ライフサイエンスコーパス: dimethylformamide

1 been crystallized from its gelling solvent (dimethylformamide).

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

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

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

5 d excess of 4-iodobutyraldehyde in anhydrous dimethylformamide.

6 ular electrocatalyst for proton reduction in dimethylformamide.

7 trifluoromethylsulfonyl)imide (BMP TFSI) and dimethylformamide.

8 pts the intermediate formic acid to generate dimethylformamide.

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

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

11 od to excellent yield, via transamidation of dimethylformamide.

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

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

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

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

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

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

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

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

20 rrogate was generated via the unification of dimethylformamide and ammonium iodide (NH(4)I).

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

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

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

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

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

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

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

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

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

30 dels for common solvents (methanol, acetone, dimethylformamide, and n-hexane).

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

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

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

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

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

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

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

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

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

40 ligand and potassium carbonate as a base in dimethylformamide at 105 degrees C.

41 n a mixture of formic acid-triethylamine and dimethylformamide at 25 degrees C.

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

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

44 t with the use of methylene chloride and N,N-dimethylformamide being particularly prevalent.

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

46 lvent in high accuracy, we demonstrated that dimethylformamide can work as an effective surface molec

47 ly investigated at glassy carbon cathodes in dimethylformamide containing 0.10 M tetra-n-butylammoniu

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

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

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

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

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

53 echo spectra we showed that solvents such as dimethylformamide, diethylformamide, 2-octanone, bromobe

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

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

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

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

58 n polar solvents (such as n-methylformamide, dimethylformamide, dimethyl sulfoxide, H(2)O) with vario

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

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

61 sponse to 3 distinct differentiating agents, dimethylformamide, dimethylsulfoxide, and retinoic acid,

62 Dimethylformamide disrupts the interfacial network of hy

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

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

65 f was prepared by the solvothermal method in dimethylformamide (dmf) and characterized by variable-te

66 ations during the guest exchange between N,N-dimethylformamide (DMF) and ethanol (EtOH)-containing 1.

67 degrees C, in polyethylene glycol (PEG-400), dimethylformamide (DMF) and in sunflower oil (SO).

68 ,4-benzenedicarboxylate) in a mixture of N,N-dimethylformamide (DMF) and methanol affords Fe(2)(dobdc

69 -1,2,3-triazol-5-yl)benzene (H3BTTri) in N,N-dimethylformamide (DMF) and methanol leads to the format

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

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

72 ly employed dipolar aprotic solvents such as dimethylformamide (DMF) and N-methyl-2-pyrrolidinone (NM

73 intertwined with harmful substances such as dimethylformamide (DMF) and PFAS-classified trifluoroace

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

75 , we demonstrate that the combination of N,N-dimethylformamide (DMF) and TU has the remarkable abilit

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

77 uced with trichlorosilane in the presence of dimethylformamide (DMF) as an organocatalyst ( 10 mol %)

78 uced with trichlorosilane in the presence of dimethylformamide (DMF) as an organocatalyst (<=10 mol %

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

80 as a base and dichloromethane (DCM) and N,N-dimethylformamide (DMF) as solvents) and relies on the u

81 Using CuBr and t-BuONa in dimethylformamide (DMF) as the optimal reaction conditio

82 xtended 2D structure by replacing water with dimethylformamide (DMF) as the solvent during the synthe

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

84 mediator, 1,1-dimethylferrocene, in dry N,N-dimethylformamide (DMF) containing oxalate (C(2)O(4)(2-)

85 ld be used for controllable synthesis of N,N-dimethylformamide (DMF) from dimethylamine and CO(2)/H(2

86 A suspension of VOTCPP-PIF-1 at 5 K in dimethylformamide (DMF) had a spin-spin relaxation time

87 ilyl-B-alkyl(aryl)-a,B-unsaturated esters in dimethylformamide (DMF) has furnished (Z)-B-substituted-

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

89 d ranitidine were tested for NDMA, NDEA, and dimethylformamide (DMF) impurities, using a liquid chrom

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

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

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

93 ains bridged by dipyrazolate linkers and N,N-dimethylformamide (DMF) ligands has been synthesized.

94 to the diffusion rate of incorporated guest dimethylformamide (DMF) molecules: slow diffusion of DMF

95 nzene (H(6)cpb) by solvothermal reactions in dimethylformamide (dmf) or dimethylacetamide (dmac) with

96 d that N, N-dimethylacetamide (DMA) and N, N-dimethylformamide (DMF) prevent inflammation-induced PTB

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

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

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

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

101 and its chemical origin from decomposed N,N-dimethylformamide (DMF) solvent.

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

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

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

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

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

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

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

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

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

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

112 MSO), N-methyl-2-pyrrolidone, verbenone, and dimethylformamide (DMF)), requiring sample sizes of only

113 rgo major restructuring upon exposure to N,N-dimethylformamide (DMF), a common perovskite precursor s

114 tion of purines with ferrocenoyl chloride in dimethylformamide (DMF), a regioselective acylation occu

115 In dimethylformamide (DMF), a solvent that disrupts hydroge

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

117 10(6) ) was achieved in the synthesis of N,N-dimethylformamide (DMF), and the solid catalysts can be

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

119 e azepane ring was efficiently formed in N,N-dimethylformamide (DMF), as the preferred aprotic solven

120 ectroscopic measurements are reported in N,N-dimethylformamide (DMF), dichloromethane (DCM), and tolu

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

122 Common solvents N,N-dimethylformamide (DMF), ethanol (EtOH), and methanol (M

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

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

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

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

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

128 e conducted on MHP thin films processed from dimethylformamide (DMF)-based solutions to which either

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

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

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

132 s for proper management of solvents like N,N-dimethylformamide (DMF).

133 hanol (EtOH), dichloromethane (DCM), and N,N-dimethylformamide (DMF).

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

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

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

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

138 7 for the PEO blocks (PS962-b-PEO227) in N,N-dimethylformamide (DMF)/water, in which water is a selec

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

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

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

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

143 comparison with the same surface treated by dimethylformamide immersion.

144 ts are assessed by comparing water with N, N-dimethylformamide, in which SBU adducts are appreciably

145 30-fold excess of 4-iodobutyraldehyde in N,N-dimethylformamide into a derivative having 2-pyrrolino-D

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

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

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

149 0, using a separation voltage of +3,000 V, a dimethylformamide medium, and a contactless conductivity

150 ment (AIEE) behavior by aggregation in H(2)O-dimethylformamide medium.

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

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

153 Isatin in a solution of dry N,N-dimethylformamide/NaClO(4) is electroreduced in the pres

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

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

156 2)) with two substituted thiobenzanilides in dimethylformamide or acetonitrile was used for the synth

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

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

159 nic solvents, for example, acetonitrile, N,N-dimethylformamide, or acetone, which indicated the excep

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

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

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

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

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

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

166 This aggregate is stable in N,N-dimethylformamide solution; however, it slowly dissociat

167 onaphthylimino group in commercial-grade N,N-dimethylformamide solvent and employs CuI or thiophene-2

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

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

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

171 ve that the choice of solvent (water and N,N-dimethylformamide), the introduction of ions (Na(+) and

172 Importantly, in dimethylformamide, the photoligation reaction did not oc

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

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

175 2, PbCl2, CdI2, or CdCl2) salts dissolved in dimethylformamide to displace oleate surface ligands and

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

177 Bu(3)MgLi at -100 degrees C and reacted with dimethylformamide to give the required fulvene dialdehyd

178 ase structures depending on the ratio of N,N-dimethylformamide to N,N-diethylformamide solvent and th

179 The stability of dimethylformamide toward reduced oxygen species is insuf

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

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

182 cleaved with tetrabutylammonium fluoride in dimethylformamide under microwave irradiation.

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

184 iron tetraphenylporphyrin (Fe(TPP)) in N, N'-dimethylformamide using decamethylferrocene as a soluble

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

186 N,N-Dimethylformamide was reacted with hexamethyldisilazane

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

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

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

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

191 azolyl))-2-hydroxy-1,3-diaminopropane; DMF = dimethylformamide) with [Fe(II){FeNO}(7)] formulation [J