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1 milar to commercial white glue based on poly(vinyl acetate).
2 nique, known under the acronym EVA (ethylene-vinyl acetate).
3 ediation of living radical polymerization of vinyl acetate.
4 hydroformylations of styrene derivatives and vinyl acetate.
5 cetate via pairwise parahydrogen addition to vinyl acetate.
6                      It allowed synthesis of vinyl acetate-1-(13) C, which is a precursor for prepara
7 duct of pairwise addition of parahydrogen to vinyl acetate-1-(13)C, resulting from zero-crossing magn
8 -phase solution of CO2, 0.15 wt % sodium bis(vinyl acetate)8 sulfosuccinate, and water, at water load
9 ospholane)] with hydroformylation substrates vinyl acetate, allyl cyanide, 1-octene, and trans-1-phen
10  ligands and six alkene substrates (styrene, vinyl acetate, allyloxy-tert-butyldimethylsilane, (E)-1-
11 ble bond in the compounds is, in the case of vinyl acetate, an alpha-ester rearrangement to produce a
12 ormed from the reactions of OH radicals with vinyl acetate and allyl acetate have been studied in a 1
13  of the transesterification reaction between vinyl acetate and allyl alcohol was significantly attenu
14 nts for cyanoisopropyl radical addition with vinyl acetate and hydrogen atom transfer to (TMP)Co(II)*
15 lderia cepacia (Amano PS-IM) in a mixture of vinyl acetate and toluene, the desired (R)-ester (99% ee
16  amides was achieved by their treatment with vinyl acetate and vinyl methacrylate in dry THF using No
17  of sophorolipid ethyl ester in dry THF with vinyl acetate and vinyl methacrylate to give the corresp
18 ovozym 435 in dry tetrahedrofuran (THF) with vinyl acetate and vinyl methacrylate to produce 6'-monoa
19 rolipid amide at 6' and 6' ' in dry THF with vinyl acetate and vinyl methacrylate using Novozym 435 a
20 this, a library of statistical copolymers of vinyl acetate and vinyl trifluoroacetate was synthesized
21                    Compatible blends of poly(vinyl acetate) and poly(methyl methacrylate) have been u
22 s such as poly(methyl methacrylate, styrene, vinyl acetate, and ethyl vinyl ether).
23 polyamide, polyester, polyethylene, ethylene vinyl acetate, and poly(methyl methacrylate).
24 esterification of racemic proxyphylline with vinyl acetate as well as (ii) hydrolysis and (iii) metha
25 linear viscoelastic regime for films of poly(vinyl acetate) at a thickness of 27.5 nanometers.
26 structurally dynamic nature in heterogeneous vinyl acetate chemistry.
27 m sorbent-phase dosing system using ethylene vinyl acetate coated vials was developed to eliminate th
28                                The resulting vinyl acetate-containing adducts are easily hydrolyzed w
29 ed on ethylene-vinyl acetate polymers with a vinyl acetate content of 28 w% (EVA28) and unprecedented
30 ergy of -3.7 kcal.mol(-1) between lipase and vinyl acetate, contributing to the highest conversion ra
31 n ASD of ritonavir with polyvinylpyrrolidone-vinyl acetate copolymers (Kollidon(R) VA64) was prepared
32 portant are the results obtained on ethylene/vinyl acetate copolymers.
33                             Poly(ethylene-co-vinyl acetate) disks containing 125I-labeled monoclonal
34 se molecules were incorporated into ethylene-vinyl acetate (ELVAX), a non-biodegradable, sustained-re
35 oteinase inhibitor, with the use of ethylene-vinyl-acetate (ELVAX) 40, a non-biodegradable, non-infla
36 onsist of micrometer-thin layers of ethylene vinyl acetate (EVA) coated onto a glass fiber filter or
37    The significance and features of ethylene-vinyl acetate (EVA) copolymers in initial research and d
38 values of the used and virgin-grade Ethylene vinyl acetate (EVA) encapsulant were found to be high, u
39 ds, placed in close contact with an ethylene vinyl acetate (EVA) film, and exposed to a light source.
40                                     Ethylene-Vinyl Acetate (EVA) is the most popular material for man
41 nd a larger MW peptide, via a novel ethylene vinyl acetate (EVA) ring transvaginal drug delivery syst
42  analysis: polyvinyl butyral (PVB), ethylene vinyl acetate (EVA), thermoplastic polyurethane (TPU), a
43  the non-water swellable elastomer, ethylene vinyl acetate (EVA-28), containing the hydrophobic small
44 LCs by subcutaneous implantation of ethylene-vinyl-acetate (EVA) polymer rods releasing macrophage in
45 low density polyethylene - LDPE and ethylene vinyl acetate - EVA lined) were determined for a period
46  hot-melt adhesives such as poly(ethylene-co-vinyl acetate) (EVA) and polyurethanes lack chemical rec
47 tide-co-glycolide) (PLGA), and poly(ethylene vinyl acetate) (EVA).
48 olecules: the technique uses a special ethyl-vinyl acetate film functionalized with strong cation/ani
49  was backed by 0.9 kg/m3 of 1.27-kg ethylene vinyl acetate foam.
50 nal diacetates showed higher reactivity than vinyl acetate for hydrolases that are sensitive to aceta
51  shown to control the catalytic formation of vinyl acetate from ethylene and acetic acid by AuPd cata
52 ed sugars, poly(propylene glycol), and oligo(vinyl acetate), have been used to generate CO2-soluble i
53 owder in transesterification of geraniol and vinyl acetate in the gas phase and maintains the initial
54 4 + 2]-annulation of N-chlorobenzamides with vinyl acetate in the presence of CoCp*(III) catalyst in
55 linear function of the mole fraction of poly(vinyl acetate) in the blend.
56 SiO2(LuPc2)) grafted with Poly(vinyl alcohol-vinyl acetate) itaconic acid (PANI(PVIA)) doped polyanil
57 nd non-degradable, implantable poly(ethylene vinyl acetate) matrices to continuously deliver BDNF to
58 on, which is different from that of previous vinyl acetate mediated C-H activation reactions.
59                                  Kinetics of vinyl acetate molecular hydrogenation and polarization t
60                                              Vinyl acetate monomer (VAM) is a crucial intermediate in
61 age on the acetoxylation of ethylene to form vinyl acetate over Pd.
62 lters to polyethylene terephthalate-ethylene vinyl acetate (PET-EVA) substrates by a temperature-driv
63 l methacrylate) [PBMA], and poly(ethylene-co-vinyl acetate) [PEVA].
64 polyisoprene, poly(vinyl stearate), ethylene-vinyl acetate, polyepoxide, paraffin wax and polycaprola
65 , a transparent thermoplastic film (ethylene vinyl acetate polymer) is applied to the surface of the
66 stems based on ethylene, vinyl chloride, and vinyl acetate polymerization.
67  and drug-loaded filaments based on ethylene-vinyl acetate polymers with a vinyl acetate content of 2
68 was replaced by gum arabic first and by poly(vinyl acetate) (PVAC) later.
69 e to carbon black-polymer composites of poly(vinyl acetate) (PVAc) or of poly(N-vinylpyrrolidone).
70 cture of poly(vinyl n-octadecyl carbamate-co-vinyl acetate) (PVNODC) or poly(octadecyl acrylate) (PA-
71 inhomogeneous ritonavir/polyvinylpyrrolidone-vinyl acetate (PVPVA) amorphous dispersions.
72  model polymer was poly (vinylpyrrolidone-co-vinyl acetate) (PVPVA).
73 hydroxyethyl acrylate and ethyl acetate from vinyl acetate, respectively.
74 he versatile new poly(oligo(ethylene glycol) vinyl acetate)s are presented with excellent control ove
75                Furthermore, poly(ethylene-co-vinyl acetate) scaffolds containing NSC23766 attenuated
76  mimics that performed similarly to ethylene-vinyl acetate shoe materials in quasi-static loading.
77 teps in the Samanos and Moiseev pathways for vinyl acetate synthesis carried out on acetate-saturated
78 industrial process, palladium (Pd)-catalyzed vinyl acetate synthesis, proceeds via interconversion of
79           For certain reactions, for example vinyl acetate synthesis, this effect is responsible for
80  2) sites, which are known to be optimal for vinyl acetate synthesis.
81 ystems, only surfactants with the oligomeric vinyl acetate tails exhibited spectroscopic evidence of
82                             Surfactants with vinyl acetate tails yielded the most promising results,
83 III-174) within a matrix of poly(ethylene-co-vinyl acetate); these disks released 2 to 40 micrograms/
84 tion of enamides with the feedstock chemical vinyl acetate to access diverse functionalized ketones.
85  a cerium-catalyzed reaction with alpha-aryl vinyl acetates under oxidative conditions.
86 d electronically similar alkenes-enamide and vinyl acetate-underwent selective cross-coupling through
87                                              Vinyl acetate (VA) and vinyl trifluoroacetate (VA(f)) re
88 onometallic supported Cu and Pd catalysts to vinyl acetate (VA) synthesis reaction conditions.
89                 Acetoxylation of ethylene to vinyl acetate (VA) was used to investigate the mechanism
90 tetramesityl porphyrin ((TMP)Co(II)*, 1) and vinyl acetate (VAc) in benzene and react to produce tran
91 le, a sodium sulfate with single, oligomeric vinyl acetate (VAc) tails consisting of 10 VAc repeat un
92 ach of four polar monomers: methyl acrylate, vinyl acetate, vinyl chloride, and acrylonitrile.
93 ation study of eight corks, made of ethylene-vinyl acetate, was carried out to identify any non-volat
94 y products formed in the reaction of OH with vinyl acetate were: formic acetic anhydride (84 +/- 11)%