ライフサイエンスコーパス: propanol

1 ., trifluoroethanol) to hydrophobic (e.g., n-propanol).

2 precursor of 3-phenylpropanal and 3-phenyl-1-propanol.

3 oxymethyl group (-CH(2)OH) of the produced 1-propanol.

4 couple with CO leading to the formation of 1-propanol.

5 ric transfer hydrogenation of benzils from 2-propanol.

6 ation are propionaldehyde, propionate, and 1-propanol.

7 t on substrate, and inversely dependent on 2-propanol.

8 of zirconium(IV)-n-propoxide solutions in 1-propanol.

9 sing a buffered mobile phase containing 5% 2-propanol.

10 ut had no effect on growth with acetone or n-propanol.

11 -2-octanol being 1700 times lower than for 2-propanol.

12 n the elution of LF from the column at 30% N-propanol.

13 MPD is significantly more excluded than 2-propanol.

14 ) = 78.7 s(-1) in benzene containing 0.8 M 2-propanol.

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

16 es between 96% (R) and 75% (S) of 1-phenyl-1-propanol.

17 including 4-vinylcyclohexene and 2-phenyl-2-propanol.

18 yoxal, a toxic byproduct of glycolysis, as 1-propanol.

19 methanol in THF and is also viable in neat 2-propanol.

20 wn for the apolar hydrocarbon solvents and 2-propanol.

21 acids, alcohols, ethyl esters and 3-ethoxy-1-propanol.

22 formed from monomeric and dimeric adsorbed 1-propanol.

23 ice and adult human non-smokers as carnosine-propanols.

24 ed acid-catalyzed gas-phase dehydration of 1-propanol (0.075-4 kPa) was studied on zeolite H-MFI (Si/

25 n using a mobile phase of 0.05M SDS - 7.5% 1-propanol - 0.5% triethylamine buffered at pH 3, running

26 nces using mobile phase of 0.05M SDS/12.5% 1-propanol/0.5% triethylamine at pH 3, running at 1mL/min

27 iperazinyl)phen yl)-1,1,1,3,3,3-hexafluoro-2-propanol (1, AMG-3969), a compound that effectively enha

28 propane-1,2-diol (3-MCPD) and 1,3-dichloro-2-propanol (1,3-DCP) were found in domestically manufactur

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

30 lectrooxidation of four alcohols (ethanol, 1-propanol, 1-butanol, and 1-pentanol) to the correspondin

31 2-Propanol (10%-25% gradient) replaced the previously used

32 phase system consisted of 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 5% methanol (mobile

33 anol (mobile phase A) and 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 90% methanol (mobile

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

35 b, demonstrating that the R-chirality at the propanol 2-position is key to high potency in this serie

36 Microwave reactions of 2-amino-2-methyl-1-propanol (2) or 2-aminoethanethiol hydrochloride (4) wit

37 buffer solvent with added methanol (MeOH), 2-propanol (2-PrOH), and dimethyl sulfoxide (DMSO) reveal

38 After baking, 2,3-butanedione, 1-propanol, 2-methyl-1-propanol, 3/2-methyl-1-butanol and

39 of the alcohol chain (C1-C3) and geometry (1-propanol, 2-propanol) as well as their polarity on the s

40 of volatile compounds and fusel alcohols (1-propanol, 2-propanol, acetone, and acetaldehyde) was fou

41 such as type and concentration of alcohol (1-propanol, 2-propanol, and ethanol), type of salt (sodium

42 KIE = 1.7), ethanol (14.3 ps, KIE = 1.8), 2-propanol (28 ps, KIE = 1.4), and 2,2,2-trifluoroethanol

43 1 to 100 mM 2-nitroethanol (2ne), 2-nitro-1-propanol (2nprop), and 3-nitro-2-pentanol (3n2pent) at p

44 troalcohols (2-nitroethanol [2ne], 2-nitro-1-propanol [2nprop]), and 3-nitro-2-pentanol [3n2pent]).

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

46 H terminating head group, i.e., 3-mercapto-1-propanol (3-MPL), 6-mercapto-1-hexanol (6-MHL), 8-mercap

47 using 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol and

48 ent of 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1-butanol and 2-methyl-1-butanol was

49 ted samples with the exception of 2-methyl-1-propanol, 3-methyl-1-butanol and 2-phenylethyl alcohol,

50 ing, 2,3-butanedione, 1-propanol, 2-methyl-1-propanol, 3/2-methyl-1-butanol and ethyl octanoate were

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

52 ectroscopic studies revealed that 2-methyl-2-propanol (4) competes with substrates for binding to the

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

54 poly(1,5-pentanediol diacrylate-co-3-amino-1-propanol) ('536') at a 25 polymer-to-DNA weight-to-weigh

55 that defatting with WSB (20 degrees C) or 2-propanol (75 degrees C) decreased the gliadin and increa

56 erchange reactions, caused either by heat (2-propanol, 75 degrees C) or by the solvent WSB, which aff

57 ips among 6, 7, and 2-(acetylamino)-2-methyl propanol (8) in acidified MeCN solution.

58 1-hexnaol, the intercalation rate peaks in 1-propanol (80 times faster than the slowest case in metha

59 R)-d-erythro-2-(N-myristoylamino)-1-phenyl-1-propanol, a ceramidase inhibitor, and TNFalpha, a homolo

60 covalently linked monolayer of 3-mercapto-1-propanol, a modified surface that blocks the oxidation o

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

62 ompetitive adsorption of the studied VOCs (2-propanol, acetone, n-butanol, toluene, 1,2,4-trimethylbe

63 ilizing titanium tetraisopropoxide, BINOL, 2-propanol additive, and tetraallylstannane as allylating

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

65 an for the primary amines 2-amino-2-methyl-1-propanol (AMP) and monoethanolamine (MEA) and the tertia

66 DEA) carbamate as well as 2-amino-2-methyl-1-propanol (AMP) carbamate were obtained in crystalline fo

67 ent chemoselectivity in bulk oxidations of 2-propanol and 1,2-benzenedimethanol in THF and is also vi

68 formation of 3-methyl-1-butanol, 2-methyl-1-propanol and 3-(methylsulfanyl)-propanal, whereas hexana

69 rbon feedstocks such as ethylene, ethanol, n-propanol and acetate, most efforts have been devoted to

70 ation of sulfide radical cations (2-phenyl-2-propanol and diaryl disulfides).

71 d, or aliphatic aldehydes 2a-i mediated by 2-propanol and employing a cyclometalated iridium C,O-benz

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

73 By washing with iso-propanol and hexane the immobilised lipase could be reus

74 ence of methanol, ethanol, 1-propanol, and 2-propanol and K(3)PO(4), K(2)HPO(4) or KH(2)PO(4)/K(2)HPO

75 Plant tissue is extracted in aqueous 1-propanol and mixed with dichloromethane.

76 igh concentrations of methanol, ethanol, and propanol and moderate concentrations of trifluoroethanol

77 lcohols 2-methyl-2,4-pentanediol (MPD) and 2-propanol and of glycerol with condensed spermidine(3+)-D

78 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol and phospholipase C), we demonstrated that PSV

79 The architecture yields the formation of n-propanol and propionaldehyde at potentials as low as -0.

80 ionate accumulated stoichiometrically when 1-propanol and propionaldehyde were added to butane- and e

81 primarily by conversion to propionate and 1-propanol and secondarily due to volatility.

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

83 Replacement of ethanol with 1-propanol and use of a surfactant increased the signal.

84 ence of the competitive adsorption between 1-propanol and water.

85 or D-erythro-2-tetradecanoylamino-1-phenyl-1-propanol and, to a much lesser extent, by L-cycloserine,

86 HMPA and proton donors (methanol, 2-methyl-2-propanol, and 2,2,2-trifluoroethanol) on SmI2-initiated

87 The influence of methanol, ethanol, 1-propanol, and 2-propanol and K(3)PO(4), K(2)HPO(4) or KH

88 of different alcohols (methanol, ethanol, 1-propanol, and 2-propanol) adsorbed into Cu-BTC thin film

89 ffinity subsite: 4-aminobutanol, guanidine-3-propanol, and 4-hydroxymethylbenzamidine.

90 enzenediazonium in water, methanol, ethanol, propanol, and acetonitrile were similar, but measured pr

91 3-Phenylpropanal, 3-phenyl-1-propanol, and benzyl alcohol were identified as potent a

92 lcholine bilayer when solvated with ethanol, propanol, and butanol solutions.

93 ibitory effects were observed with methanol, propanol, and butanol, with ethanol being the most poten

94 lex was then purified, dried, dissolved in 2-propanol, and cast onto a glass slide to form a self-sta

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

96 philic asthma, the combination of nonanal, 1-propanol, and hexane had a classification performance si

97 tested alcoholic vapors (ethanol, methanol, propanol, and isopropanol).

98 on of guest size, i.e., methanol, ethanol, n-propanol, and isopropanol, showing that fine control ove

99 50 mumol L(-1) were obtained for ethanol, n-propanol, and methanol, respectively.

100 on of two polar molecules, acetic acid and 2-propanol, and one nonpolar molecule, dodecane, on LiNbO3

101 e photoreactions in cyclopentane, 2-methyl-2-propanol, and the gas phase occurred exclusively through

102 nt of CdSe nanocrystals (NCs) in a 3-amino-1-propanol (APOL)/water (v/v = 10:1) mixture at 80 degrees

103 Ethylene, ethanol, and n-propanol are the major C2-C3 products with onset potenti

104 ituted N-benzyl-N-phenyl-trifluoro-3-amino-2-propanols are described that reversibly inhibit choleste

105 ed techniques, it was possible to identify n-propanol as a possible volatile compound released during

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

107 owing a lag period, producing propionate and propanol as additional fermentation products.

108 The use of 1,1,1,3,3,3-hexafluoro-2-propanol as solvent significantly extended the reaction

109 ol chain (C1-C3) and geometry (1-propanol, 2-propanol) as well as their polarity on the sensing perfo

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

111 king test, using wheat flour defatted with 2-propanol at 20 degrees C, was established to determine t

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

113 e compared to control flour extracted with 2-propanol at 20 degrees C.

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

115 Exposure of the nanoparticles to 2-propanol at 30 degrees C leads to immediate partial redu

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

117 benign polar solvents, such as ethanol or n-propanol, at high concentrations (up to 200 mg/mL) is de

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

119 nts showed that 3-phenylpropanal, 3-phenyl-1-propanol, benzyl alcohol, methyl 3-phenylpropionate, met

120 In the presence of 2-propanol, but under otherwise identical conditions, viny

121 In the absence of 2-propanol, but under otherwise identical reaction conditi

122 as a regular single left-handed helix from a propanol, butanol, or iodine solution.

123 te determining step for C2 products, while n-propanol (C3) production seems to have a discrete pathwa

124 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol), C9DGJ (N-nonyl-deoxygalactonojirimycin) or C4

125 action procedures (e.g., chaotropic salts, 2-propanol) can be avoided, making the method more conduci

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

127 e of (4.5 +/- 0.1) mA cm(-2), and a record n-propanol cathodic energy conversion efficiency (EE(catho

128 as increasing concentrations of ethanol or 2-propanol cause the helices of the alpha 4H tetramer firs

129 yric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed.

130 T was used, such as 1,1,1,3,3,3-hexafluoro-2-propanol (commonly referred to as HFIP), as the sample p

131 al conformation at high TFE and hexafluoro-2-propanol concentrations.

132 es from the reactant CO, while ethanol and n-propanol contained mainly solvent oxygen.

133 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), an inhibitor of glucosylceramide synt

134 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (D-PDMP), solubilized in vehicle (5% Tween-80 i

135 lenamide 1e to aldehyde 2a conducted using 2-propanol-d(8) as the terminal reductant delivers deuteri

136 ctivity was developed using 3-diethylamino-1-propanol (deapH) in lieu of BnOH and NEt(3).

137 the presence of aldehydes 2a-i mediated by 2-propanol delivers products of (trimethylsilyl)allylation

138 Interestingly, 1-propanol, delta-butyrolactone and ethyl lactate concentr

139 noic acid derivatives were reduced to give 3-propanol derivatives, which were readily oxidised to tar

140 l-4-trifluoromethyl -2-imidazolyl)phenoxy]-2-propanol dihydrochloride (CGP-20712A) prevented isoprote

141 BV2), of which dimercaprol (2,3-dimercapto-1-propanol (DMP)) was found to be the most effective compo

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

143 ine-Ru(II) complex combined with t-BuOK in 2-propanol effectively catalyzes enantioselective hydrogen

144 s alcohols trifluoroethanol and hexafluoro-2-propanol efficiently promote the cyclocondensation of o-

145 ent relative to previously-published CO-to-n-propanol electroreduction reports.

146 In the absence of 2-propanol, enantioselective carbonyl reverse prenylation

147 Ethanol and propanol enhanced fusion, butanol also enhanced fusion b

148 ioxy)phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (EtDO-P4) greatly reduced GSL and monosialotetr

149 ioxy)phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (EtDO-P4), the glucosylceramide (GlcCer) syntha

150 The content of 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1

151 r, gold, aged and extra-aged tequila using 1-propanol, ethyl acetate, 2-methyl-1-propanol, 3-methyl-1

152 cs of five hydraulic fracturing compounds (2-propanol, ethylene glycol, propargyl alcohol, 2-butoxyet

153 Four compounds (2-propanol, ethylene glycol, propargyl alcohol, and 2-buto

154 A single n-hexane/2-propanol extract containing both types of compounds was

155 tanol (WSB; extracted at 20 degrees C) and 2-propanol (extracted at 75 degrees C) had inferior extens

156 A single dilution of seed oils in 2-propanol facilitated the direct use samples in the DPPH

157 We achieve a record n-propanol Faradaic efficiency (FE) of (33 +/- 1)% with a

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

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

160 licit water as well as explicit hexane and 1-propanol for the nanomer.

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

162 ha-d-glucopyranosyl fluoride in hexafluoro-2-propanol gives two products, 1,1,1,3,3,3-hexafluoropropa

163 ll section can be selectively dissolved by 2-propanol, giving yolk-shell nanostructures and, thus, ma

164 ydrophobic chromatography with a 10 to 60% N-propanol gradient in 0.1 M ammonium acetate, resulting i

165 and increasing area per molecule was butanol>propanol>ethanol>methanol, although the lysis strain was

166 Propanal-propanol-H(2) equilibration is mediated by their chemiso

167 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol.HCI (PDMP), a glucosylceramide synthase and Lac

168 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol-HCl, also results in a significant decrease in

169 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol.HCl (PDMP), a glucosylceramide synthase and Lac

170 eparated using a chiral column eluted with 2-propanol:hexane.

171 and 3-methylbutanoic acid; 3-(methylthio)-1-propanol; hexanoic acid; beta-damascenone; and ethyl-3-p

172 hloric acid in a 1:1 mixture of hexafluoro-2-propanol (HFIP) and methylene chloride (DCM) is describe

173 n forming peptide, MrH3a, in 8% hexafluoro-2-propanol (HFIP) and the dynamics of its refolding follow

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

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

176 ith triflic acid in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at 0 degrees C generated in situ the cor

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

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

179 und that the use of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) or dimethyl sulfoxide (DMSO) significant

180 olvent of water and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), polyene cyclizations using allylic alco

181 a unique additive, 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), to achieve highly efficient separation

182 taining triethylamine (TEA) and hexafluoro-2-propanol (HFIP).

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

184 dium dodecyl sulfate (SDS), and hexafluoro-2-propanol (HFIP).

185 3,4-tetrahydro-1-naphthalenyl]amino]-(2S)- 2-propanol hydrochloride [SR 59230A]) stimulated responses

186 ents to examine interactions of hexafluoro-2-propanol in a 30% fluoro alcohol-50 mM phosphate buffer

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

188 ile phase containing acetonitrile:methanol:2-propanol in the ratio of 85:15:33 with 0.01% ammonium ac

189 nosine-propanals were converted to carnosine-propanols in the lysates of heart, skeletal muscle, and

190 nti-Lewisite, also known as 2,3-dimercapto-1-propanol) inhibits S6K1 phosphorylation and stabilizes t

191 When transferred from propanol into 40:60 propanol:water under acidic conditio

192 he formation of 2-propanol, propylene, and 1-propanol involving the oxidation of Fe(II) to Fe(III) vi

193 ur small Pt particles for the oxidation of 2-propanol is attributed to the large amount of edge and c

194 ids at room temperature in technical grade 2-propanol is described.

195 2.2]octanes from 3-bromo-2,2-bis(bromomethyl)propanol is developed, making a diverse set of mass-diff

196 hyde, only a minor fraction (up to 36%) of 1-propanol is from this pathway, and the majority of it is

197 yl]-N-(3-phenoxyphenyl)-trifluoro-3-am ino-2-propanols is described which potently and reversibly inh

198 teen model VOCs (tetrahydrofuran, butanol, n-propanol, iso-propano, acetone, methanol, ethanol, tolue

199 significantly changes the wine content in 1-propanol, isobutanol, acetaldehyde, 1,1-diethoxiethane a

200 y were: n-butanol, acetonitrile, methanol, n-propanol, isopropanol, and isobutanol.

201 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (L-PDMP) in two mouse models of Parkinsonism pr

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

203 in the order water > methanol > ethanol > 2-propanol, linearly according to empirical scales of solv

204 ctive species for the partial oxidation of 2-propanol (<140 degrees C), while the complete oxidation

205 ed in cyclopentane, methanol, and 2-methyl-2-propanol, media with differing polarities and viscositie

206 Related 2-propanol mediated reductive couplings also are described

207 complexes modified by SEGPHOS catalyze the 2-propanol-mediated reductive coupling of branched allylic

208 al phosphine ligand PhanePhos catalyze the 2-propanol-mediated reductive coupling of diverse 1,1-disu

209 enium(II)-catalyzed hydrogen transfer from 2-propanol mediates reductive coupling of 1,1-disubstitute

210 e effects of different solvents, including 2-propanol, methanol, and acetonitrile, pure or as mixture

211 ifferences in the concentrations of ethanol, propanol, methyl phenol, and ethyl phenol were not signi

212 eters report heat changes generated in water/propanol mixing and in ligand/protein binding.

213 ected in series using a gradient of hexane-2-propanol mobile phase.

214 tionally restricted version of the 3-amino-1-propanol moiety common to the many previously described

215 e change in the alcohol's orientation with 2-propanol mole fraction closely tracked changes in its bu

216 onsiders the transient binding of a single 2-propanol molecule during mobility measurements.

217 er of a proton from a solvating hexafluoro-2-propanol molecule.

218 Water stabilizes the adsorbed 1-propanol monomer significantly more than the elimination

219 -propanol stabilizes the adsorbed state of 1-propanol more than the elimination transition state.

220 1,3-propanediol (NT = nitrotriol), 2-nitro-1-propanol (NP)] against 5 different microbial pathogens i

221 methanol-O-d (16 ps), ethanol-O-d (26 ps), 2-propanol-OD (40 ps), and 2,2,2-trifluoroethanol-O-d (14

222 The ACOD radical reacts with TPZ in 2-propanol-OD with an absolute rate constant of (6.7 +/- 0

223 s using different proportions of lecithin, 1-propanol, olive oil and water to examine their abilities

224 ng 5 g microemulsion composed of lecithin: 1-propanol: olive oil: water (53.33:26.67:10:10 wt%) resul

225 itive adsorption isotherms of rac-1-phenyl-1-propanol on cellulose tribenzoate were measured by compe

226 fluenced the rise of the level of 3-ethoxy-1-propanol only.

227 ially available solvent, 2-trifluoromethyl-2-propanol, optimally balances monomer, polymer, and catal

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

229 )-1,2,3,4-tetrahydronaphth-1-ylamino]-(2S)-2-propanol oxalate).

230 eo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4), or reduction of CD82 expression by RNA in

231 eo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol (P4).

232 itor 1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP) resulted in the production of virus part

233 hreo-1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP), increased caspase activity to the same

234 s responsible for synthesizing (R)-1-amino-2-propanol phosphate which is the precursor for the linkag

235 resolution of racemic mixtures of 1-phenyl-1-propanol (PP) was studied by varying time, temperature,

236 reo-1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (PPMP), an inhibitor of glucosylceramide synthe

237 tor 1-phenyl-2-palmitoylamino-3-morpholino-1-propanol (PPMP, 5.0 micromol/L, 4 days) decreased gangli

238 1-phenyl-2-hexadecanoylamino-3-pyrrolidino-1-propanol (PPPP) each partially inhibited the ability of

239 The kinetic effects of H(2), propanal, and propanol pressures on turnover rates, taken together wit

240 Bchl a on stirring with KOH/propanol produced an "unstable bacteriochlorin", which d

241 efficient and an unprecedented hexafluoro-2-propanol, promoting low-temperature aromatic nucleophili

242 ully convert 1,3-propanediol to equilibrated propanol-propanal intermediates that subsequently form l

243 a reaction mechanism for the formation of 2-propanol, propylene, and 1-propanol involving the oxidat

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

245 cceleration of this reaction by hexafluoro-2-propanol reinforces this view by altering the relative s

246 The stronger adsorption of 1-propanol relative to water indicates that the reduced de

247 l was higher than 0.68, the orientation of 2-propanol remained almost constant.

248 kyl alicyclic amines, where the piperazine-2-propanol scaffold was modified, were designed, synthesiz

249 centration of the alcohol in the ethanol and propanol simulations does not have a significant influen

250 e other six oxygen atoms for the ethanol and propanol simulations.

251 relative reduction (abundance of SH) of the propanol soluble proteins (hordein I fraction); and (iv)

252 ied using the (13)C NMR resonances for the 2-propanol solvent, whose chemical shifts report on the in

253 In a similar manner, an excess of 1-propanol stabilizes the adsorbed state of 1-propanol mor

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

255 methyl sulfoxide or 1,1,1,3,3,3-hexafluoro-2-propanol, synthetic human Abeta(1-42) readily forms olig

256 ysis was confirmed for the phenolate/AlMe3/2-propanol system.

257 an the inversion S(N)2 counterpart for the 2-propanol system.

258 ce by all drugs tested: ethanol, methanol, n-propanol, t-butanol, pentobarbital, diazepam, and allopr

259 ization, and the formation of propionate and propanol that are up-regulated during growth on fucose.

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

261 2-(hydroxymethyl)-(2S,3S)-1,4-benzodiox in-6-propanol, threo and erythro 3-methoxy-8,4'-oxyneolignan-

262 ied 2-butanol, 2-butanone, 2-pentanone and 1-propanol to be possibly elevated in the ALF stage.

263 O below 90 degrees C, and the oxidation of 2-propanol to carboxylates only occurs in the presence of

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

265 yrroles (2 equiv) in refluxing acetic acid/2-propanol to give tripyrrane analogues, and following a d

266 completeness of the reaction increases from propanol to methanol.

267 tide is selectively solvated by hexafluoro-2-propanol to the extent that the fluoro alcohol concentra

268 t can be photoactivated in the presence of 2-propanol to transfer electrons to (99)TcO(4)(-) and inco

269 thyl-2-aminopropane, methanol, or 2-methyl-2-propanol) to form the corresponding alkane-substituted a

270 primarily formed 3-(methylamino)-1-phenyl-1-propanol (TP 166) and 4-(trifluoromethyl)phenol, by hydr

271 eo-1-phenyl-2-palmitoylamino-3-pyrrolidino-1-propanol) treatment or by knockdown of CD9 by the RNA in

272 l(2)O(3) during the catalytic oxidation of 2-propanol using X-ray absorption fine-structure spectrosc

273 ne micelles and 25% 1,1,1,3,3,3-hexafluoro-2-propanol (v/v) confirmed folding of the complete 2F5 epi

274 2-Propanol vapors were introduced in one of the stages to

275 es were measured for saturated toluene and 2-propanol vapors.

276 ned in exposure to the methanol, ethanol and propanol vapours, respectively, in the atmosphere condit

277 production of C3 oxygenates (propanal and 1-propanol) via the heterogeneous hydroformylation reactio

278 This concentration of 2-propanol was crucial not only to enhance the solubility

279 oxy-1,1'-binapthyl ((S)-BINOL), AlMe3, and 2-propanol was established through 1H and 27Al NMR spectro

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

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

282 When the mole fraction of 2-propanol was higher than 0.68, the orientation of 2-prop

283 re and conductivity, while the response to 2-propanol was less predictable.

284 The free hydroxyl group of the propanol was required for high potency, since acylation

285 n-Propanol was used as an internal standard and the three

286 WT mice, the urinary excretion of carnosine-propanols was decreased in AR-null mice.

287 -stage, dual-phase microdevice allowed the 2-propanol wash step, typically required to remove protein

288 e matrix eliminates both guanidine and the 2-propanol wash that can inhibit downstream PCR and compet

289 pyl group at the liquid/vapor interface in 2-propanol/water binary mixtures was studied by vibrationa

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

291 15 degrees ) in 35% 1,1,1,3,3,3-hexafluoro-2-propanol/water is smaller than the angle found in other

292 nary phase diagrams of canola oil/lecithin:n-propanol/water microemulsions in the presence of differe

293 When transferred from propanol into 40:60 propanol:water under acidic conditions, a remarkably slo

294 for the solvolysis reaction in hexafluoro-2-propanol, we synthesized a series of isotopically labele

295 ombinations, we established that ethanol and propanol were both highly suitable for chain elongation.

296 l-4-trifluoromethy l-2-imidazolyl)phenoxy]-2-propanol], which showed no agonistic activity, had only

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

298 Ab initio calculations on 2-propanol with or without a hydrogen bonding partner, in

299 ion but deflated on the beta-C position in 2-propanol with respect to the values predicted by the sem

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