ライフサイエンスコーパス: maleic anhydride

1 ty was exclusive with N-phenyl maleimide and maleic anhydride.

2 erenes can be recovered by displacement with maleic anhydride.

3 amines (3-arylallylamines), maleimides, and maleic anhydride.

4 iosynthesis of the tropolone class of fungal maleic anhydrides.

5 s-Alder adduct 24 of 2,5-dimethylfuran 7 and maleic anhydride 23 in 8 steps.

6 2,4-dien-1-yldimethyl(phenyl)silane (8) with maleic anhydride (3) to afford the tricyclic anhydride 1

7 Maleic anhydride, a precursor to polyester resins, is ma

8 ethyl]lysine (BCML), was easily coupled to a maleic anhydride-activated polystyrene microtiter plate.

9 l/mol) than that previously measured for the maleic anhydride adduct 1, and this was attributed to th

10 reaction under the flash-vacuum pyrolysis of maleic anhydride adducts is developed.

11 gs (stearic acid (SA), oleic acid (OA), poly(maleic anhydride-alt-1-octadecene) (PMAO), linear polyet

12 oly(gamma-glutamic acid) (gammaPGA) and poly(maleic anhydride-alt-1-octadecene) (PMHC18).

13 with amphiphilic polymer prepared from poly(maleic anhydride-alt-1-octadecene) and Jeffamine ED-2003

14 l) (PAA-EG), polyethylenimine (PEI) and poly(maleic anhydride-alt-1-octadecene)-poly(ethylene glycol)

15 cyclooctatetraene (COT) with the dienophiles maleic anhydride and 4-phenyl-1,2,4-triazoline-3,5-dione

16 d with the isotopically enriched dienophiles maleic anhydride and a C18-alkyl chain-modified maleimid

17 Using terpenes from turpentine, maleic anhydride and allyl chloride as reactants, the sy

18 through the ring-opening copolymerization of maleic anhydride and an oligo(ethylene glycol)-functiona

19 Energetics are compared to the reaction of maleic anhydride and ethylene.

20 subsequent functionalization of n-butane to maleic anhydride and found that the overall barrier does

21 The method works effectively for maleic anhydride and maleic acid as well.

22 oadditions with alpha-substituted acroleins, maleic anhydride and N-phenylmaleimide.

23 inetically significant for the production of maleic anhydride and not just for the production of by-p

24 The ring-opening copolymerization of maleic anhydride and propylene oxide, using a functional

25 utyl 4-vinylbenzoate were copolymerized with maleic anhydride and tert-butyl 4-maleimidobenzoate, ind

26 iels-Alder adducts of furan: one formed with maleic anhydride and the other with N-methylmaleimide.

27 ate interfacial forces, polymers composed of maleic anhydride and two other components have been desi

28 d upon reversible amidation reaction between maleic anhydrides and secondary amines.

29 dition reaction between poly(isobutylene-alt-maleic anhydride) and distinct amine-containing function

30 g enophile molecules (e.g., methylmaleimide, maleic anhydride, and 4-cyclopentene-1,3-dione) with an

31 ized with a backbone of poly[isobutylene-alt-maleic anhydride] and pendant dodecyl alkyl chains, Luci

32 N-Arylitaconimides, accessible from maleic anhydride, anilines, and paraformaldehyde, react

33 ectron-poor butenolides leans toward that of maleic anhydride, another essential monomer that does no

34 um was used as insect repellent compound and maleic anhydride as compatibilizer.

35 proposed cyclobutadiene intermediates using maleic anhydride as dienophile as well as kinetic studie

36 he Diels-Alder adduct of alpha-terpinene and maleic anhydride as the cyclic anhydride comonomer resul

37 of a 1-aminoethyl-substituted butadiene with maleic anhydride at 0 degrees C to room temperature for

38 cial attention was focused on development of maleic anhydride-based amphiphilic polymers for QDs solu

39 inated poly(amido amine) dendrimers and poly(maleic anhydride)-c-poly(methyl vinyl ether) (Gantrez).

40 mechanism in which amide-acids derived from maleic anhydride can reversibly form free amine and cycl

41 functionalities, onto a poly(isobutylene-alt-maleic anhydride) chain via a one-step nucleophilic addi

42 ion of a bioadhesive coating, poly(butadiene-maleic anhydride-co-L-DOPA) (PBMAD), to non-bioadhesive

43 er disks formed by phospholipids and styrene maleic anhydride copolymer preserve the functional and s

44 These copolymers are generated using a maleic anhydride coupling scheme that permits the coupli

45 to both maleic anhydride-cyclopentadiene and maleic anhydride-cyclohexadiene adducts was accomplished

46 nucleophilic addition of PhSCF2SiMe3 to both maleic anhydride-cyclopentadiene and maleic anhydride-cy

47 -bromophenylhydrazine (7b) and the exo-furan/maleic anhydride Diels-Alder adduct (8) in acetic acid t

48 er to reversion-while the adduct formed with maleic anhydride experiences a larger change in dipole d

49 nterconversion of this and the corresponding maleic anhydride, followed by decarboxylation of the dia

50 talysts are exposed to n-butane, the rate of maleic anhydride formation is proportional to the rate o

51 ic copolymers consisting of hydrocarbons and maleic anhydride groups.

52 ural and unnatural conjugated alkenyl(methyl)maleic anhydrides have been described.

53 stitute a missing link between acrylates and maleic anhydride in radical polymerization.

54 In contrast to previous results with maleic anhydride, in this case potassium 3-furanyltriflu

55 We show that the lysine modifier maleic anhydride inhibits leader peptidase by reacting w

56 ess consists of N-acylation of the amines by maleic anhydride, intramolecular [4 + 2] cycloaddition i

57 uggish Diels-Alder reaction of perylene with maleic anhydride is accelerated by the addition of chlor

58 f a phomoidride D precursor lacking only the maleic anhydride is described, and the prospects for the

59 lkenyl boronic derivatives and maleimides or maleic anhydride is described.

60 harboring a maleimide moiety in place of the maleic anhydride is presented.

61 exposure and, in addition to TMLA, excludes maleic anhydride (MA) and phthalic anhydride (PA).

62 racene (MeA), tetracyanoethylene (TCNE), and maleic anhydride (MA) with graphene models have been inv

63 solid polymer materials, a nylon film and a maleic anhydride (MAH) grafted poly(ethylene-octene) (MA

64 H, which regioselectively reduces one of the maleic anhydride moieties in rubratoxin B to the gamma-h

65 9-membered carbocycles with one or two fused maleic anhydride moieties.

66 t of methodology for the construction of the maleic anhydride moiety of the CP-molecules are describe

67 study the mechanism of n-butane oxidation to maleic anhydride on the vanadium phosphorus oxide (VPO)

68 In reactions with maleic anhydride or maleimides, phenoxyacetic acid produ

69 solubilizing motifs on poly(isobutylene-alt-maleic anhydride), PIMA, via nucleophilic addition react

70 reaction of a 5,5,7-tricyclic compound with maleic anhydride produced a 5,5,7,6-polycyclic product.

71 microarray was prepared on a poly(styrene-co-maleic anhydride) (PS-MA)-coated glass slide.

72 tional theory (L = PH3, PMe3, PF3, ethylene, maleic anhydride, pyridine, imidazol-2-ylidene).

73 nges in solvent while the adduct formed with maleic anhydride responds more strongly to changes in so

74 h-Quinox), 2,3-pyrazine ((S,S)-Ph-Pyrazine), maleic anhydride ((S,S)-Ph-MalPhos), and 1,1'-ferrocene

75 ylene-styrene terpolymer functionalized with maleic anhydride (SEBS-g-MA), a thermal modifier and tou

76 tion of VOCs with furan (primary BB VOC) and maleic anhydride (secondary BB VOC) can indicate the ori

77 A maleic anhydride-styrene-glycidyl methacrylate (MA-St-GM

78 between an aminoethyl-substituted diene and maleic anhydride to afford an N-substituted octahydroiso

79 termediate for the conversion of n-butane to maleic anhydride under typical industrial conditions.

80 duct derived from reaction of pyrazinone and maleic anhydride underwent selective anhydride ring open

81 sequential single-electron reductions of the maleic anhydride using electrons derived from NADH and t

82 e transformed into conjugated alkenyl(methyl)maleic anhydrides via oxidation followed by a Horner-Wad

83 report the ring-opening copolymerization of maleic anhydride with a variety of epoxides catalyzed by