

277 traction of metabolites was carried out with acetonitrile-water-formic acid (80:19:1, v/v/v).

278 Samples were extracted with a mixture of acetonitrile/water followed by salt-induced partitioning

279 extraction techniques (such as cold methanol/acetonitrile/water, hot water, and boiling ethanol/water

280 The method was based on extraction with acetonitrile/water/formic acid, ten-fold dilution and an

281 etate; D, methanol: water (1:1, v/v); and E, acetonitrile: water (1:1, v/v).

282 at the extraction solvents with isopropanol: acetonitrile: water (3:2:2 ratio) and 80% methanol were

283 Acetonitrile: water (75:25, v/v) is proposed as a mobile

284 4.6mm, 5micro) using mobile phase consist of acetonitrile: water (90:10, v/v) at flow rate 1.0mL/min

285 dition for the liquid desorption was 150 muL acetonitrile:water (50:50 v/v) and desorption time of 20

286 les were extracted using 0.1% formic acid in acetonitrile:water (8:2) with the addition of EDTA and c

287 Extraction efficiency was evaluated by using acetonitrile:water and ethanol:water mixtures.

288 ontaining 12.5mgmL(-1) of ferulic acid in an acetonitrile:water:formic acid 50:33:17 v/v/v mixture.

289 thylstannane by 1,2,4,5-tetracyanobenzene in acetonitrile were found to depend on the codonor used to

290 ons with several hydride acceptors/donors in acetonitrile, were determined.

291 3]X (X = Cl or Br) with NaOCl in methanol or acetonitrile (where L = 1,4,7-trimethyl-1,4,7-triazacycl

292 ls in organic solvents such as chloroform or acetonitrile, which can then be analyzed by a number of

293 supported very high (pKa > 40) basicities in acetonitrile, which cannot be directly measured.

294 using tris(4-methoxyphenyl)phosphine (L3) in acetonitrile, while branched amides were obtained in hig

295 ss at 77 K as well as at room temperature in acetonitrile with 1.8 x 10(-4)% quantum yield (ddpd = N,

296 etones using calcium hypochlorite in aqueous acetonitrile with acetic acid as activator.

297 arison of experimental data obtained in neat acetonitrile with data from acidic solutions suggests th

298 mpounds was performed using C18 and methanol-acetonitrile with gradient elution system.

299 The mobile phase consisted of water and acetonitrile, with a flow rate of 0.5mL/min in gradient

300 ability to electrochemical cycling at 1 M in acetonitrile without a supporting electrolyte in a symme