ライフサイエンスコーパス: propanol

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

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

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

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

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

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

7 -2-octanol being 1700 times lower than for 2-propanol.

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

9 MPD is significantly more excluded than 2-propanol.

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

11 ) = 78.7 s(-1) in benzene containing 0.8 M 2-propanol.

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

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

14 roxamic acid by treatment with Nafion-H in 2-propanol.

15 tetramethoxyquinolizine 9 with neat 3-iodo-1-propanol.

16 and acetonitrile--water in the presence of 1-propanol.

17 various concentrations of 2-amino-3-phenyl-1-propanol.

18 antiomeric composition of 2-amino-3-phenyl-1-propanol.

19 e liquid chromatography in the presence of 1-propanol.

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

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

22 formed from monomeric and dimeric adsorbed 1-propanol.

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

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

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

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

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

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

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

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

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

32 2-Propanol (10%-25% gradient) replaced the previously used

33 afford the corresponding (S)-1-substituted 1-propanols 10a-n with a mean enantiomeric excess of 92%.

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

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

36 onditions generated cis-dibenzoquinolizinium propanol 15 in 85% yield with >94% cis-selectivity.

37 Dibenzo[a,g]quinolizinium propanol 15 was prepared enantioselectively in three ste

38 ation of the unique cis-dibenzoquinolizinium propanols 15 and 16and their transformation into bis- an

39 The cis-dibenzo[a,h]quinolizinium propanol 16 was obtained as a single stereoisomer by rea

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

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

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

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

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

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

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

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

48 1 to 100 mM 2-nitroethanol (2ne), 2-nitro-1-propanol (2nprop), and 3-nitro-2-pentanol (3n2pent) at p

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

65 following: acetaldehyde, acetone, butanal, 2-propanol, acetic acid, 2-hexanol, benzoic acid, benzalde

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

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

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

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

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

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

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

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

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

75 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

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

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

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

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

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

92 3-Phenylpropanal, 3-phenyl-1-propanol, and benzyl alcohol were identified as potent a

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

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

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

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

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

98 50 mumol L(-1) were obtained for ethanol, n-propanol, and methanol, respectively.

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

100 r seems to be inhibited in the presence of 1-propanol, and partitioning is the predominant solute ret

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 ent behavior from that of the C18 phase, and propanol appears to disrupt the pi-stacking interactions

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

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

106 f dibenzoquinolizines 9 and 14 with 3-halo-1-propanols are highly cis-selective (94-100% cis), result

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 ndioxyphenyl-2-palmitoylamino-3-pyrrolidi no-propanol (D-t-EtDO-P4) showed a concentration-dependent

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

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

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

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

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

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

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

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

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

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

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), the glucosylceramide (GlcCer) syntha

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

166 The presence of a small amount of 1-propanol has been shown to affect mainly the polarity pr

167 -phenyl-2-hexadecanoylamino-3 -pyrrolidino-1-propanol-HC l (glucosylceramide synthase), which deplete

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

169 reo-1-phenyl-2-decanolylamine-3-morpholino-1-propanol HCl, an inhibitor of glucosylceramide synthase,

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

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

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

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

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

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

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

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

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

179 1,1,1,3, 3,3-Hexafluoro-2-propanol (HFIP) was found to be the best solvent for sol

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

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

184 Two model tyrosinase prodrugs, hydroxyphenyl-propanol (HPP) and N-acetyl-4-S-cysteaminylphenol (NAcSC

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

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

194 2.2]octanes from 3-bromo-2,2-bis(bromomethyl)propanol is developed, making a diverse set of mass-diff

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

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

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

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

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

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

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

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

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

204 Related 2-propanol mediated reductive couplings also are described

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

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

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

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

209 2-Propanol modifier displayed more efficient displacement

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

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

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

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

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

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

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

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

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

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

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

221 dified Curtius rearrangement with 2-methyl-2-propanol or 2-(trimethylsilyl)ethanol to form the stable

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

223 )-1,2,3,4-tetrahydronaphth-1-ylamino]-(2S)-2-propanol oxalate).

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

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

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

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

228 hreo 1-phenyl-2-decanoylamino-3-morpholino-1-propanol (PDMP), which inhibits acid ceramidase or gluco

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

230 Shorter chain alcohols from methanol to n-propanol potentiated acetylcholine (ACh)-induced current

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

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

233 1-phenyl-2-hexadecanoylamino-3-morpholino-1-propanol (PPMP), blocked target membrane glycosphingolip

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

235 1-phenyl-2-hexadecanoylamino-3-pyrrolidino-1-propanol (PPPP) each partially inhibited the ability of

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

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

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

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

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

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

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

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

244 ng probe molecules n-heptane, toluene, and 2-propanol, showed that slow diffusion occurs within the m

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

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

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

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

249 rotational equilibrium isotope effects in 2-propanol strongly imply a hyperconjugative mechanism for

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

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

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

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

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

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

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

257 2-(hydroxymethyl)-(2S,3S)-1,4-benzodiox in-6-propanol, threo and erythro 3-methoxy-8,4'-oxyneolignan-

258 methylpyrroles 10 in refluxing acetic acid-2-propanol to afford tripyrranes 11.

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

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

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

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

263 completeness of the reaction increases from propanol to methanol.

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

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

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

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

268 Quaternization of 14 with 3-chloro-1-propanol under Finkelstein conditions generated cis-dibe

269 cy of methanol, acetonitrile, ethanol, and 1-propanol used as modifiers in packed-column SFC.

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

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

272 2-Propanol vapors were introduced in one of the stages to

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

274 Adsorption of 2-propanol was best modeled by a single Langmuir isotherm

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

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

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

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

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

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

281 ce in adsorption energy for the two sites; 2-propanol was shown to easily displace ethyl acetate from

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

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

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

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

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

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

288 15 degrees ) in 35% 1,1,1,3,3,3-hexafluoro-2-propanol/water is smaller than the angle found in other

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

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

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

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

293 t modifiers such as methanol, ethanol, and 2-propanol were used.

294 chiral N,N-disubstituted trifluoro-3-amino-2-propanols were found to associate with both LDL and HDL,

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

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

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

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

299 favored omega-hydroxy metabolite, 2-phenyl-1-propanol, with product stereoselectivity for the (S)-ena

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