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1 lic vapors (ethanol, methanol, propanol, and isopropanol).
2 d in silica-based extractions (guanidine and isopropanol).
3  cyclohexane molecules, but did reveal bound isopropanol.
4 n, VA cells were cultured in the presence of isopropanol.
5 acrylate-block-polystyrene nanoassemblies in isopropanol.
6 lization capacity was achieved with absolute isopropanol.
7  a representative reaction, the oxidation of isopropanol.
8 y in MS and elution with a gradient of water/isopropanol.
9  formate salts as hydrogen donors in aqueous isopropanol.
10 nsfer hydrogenation of acetophenone in basic isopropanol.
11  isomalt glass (2.6 x 10(-6)) than in liquid isopropanol (1.1 x 10(-5)).
12  electrochemical allylic alkylation in water/isopropanol (1:1 v/v) and 0.2 m KHCO(3) solution at room
13 n MS-compatible mobile phase (59% water, 40% isopropanol, 1% formic acid) was used to remove the resi
14 nation rates were reduced from 3.04% for 70% isopropanol-1% iodine (control antiseptic) to 1.04% for
15 iodine (control antiseptic) to 1.04% for 70% isopropanol-1% iodine-5% DMSO (P < 0.01).
16 improved microscale synthesis of 2-tritiated isopropanol ([2-3H]iPrOH) and R-tritiated reduced beta-n
17        Hexane (hex) or the more polar hexane:isopropanol (3:2 v/v) (hex:isoprop) were used to impact
18    Maceration using the binary system hexane/isopropanol (50/50) was found to be the most efficient p
19 hest lipid removal (87%), followed by hexane/isopropanol (78%).
20 imethylformamide, 80% 5-hexene-1,2-diol, 80% isopropanol, 80% ethanol and 40% trifluoroethanol showed
21 tion under the coupling conditions, although isopropanol, a secondary alcohol, may serve as terminal
22                This study evaluated ethanol, isopropanol, acetone, and ethyl acetate for extracting o
23 hown for NH(3)/ethanol, acetone/ethanol, and isopropanol/acetone mixtures, which are relevant in view
24 e., methanol, acetonitrile, isopropanol, and isopropanol-acetonitrile) and four liquid-liquid extract
25  HPLC and a solvent system containing hexane/isopropanol/acetonitrile/acetic acid (800/8/30/1, v/v) u
26 monstrated that the extraction solvents with isopropanol: acetonitrile: water (3:2:2 ratio) and 80% m
27 ed pyridine aggregation but had no effect on isopropanol aggregation.
28  reaction conditions, but in the presence of isopropanol, aldehydes 3a-3i are converted to an equival
29  from gut microbiota (formate, methanol, and isopropanol; all elevated).
30 res of 40% benzene or 40% cyclohexane in 50% isopropanol and 10% water showed no bound benzene or cyc
31 ward a broad array of substrates including n-isopropanol and beta-estradiol.
32  RNA is then recovered by precipitation with isopropanol and can be used for several applications.
33                             Use of propanol, isopropanol and chlorhexidine can significantly decrease
34 g the molecules in organic solvents, such as isopropanol and dimethylsulfoxide or by enzymatic cleava
35                The oils extracted by ethanol/isopropanol and ethanol/n-hexane significantly showed th
36 e reagents used for conventional extraction (isopropanol and guanadinium hydrochloride), which are po
37           Both TPA6 and TPA7 were soluble in isopropanol and had a M(w) of 3.9 and 4.2 kDa respective
38                        SANS data showed that isopropanol and pyridine both form clusters in water res
39 de in water mixtures with methanol, ethanol, isopropanol and t-butyl alcohol.
40 rkers such as acetone, ammonia, ethanol, and isopropanol and test sensor system capabilities for alco
41                   Competition reactions with isopropanol and trimethyl(methallyl)silane are interpret
42 id of PCR inhibitors that are reagent-based (isopropanol) and sample-based (indigo dye), both of whic
43 ganic solvents (i.e., n-hexane, ethanol, and isopropanol) and their binary mixtures was evaluated bas
44  n-butanol, 1,3-propanediol, 1,3-butanediol, isopropanol, and butyrate.
45 butanol, acetonitrile, methanol, n-propanol, isopropanol, and isobutanol.
46 ation methods (i.e., methanol, acetonitrile, isopropanol, and isopropanol-acetonitrile) and four liqu
47 nd compare it to photolysis in liquid water, isopropanol, and octanol.
48 sters of methanol, ethanol, ethylene glycol, isopropanol, and propylene glycol are obtained with grea
49 BS increased in the presence of sorbic acid, isopropanol, and sodium azide.
50 tion, PLA conditioning of the cartridge with isopropanol, and solvent volume introduced into the rese
51 um were recovered by means of formaldehyde-, isopropanol- and ethanol-based extractions and analyzed
52                                Additionally, isopropanol appeared to be the most straightforward and
53 e used as substrates; N-benzoyloxyamines and isopropanol are employed as the amine source (oxidant) a
54 in the presence of various concentrations of isopropanol as a function of time.
55 EP under identical conditions, but employing isopropanol as a hydrogen donor.
56 tion with dioxazolone amidating reagents and isopropanol as an environmentally friendly hydride sourc
57 latin can be used for such analyses by using isopropanol as precipitating reagent.
58                                    Employing isopropanol as terminal reductant, exposure of allyl ace
59  transfer hydrogenation conditions employing isopropanol as terminal reductant, isoprene couples to a
60  in combination with K(2)CO(3) (4 mol %) and isopropanol as the hydrogen donor.
61 -2j under the same conditions, but employing isopropanol as the terminal reductant.
62 olar protic solvents (methanol, ethanol, and isopropanol) as well as using solely the nebulizing gas
63 opha enabled production of the fusel alcohol isopropanol at up to 216 mg/L, the highest bioelectroche
64 in produced advanced biofuels, n-butanol and isopropanol, at high yield (0.31 g g(-1)), titre (15.4 g
65 point using solid carbon dioxide (CO2) in an isopropanol bath.
66 , indicating that surface species leading to isopropanol become more strongly adsorbed on the surface
67 rogressors demonstrated enhanced activity in isopropanol biosynthesis, biotin biosynthesis II, and ph
68 ous denaturation and chromophore trapping by isopropanol/borohydride, followed by exhaustive protein
69                            The metabolism of isopropanol by VA cells resulted in very little reductio
70 ture using hexane/ethanol (COBio) and hexane/isopropanol (COHar).
71                                   Increasing isopropanol concentration above 40% resulted in a decrea
72 enase and trypsin inhibitors, as compared to isopropanol containing solvents (P<0.05).
73 the non-defatted flour and those defatted by isopropanol containing solvents throughout the storage (
74  low dielectric solvents (acetone, methanol, isopropanol, DMF, DMSO, chloroform, and CCl(4)).
75 se data indicate that live-cell PCR and LiCl-isopropanol DNA precipitation are ideal to prepare DNA f
76  melting curve analysis, we showed that LiCl-isopropanol DNA precipitation removed primers and small,
77 omous studies of TEMPO-catalyzed ethanol and isopropanol electro-oxidation, demonstrating rapid ident
78 trolysis studies confirm that the product of isopropanol electrooxidation is acetone, generated with
79                               In conclusion, isopropanol enriched DEN gas greatly improves the detect
80 t extraction of soybean seed powder with 40% isopropanol enriches lower abundance proteins and is a s
81 out fluid or in large molecule fluids (e.g., isopropanol, ethanol, or fluorinert), the high-pressure
82      Bioactivity guided isolation of rhizome isopropanol extract led to the identification by HPLC an
83                                              Isopropanol-extracted avocado pulp oil (APO) showed the
84                      We investigated whether isopropanol extraction could facilitate resolution of th
85   Results on FA composition using the hexane/isopropanol extraction method were the same in terms of
86 ntaminants were removed by phenol-chloroform-isopropanol extraction prior to DNA precipitation.
87                                              Isopropanol extraction was the method of choice for lipi
88 ction procedure were clearly seen in the 40% isopropanol extracts.
89 lamide gels by pretreating the gels with 50% isopropanol followed by distilled water treatment.
90 hted by evaluating the transient response of isopropanol formation following either removal of the re
91 industrially important chemicals acetone and isopropanol from abundant, low-cost waste gas feedstocks
92                       The samples grafted in isopropanol gave colors and lambdamax intermediate betwe
93                  Suspensions of acetone- and isopropanol-grown R. rhodochrous readily metabolized ace
94         Surface samples were collected using isopropanol imbued non-woven wipes from hard surfaces an
95 tion producing longer-range structuring than isopropanol in 3 m solutions.
96 ectrometry, we optimized solvent conditions: isopropanol in a triethylamine/hexafluoroisopropanol mix
97 and 2 are active for the electrooxidation of isopropanol in the presence of strong base (potassium t-
98 atom transfer (HAT) of the alpha-C-H bond in isopropanol, in contrast to that of TiO(2) or CuO, which
99 ies of the GO doped isotropic media, such as isopropanol IPA, were observed to be much lower than the
100 turing (aggregation) of aqueous solutions of isopropanol (IPA) and pyridine and the effect on structu
101 ic materials common in bioparticle analysis: isopropanol (IPA) and sucrose.
102                               We screened an isopropanol (IPA) extract of the plant commensal Bacillu
103 f product per mol of cells) to biofuels like isopropanol (IPA), 2,3-butanediol (BDO), C(11)-C(15) met
104 l, ethylene glycol (EG), ethyl acetate (EA), isopropanol (IPA), propylene glycol (PG), polyethylene g
105 ddition of organic solvents (ethanol (EtOH), isopropanol (IPA), tert-butanol (TBA) and tetrahydrofura
106 with acid vapor from propionic acid (PA) and isopropanol (IPA), the ion suppression effects from trif
107 xtures were compared using methanol (MeOH)-, isopropanol (IPA)-, and acetonitrile (ACN)-based PCMF at
108 ), n-butanol (nBuOH), ethyl acetate (EtOAc), isopropanol (iPrOH), and tetrahydrofuran (THF).
109 solvents including tetrahydrofuran (THF) and isopropanol (iPrOH).
110 eover, selective tandem double alkylation of isopropanol is achieved by sequential addition of differ
111  where an aerosol of a pure solvent, such as isopropanol, is mixed with the sample aerosol generated
112 ile alcohols, such as methanol, ethanol, and isopropanol lead to a significant reduction in sodium io
113 cantly contribute; however, alcohols such as isopropanol may inhibit degradation by quenching ROT exc
114         Identical products are obtained upon isopropanol-mediated transfer hydrogenation of donor-acc
115 ctivity modifications, and a high-performing isopropanol metabolic pathway, are isolated from librari
116 ne glycol, dimethylsilanediol, formaldehyde, isopropanol, methanol, methylethyl ketone, methylsulfone
117                                          The isopropanol method extracted 937 lipid species from 20 m
118          Here, we compared a simple one-step isopropanol method to a two-step methyl-tert-butyl ether
119                                  The ethanol/isopropanol mixture would be a promising solvent for n-h
120 ed of a solvent extraction with a hexane and isopropanol mixture, and a further clean-up step.
121 rried out upon its immobilization from water-isopropanol mixtures with the high (90%) content of orga
122 rogen bonding of the Oligomycin A side-chain isopropanol moiety with the carbonyl group of the dienop
123                      Ethyl acetate, ethanol, isopropanol, n-heptane and cyclopentyl methyl ether (CPM
124 (VM) heating prior to UAE using a mixture of isopropanol/n-hexane (1:1) as solvent.
125 , or n-octane as nonclustering modifiers and isopropanol or ethanol as clustering modifiers.
126 ion, which is typically 1.5-3 mol % ratio of isopropanol or ethanol in nitrogen.
127 chiral SFC (Chiralcel OJ-3 and Chiralpak IB, isopropanol or ethanol with 25 mM isobutylamine/carbon d
128  organometallic catalysts most often rely on isopropanol or formate to generate the reactive hydride
129 thod and liquid-solid extraction with hexane/isopropanol or with hexane/acetone were investigated, as
130 urnover frequencies of 3.2 and 4.8 s(-1) for isopropanol oxidation are achieved with 1 and 2, respect
131                 Water substantially promotes isopropanol oxidation in the liquid phase.
132 dox changes, but the metabolic by-product of isopropanol oxidation is acetone.
133  nm and use them as model catalysts to study isopropanol oxidation to acetone in both the liquid and
134 As)--N-ethanol palythine (= asterina-330), N-isopropanol palythine (= aplysiapalythine A), and N-ethy
135 nto the chromosome together with a synthetic isopropanol pathway.
136                  (i) Silica-assisted ethanol/isopropanol precipitation ensures reproducible and effic
137 hat lipid profiling greatly benefits from an isopropanol precipitation in terms of simplicity, protei
138               These results demonstrate that isopropanol precipitation is an excellent sample prepara
139                                              Isopropanol precipitation is not limited to untargeted p
140                         Chaotropic lysis and isopropanol precipitation were used to extract RNA from
141 w how live E coli cell PCR and one-step LiCl-isopropanol purification can streamline DNA engineering.
142                             The oxidation of isopropanol results in similar redox changes, but the me
143                    Trapping studies using d8-isopropanol showed deuterium incorporation in 5-chloro-2
144 0%, 20%, 30%, 40%, 50%, 60%, 70% and 80%) of isopropanol showed that greater than 30% isopropanol was
145 standard acetonitrile enriched nitrogen gas, isopropanol showed the highest increase in regards to pe
146 of WGO and PGO delivered in organic solvent (isopropanol) showed dose-dependent antimicrobial activit
147 ze, i.e., methanol, ethanol, n-propanol, and isopropanol, showing that fine control over the thermal
148 cavenging and quenching agents (sorbic acid, isopropanol, sodium azide, and tert-butanol) that are co
149                                           In isopropanol solution, most products appeared to result f
150 gated the effects of post-column addition of isopropanol solutions of formaldehyde, 2,2-dimethylpropa
151       Interestingly, however, while in polar isopropanol solvent at low concentration, NTA shows a ty
152                          The dichloromethane/isopropanol solvent has been identified as an optimal sp
153  solvothermal treatment of Co and Mn ions in isopropanol solvent mixed with glycerol.
154                                          The isopropanol solvent plays several crucial roles: activat
155  exceptional selectivity in the oxidation of isopropanol to acetone, with a hydrogen production rate
156      The transformation uses copper wire and isopropanol to promote the reaction.
157 -helix forms on addition of small amounts of isopropanol to the aqueous subphase, and appears to be a
158 atalyzed a hydride transfer from C-2-labeled isopropanol to the re face of oxidized nicotinamide aden
159 t VOCs including acetone, methanol, ethanol, isopropanol, toluene and xylene at concentrations rangin
160 rystallographic experiments (low pH and 26 % isopropanol), two symmetrically related monomers form a
161 r the transfer hydrogenation of ketones with isopropanol under ambient conditions.
162                           In the presence of isopropanol under otherwise identical conditions, aldehy
163  of isopropanol showed that greater than 30% isopropanol was suitable for preferential enrichment of
164   Efficacy in defatting was higher than when isopropanol was used.
165             Using a radical scavenger (i.e., isopropanol), we determined that halogenated products of
166 nging the dielectric environment from air to isopropanol, we observe a 25% reduction in the transport
167                        For that, ethanol and isopropanol were evaluated in terms of their suitability
168                 Low concentrations (0.1%) of isopropanol were found to improve resolution and sensiti
169 ts, and protic solvents such as methanol and isopropanol were identified as optimal.
170  intermediates that lead to the formation of isopropanol were removed from the catalytic surface was
171 teractions involving the aliphatic groups of isopropanol were unaffected by GdmCl, indicating that th
172 action protocols (methyl tertbutyl-ether and isopropanol) were assessed.
173 milar extent by propofol, phenylethanol, and isopropanol when added at anesthetic concentrations, but
174 was achieved by treating the microarray with isopropanol, which prevents nucleic acids from dissolvin
175                                              Isopropanol with 1.0% trichloroacetic acid was found to
176 loromethane, and methyl-tert butyl ether and isopropanol with hexane).
177          Using a binary mixture of water and isopropanol, with the latter serving as a surrogate for

 
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