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1  +/- 4.7% (decay-corrected to starting (11)C-methyl iodide).
2 1.7% 4.7% (decay-corrected to starting (11)C-methyl iodide).
3 m cyclotron-produced (11)C-methane via (11)C-methyl iodide.
4 ssociation spectroscopy and was trapped with methyl iodide.
5 stereoselectivity during the alkylation with methyl iodide.
6 ation of the desmethyl precursor using (11)C-methyl iodide.
7  by reacting the phenol precursor with (11)C-methyl iodide.
8  of the synthesis was achieved using labeled methyl iodide.
9 ation of its phenol precursor 25 with [(11)C]methyl iodide.
10 is too short to fold and thus unable to bind methyl iodide.
11 form in the reaction of the silver salt with methyl iodide.
12  by reacting the phenol precursor with (11)C-methyl iodide.
13 tes from the corresponding alpha-substituted methyl iodides.
14 pled Nd: YAG laser on samples of NO, O2, and methyl iodide; a useful resolution (> 10) was achieved w
15 o[3,4-b]indole 9c followed by treatment with methyl iodide affords disubstituted furo[3,4-b]indole 10
16 ectrophiles, e.g., phenylselenenyl chloride, methyl iodide, allyl bromide, and NFSI, gave predominate
17 olyl carboxamides with alpha-haloacetate and methyl iodide and applications in the stereoselective sy
18                        Alkylation of 14 with methyl iodide and benzyl bromide gave good yields of the
19 the blooms, revealing that concentrations of methyl iodide and dimethylsulfide were significantly red
20 ior in the presence of electrophiles such as methyl iodide and group 11 metal chlorides, akin to the
21 oacetate with nitroarenes, were reacted with methyl iodide and KOH in DMSO to give N-methylpyrroles a
22                              Alkylation with methyl iodide and potassium carbonate gave a 22-methyl d
23      When the carbachlorin was refluxed with methyl iodide and potassium carbonate in acetone, the 22
24          The per-O-methylation reaction with methyl iodide and solid sodium hydroxide in methyl sulfo
25 orresponding sulfonium ion by treatment with methyl iodide and subsequently displaced with iodide.
26  and platinum-catalyzed C-C coupling between methyl iodide and tetramethyltin.
27 The Co(I) corrinoid could be remethylated by methyl iodide, and the protein catalyzed a methyl iodide
28                  Al(n)I(x)- are reacted with methyl iodide, and the reaction mechanisms and products
29 rast, carbon-based electrophiles larger than methyl iodide approach from the convex (exo) face.
30  atmospheric methyl bromide and 5 percent of methyl iodide arise from rice fields worldwide.
31  by trapping of the Pt(II) intermediate with methyl iodide as the methylating reagent.
32 oalkylbacteriochlorins were quaternized with methyl iodide at two or four amine sites per molecule, w
33 mpetitive inhibition experiments reveal that methyl iodide binds weakly within the oligomer cavity wi
34 equent Coulomb explosion of fully deuterated methyl iodide, CD(3)I, irradiated with hard X-rays has b
35 y catalyze the destruction of ozone, whereas methyl iodide (CH(3)I) influences aerosol formation and
36 s in concentrations of carbon monoxide (CO), methyl iodide (CH(3)I), and CO(2) observed during the So
37  and isoprene, while the LMA species removed methyl iodide (CH(3)I), DMS, and isoprene depending on t
38            Efficiently capturing radioactive methyl iodide (CH(3)I), present at low concentrations in
39 hyl-MMCP to CoM was mediated by MT2-A, since methyl iodide:CoM methyl transfer by MMCP and MT2-A did
40 y methyl iodide, and the protein catalyzed a methyl iodide:CoM transmethylation reaction at a rate of
41 on constant K(a) = 2 M(-1), and the oligomer-methyl iodide complex reacts with unimolecular rate cons
42                   It was found that at 300 K methyl iodide decomposes on the Al(111) surface, forming
43 S(N)2-type oxidative addition mechanism with methyl iodide followed by a reductive elimination.
44 Desmethyl precursor 2 was reacted with (11)C-methyl iodide followed by deprotection and high-performa
45    Compound 3 underwent treatment with (11)C-methyl iodide followed by high-performance liquid chroma
46 ohydrate dissolved in dimethyl sulfoxide and methyl iodide, followed by reaction with the base.
47 ions of methyl chloride, methyl bromide, and methyl iodide from flooded California rice fields, we es
48 eaction of the phenolic precursor with (11)C-methyl iodide, giving a radiochemical yield of 51.7% +/-
49 eaction of the phenolic precursor with (11)C-methyl iodide, giving a radiochemical yield of 51.7% 4.7
50 ppe), and Ph(2)PCH(2)P(O)Ph(2) (dppmo)] with methyl iodide have been undertaken.
51 of their corresponding nortropanes with [11C]methyl iodide in approximately 30% radiochemical yield (
52        The reaction between carbohydrate and methyl iodide in dimethyl sulfoxide can result in a comp
53  of carbohydrates in dimethyl sulfoxide with methyl iodide in the presence of base is described.
54 e, however, their subsequent alkylation with methyl iodide in the presence of potassium carbonate aff
55                                Reaction with methyl iodide in the presence of potassium carbonate gav
56  of carbohydrates in dimethyl sulfoxide with methyl iodide in the presence of solid sodium hydroxide
57 o these complexes but slowed the addition of methyl iodide, indicating that the oxidative addition me
58                                              Methyl iodide is a toxic halocarbon with diverse industr
59 reactions between bare aluminum clusters and methyl iodide is addressed, and the chemical differences
60 cysteine and reactive electrophiles, such as methyl iodide (MeI) and methyl toluene sulfonate (MeOTs)
61 approach involved treatment of polymers with methyl iodide (MeI), an alkylating agent, to convert pol
62 s and trans isomers), chloropicrin (CP), and methyl iodide (MeI), have been widely used.
63 equiv of n-butyllithium (n-BuLi) followed by methyl iodide (MeI), or reacting iPrN:BH(3) with 1 equiv
64 ivalent with different alkyl halides such as methyl iodide, methoxymethyl chloride, benzyl bromide, p
65         Methylation of 4a, 14a, and 26a with methyl iodide occurred exclusively at the site of the in
66 e or carboxylic acid precursors using [(11)C]methyl iodide or [(11)C]methyl triflate (generated from
67                                              Methyl iodide or iodomethane (CH3I) has recently been re
68  trace of water in dimethyl sulfoxide before methyl iodide, or by using N,N-dimethylacetamide as the
69  of sorbicillactone A, alkylations involving methyl iodide proceed from the concave (endo) face of th
70                    Radiolabeling with [(11)C]methyl iodide produced [methylpiperazine-(11)C]brigatini
71 this temperature and in this coverage range, methyl iodide produces adsorbed methyl (CH(3,ad)) plus a
72               In hexanes, the reaction using methyl iodide produces aminoborane and methane, whereas
73 olabeling with high specific activity [(11)C]methyl iodide provided derivatives for in vivo evaluatio
74 nt reaction with potassium tert-butoxide and methyl iodide provided the corresponding N-methylated ta
75           Treatment of labeled proteins with methyl iodide released isoprenes that were identified by
76 lamide and reacted with carbon disulfide and methyl iodide to afford a dihydrothiophene derivative.
77                                  Addition of methyl iodide to the intermediate hafnocene resulted in
78 helate ligands promote oxidative addition of methyl iodide to the square planar M(I) centers, by fact
79 l tosylate in situ into the active reactant, methyl iodide, to promote the hydromethylation.
80 dianion intermediate, which upon addition of methyl iodide, trimethylsilyl chloride, or tributyltin c
81 onding lithium aminoborohydrides (LABs) with methyl iodide, trimethylsilylchloride (TMS-Cl), or benzy
82 ered sodium hydroxide before introduction of methyl iodide under nonanhydrous conditions, or by addin
83 esized from high-specific radioactivity [11C]methyl iodide using a high-temperature/high-pressure tec
84 a alkylation of the norprecursors with (11)C-methyl iodide using literature methods.
85 pyridyl trifluoroborate precursor with (11)C-methyl iodide via the Suzuki-Miyaura cross-coupling meth
86                                              Methyl iodide was found to be critical for this dispersi
87 obability for the dissociative adsorption of methyl iodide were measured on Pt(111) at 320 K and at l
88 synthesis of acetyl-CoA when CH3-H4folate or methyl iodide were provided as methyl donors and CO and
89 iol form or modified with iodoacetic acid or methyl iodide, were grown into amyloid fibrils, and the
90 ggish, the Mannich base was quaternized with methyl iodide which afforded much faster exchange reacti
91  degradation can be accelerated by replacing methyl iodide with dimethyl sulfate.
92                              The reaction of methyl iodide with the Al(111) surface was studied by ro