ライフサイエンスコーパス: methyl acrylate

1 nthesized and used as a cross-linker in poly(methyl acrylate).

2 n aryl diazonium salts generated in situ and methyl acrylate.

3 ncrease in the order DMAA < AcAMEA < NIPAM < methyl acrylate.

4 tes formed by nucleophilic attack of PCy3 on methyl acrylate.

5 c methods and 1,3-dipolar cycloaddition with methyl acrylate.

6 g it necessary to add more base catalyst and methyl acrylate.

7 rohydroxyalkylation, vicinal diols 1a-1l and methyl acrylate 2a are converted to the corresponding la

8 The reactions of methyl acrylate 2a with hydrobenzoin 1f, benzoin didehyd

9 In the case of methyl acrylate a pathway leading to the two diastereois

10 (tetramethylethylene, cyclohexene, 1-hexene, methyl acrylate, acrylonitrile, and alpha-chloroacryloni

11 The corresponding reaction of 5 with methyl acrylate, acrylonitrile, and phenyl vinyl sulfone

12 n of a preorganized tetraamine using various methyl acrylate analogues.

13 ee stereocenters is a [3+2] cycloaddition of methyl acrylate and an imino ester prepared from l-leuci

14 These mixtures, which contain methyl acrylate and ethyl acrylate at amount fractions b

15 The stability of methyl acrylate and ethyl acrylate in gas sampling bags

16 nge in the forward (ethylene displacement by methyl acrylate) and reverse directions, respectively.

17 ement of the slow equilibration of ethylene, methyl acrylate, and 4-methoxystyrene in cyclophane-base

18 es for DMC additions to 2-ethyl-1-butene and methyl acrylate are computed and observed to be negative

19 ion energy and enthalpy for addition of 1 to methyl acrylate are the most negative values yet encount

20 s, different products are also obtained with methyl acrylate as a substrate.

21 d in diastereoselective radical additions to methyl acrylate at -78 degrees C (ds = 6/1 and 11/1, res

22 id poly-(o-phenylene ethynylene)-block-poly-(methyl acrylate) block copolymers.

23 comprised of a poly(acrylic acid)-block-poly(methyl acrylate)-block-polystyrene (PAA(90)-b-PMA(80)-b-

24 thyl allyl ether, norbornene, acrylonitrile, methyl acrylate, butadiene, methyl(vinyl)silanediamine,

25 s-Hillman reaction of various aldehydes with methyl acrylate catalyzed by 1,4-diazabicyclo[2.2.2]octa

26 oupling of azides and alkynes) within a poly(methyl acrylate) chain renders it susceptible to ultraso

27 Poly(methyl acrylate) chains of varying molecular weight were

28 ls-Alder reaction between 1,2-azaborines and methyl acrylate correlate with aromaticity trends and pl

29 erials containing an ultrathin layer of poly(methyl acrylate)-d(3) (PMA-d(3)) on silica was studied u

30 (DeltaG(double dagger) = 18.9 kcal/mol) and methyl acrylate (DeltaG(double dagger) = 16.3 kcal/mol)

31 ytic reactivity of 1 a for mild tail-to-tail methyl acrylate dimerization and for cyclobutene formati

32 ynthesis of the title compound starting from methyl acrylate, ethylenediamine, and dimethyl malonate

33 agger) = 20.6 and 16.4 kcal/mol for ethylene-methyl acrylate exchange in the forward (ethylene displa

34 man reaction of an appropriate aldehyde with methyl acrylate followed by acetylation of the resulting

35 er reaction with the less electron-deficient methyl acrylate is observed.

36 ael addition adduct formed between DABCO and methyl acrylate is the active intermediate for the Bayli

37 tion of the copolymerization of ethylene and methyl acrylate (MA) by a Pd(II) cyclophane-based alpha-

38 tereoselectivity of the first and the second methyl acrylate (MA) insertion into the Pd-Me bond of in

39 methyl ether acrylate and PEGA480 to a poly(methyl acrylate) macroinitiator without prior workup or

40 aine product, consumes both the catalyst and methyl acrylate, making it necessary to add more base ca

41 For cis-cyclooctene, indene, methyl acrylate, methyl methacrylate, vinyl methyl keton

42 Poly(methyl acrylate) of varying molecular weight was grown f

43 minal biotinylated poly(acrylic acid)-b-poly(methyl acrylate) (PAA-b-PMA) and nonbiotinylated PAA-b-P

44 low (LMW) molecular weight hydrogenated poly(methyl acrylate) (PMA) as the overlayer.

45 Silica nanoparticles grafted with poly(methyl acrylate) (PMA) chains anchored by a maleimide-an

46 diation of a molecular weight series of poly(methyl acrylate) polymers in which each macromolecule ha

47 esters from benzylic nitriles or esters and methyl acrylate promoted by potassium tert-butoxide is d

48 Methyl acrylate reacted instantly with the sulfhydryl gr

49 Poly(methyl acrylate)s (PMAs) of varying molecular weights we

50 esulfonyl-2-diazoacetyl)pyrrolidin-2-one and methyl acrylate, several indolo- and furano-fused indoli

51 A newly developed polyacrylamide-co-methyl acrylate/spiropyran (SP) hydrogel crosslinked by

52 generated in ca. 90% yield on metathesis of methyl acrylate, styrene, or ethylene in the presence of

53 , and stereoselectivities were observed with methyl acrylate, though catalysis by Ag(I) was necessary

54 chnique is demonstrated by polymerization of methyl acrylate to a range of chain lengths (DP(n) = 25-

55 The dimerization of methyl acrylate to the head-to-tail 2-methylene-pentaned

56 ha-alkylation/lactonization of alcohols with methyl acrylate via a hydrogen atom transfer mechanism.

57 e Pd-C bond for each of four polar monomers: methyl acrylate, vinyl acetate, vinyl chloride, and acry

58 bolites are sulfhydryl-containing compounds, methyl acrylate was used to stabilize these compounds in

59 ies in the Morita-Baylis-Hillman reaction of methyl acrylate with benzaldehyde derivatives.