ライフサイエンスコーパス: 2-propanol

1 (dimethyl sulfoxide, dimethylformamide, and 2-propanol).

2 dimethanol in THF and is also viable in neat 2-propanol.

3 R)-2-octanol being 1700 times lower than for 2-propanol.

4 MPD is significantly more excluded than 2-propanol.

5 K) = 78.7 s(-1) in benzene containing 0.8 M 2-propanol.

6 buffer, at high salt (0.5 M NaCl) and in 30% 2-propanol.

7 ydroxamic acid by treatment with Nafion-H in 2-propanol.

8 e chiral column using a mobile phase of 100% 2-propanol.

9 M, including 4-vinylcyclohexene and 2-phenyl-2-propanol.

10 hown for the apolar hydrocarbon solvents and 2-propanol.

11 etric transfer hydrogenation of benzils from 2-propanol.

12 using a buffered mobile phase containing 5% 2-propanol.

13 ent on substrate, and inversely dependent on 2-propanol.

14 -piperazinyl)phen yl)-1,1,1,3,3,3-hexafluoro-2-propanol (1, AMG-3969), a compound that effectively en

15 ropropane-1,2-diol (3-MCPD) and 1,3-dichloro-2-propanol (1,3-DCP) were found in domestically manufact

16 From the dichloromethane/2-propanol (1:1) extract of the Indonesian marine sponge

17 ps were similar for dehydration of alkanols (2-propanol, 1- and 2-butanol, tert-butanol) and cleavage

18 2-Propanol (10%-25% gradient) replaced the previously us

19 e phase system consisted of 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 5% methanol (mobil

20 thanol (mobile phase A) and 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 90% methanol (mobi

21 eonine formylation was found for 50% H2O/33% 2-propanol/17% formic acid.

22 n buffer solvent with added methanol (MeOH), 2-propanol (2-PrOH), and dimethyl sulfoxide (DMSO) revea

23 s, KIE = 1.7), ethanol (14.3 ps, KIE = 1.8), 2-propanol (28 ps, KIE = 1.4), and 2,2,2-trifluoroethano

24 containing sodium dodecyl sulfate (SDS) and 2-propanol (2PN).

25 ps: (1) tissue extraction using acetonitrile/2-propanol (3+1, v+v) followed by 0.1M potassium phospha

26 anolicus (W110A TESADH) in Tris buffer using 2-propanol (30%, v/v) as cosolvent and cosubstrate.

27 spectroscopic studies revealed that 2-methyl-2-propanol (4) competes with substrates for binding to t

28 ), and a negative dependence on the 2-methyl-2-propanol (4) concentration.

29 ried sample in the mobile phase (cyclohexane:2-propanol:5 mM phosphoric acid, 50:50:2.9, v/v/v).

30 ed that defatting with WSB (20 degrees C) or 2-propanol (75 degrees C) decreased the gliadin and incr

31 nterchange reactions, caused either by heat (2-propanol, 75 degrees C) or by the solvent WSB, which a

32 e following: acetaldehyde, acetone, butanal, 2-propanol, acetic acid, 2-hexanol, benzoic acid, benzal

33 le compounds and fusel alcohols (1-propanol, 2-propanol, acetone, and acetaldehyde) was found in the

34 competitive adsorption of the studied VOCs (2-propanol, acetone, n-butanol, toluene, 1,2,4-trimethyl

35 eatic acini were measured by extraction with 2-propanol/acetonitrile, followed by separation and quan

36 utilizing titanium tetraisopropoxide, BINOL, 2-propanol additive, and tetraallylstannane as allylatin

37 alcohols (methanol, ethanol, 1-propanol, and 2-propanol) adsorbed into Cu-BTC thin films.

38 cetoxymethylpyrrole in refluxing acetic acid-2-propanol afforded a series of annulated tripyrranes.

39 llent chemoselectivity in bulk oxidations of 2-propanol and 1,2-benzenedimethanol in THF and is also

40 using a combination of two of the compounds, 2-propanol and 2-butanone.

41 ipal component analysis showed that ethanol, 2-propanol and 3-methylbutanol, identified by HS-GC-IMS,

42 d to the target compound volatility, whereby 2-propanol and acetaldehyde exhibited the highest emissi

43 ntation of sulfide radical cations (2-phenyl-2-propanol and diaryl disulfides).

44 ted, or aliphatic aldehydes 2a-i mediated by 2-propanol and employing a cyclometalated iridium C,O-be

45 etention (S(N)F) mechanisms were located for 2-propanol and exo-2-norbornanol.

46 luence of methanol, ethanol, 1-propanol, and 2-propanol and K(3)PO(4), K(2)HPO(4) or KH(2)PO(4)/K(2)H

47 alcohols 2-methyl-2,4-pentanediol (MPD) and 2-propanol and of glycerol with condensed spermidine(3+)

48 Achiral 2-propanol and short-chain (R)- and (S)-2-alkanols were

49 In the presence of 2-propanol and trifluoroethanol, dearomatized adducts de

50 f HMPA and proton donors (methanol, 2-methyl-2-propanol, and 2,2,2-trifluoroethanol) on SmI2-initiate

51 organic solvents such as methanol, acetone, 2-propanol, and acetonitrile.

52 mplex was then purified, dried, dissolved in 2-propanol, and cast onto a glass slide to form a self-s

53 pe and concentration of alcohol (1-propanol, 2-propanol, and ethanol), type of salt (sodium citrate,

54 tion of two polar molecules, acetic acid and 2-propanol, and one nonpolar molecule, dodecane, on LiNb

55 The photoreactions in cyclopentane, 2-methyl-2-propanol, and the gas phase occurred exclusively throu

56 stituted N-benzyl-N-phenyl-trifluoro-3-amino-2-propanols are described that reversibly inhibit choles

57 We show, by using the conversion of 2-propanol as a probe reaction, that the surface termina

58 Using 2-propanol as a reductant, aldehydes dehydro-2a, 2l part

59 Reactions of serinol and 1,3-diamino-2-propanol as model trifunctional compounds showed parti

60 The use of 1,1,1,3,3,3-hexafluoro-2-propanol as solvent significantly extended the reactio

61 kovnikov and anti-Markovnikov alcohols using 2-propanol as the hydrogen source.

62 ohol chain (C1-C3) and geometry (1-propanol, 2-propanol) as well as their polarity on the sensing per

63 ter with ease, while larger alcohols such as 2-propanol, as well as DMSO, are excluded.

64 baking test, using wheat flour defatted with 2-propanol at 20 degrees C, was established to determine

65 ly present in dough from flour defatted with 2-propanol at 20 degrees C.

66 ume compared to control flour extracted with 2-propanol at 20 degrees C.

67 urrent drift gas of the system is doped with 2-propanol at 20 muL/h, full baseline resolution of the

68 Exposure of the nanoparticles to 2-propanol at 30 degrees C leads to immediate partial re

69 the presence of Zn(II) ions as templates in 2-propanol at 70 degrees C.

70 e capillary tip to construct a fine layer of 2-propanol-based colloidal graphite.

71 In the presence of 2-propanol, but under otherwise identical conditions, vi

72 In the absence of 2-propanol, but under otherwise identical reaction condi

73 traction procedures (e.g., chaotropic salts, 2-propanol) can be avoided, making the method more condu

74 nt in situ study of the partial oxidation of 2-propanol catalyzed with PdO nanoparticles supported on

75 reas increasing concentrations of ethanol or 2-propanol cause the helices of the alpha 4H tetramer fi

76 of organic solvents (acetonitrile, methanol, 2-propanol), chaotropic agents (6 M urea, 6 M guanidine-

77 utyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed.

78 PET was used, such as 1,1,1,3,3,3-hexafluoro-2-propanol (commonly referred to as HFIP), as the sample

79 e chiral N,N-disubstituted trifluoro-3-amino-2-propanol compounds do not affect lipoprotein structure

80 ical conformation at high TFE and hexafluoro-2-propanol concentrations.

81 allenamide 1e to aldehyde 2a conducted using 2-propanol-d(8) as the terminal reductant delivers deute

82 n the presence of aldehydes 2a-i mediated by 2-propanol delivers products of (trimethylsilyl)allylati

83 hyl-4-trifluoromethyl -2-imidazolyl)phenoxy]-2-propanol dihydrochloride (CGP-20712A) prevented isopro

84 that is intermediate in size between MPD and 2-propanol does not observably affect DNA force curves.

85 amine-Ru(II) complex combined with t-BuOK in 2-propanol effectively catalyzes enantioselective hydrog

86 ous alcohols trifluoroethanol and hexafluoro-2-propanol efficiently promote the cyclocondensation of

87 In the absence of 2-propanol, enantioselective carbonyl reverse prenylatio

88 -hydroxybenzotriazole esters, and hexafluoro-2-propanol esters.

89 tics of five hydraulic fracturing compounds (2-propanol, ethylene glycol, propargyl alcohol, 2-butoxy

90 Four compounds (2-propanol, ethylene glycol, propargyl alcohol, and 2-bu

91 A single n-hexane/2-propanol extract containing both types of compounds wa

92 butanol (WSB; extracted at 20 degrees C) and 2-propanol (extracted at 75 degrees C) had inferior exte

93 A single dilution of seed oils in 2-propanol facilitated the direct use samples in the DPP

94 For the two species examined and at a 2-propanol flow rate of 160 muL/h, MPA demonstrated the

95 Soil samples were briefly sonicated in 2-propanol, followed by direct CP-MIMS measurement.

96 ves an automated single-step extraction with 2-propanol, followed by lipid analysis using hydrophilic

97 Ethyl acetate could also displace 2-propanol from the silica, and least-squares modeling a

98 Irradiation of 4 in 2-propanol gave compounds 6 and 7 that also come from in

99 lpha-d-glucopyranosyl fluoride in hexafluoro-2-propanol gives two products, 1,1,1,3,3,3-hexafluoropro

100 hell section can be selectively dissolved by 2-propanol, giving yolk-shell nanostructures and, thus,

101 y (HPLC) using an amino column with a hexane/2-propanol gradient.

102 separated using a chiral column eluted with 2-propanol:hexane.

103 ons were performed in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and 2,2,2-trifluoroethanol (TFE) using

104 ochloric acid in a 1:1 mixture of hexafluoro-2-propanol (HFIP) and methylene chloride (DCM) is descri

105 sing a combination of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and NaOAc.

106 nating (HBD) solvents 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) and nonafluoro tert-butyl alcohol (NFT

107 pin forming peptide, MrH3a, in 8% hexafluoro-2-propanol (HFIP) and the dynamics of its refolding foll

108 ransformation employs 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as both solvent and promoter, eliminat

109 wis acid catalysis in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as solvent is described.

110 We used 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) as the activating solvent for a nitric

111 with triflic acid in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at 0 degrees C generated in situ the c

112 ns are solubilized in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at 25-30% (wt/vol) for extrusion into

113 The use of hexafluoro-2-propanol (HFIP) in the separation medium, and as an ad

114 ole of the co-solvent 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) is also revealed.

115 found that the use of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) or dimethyl sulfoxide (DMSO) significa

116 demonstrate here that 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) promotes the ring-opening reaction and

117 1,1,1,3, 3,3-Hexafluoro-2-propanol (HFIP) was found to be the best solvent for s

118 solvent of water and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), polyene cyclizations using allylic al

119 nd a unique additive, 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), to achieve highly efficient separatio

120 Hexafluoro-2-propanol (HFIP), which promotes alpha-helix formation,

121 ions of the first examples of the hexafluoro-2-propanol (HFIP)-mediated IFCEAC of readily accessible

122 at microdroplets formed in dilute hexafluoro-2-propanol (HFIP).

123 sodium dodecyl sulfate (SDS), and hexafluoro-2-propanol (HFIP).

124 ontaining triethylamine (TEA) and hexafluoro-2-propanol (HFIP).

125 2,3,4-tetrahydro-1-naphthalenyl]amino]-(2S)- 2-propanol hydrochloride [SR 59230A]) stimulated respons

126 s induced by pesticides such as 1,3-Dichloro-2-propanol, imidacloprid, permethrin, are attributed to

127 iments to examine interactions of hexafluoro-2-propanol in a 30% fluoro alcohol-50 mM phosphate buffe

128 l dehydration and alkylation of m-cresol and 2-propanol in the liquid phase, at high temperatures.

129 obile phase containing acetonitrile:methanol:2-propanol in the ratio of 85:15:33 with 0.01% ammonium

130 vestigated: methanol (MeOH), ethanol (EtOH), 2-propanol (IPA), 1-butanol (BuOH), acetonitrile (ACN) a

131 our small Pt particles for the oxidation of 2-propanol is attributed to the large amount of edge and

132 acids at room temperature in technical grade 2-propanol is described.

133 nzyl]-N-(3-phenoxyphenyl)-trifluoro-3-am ino-2-propanols is described which potently and reversibly i

134 Photolysis of 3 in argon-saturated 2-propanol led to formation of 5 via intermolecular H-at

135 es in the order water > methanol > ethanol > 2-propanol, linearly according to empirical scales of so

136 active species for the partial oxidation of 2-propanol (<140 degrees C), while the complete oxidatio

137 ined in cyclopentane, methanol, and 2-methyl-2-propanol, media with differing polarities and viscosit

138 Related 2-propanol mediated reductive couplings also are describ

139 m complexes modified by SEGPHOS catalyze the 2-propanol-mediated reductive coupling of branched allyl

140 iral phosphine ligand PhanePhos catalyze the 2-propanol-mediated reductive coupling of diverse 1,1-di

141 om [Ir(cod)Cl](2) and (R)-PhanePhos catalyze 2-propanol-mediated reductive couplings of 2-substituted

142 thenium(II)-catalyzed hydrogen transfer from 2-propanol mediates reductive coupling of 1,1-disubstitu

143 the effects of different solvents, including 2-propanol, methanol, and acetonitrile, pure or as mixtu

144 tate in a mobile phase consisting of hexane, 2-propanol, methanol, and water (5.5:8:1.5:1).

145 nnected in series using a gradient of hexane-2-propanol mobile phase.

146 2-Propanol modifier displayed more efficient displacemen

147 The change in the alcohol's orientation with 2-propanol mole fraction closely tracked changes in its

148 considers the transient binding of a single 2-propanol molecule during mobility measurements.

149 sfer of a proton from a solvating hexafluoro-2-propanol molecule.

150 threonine O-3-phosphate to yield (R)-1-amino-2-propanol O-2-phosphate.

151 n methanol-O-d (16 ps), ethanol-O-d (26 ps), 2-propanol-OD (40 ps), and 2,2,2-trifluoroethanol-O-d (1

152 The ACOD radical reacts with TPZ in 2-propanol-OD with an absolute rate constant of (6.7 +/-

153 rcially available solvent, 2-trifluoromethyl-2-propanol, optimally balances monomer, polymer, and cat

154 modified Curtius rearrangement with 2-methyl-2-propanol or 2-(trimethylsilyl)ethanol to form the stab

155 Ionization of 1,1,1,3,3,3-hexafluoro-2-propanol or benzoic acid results in the observation of

156 1S)-1,2,3,4-tetrahydronaphth-1-ylamino]-(2S)-2-propanol oxalate).

157 is responsible for synthesizing (R)-1-amino-2-propanol phosphate which is the precursor for the link

158 ly efficient and an unprecedented hexafluoro-2-propanol, promoting low-temperature aromatic nucleophi

159 te a reaction mechanism for the formation of 2-propanol, propylene, and 1-propanol involving the oxid

160 trates that lacked a sulfonate moiety [e.g., 2-propanol, (R)-2-pentanol, and (R)-2-heptanol].

161 acceleration of this reaction by hexafluoro-2-propanol reinforces this view by altering the relative

162 nol was higher than 0.68, the orientation of 2-propanol remained almost constant.

163 otide intermediates in a protic antisolvent (2-propanol), remained near quantitative.

164 Chiral N,N-disubstituted trifluoro-3-amino-2-propanols represent a recently discovered class of com

165 alkyl alicyclic amines, where the piperazine-2-propanol scaffold was modified, were designed, synthes

166 ding probe molecules n-heptane, toluene, and 2-propanol, showed that slow diffusion occurs within the

167 talyzes the phosphorylation of the 1-amino-O-2-propanol side chain of the adenosylcobinamide ring and

168 yzes both the phosphorylation of the 1-amino-2-propanol side chain of the corrin ring and the subsequ

169 ified using the (13)C NMR resonances for the 2-propanol solvent, whose chemical shifts report on the

170 al rotational equilibrium isotope effects in 2-propanol strongly imply a hyperconjugative mechanism f

171 crease on going from methanol to ethanol and 2-propanol substrates, in accord with experiment.

172 dimethyl sulfoxide or 1,1,1,3,3,3-hexafluoro-2-propanol, synthetic human Abeta(1-42) readily forms ol

173 alysis was confirmed for the phenolate/AlMe3/2-propanol system.

174 than the inversion S(N)2 counterpart for the 2-propanol system.

175 In contrast to 10% HFIP, 1,1,1-trifluoro-2-propanol (TFIP) did not inactivate prion infectivity b

176 There is evidence in 2-propanol that geminate reaction within the initial ion

177 xymethylpyrroles 10 in refluxing acetic acid-2-propanol to afford tripyrranes 11.

178 PdO below 90 degrees C, and the oxidation of 2-propanol to carboxylates only occurs in the presence o

179 inding of the substrate analogue (S)-1-amino-2-propanol to EAL eliminates the P(f) state and lowers t

180 lpyrroles (2 equiv) in refluxing acetic acid/2-propanol to give tripyrrane analogues, and following a

181 eptide is selectively solvated by hexafluoro-2-propanol to the extent that the fluoro alcohol concent

182 he study the adsorption of ethyl acetate and 2-propanol to the surface of thin silica sol-gel films i

183 hat can be photoactivated in the presence of 2-propanol to transfer electrons to (99)TcO(4)(-) and in

184 methyl-2-aminopropane, methanol, or 2-methyl-2-propanol) to form the corresponding alkane-substituted

185 omatic species (phenoxyethanol and 1-phenoxy-2-propanol), two esters (butyl butyrate and butyl acetat

186 -Al(2)O(3) during the catalytic oxidation of 2-propanol using X-ray absorption fine-structure spectro

187 line micelles and 25% 1,1,1,3,3,3-hexafluoro-2-propanol (v/v) confirmed folding of the complete 2F5 e

188 2-Propanol vapors were introduced in one of the stages t

189 ties were measured for saturated toluene and 2-propanol vapors.

190 Adsorption of 2-propanol was best modeled by a single Langmuir isother

191 This concentration of 2-propanol was crucial not only to enhance the solubilit

192 droxy-1,1'-binapthyl ((S)-BINOL), AlMe3, and 2-propanol was established through 1H and 27Al NMR spect

193 ng hydrogen-bond-donating solvent hexafluoro-2-propanol was found to be consistent with low catalyst

194 For soil sample analysis, 2-propanol was found to be the optimal PAH sampling solv

195 A calibration curve for aqueous solutions of 2-propanol was generated and a limit of detection (LOD)

196 When the mole fraction of 2-propanol was higher than 0.68, the orientation of 2-pr

197 ture and conductivity, while the response to 2-propanol was less predictable.

198 ence in adsorption energy for the two sites; 2-propanol was shown to easily displace ethyl acetate fr

199 wo-stage, dual-phase microdevice allowed the 2-propanol wash step, typically required to remove prote

200 ure matrix eliminates both guanidine and the 2-propanol wash that can inhibit downstream PCR and comp

201 ropyl group at the liquid/vapor interface in 2-propanol/water binary mixtures was studied by vibratio

202 e conformation of melittin in 35% hexafluoro-2-propanol/water is alpha-helical from residues Ile-2 to

203 - 15 degrees ) in 35% 1,1,1,3,3,3-hexafluoro-2-propanol/water is smaller than the angle found in othe

204 TS for the solvolysis reaction in hexafluoro-2-propanol, we synthesized a series of isotopically labe

205 ent modifiers such as methanol, ethanol, and 2-propanol were used.

206 e chiral N,N-disubstituted trifluoro-3-amino-2-propanols were found to associate with both LDL and HD

207 Two thiols, 2-mercaptoethanol and mercapto-2-propanol, were poorer substrates than CoM, while sever

208 in situ generation of water from hexafluoro-2-propanol which acts as a reactant for the removal of t

209 hyl-4-trifluoromethy l-2-imidazolyl)phenoxy]-2-propanol], which showed no agonistic activity, had onl

210 (4)H(c)", benzene hydrogenation catalysis in 2-propanol with added Et(3)N and at 100 degrees C and 50

211 Ab initio calculations on 2-propanol with or without a hydrogen bonding partner, i

212 ation but deflated on the beta-C position in 2-propanol with respect to the values predicted by the s

213 ysis of an oxygen-saturated solution of 3 in 2-propanol yields products 8, 9, and 10, which were all