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1 oroacetic acid, and the APs derivatized with acetic anhydride.
2 y reacting with an acyl anhydride, including acetic anhydride.
3 from cultivars of cassava were modified with acetic anhydride.
4  situ from unprotected alpha-amino acids and acetic anhydride.
5  triflate-mediated acylation of anisole with acetic anhydride.
6 hydride, and regioselective acetylation with acetic anhydride.
7 h molecular selective absorption features of acetic anhydride.
8 to acetate by treatment with BF(3)-OEt(2) in acetic anhydride.
9 a free amine, as judged by modification with acetic anhydride.
10  that were hyperacetylated by treatment with acetic anhydride.
11 )s, which can be covalently derivatized with acetic anhydride.
12 llowed by denaturation and reaction with [3H]acetic anhydride.
13 zed by acetylation of recombinant HFABP with acetic anhydride.
14 es by SNA, labeled them at the N-terminus by acetic anhydride ((1)H(6)/(2)D(6)) reagents, enzymatical
15  rate law nu approximately k 3 [Ln (3+)] (1)[acetic anhydride] (1)[anisole] (1).
16 +/- 15)% in the presence of NO(x) and formic acetic anhydride (28 +/- 5)%; acetic acid (87 +/- 12)% a
17 action of OH with vinyl acetate were: formic acetic anhydride (84 +/- 11)%; acetic acid (18 +/- 3)% a
18  reaction was carried out in the presence of acetic anhydride, a substituted 3-oxabicyclo[3.3.1]nonan
19 f the tetrahydroxytrioxocalix[4]arene 6 with acetic anhydride and 1-bromobutane, respectively, afford
20  of glycine, alanine, and phenylalanine with acetic anhydride and ammonium thiocyanate give the 1-ace
21 f free sugars with stoichiometric amounts of acetic anhydride and catalytic In(OTf)3 in the mill as n
22 -O-acetylation of sugars with stoichiometric acetic anhydride and catalytic iodine proceeds in high y
23 her the presence or absence of HS using both acetic anhydride and hexadeuterioacetic anhydride under
24 obtained by treating the imidosulfoxide with acetic anhydride and p-toluenesulfonic acid, reacts with
25 easibility of using prepolarized [1,1-(13)C] acetic anhydride and rapid chemical reactions to provide
26 [1-(13)C]acetyl salicylate or [1,1'-(13)C(2)]acetic anhydride, and the acetylated products were detec
27 r disaccharides in a mixture of pyridine and acetic anhydride are treated with acetic acid, regiosele
28 (+/-)-sec-phenylethanol as the substrate and acetic anhydride as the acylation agent.
29 ective, efficient, and scalable and requires acetic anhydride as the sole additive.
30 eased seven compounds including acetic acid, acetic anhydride, benzyl alcohol, benzyl nitrile, indole
31 ment of wild type ubiquitin with the labeled acetic anhydride but not upon treatment of the H68N muta
32  as the effect of modifying this starch with acetic anhydride by catalysis with 1, 5 or 10mM of iodin
33 ,25,26,27-tetranor-23-OH-[3 alpha-3H]D3 with acetic anhydride changed its migration on amino HPLC to
34                      Acetylation of BCA with acetic anhydride converts all 18 lysine-epsilon-NH(3)(+)
35        N-Acetylation of heparin samples with acetic anhydride-d6 is followed by exhaustive heparinase
36             Deprotonation in the presence of acetic anhydride delivers the N-acetylpyridinium complex
37  formation via interaction of Ln(OTf) 3 with acetic anhydride, followed by Ln (3+)-anisole pi-complex
38 ates the influence of acetylation (4% and 6% acetic anhydride for 10 and 20 min) on the functional, t
39                    Ethano-dC is sensitive to acetic anhydride found in the capping reagent, and multi
40 ation of N-acetylglycine with aldehyde 15 in acetic anhydride gave acetamido coumarin 16.
41 ith Raney nickel, followed by treatment with acetic anhydride, gave the amide derivative 35.
42                     3-OST-1 was treated with acetic anhydride in either the presence or absence of HS
43  Eu, Yb, Lu)-mediated anisole acylation with acetic anhydride in nitromethane reveal the rate law nu
44 de by adsorption is followed by capping with acetic anhydride in the vapor phase, and then capping wi
45 trol mitochondria with the acetylating agent acetic anhydride inhibits pyruvate uptake and pyruvate-s
46 sitive charges of lysines were eliminated by acetic anhydride instead of MDA, the acetylated BSA star
47  directly in aqueous medium with 1,1'-13C(2) acetic anhydride is a simple method that creates a high
48                                  [1,1-(13)C] acetic anhydride is an excellent substrate for DNP hyper
49  of the resulting cycloadducts to additional acetic anhydride leads to ring opening and formation of
50 ort that in thylakoid membranes treated with acetic anhydride, luminal acidification by a photosystem
51 ermally stable complexes with ethyl acetate, acetic anhydride, N-methylsuccinimide, N-acetylpyrrole,
52  amine groups preexisting in the stroma with acetic anhydride or ethyl acetimidate does not affect RF
53 ifluoroacetate) derivative by treatment with acetic anhydride or trifluoroacetic anhydride, respectiv
54 treated with either the H6 or the D6 form of acetic anhydride, peptides that contain C-terminal basic
55 (8) with the lithium acetylide 9 followed by acetic anhydride produced the propargylic acetate 10.
56 dation of 35, followed by rearrangement with acetic anhydride, produced the acetate derivative, 5-[(a
57 chitosan, a deacetylated form of chitin, and acetic anhydride produces a surface-bound film of chitin
58 ifficult to remove from the products), since acetic anhydride provided regioisomeric product mixtures
59 hydrofuran derivatives with a Lewis acid and acetic anhydride provided the corresponding ring-opened
60                             Addition of 3.5% acetic anhydride resulted in starches with DS of 1.66% a
61  diepoxide was reacted with sulfamic acid in acetic anhydride, resulting in the formation of a new br
62 e product 3 under the literature conditions (acetic anhydride/sodium acetate) affords both the indole
63 utation of Lys99 to Ala, or acetylation with acetic anhydride, specifically prevented the cleavage of
64 egrees C), catalyst load (0-2.3 g/g starch), acetic anhydride/starch weight ratio (6.5-13.5 g/g), and
65 phenolic group in resins was acetylated with acetic anhydride to afford two polymer-bound 4-acetoxybe
66  formation of indolizine products, and using acetic anhydride/triethylamine leads to indolizine produ
67 opargylic alkoxides are trapped in situ with acetic anhydride, which are susceptible to a second nucl
68 es advantage of the preferential reaction of acetic anhydride with amine nucleophiles, which occurs m
69 on (DNP) was combined with the reactivity of acetic anhydride with amines to perform rapid, high SNR
70 e monitoring and modeling of the reaction of acetic anhydride with butanol using the catalyst 4-(dime

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