戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (１語後でソート)

通し番号をクリックするとPubMedの該当ページを表示します
1 reached over the 24 h of the experiment with methanolysis.
2 n: the silyl groups are readily removed upon methanolysis.
3 the methanol was in situ consumed in the PET methanolysis.
4 olymerization, the NPr-GBMP was subjected to methanolysis, 3N hydrochloric acid in methanol for 16h a
5                The method involves mild acid methanolysis (5 mM HCl) for 3 h at 84 degrees C followed
6                                     Alkaline methanolysis abolished the binding.
7            Chemical modifications, including methanolysis, acetonide formation, and application of th
8 vides conclusive evidence for the hydrolysis/methanolysis acid-base neutralization pathway, as formul
9 yl group with 2 equiv of 9-BBN-H followed by methanolysis afforded 5-R-4-(9-BBN)-2,5-dihydro-1H-silol
10  ring-opening reaction of the heterocycle by methanolysis, although, under these reaction conditions,
11                                 A succeeding methanolysis and concomitant ring-closing reaction gives
12 of three reactions: CO(2) hydrogenation, PET methanolysis and dimethyl terephthalate (DMT) hydrogenat
13 ZnZrO(x) catalyst was also effective for the methanolysis and hydrogenolysis of C-C bonds (compared t
14 etal-organic framework as a catalyst for the methanolysis and hydrolysis of phosphate-based nerve age
15 (before fragmentation), followed by eventual methanolysis and hydrolysis of ROCH(Cl)OMe.
16 hydrogenolysis, N-Boc protection, reduction, methanolysis, and acetate protection gave methyl N,O-dia
17 steady-state kinetics, ITC binding analysis, methanolysis, and NMR study.
18               Gt alpha was also subjected to methanolysis, and the resulting fatty acyl methyl esters
19 chelic macromonomers through straightforward methanolysis, and the resulting macromonomers could be e
20 e TSP-binding lipid was purified by alkaline methanolysis, anion exchange chromatography and preparat
21 of polyethylene terephthalate by vapor phase methanolysis at relatively low temperatures.
22 cetal, a formal [2 + 2] cycloaddition, and a methanolysis cascade to efficiently generate a highly su
23 ed by formylation and finally acid-catalyzed methanolysis complete the synthesis.
24  and colominic acid were used to confirm the methanolysis depolymerization efficiency of the alpha(2
25 ethyl acetal of hexadecanal produced by acid methanolysis derivatization was no longer present.
26 ved for all serotypes by the use of a single methanolysis, derivatization, and chromatography procedu
27 Disaccharide yield over time is compared for methanolysis, ethanolysis, and butanolysis.
28 lp, NPbeta-Galp, or UDPalpha-Galp, mild acid methanolysis failed to produce any galactofuranoside.
29 Alkenyl-GP was generated by acidic and basic methanolysis from ethanolamine lysoplasmalogen, which wa
30                                              Methanolysis gave esters (RO(2)C)CH(R')(NHPh) (R' = Me(3
31                   Mild acid hydrolysis, mild methanolysis, immunoblotting and exoglycosidase digestio
32 olysaccharide or conjugate were subjected to methanolysis in 3N hydrochloric acid in methanol followe
33              Monosaccharides released during methanolysis included hexoses, uronic acids, 6-deoxy-hex
34 in CH(3)OH-H(2)O (4:1), the quantum yield of methanolysis is Phi = 0.70.
35  rings appears to have taken place in 4 upon methanolysis, leading to the corresponding ester and thi
36 d more sensitive than a previously published methanolysis method.
37                               Acid-catalyzed methanolysis of 3 followed by two-step derivatization of
38 tion of methanol at -80 degrees C results in methanolysis of 8-L (L = solvent) to form the linear die
39 rous POP that is catalytically active in the methanolysis of a nerve agent simulant.
40 lts corroborate earlier suggestions that the methanolysis of acetyl chloride does not proceed through
41 r use as catalysts for the hydroxyl-directed methanolysis of alpha-hydroxy esters in preference to al
42  T Delta S(#), accelerating the nonenzymatic methanolysis of ATP 11-fold at pH 7 and 25 degrees C.
43  changing temperature for 1) the spontaneous methanolysis of ATP and 2) reactions catalyzed by kinase
44 a H(#) and T Delta S(#) for the nonenzymatic methanolysis of ATP(2-), ATP(3-), and ATP(4-) in the abs
45                                          The methanolysis of BPA-PC and the glycolysis of PET were ac
46                     DFT yields a barrier for methanolysis of DeltaG(double dagger) = 29.7 kcal mol(-1
47 ed acid sites for efficiently catalyzing the methanolysis of epoxides.
48 terification reaction, and in particular the methanolysis of ethyl acetate with sulfuric acid as cata
49 ain of these are much more selective for the methanolysis of hydroxy esters than FPP.
50 acetate as well as (ii) hydrolysis and (iii) methanolysis of its esters.
51 ere dramatically enriched by direct alkaline methanolysis of lipid extracts followed by extraction to
52 gh DFT calculations, we show that asymmetric methanolysis of meso-cyclic anhydrides (AMMA) catalyzed
53 ptor with the second order rate constant for methanolysis of MgATP) ranged between 10(12)- and 10(14)
54                                              Methanolysis of neomycin B under acidic conditions produ
55 yzes the release of 3 equivalents of H(2) by methanolysis of phenylsilane, with a turnover number of
56 tivity was demonstrated for the solvent-free methanolysis of PLA at mild conditions with full convers
57 ethanol (CH(3)OH) in a dual role for (1) the methanolysis of polyethylene terephthalate (PET) to form
58 istence is further supported by the observed methanolysis of the alpha-1'-O-alkylamidate intermediate
59                                          The methanolysis of the Cu(II) complex of N-acetyl-N,N-bis(2
60 , through the quinine- or quinidine-promoted methanolysis of the cyclic anhydride (+/-)-10, leading t
61 mines by reaction with t-BuLi and subsequent methanolysis of the generated sulfinamide derivatives wi
62                                              Methanolysis of the indenyl acetates yields the correspo
63                                              Methanolysis of the lactone ring of the N-benzyl-N-methy
64                                  Considering methanolysis of the linear Pd-acyl species, whose energe
65 ulations indicate that energy differences of methanolysis of the linear versus branched Pd-acyls are
66 functional methods for the in-line dianionic methanolysis of the native (unsubstituted) and thio-subs
67 ciated with the highest energetic barrier is methanolysis of the Pd-acyl species.
68  to disaccharides through microwave-assisted methanolysis or enzymatic digestion for subsequent MALDI
69 clic ADPR hydrolysis, and could not catalyze methanolysis or transglycosidation.
70                  The results of partial mild methanolysis over shorter periods were consistent with i
71                            A two-factor (the methanolysis period and temperature), three-level, facto
72                                          The methanolysis procedure was performed under microwave irr
73  of 4 from refluxing methanol results in the methanolysis product 5-(4-methoxymethyl-2,5-dimethylthio
74           A synthesis of bafilomycin V(1), a methanolysis product of the macrolide natural product ba
75 esis of dimethyl sulfomycinamate, the acidic methanolysis product of the sulfomycin family of thiopep
76                         NMR analysis of MutY methanolysis products corroborates a mechanism for adeni
77                                          The methanolysis products Mealpha-Galf and Mebeta-Galf were
78 st probably via quinone methides (QMs), with methanolysis quantum efficiencies PhiR = 0.02-0.3.
79                      The main product of the methanolysis reaction was a de-N-acylated methyl glycosi
80 to a decrease in the rate of the nondirected methanolysis reaction with the ketone-derived catalysts.
81  the kinetics and reaction products of their methanolysis reactions in the presence of Cu(O(3)SCF(3))
82 The key transformation is the base-catalyzed methanolysis-rearrangement of (+/-)-6,7-exo,exo-(isoprop
83 ity for Lewis acid catalysis (regioselective methanolysis ring-opening of styrene oxide), oxidative c
84 2-C3 relative stereochemistry, followed by a methanolysis/ring-closure tandem reaction sequence.
85 ilyl-derivatives of overexpressed SKP1 after methanolysis showed the HexNAc to be GlcNAc.
86                    Lastly, we demonstrate by methanolysis study that the catalytic reaction proceeds
87      After appropriate derivatization and/or methanolysis the compounds were analyzed using capillary
88                                 The ratio of methanolysis to hydrolysis for cADPR and NAD+ catalyzed
89 ne disaccharides are readily rearmed by mild methanolysis to provide GlcN-IdoA thiophenyl disaccharid
90 jected to base hydrolysis followed by acidic methanolysis to release S- and N-linked fatty acids, res
91 ydrolysis to the hydroxyacid in 99% yield or methanolysis to the hydroxyester in 91% yield, achieving
92 ) (PET) waste to produce monomers, including methanolysis to yield dimethyl terephthalate (DMT) and g
93  (1) underwent a facile (auto) acid-mediated methanolysis to yield seco-shornephine A methyl ester (1
94 involving epoxidation of the O-methyl ether, methanolysis under mildly acidic conditions, and regiose
95         Optimisation of a microwave-assisted methanolysis was performed to obtain cafestol and kahweo
96 etone and an ester or an aldehyde, undergoes methanolysis with cleavage of one of the two activated c
97                                              Methanolysis yielded (R)-(+)-1 (169 g, 40% overall yield