ライフサイエンスコーパス: MeOH

1 MeOH and THF permeance increased when MOFs were embedded

2 MeOH displayed excellent chromatographic performance (se

3 d bound DMF molecules for methanol to give 1-MeOH, complete desolvation of the framework at 180 degre

4 aration (5min separation using acidified 10% MeOH isocratic flow in a CORTECS C18 column) to allow un

5 queous compatibility was demonstrated in 10% MeOH-H(2)O solution.

6 In 10% MeOH/H(2)O at pH 1 or 11 or in pure MeOH, assembly is dr

7 In 10% MeOH/H(2)O, the tetraphenylporphyrin (TPP) and 1,4,5,8-n

8 l3, benzene) and even in the presence of 10% MeOH.

9 ween these two groups than both 50% and 100% MeOH.

10 of some of the norbornene, but even in 100% MeOH, the norbornyl chloride products of ion pair return

11 r 1000W, extraction time 20min, solvent 100% MeOH, and solvent-to-sample ratio 10:1.

12 ed in MeOH/H2O ratios ranging from 0 to 100% MeOH and analyzed with untargeted reversed phase LC-MS s

13 ile, reacts in a similar fashion (e.g., 16 + MeOH --> 43).

14 theoretical predictions, and by employing 2% MeOH/toluene as solvent, the Heck-Matsuda reaction provi

15 stalline solid solutions (M,M')(NPBA)2(NO3)2(MeOH)2 (M, M' = Co2+, Ni2+, or Zn2+, 13-16), where mixtu

16 Molecule Magnet (SMM) [MnIII6O2(sao)6(O2CH)2(MeOH) 4] (1) (where sao2- is the dianion of salicylaldox

17 HCO2- in the molecule [MnIII6O2(sao)6(O2CH)2(MeOH)4] (1), with Et-sao2- (Et-saoH2 = 2-hydroxypropioph

18 Using small amounts of water in CO(2)/MeOH is known to be beneficial in chiral subcritical/sup

19 ciency in the presence of water in the CO(2)/MeOH system.

20 e demonstrate important aspects of the CO(2)/MeOH/H(2)O system on nine chiral stationary phases with

21 Ester hydrolysis with Ba(OH)(2)/MeOH gave the target prodrug 2a which is a substrate for

22 (THF = tetrahydrofuran) solvent mixtures, 2-MeOH is characterized by a LMCT band at lambda(max) = 51

23 pon addition of HO(2) to 1 and converts to 2-MeOH at a rate of 65(1) s(-1), which is consistent with

24 ing above -50 degrees C, 3 is converted to 2-MeOH.

25 (2a) and (Li-OPO)PdMe(L) (L = pyridine (2b); MeOH (2d); 4-(5-nonyl)pyridine) (py', 3)).

26 organic framework (MOF), [Bi(BTC)(H2O)].2H2O.MeOH denoted CAU-17, was synthesized and found to have a

27 action from soil with 90/10 volume % CHCl(3)/MeOH at 110-120 degrees C.

28 ns in urea, MD-derived structures in CHCl(3)/MeOH reveal multiple determinants of membrane interactio

29 rising urea and chloroform/methanol (CHCl(3)/MeOH) mixture.

30 In CHCl(3)/MeOH, viscumin A is in effect turned "inside out".

31 Direct ammonolysis (NH(3)/MeOH) of such intermediates or benzylation of the imidaz

32 (5), CF3COCHCOCF3(-) (6), and solvent = 0.5 MeOH (4), 2 CH2Cl2 (5).

33 M Tris, pH 8, sheath liquid containing 50/50 MeOH/10 mM HCO(2)NH(4) delivered at 5 microL/min, spray

34 used reconstitution solvent mixture of 50/50 MeOH/H2O, our results indicate that the small fraction o

35 PSPEP sorbent and elution with 100muL of 50% MeOH) were combined with a fast UHPLC separation (5min s

36 The phenolic profile of 80% MeOH extracts of the stinging nettle (Urtica dioica L.)

37 ggregate to give ((Na(5)O) subset [Ni(L)](9)(MeOH)(3))(BF(4))(2).OH.CH(3)OH, 7.

38 All peptides were more structured in 90% MeOH than in aqueous buffers.

39 by a nucleophilic attack on the nitrogen, a MeOH-assisted [1,3]-proton transfer, and subsequent loss

40 -H of the dihydropyridyl ring and the O of a MeOH and also via an N...H-O interaction between the N c

41 Mechanistic investigations of a MeOH-induced kinetic epoxide-opening spirocyclization of

42 uit samples were extracted with an acidified MeOH mixture assisted by ultrasound.

43 The epsilon in acidified MeOH and buffer pH 1 ranged between ~16,000-30,000 and ~

44 is to obtain analyte-laden eluates with ACN/MeOH (90:10, v/v) in unsupervised mode for direct inject

45 ical extract, using 80% organic solvent (ACN:MeOH:H2O 2:2:1).

46 In addition, MeOH-based nanoLC-MS/MS yielded superior results for the

47 Although MeOH also affects the magnitude of the reaction rates an

48 ves the fitting for TFE, MeCN/H(2)O 2:1, and MeOH but at the expense of that for tertiary alkanols.

49 In TFE, MeCN/H(2)O 2:1, and MeOH, the measured k(H) values were lower than expected

50 In the solvents investigated (CH(2)Cl(2) and MeOH), the most favorable mechanism is addition of perox

51 seful as food additives, such as MeOH-2, and MeOH-3, completely devoid of hepatotoxic components.

52 ea-mediated tetramer dissociation (pH 7) and MeOH-facilitated fibril formation similar to those of WT

53 nd thiophenes in combination with amines and MeOH as a C1 source.

54 strating why the presence of excess base and MeOH or H2O is required for efficient and enantioselecti

55 ed pyrrolidines using 4 N HCl in dioxane and MeOH gave the corresponding enantiomers of 2-substituted

56 The EtOAc and MeOH extracts of P. guajava showed 56.4% (COX-2) and 44.

57 The EtOAc and MeOH extracts presented higher inhibitory activity with

58 Furan and MeOH could also be employed as external nucleophiles in

59 Finally, interaction of 1+ with H2O and MeOH and 2-Me+ with H2O was also examined.

60 equently used solvent systems, ACN/H(2)O and MeOH/H(2)O, revealed that the antimony(III)-tartrate dia

61 in the solution of 10 in deuterium oxide and MeOH-d4.

62 ICl) in CH(2)Cl(2), CH(2)Cl(2)/pyridine, and MeOH are described.

63 Starting with Wat1 removed and MeOH hydrogen bonded to Asp-297-CO(2)(-), we find that M

64 the Umemoto reagent as the CF(3) source and MeOH as the reductant is disclosed.

65 d k(D)/k(T) values, is the same in water and MeOH/water mixtures, implicating similar trajectories fo

66 0 degrees C methylation procedure (anhydrous MeOH/acetyl chloride, 25:4, v/v) was performed.

67 tion species react with nucleophiles such as MeOH by clean second-order kinetics with rate constants

68 pon the addition of a proton source, such as MeOH, or by running the reaction under a hydrogen atmosp

69 extracts, useful as food additives, such as MeOH-2, and MeOH-3, completely devoid of hepatotoxic com

70 actable using more polar co-solvents such as MeOH.

71 For cpn10, both MeOH and TFE additions govern initial unfolding; however

72 e than the 6-fluoropurine compound with both MeOH/DBU/MeCN and iPentSH/DBU/MeCN and was more reactive

73 d significantly with 1 and BrCl in MeOH, but MeOH had little affect on the other reactions.

74 Likewise, complex 2 can replace acetone by MeOH and H2O to form [Fe(bpp)(H2L)](ClO4)2.1.25MeOH.0.5H

75 axane and its dumbbell precursor in a CH2Cl2/MeOH (3:2) mixed solvent and liquified by adding the oxi

76 te constant for reaction of the Cp2Ti(III)Cl-MeOH at ambient temperature was 7.5 x 10(4) M(-1) s(-1).

77 high yields (53-99%) under mild conditions (MeOH as the solvent, 80-100 degrees C, 1-24 h).

78 estigate how the adsorption of the cosolvent MeOH changes with pressure and temperature and how this

79 MeOH vapor affords [Au(im(CH(2)py)(2))(2)(Cu(MeOH))(2)](PF(6))(3) (2), which produces green luminesce

80 times of about 4.7 min for (1)H spins in [D4]MeOH are seen in this system.

81 adoxical previous observation that decreased MeOH concentration leads to increased competing intermol

82 DMF, followed by recrystallization from DMF/MeOH, yields (Et(4)N)(5)[Mo(2)(CN)(11)] x 2DMF x 2MeOH (

83 m of methylcobalamin (Me-Cbl) in a mixed DMF/MeOH solvent in 0.2 M tetrabutylammonium fluoroborate el

84 l/mol in the 40:60 and 50:50 mixtures of DMF/MeOH, respectively.

85 om 0 to -80 degrees C in 40:60 and 50:50 DMF:MeOH ratios.

86 dicated that weaker donors (THF, MeCN, DMSO, MeOH, and even H2O) likewise promote this pathway, at ra

87 ylamines (e.g., H(2)NOMe and MeHNOMe) in dry MeOH at room temperature give three different types of p

88 lly investigate the effects of simple (i.e., MeOH and EtOH) and fluorinated (i.e., trifluoroethanol,

89 ometrically rigidified by H-bonding to eight MeOH molecules and encapsulation of two benzene guests.

90 ontains a sacrificial electron donor, either MeOH or triethanolamine (TEOA), and titanium dioxide (Ti

91 re dissolved in MeOH and diluted with either MeOH (0.1% HCl) or buffers to obtain final concentration

92 e upon preparative TLC purification (eluent: MeOH/CHCl(3) saturated with NH(3)) and equilibrium studi

93 HPCCC separation under use of heptane-EtOAc-MeOH-H2O mixtures in normal-phase and reverse phase mode

94 nt systems viz. toluene/EtOAC/MeOH and EtOAC/MeOH, respectively were used for optimum separation and

95 ent systems viz.toluene/EtOAC/MeOH and EtOAC/MeOH, respectively were used for optimum separation and

96 s and two solvent systems viz. toluene/EtOAC/MeOH and EtOAC/MeOH, respectively were used for optimum

97 es and two solvent systems viz.toluene/EtOAC/MeOH and EtOAC/MeOH, respectively were used for optimum

98 roactive probe, 1,1'-ferrocenedimethanol, Fc(MeOH)2, were prepared.

99 Transport of Fc(MeOH)2 in both swollen and collapsed gels was studied us

100 The diffusion coefficient of Fc(MeOH)2 in collapsed gels was approximately 2 orders of m

101 d to measure the diffusion coefficient of Fc(MeOH)2 in gels under a wide range of experimental condit

102 t for 3.0% NIPA gel, the concentration of Fc(MeOH)2 in the collapsed phase was approximately 6 times

103 utoff of less than 232 and 295 g.mol(-1) for MeOH and THF, respectively) in all membranes.

104 d from 1.7 to 11.1 L.m(-2).h(-1).bar(-1) for MeOH/PS and THF/PS, respectively.

105 cs (QM/MM) calculations, the free energy for MeOH reduction of o-PQQ when MeOH is hydrogen bonded to

106 In addition, we found MeOH/ACN/Acetone (1:1:1, v/v/v) as extraction cocktail c

107 I(2) sorption, both from gas phase and from MeOH solution, into CTH-7 were studied by time of flight

108 Hydrogen-bonding from MeOH is critical for the hyponitrite complex formation a

109 te constant (kH) were measured on going from MeOH and TFE to isooctane (kH(isooctane)/kH(MeOH) = 5-12

110 Full MeOH reforming is achieved through the corresponding ste

111 ty of traditional Cu/ZrO(2) catalysts (159 g(MeOH)kg(cat)(-1)h(-1)).

112 ss-specific methanol formation rate of 524 g(MeOH)kg(cat)(-1)h(-1) at 220 degrees C, 3.3 times higher

113 DFT studies (B3LYP-D3/6-311++G**/MeOH) on cyclization mechanisms involving the 2-hydroxya

114 Whereas alternative protic solvents (e.g., MeOH vs HFIP) provide products of the conventional 3,6-c

115 Use of a proton source (e.g., MeOH) is not required; accordingly, synthetically versat

116 micarceplex in polar, protic solvents (e.g., MeOH).

117 SDS samples (via direct dilution with GnHCl/MeOH solution) is necessary to ensure accurate quantitat

118 olvent, e.g., hexane > toluene > DCM > THF > MeOH > H2O, an effect also noted by emission variation i

119 SA, in tert-butylbenzene (t-BuPh) and in H2O/MeOH afforded, with CF3COOH, k(d) 28-fold larger in H2O/

120 ed, with CF3COOH, k(d) 28-fold larger in H2O/MeOH than in t-BuPh, whereas it was only 4-fold larger w

121 ty, we developed HPLC and UHPLC methods (H2O/MeOH/MeCN/HCOOH) which we applied and validated by analy

122 N-alkyl nitroanilines using Zn-AcOH and HCl/MeOH, respectively.

123 haracterized with low O/C < 0.5; and hexane, MeOH, ACN, and H2O solvents increase the number and type

124 where A(-) = H2PO4(-) and CF3CO2(-) and HX = MeOH, PhOH, and Me2NOH or Et2NOH) are examined by photoe

125 (MeOH/NaOH) and methanol/ammonium hydroxide (MeOH/NH4OH)].

126 traction methods [methanol/sodium hydroxide (MeOH/NaOH) and methanol/ammonium hydroxide (MeOH/NH4OH)]

127 In MeOH, lysophosphatidic acid (LPA), a biomarker for sever

128 In MeOH/MeCN, up to 28% of exo-2-norbornyl methyl ether for

129 Upon reaction of 1 with KO(2) in MeOH at -90 degrees C, an intermediate (3) is formed, wh

130 epared halogenating agent BnNMe(3).ICl(2) in MeOH-CH(2)Cl(2).

131 oxidation of PhSH to PhSSPh with H(2)O(2) in MeOH.

132 ct with calcium hypochlorite (Ca(OCl)(2)) in MeOH to give respectively dimer-type ketals 2-(2',4',6'-

133 When using 3 in MeOH, a change in the product formation is observed, the

134 deprotection conditions [0.05 M K(2)CO(3) in MeOH, room temperature, 24 h and MeNH(2) (approximately

135 Fragmentations of 5 and 6 in MeOH afford chlorides 3g and 4g as well as the correspon

136 eoside and its reaction with an arylamine in MeOH in the absence of added metal catalyst.

137 r increased significantly with 1 and BrCl in MeOH, but MeOH had little affect on the other reactions.

138 le beta-formyl ester 21, whereas cleavage in MeOH followed by reduction with thiourea led to hemiacet

139 Ph2P-(C6H4) (2-F) with a binding constant in MeOH exceeding that of 1-Mes2B-4-MePh2P-(C6H4) ([1]+) by

140 Pigments were dissolved in MeOH and diluted with either MeOH (0.1% HCl) or buffers

141 peared better in samples reduced with DTT in MeOH.

142 W), time (5-15min), solvent (10-90% EtOAc in MeOH) and solvent-to-sample ratio (10:1 to 20:1).

143 meters such as solvent composition (EtOAc in MeOH), extraction temperature, pressure, flushing, stati

144 thyl derivatives by treatment with NH(4)F in MeOH.

145 ng D-aldopentoses by reaction with NH3(g) in MeOH solvent, isolated in solid form, and characterized

146 wing the Ugi reaction, treatment with HCl in MeOH achieves deprotection of the isopropylidene group a

147 Treatment of compound 34 with HCl in MeOH effected spiro-lactal formation and provided (+/-)-

148 of NEM compared with samples homogenized in MeOH containing NEM.

149 Thermal isomerization of the latter in MeOH occurred via a four-centered activated complex, and

150 guanidine to a 6-methylhexahydroindenone in MeOH at 85 degrees C afforded 7-epineoptilocaulin.

151 ubsequent dihydroxylation, using OsO4/NMO in MeOH conditions, resulted in an exceedingly diastereo- a

152 generic modifier (0.2% NH(4)OH, 5% H(2)O in MeOH) that enables the widespread transition of SFC to d

153 techol moieties, and inverse second order in MeOH concentration.

154 s undergo cyclization to 2-oxazolidinones in MeOH.

155 In the first step, anodic oxidation in MeOH using a repurposed power source provides a convenie

156 SO2, CF3SO2) react with hydrogen peroxide in MeOH, THF, MeCN or AcOH to form the corresponding C-N co

157 c) = 1.9 h, rt), and with a moderate rate in MeOH (t1/2(rac) = 30.5 h, rt).

158 sogeny Broth medium samples reconstituted in MeOH/H2O ratios ranging from 0 to 100% MeOH and analyzed

159 NPs suspended in MeOH under constant illumination produce valence-band ho

160 Toward 3,6-diphenyl-s-tetrazine in MeOH at 25 degrees C, the strained derivative is 160 tim

161 Toward 3,6-dipyridyl-s-tetrazine in MeOH at 25 degrees C, the strained derivative is 19 and

162 f M(2+), TPyA, H(2)DBQ, and triethylamine in MeOH solution.

163 4)(2).6H2O, TPyA, H2CA, and triethylamine in MeOH solution.

164 asic than a-PhobPH by about 2 pK(a) units in MeOH.

165 malononitriles 13 in 84-92% yields, while in MeOH the (Z)-2-[2-phenyl-4-(arylimino)-1H-imidazol-5(4H)

166 nding thiophenes 6 in good to high yields in MeOH as the solvent at 50-100 degrees C in the presence

167 -7-one core with good to excellent yields in MeOH.

168 MeOH and TFE to isooctane (kH(isooctane)/kH(MeOH) = 5-12; kH(isooctane)/kH(TFE) > 80).

169 iables quantity of sample (g), volume of KOH/MeOH (mL) and ultrasound time (s) were investigated in t

170 xime or 2-hydroxybenzaldeyhyde oxime and L = MeOH, EtOH) via the use of derivatized oxime ligands and

171 icities of [Rh2(micro-O2CCH3)2(eta1-O2CCH3)L(MeOH)]+ (L=dppz, 7; L=dppn, 8) relative to [Rh2(micro-O2

172 l sites of Ni(II) to give the complex [Ni(L)(MeOH)(2)] in which a Ni(II) center is bound in an octahe

173 n be achieved using weak proton sources like MeOH and PhOH, the facile heterolytic cleavage of the C-

174 Reaction of 1 with either liquid MeOH or MeOH vapor affords [Au(im(CH(2)py)(2))(2)(Cu(MeO

175 Maximum yield was obtained at ca.0.2 M MeOH.

176 sensitivity and shorter gradient times make MeOH an excellent organic modifier for the use in nanoLC

177 Deacetylation of 4b and 4e with MeONa/MeOH gave beta-glucuronides 5b and 5e.

178 phenolic compounds with O/C > 0.5; methanol (MeOH) has higher selectivity toward compounds characteri

179 ir spectral behaviors in acidified methanol (MeOH) and buffers pH 1-9.

180 TBP), in buffer solvent with added methanol (MeOH), 2-propanol (2-PrOH), and dimethyl sulfoxide (DMSO

181 amines to formate, formamides, and methanol (MeOH) is a promising approach to streamlining carbon cap

182 lohexane, acetonitrile (MeCN), and methanol (MeOH) was investigated under steady-state conditions.

183 such as trifluoroethanol (TFE) and methanol (MeOH), indicating a lower propensity of the oxidized pro

184 reductively couples NO(g) at RT in methanol (MeOH), giving a structurally characterized hyponitrito-d

185 tion was evaluated on the basis of methanol (MeOH) and tetrahydrofuran (THF) permeances and rejection

186 rt, we demonstrate that the use of methanol (MeOH) as the organic modifier improves the detection lim

187 obile phases, aqueous solutions of methanol (MeOH/H(2)O = 40/60 and 30/70, v/v) and aqueous solutions

188 aride mixtures were compared using methanol (MeOH)-, isopropanol (IPA)-, and acetonitrile (ACN)-based

189 ies into chloroform (CHCl(3)) with methanol (MeOH) as cosolvent, consistent with MeOH competitively d

190 es of the ethyl acetate (EtOAc), methanolic (MeOH) and aqueous extracts from the Micromeria nervosa a

191 the used 2-MeTHF, scale-up, ratio of 2-MeTHF/MeOH, utilized hydroxide, temperature, and reaction time

192 Mg/MeOH is significantly more reactive than Me(2)S or PPh(3

193 nyl, UO2Ac(H2O)n(MeOH)m(+), and UO2Ac2(H2O)n(MeOH)(m)H(+) (n = 1, 2, 3,...; m = 1, 2, 3,...).

194 : inorganic (nonligated) uranyl, UO2Ac(H2O)n(MeOH)m(+), and UO2Ac2(H2O)n(MeOH)(m)H(+) (n = 1, 2, 3,..

195 ion, and a unique ester reduction with NaBH4-MeOH catalyzed by NaB(OAc)3H that not only achieves exce

196 o form 100% of the 9-cation, then with NaOMe-MeOH, provided 29% of re-formed substrate (configuration

197 cycloadducts has been demonstrated by an NBS-MeOH mediated stereospecific efficient access to fully s

198 3 via a Dimroth rearrangement in either neat MeOH or in DCM with DBU.

199 its porfiromycin activation and nucleophile (MeOH, DNA) adduction.

200 itation with an appropriate solvent (Et(2)O, MeOH, or EtOAc), followed by filtration through a SPE pr

201 2-electron transfer and extrusion of H(2)O, MeOH, or MeOMe to give [Os(II)-N(2)].

202 ic acid-base titrations carried out in H(2)O/MeOH (9:1 vol.) afford pK(R+) values of 7.3(+/-0.07) for

203 ion, fluoride titration experiments in H(2)O/MeOH (9:1 vol.) show that the fluoride binding constants

204 )(2) reacted in DMF, followed by addition of MeOH and H(2)O, respectively.

205 pathway depends on the alcohol: addition of MeOH induces a transition to a superhelical structure th

206 ing in peak area response by the addition of MeOH to H2O, 5%, is outweighed by the fraction of compou

207 ion, and spontaneous oxa-Michael addition of MeOH.

208 ta-sulfido carbonyl compounds by addition of MeOH.

209 ial unfolding; however, further additions of MeOH result in the formation of a non-native beta-struct

210 lts in significant changes in the amounts of MeOH adsorbed to the stationary phase.

211 dies also indicate that the concentration of MeOH produced is independent of catalyst concentration,

212 s pulled such that the overall conversion of MeOH to CH(2)(OH)(2) is exothermic.

213 ulting 2-arylchromen-2-ols in a cosolvent of MeOH and THF at rt for 1 h.

214 a clear impact on the metabolome coverage of MeOH extracted biological samples, highlighting the impo

215 lato)diboron [B(2)(pin)(2)] and 1.1 equiv of MeOH at -50 to -15 degrees C in 3-24 h.

216 data is proposed in which one equivalent of MeOH activates the epoxide electrophile via a hydrogen b

217 a hydrogen bond while a second equivalent of MeOH chelates the side-chain nucleophile and glycal ring

218 ratios as a function of the mole fraction of MeOH in dichloroethane showed that the homoadamantyl chl

219 f 2 to atmosphere produces a partial loss of MeOH accompanied by a luminescence color change to yello

220 The uptake and loss of MeOH vapor is rapid and reversible.

221 sure of 2 to vacuum affords complete loss of MeOH, and the luminescence changes to yellow-orange (lam

222 roduce, in combined high yield, a mixture of MeOH, C2H6, and MeOOH along with water-soluble n-Pr4N[(d

223 In a mixture of MeOH/CHCl3, the domino cyclization of 1 further affords

224 t pH 4.0, followed by elution with 2.0 mL of MeOH:CH(2)Cl(2):HAc (34:62:4, v/v).

225 PEC nature and are due to photooxidation of MeOH by the NPs at the electrode surface.

226 We use photooxidation of MeOH by TiO2 NPs as a model system of photocatalysis in

227 ally demanding achiral NHCs, the presence of MeOH is required for high efficiency.

228 ethylbenzene) with SmI(2) in the presence of MeOH or TFE was studied.

229 yclic carbene (NHC) complex; the presence of MeOH promotes in situ protonation of the C-Cu bond and l

230 by reaction of 2 with KF in the presence of MeOH.

231 gate the topic of the ruthenium promotion of MeOH electro-oxidation over nanoscale platinum catalysts

232 lear relationship between the sensitivity of MeOH adsorption to the stationary phase and the robustne

233 zation reaction is second-order dependent on MeOH, and the glycal ring oxygen is required for second-

234 de reaction is only first-order dependent on MeOH.

235 Previous work from our laboratory optimized MeOH-inducible expression of the P. falciparum malarial

236 nduct its further hydrogenation to CH(4) (or MeOH), for which Ni clusters are needed.

237 in disulfides suspended in NaPO(4) buffer or MeOH was assessed, and no differences in total normalize

238 Reaction of 1 with either liquid MeOH or MeOH vapor affords [Au(im(CH(2)py)(2))(2)(Cu(MeOH))(2)](

239 f the resulting sulfonyl chalcones in THF or MeOH/THF at 25 degrees C; and then (iii) Amberlyst-15 me

240 conventional techniques (e.g., using TMS or MeOH/benzene dual referencing) is demonstrated to be imp

241 cal ring oxygen is required for second-order MeOH catalysis.

242 n the electrode is able to decompose/oxidize MeOH to form (adsorbed) methoxy groups that can further

243 tion produce valence-band holes that oxidize MeOH.

244 ntegral to the catalytic cycle that produces MeOH.

245 n be converted into 5 with CuBr(2) in i-PrOH/MeOH/H(2)O.

246 In 10% MeOH/H(2)O at pH 1 or 11 or in pure MeOH, assembly is driven exclusively by the TPP ring, le

247 The retention order of PY-MeOH, PY-BuOH, and PY in CEC is determined by their inte

248 ibution of pyrene (PY), 1-pyrenemethanol (PY-MeOH), and 1-pyrenebutanol (PY-BuOH) into the C18 statio

249 e related reduced iron complex, [Fe(II)(PY5)(MeOH)](2+).

250 (2) and the ferrous end-product [Fe(II)(PY5)(MeOH)](OTf)(2) estimates the strength of the O-H bond in

251 )O}(n) (1-SS) and {[Co(II)((R,R)-iPr-Pybox) (MeOH)](3)[W(V)(CN)(8)](2).5.5MeOH.0.5H(2)O}(n) (1-RR).

252 no-bridged chains, {[Co(II)((S,S)-iPr-Pybox)(MeOH)](3)[W(V)(CN)(8)](2).5.5MeOH.0.5H(2)O}(n) (1-SS) an

253 Br and Cl), R = CNH+ (with X = Cl), and R = MeOH+ (with X = Br), the corresponding beta-aryl-alpha-h

254 n addition, the use of NH(4)OH in water-rich MeOH modifiers was compared to other commonly used basic

255 , Zn2+, Mn2+, Cu2+, Ag+; A = NO3-, OAc-; S = MeOH, H2O; a = 0, 1, 2; b = 0, 1, 2, 4; and c = 0, 2.

256 The (PPN){[Mn(III)(salphen)(MeOH)]2[Co(III)(CN)6]}.7MeOH (Mn2Co.7MeOH) analogue with

257 and the mixed Co/Os (PPN){[Mn(III)(salphen)(MeOH)]2[Co(III)0.92Os(III)0.08(CN)6]}.7MeOH (Mn2Co/Os.7M

258 metal Co/Os analogue (PPN){[Mn(III)(salphen)(MeOH)]2[Co(III)0.92Os(III)0.08(CN)6]}.7MeOH were underta

259 r new complex salts, (PPN){[Mn(III)(salphen)(MeOH)]2[M(III)(CN)6]}.7MeOH (Mn2M.7MeOH) (M = Fe, Ru, Os

260 The pristine (PPN){[Mn(salphen)(MeOH)]2[Os(CN)6]}.7MeOH (Mn2Os.7MeOH) behaves as an SMM

261 r of a pyridine ring and the H-O of a second MeOH molecule.

262 caffolds have unique potential for selective MeOH detection from other solvents, especially EtOH.

263 of temperature (100 degrees C) and solvent (MeOH).

264 sily removed by treatment with MeMgBr or TFA/MeOH, which affords the NH-aziridines in good yield.

265 gen bonded to Asp-297-CO(2)(-), we find that MeOH returns to be hydrogen bonded to Glu-171-CO(2)(-) a

266 2) to formate with a mild base, we show that MeOH is produced when using a strong base.

267 However, dopants became unnecessary for the MeOH mobile phase when the Ar lamp was used.

268 We further integrated the MeOH/ACN/Acetone extraction with the HILIC-FTMS method f

269 The lower the pressure, the stronger the MeOH adsorption to the stationary phase; in addition, at

270 erall identified 33% fewer proteins than the MeOH-based procedure.

271 While the MeOH/NaOH solvent yielded more efficient recovery rates

272 nd quaternary ammonium was improved with the MeOH/NaOH based method.

273 CN to solution and solid-phase esters in THF/MeOH/50% aqueous NH2OH increases the efficiency of their

274 Kinetic measurements in 9:1 THF:MeOH at 25 degrees C indicate that 3 is formed near the

275 D) showed that the ZnCar framework adapts to MeOH and H2 O guests because of the torsional flexibilit

276 ounterion, produces the free NHC H-bonded to MeOH with a weakly associated CO2.

277 ders of magnitude on going from isooctane to MeOH.

278 Simply switching the solvent (from MeCN to MeOH) or chelating unit (from bidentate to tridentate) i

279 ts with different polarities (i.e., toluene, MeOH, DMF, and DMSO).

280 -methylation of nitroarenes and amines using MeOH as both a C1 and a H(2) source.

281 imated to be approximately 10(13) in 60% v/v MeOH/water at 0.1 M ionic strength.

282 The calculated DeltaG++ when MeOH is hydrogen bonded to Asp-297-CO(2)(-) is >50 kcal/

283 free energy for MeOH reduction of o-PQQ when MeOH is hydrogen bonded to Glu-171-CO(2)(-) and the crys

284 ts did enhance Kr lamp APPI sensitivity when MeOH was used as the mobile phase.

285 20 and 21 resulting from trapping of 13 with MeOH.

286 Reaction of 6 with MeOH yielded 9,9'-digerma-9,9'-bifluorene (7).

287 f a few hundred attomoles were achieved with MeOH; those levels could not be achieved with ACN.

288 and for acceptorless coupling of amines with MeOH and EtOH affording formamides and acetamides.

289 NH(4)OH and H(2)O levels in conjunction with MeOH/CO(2) served to furnish a generic modifier (0.2% NH

290 ethanol (MeOH) as cosolvent, consistent with MeOH competitively displacing PBAT from H-bond donating

291 Treatment of D with MeOH affords two isomeric dimers, MD1 and MD2, both of w

292 an octahedral coordination environment with MeOH ligands occupying the axial sites.

293 ion of 1 in solution, although exchange with MeOH was shown to be slow by an EXSY study.

294 NH2/MeCN), F > Cl approximately Br > I (with MeOH/1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)/MeCN), and

295 success rate of protein identification with MeOH-based nanoLC-ESI-MS/MS was 100%, with multiple prot

296 2-methyltetrahydrofuran (2-MeTHF) mixed with MeOH.

297 shown that all aldoxime ethers reacted with MeOH by clean second-order kinetics with rate constants

298 possible for chromatographic separation with MeOH versus ACN.

299 s spectrometry, and 13 has been trapped with MeOH to afford methyl 1,3-cyclopentadiene-1- and -2-carb

300 ed and reused multiple times by washing with MeOH.