ライフサイエンスコーパス: dimethylformamide

1 entrated graphene ink (10 mg mL(-1), in N,N'-dimethylformamide).

2 enzoyl-AMP under anhydrous conditions in N,N-dimethylformamide.

3 d excess of 4-iodobutyraldehyde in anhydrous dimethylformamide.

4 pts the intermediate formic acid to generate dimethylformamide.

5 was achieved to form a mixture of CH3OH and dimethylformamide.

6 re than 10-fold quenching of fluorescence in dimethylformamide.

7 od to excellent yield, via transamidation of dimethylformamide.

8 e suppressed upon adsorption of CO2 and N,N'-dimethylformamide.

9 trifluoromethylsulfonyl)imide (BMP TFSI) and dimethylformamide.

10 eat treatment in the presence of urea or N,N-dimethylformamide.

11 e hydrazone with an excess of piperidine-N,N-dimethylformamide (1:1) released the piperidine-dibenzof

12 been studied in acetonitrile (6 and 7), N,N-dimethylformamide (6), and acetonitrile containing water

13 stase in neat acetonitrile, 95% acetone, 55% dimethylformamide, 80% 5-hexene-1,2-diol, 80% isopropano

14 onitrile (9360 cm(-1)) and those observed in dimethylformamide (8100 cm(-1)) and butyronitrile (8040

15 or poly(methyl methacrylate) substrates or a dimethylformamide/acetone mixture for polystyrene.

16 fluorescence was measured to be 14 ns in N,N-dimethylformamide, an average of 7 ns in Bold's basal me

17 differential pulse voltammetry (DPV) in N,N'-dimethylformamide and acetonitrile.

18 and comparisons were also carried out using dimethylformamide and butyronitrile as solvents.

19 t saturated solvent vapor atmospheres, e.g., dimethylformamide and dimethylsufoxide, dramatic film mo

20 onal dispersibility (0.24 mg mL(-1) ) in N,N-dimethylformamide and for conjugation with amines.

21 n) were extracted from hair samples with N,N-dimethylformamide and subsequently analyzed by liquid ch

22 ylic acid, l-lac = l-lactic acid, dmf = N,N'-dimethylformamide) and observed an increase in enantiome

23 vents miscible in water (dimethyl sulfoxide, dimethylformamide, and 2-propanol).

24 ture of equal volumes of dimethyl sulfoxide, dimethylformamide, and acetonitrile at -50 degrees C.

25 tants (methanol, dimethyl sulfoxide, aqueous dimethylformamide, and deuterium oxide).

26 in aqueous solutions of dimethyl sulfoxide, dimethylformamide, and methanol, at GSSG concentrations

27 of anions with iodomethane in methanol, N,N-dimethylformamide, and water.

28 ene, and 2,7- and 1,8-dinitrobiphenylene) in dimethylformamide are reported and analyzed.

29 Ps in polar solvents (e.g., acetonitrile and dimethylformamide) are crucial to provide repulsive inte

30 trichloride heptahydrate as a cocatalyst in dimethylformamide as a solvent at 60 degrees C.

31 ols has been studied in acetonitrile and N,N-dimethylformamide as solvents.

32 Here, we investigate dimethylformamide as the basis of an electrolyte.

33 yzes the production of H(2) using protonated dimethylformamide as the proton source, with turnover fr

34 zyl esterase variant performs as well in 30% dimethylformamide as the wildtype enzyme in water, refle

35 yrin IX dimethyl ester were then coupled (in dimethylformamide at 100 degrees C) to the Pd-containing

36 constant is 9.5 x 10(5) M(-1) s(-1) in N,N'-dimethylformamide at 298 K, a value within the range of

37 e ylide precursor (4 mg) with (18)F-Et4NF in dimethylformamide at 80 degrees C for 5 min and formulat

38 Moreover, the graphene ink prepared in dimethylformamide can exhibit concentrations as high as

39 -dimethoxycoumarin (5) at carbon cathodes in dimethylformamide containing 0.10 M tetra-n-butylammoniu

40 e(I) electrogenerated at a carbon cathode in dimethylformamide containing tetramethylammonium tetrafl

41 diation of the hydrocarbons in a solution of dimethylformamide-d7 containing potassium tert-butoxide

42 ompound 1 was effected by treatment with N,N-dimethylformamide di-tert-butyl acetal to provide compou

43 -carbonyl glycinate (3) catalyzed by bis(N,N-dimethylformamide)dichlorodioxomolybdenum(VI).

44 Sequential reaction of a keto-dioxinone with dimethylformamide dimethyl acetal and a range of magnesi

45 mylation of a beta-ketosulfonamide employing dimethylformamide dimethyl acetal to afford an enaminone

46 on of triethylene tetraamine (TETA) with N,N-dimethylformamide dimethyl acetal, gave the twelve-membe

47 N-sulfinyl delta-amino beta-ketoesters with dimethylformamide dimethyl acetal.

48 etamide (MTBSTFA) as silylating reagent, N,N-dimethylformamide dimethylacetal (DMF-DMA) and tetrameth

49 h the separation of aliphatic amines in pure dimethylformamide, dimethylacetamide, dimethyl sulfoxide

50 sidase or GFP) in a solvent mixture [94% N,N-dimethylformamide (DMF) + 6% 1x TE buffer] and subsequen

51 f [(dippe)NiH]2 with 2M3BN in decane and N,N-dimethylformamide (DMF) allowed for the calculation of E

52 ,4-benzenedicarboxylate) in a mixture of N,N-dimethylformamide (DMF) and methanol affords Fe(2)(dobdc

53 -1,2,3-triazol-5-yl)benzene (H3BTTri) in N,N-dimethylformamide (DMF) and methanol leads to the format

54 of the cumyloxyl radical (CumO(*)) with N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA)

55 n of hydrogen abstraction reactions from N,N-dimethylformamide (DMF) and N,N-dimethylacetamide (DMA)

56 smeier-Haack reagents is possible using only dimethylformamide (DMF) and tetrabromomethane (CBr4) in

57 (Fe(III)-IL) as desulfurizer, Fe(II) and N,N-dimethylformamide (DMF) are introduced to Fe(III)-IL to

58 We report here on the use of N,N-dimethylformamide (DMF) as both solvent and reductant in

59 antly faster in Lewis basic solvents such as dimethylformamide (DMF) compared with those in chlorofor

60 Moreover, polar aprotic dimethylformamide (DMF) improves chromatographic separat

61 A Heck coupling reaction is performed in N,N-dimethylformamide (DMF) in a continuous membrane reactor

62 the corresponding imidazole linker, and N,N dimethylformamide (DMF) in the case of ZIF-4.DMF.

63 ylphenyl-N'-methylformamidine (DMPF) and 2,4-dimethylformamide (DMF) into 2,4-dimethylaniline (DMA),

64 Filling the MOF pores with dimethylformamide (DMF) slows the structural fluctuation

65 The title anion was synthesized by heating dimethylformamide (DMF) solution of the known Ni-centere

66 al levels of theory in the gas phase, in N,N-dimethylformamide (DMF) solution, and in DMF solution in

67 epared directly by solution casting of their dimethylformamide (DMF) solutions under ambient conditio

68 zed single-walled CNTs were assembled from a dimethylformamide (DMF) suspension onto a carbon-fiber d

69 d by the previously unknown breakdown of N,N-dimethylformamide (DMF) to formaldehyde at high temperat

70 acid (H(3)BTB), copper(II) nitrate, and N,N'-dimethylformamide (DMF) to prepare Cu(3)(BTB)(2)(H(2)O)(

71 bes (MWNT) by ultrasonication of graphite in dimethylformamide (DMF) upon addition of ferrocene aldeh

72 ontaining N,N-dimethylacetamide (DMA) or N,N-dimethylformamide (DMF) was used to improve the separati

73 amide (FA), N-methylformamide (NMF), and N,N-dimethylformamide (DMF) were compared to those in pure w

74 ctions employing Ni(COD)2/(t)Bu-Terpy in N,N-dimethylformamide (DMF) were typically high yielding and

75 over the control value (P<0.5), whereas 10% dimethylformamide (DMF) with or without CAT did not (P>0

76 quantitative determination of CO2(*-) in N,N-dimethylformamide (DMF) with the tip generation/substrat

77 ne dicarboxylic acid and zinc nitrate in N,N-dimethylformamide (DMF) yielded a dense 2-D network, 1,

78 ts for the silane, R(3)SiH, reduction of N,N-dimethylformamide (DMF), and N,N-diethylformamide (DEF),

79 solvent (N,N-dimethylacetamide (DMA) and N,N-dimethylformamide (DMF), as the background electrolyte (

80 ne sheets in N-methylpyrrolidone (NMP), N,N'-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), gamm

81 amples containing dimethyl sulfoxide (DMSO), dimethylformamide (DMF), methyl salicylate, caffeine, l-

82 factant system of dodecyl maltoside (DDM) in dimethylformamide (DMF), micelle formation can be induce

83 tom transfer (HAT) from the C-H bonds of N,N-dimethylformamide (DMF), N,N-dimethylacetamide (DMA), N-

84 addition, NDMA formation during ozonation of dimethylformamide (DMF), the other model precursor used

85 c strategy, involving a cooperative solvent, dimethylformamide (DMF), to synthesize core/shell archit

86 ry mixtures of water with 1,4-dioxane or N,N-dimethylformamide (DMF).

87 nm of a 1.5 mg/ml solution of DTPA-A in dry dimethylformamide (DMF).

88 occur for other guest molecules, such as N,N-dimethylformamide (DMF).

89 rature in dimethyl sulfoxide (DMSO) and N,N'-dimethylformamide (DMF).

90 ency was improved by the presence of 25% N,N-dimethylformamide (DMF).

91 Fe(3+) preferentially binds with NR in dimethylformamide (DMF)/water (1:1) solution over other

92 lective for the production of formic acid in dimethylformamide (DMF)/water mixtures (Faradaic efficie

93 7 for the PEO blocks (PS962-b-PEO227) in N,N-dimethylformamide (DMF)/water, in which water is a selec

94 zinc coproporphyrin III in a glassy solvent (dimethylformamide/ethylene glycol) or in poly(vinyl chlo

95 and expand again upon adsorption of DMF (N,N-dimethylformamide), EtOH, or CO(2), etc., while N(2) is

96 and aliphatic ketones can be carried out in dimethylformamide even without the use of any catalyst.

97 (3)O(MeCOO)(6)(H(2)O)(3) with formic acid in dimethylformamide exposed to air at 110 degrees C afford

98 30-fold excess of 4-iodobutyraldehyde in N,N-dimethylformamide into a derivative having 2-pyrrolino-D

99 ic sodium ion electrolyte NaClO4 (DMF)3 (DMF=dimethylformamide) is described.

100 ized in good yield through cyanuric chloride-dimethylformamide mediated cleavage of different spiro-4

101 tol structures are effectively methylated in dimethylformamide medium to avoid artefacts in MS measur

102 0, using a separation voltage of +3,000 V, a dimethylformamide medium, and a contactless conductivity

103 ar cyclization of several dialdimines in N,N-dimethylformamide, methanol, or methylene chloride/water

104 yields (up to 40%) in organic solvents (N,N-dimethylformamide, N,N-dimethylacetamide and N-methyl-2-

105 With dimethylformamide, only part of the penta-coordinated Co

106 results in the formation of byproducts when dimethylformamide or acetonitrile are used as solvents f

107 c pH's in water and in organic solvents like dimethylformamide or dichloromethane.

108 H(2)TCNQ deprotonates slowly, whereas in N,N-dimethylformamide or tetrahydrofuran, rapid deprotonatio

109 following treatment with PMA, retinoic acid/dimethylformamide, or IFN-gamma, but not in similarly tr

110 A solution of poly(vinylidene fluoride)/dimethylformamide (PVDF/DMF) was used to coat the tip of

111 hydrazine, and its co-intercalation with N,N-dimethylformamide, resulted in increases of the c-lattic

112 nd O-H bonds in 9,10-dihydroanthracene (S1), dimethylformamide (S2), 1,2-diphenylhydrazine (S3), p-me

113 maging paclitaxel molecules dissolved in N,N-dimethylformamide solution.

114 , propyl; X(-) = perchlorate) electrolyte in dimethylformamide solution.

115 solvents: acetonitrile, methylene chloride, dimethylformamide, tetrahydrofuran, dimethylsulfoxide, c

116 DMF=N,N-dimethylformamide, Tf=trifluoromethanesulfonyl, TIPS=tri

117 DEA=diethanolamine, DMF=N,N'-dimethylformamide, Tf=trifluoromethanesulfonyl.

118 may be converted into ethyl formate and N,N-dimethylformamide, thereby providing a means for utilizi

119 ation of either functionalized aziridines in dimethylformamide (through direct bromide displacement)

120 2, PbCl2, CdI2, or CdCl2) salts dissolved in dimethylformamide to displace oleate surface ligands and

121 intercalated graphites readily exfoliate in dimethylformamide to give suspensions of crystalline sin

122 The stability of dimethylformamide toward reduced oxygen species is insuf

123 N,N-Dimethylformamide-treated poly(3,4-ethylenedioxythiophen

124 PMDI subunits, forms-in the presence of N,N-dimethylformamide-two different types of intermolecular

125 cleaved with tetrabutylammonium fluoride in dimethylformamide under microwave irradiation.

126 O (BDC=benzene-1,4-dicarboxylate and DMF=N,N-dimethylformamide) under solvothermal conditions, from m

127 th low polydispersities were prepared in N,N-dimethylformamide using small seed initiators via living

128 ve the interaction with Pd clusters, and N,N-dimethylformamide was used as solvent and capping agent

129 ion from decomposition of peroxynitrite in a dimethylformamide/water mixture was obtained by electron

130 he relatively polar solvents acetone and N,N-dimethylformamide, which have dielectric constants (epsi

131 sible-light-driven reduction of CO2 to CO in dimethylformamide with triethanolamine (TEOA) as sacrifi