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1 d into thiol-terminated microspheres through aminolysis.
2 -methylpyridinium iodide (CMPI), followed by aminolysis.
3 her the catalytic acid or catalytic base for aminolysis.
4 ated by air plasma treatment, hydrolysis, or aminolysis.
5 ach is presented here based on aqueous-phase aminolysis.
6 during a Sonogashira coupling and subsequent aminolysis.
7  synthesis of cyclo-tetrapeptides via direct aminolysis.
8 es the UFM1-conjugating E2 enzyme, UFC1, for aminolysis.
9 mations include DABAL-Me(3)-mediated lactone aminolysis and a mild TBD/ethyl trifluoroacetate mediate
10 After Boc protection, these products undergo aminolysis and acidic deprotection to generate 2-imino-5
11 ns of glyceryl esters, including hydrolysis, aminolysis, and transesterification; oxidation reactions
12 ydrolysis at the sulfonyl center rather than aminolysis at either the sulfonyl or acyl center.
13 rmore, a strategic sequence comprising ester aminolysis, aza-Michael addition, and a Pictet-Spengler
14  ubiquitin chains seems to be mediated by an aminolysis-based transfer reaction between two Ube2g2 mo
15 inhibitor was accomplished by a mild lactone aminolysis between an orthogonally protected bis-benzyli
16 the LRR domain selectively blocks productive aminolysis, but not the nonproductive discharge of Ub fr
17 beta-lactam ring opening with intramolecular aminolysis by a reaction similar to that for cephalexin
18 tioning of the acyl-enzyme intermediate, the aminolysis by D-phenylalanine of a cognate pair of depsi
19 l calculations rationalize the observed slow aminolysis by demonstrating that the diazeniumdiolate gr
20 netic isotope effects were also measured for aminolysis by hydroxylamine to study a reaction similar
21  This then partitions between hydrolysis and aminolysis by Lys 315, the latter to form an inactive, c
22 w molar mass fragments (<6.5 kDa) under mild aminolysis conditions.
23 he activation energy for the epichlorohydrin aminolysis due to the better control of mass and heat tr
24          However, the rate of intramolecular aminolysis for the S-analogue is 3 orders of magnitude g
25 , such as hydrogen exchange, alcoholysis and aminolysis, hydrogen evolution, hydrogenation, and dehyd
26 transformed into tenofovir through "one-pot" aminolysis-hydrolysis of (R)-acetate in NH(3)-saturated
27 c sulfonamides, beta-sultams, do not undergo aminolysis in aqueous solution but preferentially react
28 s serve to hamper their intermolecular cross-aminolysis in bulk water.
29 rthermore, unlike cephalexin, intramolecular aminolysis in the S-analogue occurs up to pH 14 with no
30                      Prevention of polyimide aminolysis is achieved by using weakly alkaline ammonia
31 tep preparation of hybrid compounds involved aminolysis of 2-(chloroseleno)benzoyl chloride with the
32 kinetics and mechanism of the hydrolysis and aminolysis of a series of acyclic depsipeptides, catalyz
33 pstream splice junction, consistent with the aminolysis of a thioester.
34 hydrolysis, activation of Glu-tRNA(Gln), and aminolysis of activated tRNA by Gln-derived NH(3).
35 olipids appears to arise from base-catalyzed aminolysis of arachidonate-containing glycerolipids, bec
36 resented in the literature, including direct aminolysis of aromatic methyl esters to give carboxamide
37                   The first enantioselective aminolysis of aromatic trans-2,3-epoxy sulfonamides has
38 generate benzylamides of D-diphenylAlaPro by aminolysis of Boc dipeptide Kaiser resin.
39  ring strain is relieved upon the sequential aminolysis of both BTF and BTP, it is only for the forme
40                                          The aminolysis of both the aryl the alkyl esters by D-phenyl
41 TF and BTP, the unusually fast and selective aminolysis of BTF is only fully explained through synerg
42 nding proteins, catalyzes the hydrolysis and aminolysis of d-alanyl-d-alanine-terminating peptides by
43 putational study and kinetic analysis of the aminolysis of dithioates, dithiobenzoates, trithiocarbon
44   We demonstrate this concept by testing the aminolysis of epoxides with a family of isostructural me
45 in aqueous solution and in the ribosome, the aminolysis of esters in aqueous solution has been the su
46                 Quantitative rate studies of aminolysis of methyl benzoate by NaPTA revealed a 47,000
47                                              Aminolysis of methyl benzoate with dialkylamines mediate
48 y describe experimental observations for the aminolysis of N-acetyl-dl-homocysteine thiolactone with
49                   The rate of intermolecular aminolysis of natural cephalosporins is dominated by a s
50 ations, we have investigated azole-catalyzed aminolysis of p-fluorophenyl acetate.
51 hanism of the uncatalyzed and base-catalyzed aminolysis of phenyl N-phenylcarbamate by theoretical qu
52 iously been shown to catalyze hydrolysis and aminolysis of small D-alanyl-D-alanine terminating pepti
53                                              Aminolysis of telechelic macromonomers with a small amou
54 to isolate its O(2)-benzylated derivative by aminolysis of the C horizontal lineN bond in PhC(NH2) ho
55  molecules and susceptible to hydrolysis and aminolysis of the four membered B-lactam ring present.
56 ential events consisted of lactonization and aminolysis of the lactone ring, which ultimately furnish
57                                              Aminolysis of the latter entity with an amino alcohol li
58 go ring-opening with benzylamine followed by aminolysis of the resulting CCl3 ketone to form a range
59 kane bridge to amide bonds formed during the aminolysis of the surface ester functionalities.
60                                              Aminolysis of the urea products provides enantioenriched
61 he integrity of fused-silica capillaries via aminolysis of their outer polyimide coating.
62               The Bronsted beta(nuc) for the aminolysis of thioxo-cephalosporin is +0.39, indicative
63                                          The aminolysis of three differently alpha-substituted gamma-
64         The first catalytic enantioselective aminolysis of trans-2,3-epoxy alcohols has been accompli
65  proved remarkably sluggish in comparison to aminolysis of unsubstituted benzamidine, and the desired
66                          The transamidation (aminolysis) of phthalimide with primary and secondary al
67                      Non-epimerizable direct aminolysis offers a practical solution for constrained p
68 the influence of degradation (hydrolysis and aminolysis) on the electrochemical fingerprint has to be
69 gradation of the backbone thioesters through aminolysis or thiolysis led to the full dissolution of t
70 ree amine can be liberated under mild Zincke aminolysis, or the amination and cleavage can be telesco
71             In this work, the procedures for aminolysis, photografting of linear polyacrylamide, and
72 f (phenylacetyl)-glycyl-D-thiolactate by the aminolysis product (phenylacetyl)glycyl-D-phenylalanine
73 action conditions, including alcoholysis and aminolysis protocols.
74 established that contributes to the stepwise aminolysis rate differences and enhanced selectivity.
75 is weakened by N-phosphorylation, leading to aminolysis rather than the expected deoxygenative aminat
76 ate saturation conditions, and therefore the aminolysis reaction can be directly studied.
77 t differs in its details from an uncatalyzed aminolysis reaction in solution.
78 substituted phenyl N-phenylcarbamates in the aminolysis reaction was rationalized using theoretical a
79 the monoanion of alpha,omega-diaminoalkanes (aminolysis reaction) to yield amine-terminated PMMA surf
80 rors the coupling between Gln hydrolysis and aminolysis reactions during productive transamidation.
81 y to undergo highly selective and sequential aminolysis reactions in one-pot to afford multifunctiona
82 y smaller than that reported for uncatalyzed aminolysis reactions, which has important mechanistic im
83 ning a hydrolyzed end) for each protein, the aminolysis reactivity of each modified lysyl side chain
84 methods of constructing amide bonds, lactone aminolysis remains one of the most atom economical.
85 m indicates that the selectivity-determining aminolysis step occurs via a novel concerted pathway in
86  a one-pot TEMPO-induced radical cyclization/aminolysis that forms the C ring of 1.
87 e (TBD) as an effective catalyst for lactone aminolysis under mild conditions.
88 n the synthesis of homopropargylic amides-by aminolysis using AlMe3, as well as of ketones-through th
89 se-catalyzed acylation, followed by chemical aminolysis, was used to generate vinyl carbonate and vin
90 tives, similar to acyl ones, usually undergo aminolysis with amines in water as nucleophilic attack b
91 ophosphate with ethyl isocyanate followed by aminolysis with ammonium hydroxide to form the desired p