ライフサイエンスコーパス: vinyl acetate

1 ediation of living radical polymerization of vinyl acetate.

2 hydroformylations of styrene derivatives and vinyl acetate.

3 It allowed synthesis of vinyl acetate-1-(13) C, which is a precursor for prepara

4 -phase solution of CO2, 0.15 wt % sodium bis(vinyl acetate)8 sulfosuccinate, and water, at water load

5 ospholane)] with hydroformylation substrates vinyl acetate, allyl cyanide, 1-octene, and trans-1-phen

6 ligands and six alkene substrates (styrene, vinyl acetate, allyloxy-tert-butyldimethylsilane, (E)-1-

7 ble bond in the compounds is, in the case of vinyl acetate, an alpha-ester rearrangement to produce a

8 ormed from the reactions of OH radicals with vinyl acetate and allyl acetate have been studied in a 1

9 of the transesterification reaction between vinyl acetate and allyl alcohol was significantly attenu

10 nts for cyanoisopropyl radical addition with vinyl acetate and hydrogen atom transfer to (TMP)Co(II)*

11 amides was achieved by their treatment with vinyl acetate and vinyl methacrylate in dry THF using No

12 of sophorolipid ethyl ester in dry THF with vinyl acetate and vinyl methacrylate to give the corresp

13 ovozym 435 in dry tetrahedrofuran (THF) with vinyl acetate and vinyl methacrylate to produce 6'-monoa

14 rolipid amide at 6' and 6' ' in dry THF with vinyl acetate and vinyl methacrylate using Novozym 435 a

15 this, a library of statistical copolymers of vinyl acetate and vinyl trifluoroacetate was synthesized

16 Compatible blends of poly(vinyl acetate) and poly(methyl methacrylate) have been u

17 s such as poly(methyl methacrylate, styrene, vinyl acetate, and ethyl vinyl ether).

18 esterification of racemic proxyphylline with vinyl acetate as well as (ii) hydrolysis and (iii) metha

19 linear viscoelastic regime for films of poly(vinyl acetate) at a thickness of 27.5 nanometers.

20 m sorbent-phase dosing system using ethylene vinyl acetate coated vials was developed to eliminate th

21 The resulting vinyl acetate-containing adducts are easily hydrolyzed w

22 portant are the results obtained on ethylene/vinyl acetate copolymers.

23 Poly(ethylene-co-vinyl acetate) disks containing 125I-labeled monoclonal

24 se molecules were incorporated into ethylene-vinyl acetate (ELVAX), a non-biodegradable, sustained-re

25 oteinase inhibitor, with the use of ethylene-vinyl-acetate (ELVAX) 40, a non-biodegradable, non-infla

26 onsist of micrometer-thin layers of ethylene vinyl acetate (EVA) coated onto a glass fiber filter or

27 The significance and features of ethylene-vinyl acetate (EVA) copolymers in initial research and d

28 ds, placed in close contact with an ethylene vinyl acetate (EVA) film, and exposed to a light source.

29 nd a larger MW peptide, via a novel ethylene vinyl acetate (EVA) ring transvaginal drug delivery syst

30 the non-water swellable elastomer, ethylene vinyl acetate (EVA-28), containing the hydrophobic small

31 LCs by subcutaneous implantation of ethylene-vinyl-acetate (EVA) polymer rods releasing macrophage in

32 low density polyethylene - LDPE and ethylene vinyl acetate - EVA lined) were determined for a period

33 olecules: the technique uses a special ethyl-vinyl acetate film functionalized with strong cation/ani

34 was backed by 0.9 kg/m3 of 1.27-kg ethylene vinyl acetate foam.

35 shown to control the catalytic formation of vinyl acetate from ethylene and acetic acid by AuPd cata

36 ed sugars, poly(propylene glycol), and oligo(vinyl acetate), have been used to generate CO2-soluble i

37 linear function of the mole fraction of poly(vinyl acetate) in the blend.

38 SiO2(LuPc2)) grafted with Poly(vinyl alcohol-vinyl acetate) itaconic acid (PANI(PVIA)) doped polyanil

39 nd non-degradable, implantable poly(ethylene vinyl acetate) matrices to continuously deliver BDNF to

40 Kinetics of vinyl acetate molecular hydrogenation and polarization t

41 age on the acetoxylation of ethylene to form vinyl acetate over Pd.

42 l methacrylate) [PBMA], and poly(ethylene-co-vinyl acetate) [PEVA].

43 polyisoprene, poly(vinyl stearate), ethylene-vinyl acetate, polyepoxide, paraffin wax and polycaprola

44 , a transparent thermoplastic film (ethylene vinyl acetate polymer) is applied to the surface of the

45 was replaced by gum arabic first and by poly(vinyl acetate) (PVAC) later.

46 e to carbon black-polymer composites of poly(vinyl acetate) (PVAc) or of poly(N-vinylpyrrolidone).

47 cture of poly(vinyl n-octadecyl carbamate-co-vinyl acetate) (PVNODC) or poly(octadecyl acrylate) (PA-

48 hydroxyethyl acrylate and ethyl acetate from vinyl acetate, respectively.

49 he versatile new poly(oligo(ethylene glycol) vinyl acetate)s are presented with excellent control ove

50 Furthermore, poly(ethylene-co-vinyl acetate) scaffolds containing NSC23766 attenuated

51 teps in the Samanos and Moiseev pathways for vinyl acetate synthesis carried out on acetate-saturated

52 For certain reactions, for example vinyl acetate synthesis, this effect is responsible for

53 2) sites, which are known to be optimal for vinyl acetate synthesis.

54 ystems, only surfactants with the oligomeric vinyl acetate tails exhibited spectroscopic evidence of

55 Surfactants with vinyl acetate tails yielded the most promising results,

56 III-174) within a matrix of poly(ethylene-co-vinyl acetate); these disks released 2 to 40 micrograms/

57 a cerium-catalyzed reaction with alpha-aryl vinyl acetates under oxidative conditions.

58 Vinyl acetate (VA) and vinyl trifluoroacetate (VA(f)) re

59 Acetoxylation of ethylene to vinyl acetate (VA) was used to investigate the mechanism

60 tetramesityl porphyrin ((TMP)Co(II)*, 1) and vinyl acetate (VAc) in benzene and react to produce tran

61 le, a sodium sulfate with single, oligomeric vinyl acetate (VAc) tails consisting of 10 VAc repeat un

62 ach of four polar monomers: methyl acrylate, vinyl acetate, vinyl chloride, and acrylonitrile.

63 y products formed in the reaction of OH with vinyl acetate were: formic acetic anhydride (84 +/- 11)%