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1 n of alcohols were studied on the example of cyclohexanol.
2 he enantiopure (1S,2S)-2-(1-H-imidazol-1-yl)-cyclohexanol.
3 olvent consisting of 70% 1-dodecanol and 30% cyclohexanol.
4 ot by the addition of an equimolar amount of cyclohexanol.
5 hat is observed at optimal concentrations of cyclohexanol.
6 ation of one insecticide solvent metabolite, cyclohexanol.
7 te for alcoholysis of phenyl isocyanate with cyclohexanol.
8 exanol but EPPs were more prolonged in 20 mM cyclohexanol.
9 e more complex reaction pathways than simple cyclohexanol.
10 es a strongly nonideal solvation behavior of cyclohexanol.
11 arged transition state in the dehydration of cyclohexanol.
12 thylheptyl)phenyl]-trans-4-(3-hydroxyprop yl)cyclohexanol].
13                                              Cyclohexanol (10-20 mM) also caused prolonged episodes o
14                                              Cyclohexanol (10-25 mM) reduced endplate potential (EPP)
15 he oxidation of cyclohexane to cyclohexanone/cyclohexanol (100 degrees C, conversion: 17.7%) is super
16                                     Volatile cyclohexanol (23 mV; 2575th, 19-38), 3-hydroxy-2-butanon
17 thylheptyl)phenyl]-trans-4-(3-hydroxyp ropyl)cyclohexanol ([3H]CP55,940) in a concentration-dependent
18  (HNuc(1)), such as an alcohol (neopentanol, cyclohexanol, 4-methylumbelliferone, and Boc-Tyr-OMe), a
19 ion, phenol could be hydrogenated to furnish cyclohexanol (93-95% yield) at ambient pressure at 50 de
20 ol (AH5183; (-)-trans-2-[4-phenylpiperidino] cyclohexanol), a drug which blocks the refilling of syna
21 trans-4-[(2,4-dibromanilin-6-yl)-methyamino]-cyclohexanol, a mucolytic drug applied by inhalation, su
22 ,1-dimethylheptyl)phenyl]-4-(3-hydroxypropyl)cyclohexanol], a potent cannabinoid that binds with simi
23 hibits the well-known reduction of phenol to cyclohexanol, affording control of product ring saturati
24  functionalized stereoselectively to provide cyclohexanols after oxidation of the carbon-silicon bond
25                                              Cyclohexanol also increased quantal content of evoked tr
26 , associated with increased plasma levels of cyclohexanol, an insecticide solvent metabolite.
27 l methacrylate in the presence of mixture of cyclohexanol and 1-dodecanol as a porogenic solvent.
28 ith formaldehyde or methane, and on ethanol, cyclohexanol and 1-hydroxymethyl-tetrahydropyran are pre
29 ties >95% are obtained with trans-2-phenyl-1-cyclohexanol and 2,2-diphenylcyclopentanol vinyl ethers.
30        Here, the oxidation of cyclohexane to cyclohexanol and cyclohexanone is used as a model reacti
31  solid-acid-catalyzed phenol alkylation with cyclohexanol and cyclohexene in the apolar solvent decal
32 ized by replacement of H in the -OH group of cyclohexanol and phenol with alkali or alkaline earth me
33 ignificant migration of the hydroxy group in cyclohexanol and the double bond in cyclohexene with res
34 aturation kinetics for oxidation of ethanol, cyclohexanol, and 1-butanol are quantitatively explained
35 dustrial wastewater bioreactor that utilized cyclohexanol as a sole carbon source.
36 e HBEA catalyse aqueous phase dehydration of cyclohexanol at a rate significantly higher than hydroni
37                          Modelling indicated cyclohexanol binding (-3.8 kcal/mol) to voltage-sensitiv
38                Molecular modelling indicated cyclohexanol binding (-6 kcal/mol) to a previously ident
39  blocked K(+) channels more effectively than cyclohexanol but EPPs were more prolonged in 20 mM cyclo
40 ot caused by the limited access of phenol to cyclohexanol, but is due to the absence of a reactive el
41 her with molecular modelling, indicated that cyclohexanol causes selective, allosteric antagonism of
42 iation of NADH from the abortive enzyme-NADH-cyclohexanol complex than from the enzyme-NADH complex.
43                   For liquid-phase catalytic cyclohexanol dehydration, these SiO(x) sites exhibit up
44 yoxy-methyl-1-cyclo-hexanone to give a vinyl cyclohexanol derivative and (2) a highly stereoselective
45     Thus, it is demonstrated that protonated cyclohexanol dimers dehydrate without the formation of a
46 y accounts for the initial rates of 1-(13) C-cyclohexanol disappearance and the appearance of the dif
47  for the synthesis of densely functionalized cyclohexanols establishes five contiguous stereocenters
48         Synthesis and testing of a series of cyclohexanol ethylpiperazines identified ( S)-(-)- 17i (
49  g(cat)(-1) at 170-175 degrees C), such that cyclohexanol formation is significant only at higher tem
50           Consistent with a previous report, cyclohexanol forms initially but then esterifies to cycl
51 acetophenone from 1-phenylethanol oxidation, cyclohexanol from cyclohexane hydroxylation, and cyclohe
52 ethyl-heptyl)-2,6-dimethoxy-phenyl]-3-methyl-cyclohexanol), greatly attenuated leukocyte adhesion in
53                                              Cyclohexanol inhibited whole-cell currents recorded from
54     Transient kinetics experiments show that cyclohexanol inhibition is due to a slower rate of disso
55 ial rearrangement between hydronium ions and cyclohexanols inhibits further increases in the reaction
56 r condensation, one chiral separation of the cyclohexanol intermediate, an ether formation using a tr
57 in cyclohexanolate, which indicates that the cyclohexanol is activated upon metal substitution.
58 yclohexanol sets in only after a majority of cyclohexanol is dehydrated to cyclohexene.
59 rophile as long as a significant fraction of cyclohexanol is present.
60 exemplified by intramolecular dehydration of cyclohexanol, is markedly influenced by steric constrain
61                           In the presence of cyclohexanol, its protonated dimers at Bronsted acid sit
62  occurs with myo-inositol-d-galactopyranose, cyclohexanol, mannitol, or glycerol as acyl acceptor.
63 ing cyclohexanol precursors and suggest that cyclohexanol may facilitate investigation of mechanisms
64 echanism; for both cases, the dehydration of cyclohexanol occurs via an E1 mechanism with the cleavag
65  C spectra show that dehydration of 1-(13) C-cyclohexanol occurs with significant migration of the hy
66      Using the intramolecular dehydration of cyclohexanol on H-MFI zeolites in water, we quantitative
67 ic and mechanistic study of the reactions of cyclohexanol on zeolite HBEA in 130 degrees C water.
68 sertion in each of the ORFs was screened for cyclohexanol oxidation in E. coli.
69  transposon mutants accumulated a variety of cyclohexanol oxidation intermediates.
70              A region that was essential for cyclohexanol oxidation was localized to a 14-kb fragment
71                                              Cyclohexanol, phenol, benzoic acid, and phenanthrene fra
72  of organophosphorus insecticides containing cyclohexanol precursors and suggest that cyclohexanol ma
73          In contrast, high concentrations of cyclohexanol produce noncompetitive substrate inhibition
74  endplate voltages and currents, showed that cyclohexanol reduced postsynaptic sensitivity to acetylc
75 sandwiched between the two methylenes in the cyclohexanol ring and the hydroxyl group of ethanol hydr
76 oiety and the two flanking methylenes in the cyclohexanol ring of cholesterol.
77                   In perineurial recordings, cyclohexanol selectively inhibited presynaptic K(+) curr
78                       Phenol alkylation with cyclohexanol sets in only after a majority of cyclohexan
79                                As phenol and cyclohexanol show similar adsorption strength, this stri
80 netobacter sp. strain SE19, and oxidation of cyclohexanol to adipic acid was demonstrated in recombin
81  encode enzymes catalyzing the conversion of cyclohexanol to adipic acid were identified.
82 he 4-O-5 linkage) is hydrogenated to produce cyclohexanol under conditions investigated.
83 trace [(3)H]-(-)-trans-2-(4-phenylpiperidino)cyclohexanol (vesamicol) with ACh, and Michaelis-Menten
84 potent anticholinergic 2-(4-phenylpiperidino)cyclohexanol (vesamicol, 1) in which the cyclohexyl frag
85 ine transporter ligand 2-(4-phenylpiperidino)cyclohexanol (vesamicol, 1), 22 N-hydroxy(phenyl)alkyl d
86 value up to 98%) synthesis of trisubstituted cyclohexanols was achieved by using a tandem Henry--Mich
87 picomoles of norbenzphetamine and 21 pmol of cyclohexanol were formed per nmol of cyt P450.
88  500 pmol of norbenzphetamine and 58 pmol of cyclohexanol were formed per nmol of cyt P450.
89 ectly produces trans-2-(dimethylphenylsilyl)-cyclohexanol, whereas the less favored boat-like transit
90 )-vesamicol [(-)-trans-2-(4-phenylpiperidino)cyclohexanol], which binds tightly to an allosteric site
91                Acetic acid, butyric acid and cyclohexanol with vinegar, cheese and camphor odours wer