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1  (dimethyl sulfoxide, dimethylformamide, and 2-propanol).
2 R)-2-octanol being 1700 times lower than for 2-propanol.
3      MPD is significantly more excluded than 2-propanol.
4  K) = 78.7 s(-1) in benzene containing 0.8 M 2-propanol.
5 buffer, at high salt (0.5 M NaCl) and in 30% 2-propanol.
6 ydroxamic acid by treatment with Nafion-H in 2-propanol.
7 e chiral column using a mobile phase of 100% 2-propanol.
8 hown for the apolar hydrocarbon solvents and 2-propanol.
9 ent on substrate, and inversely dependent on 2-propanol.
10 -piperazinyl)phen yl)-1,1,1,3,3,3-hexafluoro-2-propanol (1, AMG-3969), a compound that effectively en
11                     From the dichloromethane/2-propanol (1:1) extract of the Indonesian marine sponge
12 ps were similar for dehydration of alkanols (2-propanol, 1- and 2-butanol, tert-butanol) and cleavage
13                                              2-Propanol (10%-25% gradient) replaced the previously us
14 e phase system consisted of 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 5% methanol (mobil
15 thanol (mobile phase A) and 385mM hexafluoro-2-propanol, 14.5mM triethylamine, and 90% methanol (mobi
16 eonine formylation was found for 50% H2O/33% 2-propanol/17% formic acid.
17 n buffer solvent with added methanol (MeOH), 2-propanol (2-PrOH), and dimethyl sulfoxide (DMSO) revea
18 s, KIE = 1.7), ethanol (14.3 ps, KIE = 1.8), 2-propanol (28 ps, KIE = 1.4), and 2,2,2-trifluoroethano
19  containing sodium dodecyl sulfate (SDS) and 2-propanol (2PN).
20 ps: (1) tissue extraction using acetonitrile/2-propanol (3+1, v+v) followed by 0.1M potassium phospha
21 anolicus (W110A TESADH) in Tris buffer using 2-propanol (30%, v/v) as cosolvent and cosubstrate.
22 spectroscopic studies revealed that 2-methyl-2-propanol (4) competes with substrates for binding to t
23 ), and a negative dependence on the 2-methyl-2-propanol (4) concentration.
24 ried sample in the mobile phase (cyclohexane:2-propanol:5 mM phosphoric acid, 50:50:2.9, v/v/v).
25 ed that defatting with WSB (20 degrees C) or 2-propanol (75 degrees C) decreased the gliadin and incr
26 nterchange reactions, caused either by heat (2-propanol, 75 degrees C) or by the solvent WSB, which a
27 e following: acetaldehyde, acetone, butanal, 2-propanol, acetic acid, 2-hexanol, benzoic acid, benzal
28 eatic acini were measured by extraction with 2-propanol/acetonitrile, followed by separation and quan
29 utilizing titanium tetraisopropoxide, BINOL, 2-propanol additive, and tetraallylstannane as allylatin
30 alcohols (methanol, ethanol, 1-propanol, and 2-propanol) adsorbed into Cu-BTC thin films.
31 ntation of sulfide radical cations (2-phenyl-2-propanol and diaryl disulfides).
32 ted, or aliphatic aldehydes 2a-i mediated by 2-propanol and employing a cyclometalated iridium C,O-be
33 etention (S(N)F) mechanisms were located for 2-propanol and exo-2-norbornanol.
34 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
35  alcohols 2-methyl-2,4-pentanediol (MPD) and 2-propanol and of glycerol with condensed spermidine(3+)
36                                      Achiral 2-propanol and short-chain (R)- and (S)-2-alkanols were
37 f HMPA and proton donors (methanol, 2-methyl-2-propanol, and 2,2,2-trifluoroethanol) on SmI2-initiate
38  organic solvents such as methanol, acetone, 2-propanol, and acetonitrile.
39 mplex was then purified, dried, dissolved in 2-propanol, and cast onto a glass slide to form a self-s
40 pe and concentration of alcohol (1-propanol, 2-propanol, and ethanol), type of salt (sodium citrate,
41 tion of two polar molecules, acetic acid and 2-propanol, and one nonpolar molecule, dodecane, on LiNb
42 The photoreactions in cyclopentane, 2-methyl-2-propanol, and the gas phase occurred exclusively throu
43 stituted N-benzyl-N-phenyl-trifluoro-3-amino-2-propanols are described that reversibly inhibit choles
44          We show, by using the conversion of 2-propanol as a probe reaction, that the surface termina
45 ohol chain (C1-C3) and geometry (1-propanol, 2-propanol) as well as their polarity on the sensing per
46 ter with ease, while larger alcohols such as 2-propanol, as well as DMSO, are excluded.
47 baking test, using wheat flour defatted with 2-propanol at 20 degrees C, was established to determine
48 ly present in dough from flour defatted with 2-propanol at 20 degrees C.
49 ume compared to control flour extracted with 2-propanol at 20 degrees C.
50 urrent drift gas of the system is doped with 2-propanol at 20 muL/h, full baseline resolution of the
51             Exposure of the nanoparticles to 2-propanol at 30 degrees C leads to immediate partial re
52  the presence of Zn(II) ions as templates in 2-propanol at 70 degrees C.
53 e capillary tip to construct a fine layer of 2-propanol-based colloidal graphite.
54                           In the presence of 2-propanol, but under otherwise identical conditions, vi
55                            In the absence of 2-propanol, but under otherwise identical reaction condi
56 traction procedures (e.g., chaotropic salts, 2-propanol) can be avoided, making the method more condu
57 nt in situ study of the partial oxidation of 2-propanol catalyzed with PdO nanoparticles supported on
58 reas increasing concentrations of ethanol or 2-propanol cause the helices of the alpha 4H tetramer fi
59 of organic solvents (acetonitrile, methanol, 2-propanol), chaotropic agents (6 M urea, 6 M guanidine-
60 utyric acid 2 using 1,1,1-trichloro-2-methyl-2-propanol (chloretone) was developed.
61 PET was used, such as 1,1,1,3,3,3-hexafluoro-2-propanol (commonly referred to as HFIP), as the sample
62 e chiral N,N-disubstituted trifluoro-3-amino-2-propanol compounds do not affect lipoprotein structure
63 ical conformation at high TFE and hexafluoro-2-propanol concentrations.
64 allenamide 1e to aldehyde 2a conducted using 2-propanol-d(8) as the terminal reductant delivers deute
65 n the presence of aldehydes 2a-i mediated by 2-propanol delivers products of (trimethylsilyl)allylati
66 hyl-4-trifluoromethyl -2-imidazolyl)phenoxy]-2-propanol dihydrochloride (CGP-20712A) prevented isopro
67 that is intermediate in size between MPD and 2-propanol does not observably affect DNA force curves.
68 amine-Ru(II) complex combined with t-BuOK in 2-propanol effectively catalyzes enantioselective hydrog
69 ous alcohols trifluoroethanol and hexafluoro-2-propanol efficiently promote the cyclocondensation of
70                            In the absence of 2-propanol, enantioselective carbonyl reverse prenylatio
71 tics of five hydraulic fracturing compounds (2-propanol, ethylene glycol, propargyl alcohol, 2-butoxy
72                              Four compounds (2-propanol, ethylene glycol, propargyl alcohol, and 2-bu
73                            A single n-hexane/2-propanol extract containing both types of compounds wa
74 butanol (WSB; extracted at 20 degrees C) and 2-propanol (extracted at 75 degrees C) had inferior exte
75            A single dilution of seed oils in 2-propanol facilitated the direct use samples in the DPP
76        For the two species examined and at a 2-propanol flow rate of 160 muL/h, MPA demonstrated the
77            Ethyl acetate could also displace 2-propanol from the silica, and least-squares modeling a
78                          Irradiation of 4 in 2-propanol gave compounds 6 and 7 that also come from in
79 lpha-d-glucopyranosyl fluoride in hexafluoro-2-propanol gives two products, 1,1,1,3,3,3-hexafluoropro
80 hell section can be selectively dissolved by 2-propanol, giving yolk-shell nanostructures and, thus,
81 y (HPLC) using an amino column with a hexane/2-propanol gradient.
82  separated using a chiral column eluted with 2-propanol:hexane.
83 ochloric acid in a 1:1 mixture of hexafluoro-2-propanol (HFIP) and methylene chloride (DCM) is descri
84 pin forming peptide, MrH3a, in 8% hexafluoro-2-propanol (HFIP) and the dynamics of its refolding foll
85 ns are solubilized in 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) at 25-30% (wt/vol) for extrusion into
86                        The use of hexafluoro-2-propanol (HFIP) in the separation medium, and as an ad
87 found that the use of 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP) or dimethyl sulfoxide (DMSO) significa
88                      1,1,1,3, 3,3-Hexafluoro-2-propanol (HFIP) was found to be the best solvent for s
89  solvent of water and 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), polyene cyclizations using allylic al
90 nd a unique additive, 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP), to achieve highly efficient separatio
91                                   Hexafluoro-2-propanol (HFIP), which promotes alpha-helix formation,
92 sodium dodecyl sulfate (SDS), and hexafluoro-2-propanol (HFIP).
93 at microdroplets formed in dilute hexafluoro-2-propanol (HFIP).
94 2,3,4-tetrahydro-1-naphthalenyl]amino]-(2S)- 2-propanol hydrochloride [SR 59230A]) stimulated respons
95 iments to examine interactions of hexafluoro-2-propanol in a 30% fluoro alcohol-50 mM phosphate buffe
96 l dehydration and alkylation of m-cresol and 2-propanol in the liquid phase, at high temperatures.
97 obile phase containing acetonitrile:methanol:2-propanol in the ratio of 85:15:33 with 0.01% ammonium
98  our small Pt particles for the oxidation of 2-propanol is attributed to the large amount of edge and
99 acids at room temperature in technical grade 2-propanol is described.
100 nzyl]-N-(3-phenoxyphenyl)-trifluoro-3-am ino-2-propanols is described which potently and reversibly i
101           Photolysis of 3 in argon-saturated 2-propanol led to formation of 5 via intermolecular H-at
102 es in the order water > methanol > ethanol > 2-propanol, linearly according to empirical scales of so
103  active species for the partial oxidation of 2-propanol (<140 degrees C), while the complete oxidatio
104 ined in cyclopentane, methanol, and 2-methyl-2-propanol, media with differing polarities and viscosit
105                                      Related 2-propanol mediated reductive couplings also are describ
106 m complexes modified by SEGPHOS catalyze the 2-propanol-mediated reductive coupling of branched allyl
107 thenium(II)-catalyzed hydrogen transfer from 2-propanol mediates reductive coupling of 1,1-disubstitu
108 tate in a mobile phase consisting of hexane, 2-propanol, methanol, and water (5.5:8:1.5:1).
109 nnected in series using a gradient of hexane-2-propanol mobile phase.
110                                              2-Propanol modifier displayed more efficient displacemen
111 The change in the alcohol's orientation with 2-propanol mole fraction closely tracked changes in its
112  considers the transient binding of a single 2-propanol molecule during mobility measurements.
113 sfer of a proton from a solvating hexafluoro-2-propanol molecule.
114 threonine O-3-phosphate to yield (R)-1-amino-2-propanol O-2-phosphate.
115 n methanol-O-d (16 ps), ethanol-O-d (26 ps), 2-propanol-OD (40 ps), and 2,2,2-trifluoroethanol-O-d (1
116          The ACOD radical reacts with TPZ in 2-propanol-OD with an absolute rate constant of (6.7 +/-
117 rcially available solvent, 2-trifluoromethyl-2-propanol, optimally balances monomer, polymer, and cat
118 modified Curtius rearrangement with 2-methyl-2-propanol or 2-(trimethylsilyl)ethanol to form the stab
119         Ionization of 1,1,1,3,3,3-hexafluoro-2-propanol or benzoic acid results in the observation of
120 1S)-1,2,3,4-tetrahydronaphth-1-ylamino]-(2S)-2-propanol oxalate).
121  is responsible for synthesizing (R)-1-amino-2-propanol phosphate which is the precursor for the link
122 trates that lacked a sulfonate moiety [e.g., 2-propanol, (R)-2-pentanol, and (R)-2-heptanol].
123  acceleration of this reaction by hexafluoro-2-propanol reinforces this view by altering the relative
124 nol was higher than 0.68, the orientation of 2-propanol remained almost constant.
125   Chiral N,N-disubstituted trifluoro-3-amino-2-propanols represent a recently discovered class of com
126 ding probe molecules n-heptane, toluene, and 2-propanol, showed that slow diffusion occurs within the
127 talyzes the phosphorylation of the 1-amino-O-2-propanol side chain of the adenosylcobinamide ring and
128 yzes both the phosphorylation of the 1-amino-2-propanol side chain of the corrin ring and the subsequ
129 al rotational equilibrium isotope effects in 2-propanol strongly imply a hyperconjugative mechanism f
130 crease on going from methanol to ethanol and 2-propanol substrates, in accord with experiment.
131 dimethyl sulfoxide or 1,1,1,3,3,3-hexafluoro-2-propanol, synthetic human Abeta(1-42) readily forms ol
132 than the inversion S(N)2 counterpart for the 2-propanol system.
133 alysis was confirmed for the phenolate/AlMe3/2-propanol system.
134     In contrast to 10% HFIP, 1,1,1-trifluoro-2-propanol (TFIP) did not inactivate prion infectivity b
135                         There is evidence in 2-propanol that geminate reaction within the initial ion
136 xymethylpyrroles 10 in refluxing acetic acid-2-propanol to afford tripyrranes 11.
137 PdO below 90 degrees C, and the oxidation of 2-propanol to carboxylates only occurs in the presence o
138 inding of the substrate analogue (S)-1-amino-2-propanol to EAL eliminates the P(f) state and lowers t
139 lpyrroles (2 equiv) in refluxing acetic acid/2-propanol to give tripyrrane analogues, and following a
140 eptide is selectively solvated by hexafluoro-2-propanol to the extent that the fluoro alcohol concent
141 he study the adsorption of ethyl acetate and 2-propanol to the surface of thin silica sol-gel films i
142 hat can be photoactivated in the presence of 2-propanol to transfer electrons to (99)TcO(4)(-) and in
143 methyl-2-aminopropane, methanol, or 2-methyl-2-propanol) to form the corresponding alkane-substituted
144 -Al(2)O(3) during the catalytic oxidation of 2-propanol using X-ray absorption fine-structure spectro
145 line micelles and 25% 1,1,1,3,3,3-hexafluoro-2-propanol (v/v) confirmed folding of the complete 2F5 e
146                                              2-Propanol vapors were introduced in one of the stages t
147 ties were measured for saturated toluene and 2-propanol vapors.
148                                Adsorption of 2-propanol was best modeled by a single Langmuir isother
149                        This concentration of 2-propanol was crucial not only to enhance the solubilit
150 droxy-1,1'-binapthyl ((S)-BINOL), AlMe3, and 2-propanol was established through 1H and 27Al NMR spect
151 ng hydrogen-bond-donating solvent hexafluoro-2-propanol was found to be consistent with low catalyst
152 A calibration curve for aqueous solutions of 2-propanol was generated and a limit of detection (LOD)
153                    When the mole fraction of 2-propanol was higher than 0.68, the orientation of 2-pr
154 ture and conductivity, while the response to 2-propanol was less predictable.
155 ence in adsorption energy for the two sites; 2-propanol was shown to easily displace ethyl acetate fr
156 wo-stage, dual-phase microdevice allowed the 2-propanol wash step, typically required to remove prote
157 ure matrix eliminates both guanidine and the 2-propanol wash that can inhibit downstream PCR and comp
158 ropyl group at the liquid/vapor interface in 2-propanol/water binary mixtures was studied by vibratio
159 e conformation of melittin in 35% hexafluoro-2-propanol/water is alpha-helical from residues Ile-2 to
160 - 15 degrees ) in 35% 1,1,1,3,3,3-hexafluoro-2-propanol/water is smaller than the angle found in othe
161 TS for the solvolysis reaction in hexafluoro-2-propanol, we synthesized a series of isotopically labe
162 ent modifiers such as methanol, ethanol, and 2-propanol were used.
163 e chiral N,N-disubstituted trifluoro-3-amino-2-propanols were found to associate with both LDL and HD
164   Two thiols, 2-mercaptoethanol and mercapto-2-propanol, were poorer substrates than CoM, while sever
165 hyl-4-trifluoromethy l-2-imidazolyl)phenoxy]-2-propanol], which showed no agonistic activity, had onl
166 (4)H(c)", benzene hydrogenation catalysis in 2-propanol with added Et(3)N and at 100 degrees C and 50
167                    Ab initio calculations on 2-propanol with or without a hydrogen bonding partner, i
168 ation but deflated on the beta-C position in 2-propanol with respect to the values predicted by the s
169 ysis of an oxygen-saturated solution of 3 in 2-propanol yields products 8, 9, and 10, which were all

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