ライフサイエンスコーパス: dichloromethane

1 apsules than the resorcinarenes (1.0% v/v in dichloromethane).

2 ilane 6 (treatment with hydrogen chloride in dichloromethane).

3 ient temperature, while 1 day is required in dichloromethane.

4 ], and is markedly faster in toluene than in dichloromethane.

5 e then desorbed by treatment with 200 muL of dichloromethane.

6 n organic solvents like dimethylformamide or dichloromethane.

7 phoma, as well as marginal zone lymphoma for dichloromethane.

8 uantitatively removed in <5 min by 3% TFA in dichloromethane.

9 dimer shows the appearance of four waves in dichloromethane.

10 paced one-electron transfers on oxidation in dichloromethane.

11 These derivatives were then extracted with dichloromethane.

12 -0.89; tau(F) approximately 2.09-3.91 ns) in dichloromethane.

13 n situ activation method at -40 degrees C in dichloromethane.

14 promotion gives beta-selective couplings in dichloromethane.

15 (3v) symmetry is minor for bases weaker than dichloromethane.

16 and eluting target analytes and lipids with dichloromethane.

17 e cleaved from polymer beads with 50% TFA in dichloromethane.

18 tracted in aqueous 1-propanol and mixed with dichloromethane.

19 loroethane or a cosolvent mixture of 1/9 THF/dichloromethane.

20 reactivity in dioxane but low reactivity in dichloromethane.

21 xane, tert-butyl methyl ether, n-pentane and dichloromethane.

22 mo-2-methoxypropane with diisopropylamine in dichloromethane.

23 sed disk is extracted with a small volume of dichloromethane.

24 olymerization of N-carboxyanhydride (NCA) in dichloromethane.

25 g soil), 75% of which was not extractable by dichloromethane.

26 ne (H.G1 and H.G2) in a nonpolar medium like dichloromethane.

27 cceptor using non-H-bonding solvents such as dichloromethane.

28 etabolites and a mixture of acetonitrile and dichloromethane (1:1, v/v) for PCP.

29 From the dichloromethane/2-propanol (1:1) extract of the Indonesi

30 and diorganyl dichalcogenides (1.0 equiv) in dichloromethane (3 mL) at room temperature.

31 leaved with TFA, and following dilution with dichloromethane, "3 + 1" condensation with a pyrrole dia

32 ploying 300 muL of brewed coffee, 100 muL of dichloromethane, 400 muL of acetonitrile and without sod

33 using a mixture of n-hexane, chloroform, and dichloromethane (70 mL) for extraction.

34 near relationship at high concentrations for dichloromethane, a highly volatile compound.

35 In dichloromethane, a strong dependence on the countercatio

36 Relative energies in THF, dichloromethane, acetone, and DMSO have been estimated w

37 on (C(2) or C(6)), and solvent (1,4-dioxane, dichloromethane, acetonitrile, methanol, and in some cas

38 = 400, DeltaGalpha = -15 kJ mol(-1)) in 4:1 dichloromethane-acetonitrile.

39 ed to stabilize myoglobin against unfolding, dichloromethane actually destabilized myoglobin at all e

40 ure with a thiophene dialcohol in 2% ethanol-dichloromethane afforded a tetraphenylthiapyreniporphyri

41 Acetonitrile and dichloromethane afforded lower regioselectivity (50:50 a

42 '(4)(-) (4, Ar' = 3,5-C(6)H(3)(CF(3))(2)) in dichloromethane afforded the nonclassical polyhydride co

43 ations show the atmospheric concentration of dichloromethane-an ozone-depleting gas not controlled by

44 inimide and trifluoromethanesulfonic acid in dichloromethane and acetonitrile at -78 degrees C in the

45 of BpCCOCH3 is faster in cyclohexane than in dichloromethane and acetonitrile because of intimate sol

46 is dominantly formed in non-aqueous solvents dichloromethane and acetonitrile.

47 ixture design consisted of ethanol, acetone, dichloromethane and chloroform solvents and their binary

48 In dichloromethane and chloroform without an additive the 2

49 ts of a Soxhlet extraction with a mixture of dichloromethane and diethyl ether containing lipases and

50 PSA and TRH were dissolved in a mixture of dichloromethane and ethanol and added dropwise to a disp

51 r 17 individual PAHs through extraction with dichloromethane and gas chromatograph-mass spectrometer

52 ueezed calamansi juices were extracted using dichloromethane and headspace solid-phase microextractio

53 Philippines and Vietnam were extracted with dichloromethane and hexane, and then analysed by gas chr

54 ructed of appropriate reference compounds in dichloromethane and in acetonitrile that can be used to

55 The catalyst operates in both dichloromethane and ionic liquids and undergoes no decom

56 ternal energies of ions produced by ESI from dichloromethane and methanol solutions under standard co

57 Screening of antioxidant potential of dichloromethane and methanolic extracts of twenty-seven

58 more, novel biological activities of hexane, dichloromethane and methanolic extracts were assessed.

59 The procedure involves three parts: dichloromethane and PEG are first dried; the reaction st

60 with a dilute solution in 1:1 n-pentane and dichloromethane and pumping away the solvent.

61 xtraction solvent ratios, varying amounts of dichloromethane and salts were performed with fifty repr

62 s were 1840muL of acetonitrile and 160muL of dichloromethane and the re-suspended mixture consisting

63 solvent basicity bounded at the lower end by dichloromethane and the upper end by tributyl phosphate,

64 eaction in Scholl precursors in a mixture of dichloromethane and various acids (10% v/v).

65 gh singlet-oxygen-generation ability both in dichloromethane and water.

66 ed by the reaction of sodium salt and CsF in dichloromethane and water.

67 Thus, dichloromethane and xenon have opposite effects on myogl

68 MCRred1 reacts with chloroform and dichloromethane and, like F(430), can catalyze dehalogen

69 ction by diethyl ether instead of more toxic dichloromethane, and (3) concentration by vacuum automat

70 tained in the weakly basic solvents benzene, dichloromethane, and 1,2-dichloroethane.

71 d in acetonitrile, benzene, tetrahydrofuran, dichloromethane, and halobenzene solvents relative to cy

72 as a singlet ground state in cyclohexane, in dichloromethane, and in acetonitrile and decays by WR to

73 ns (i.e., methanol combined with chloroform, dichloromethane, and methyl-tert butyl ether and isoprop

74 g from polar to nonpolar (methanol, acetone, dichloromethane, and n-hexane) were selected to maximize

75 ck of a quinone oxidant, avoidance of use of dichloromethane, and the increased yield of macrocycle f

76 e are added dropwise to a solution of PEG in dichloromethane; and finally, the product solution is fi

77 Xenon and dichloromethane are inhalational anesthetic agents whose

78 d encapsulation efficiency compared to using dichloromethane as core and shell solvents.

79 LLE using dichloromethane as organic phase was combined with the d

80 Using ethyl acetate and dichloromethane as shell- and core-phase solvents, respe

81 ryldiazoacetates, and its compatibility with dichloromethane as solvent.

82 ne transfer and allows the strain to grow on dichloromethane as the sole carbon and energy source.

83 and diorganyl diselenides (1.0 equiv), using dichloromethane as the solvent, at room temperature, 4-m

84 dered using a Polarized Continuum Model with dichloromethane as the solvent.

85 e, and trifluoromethanesulfonic anhydride in dichloromethane at -55 degrees C, reaction with glycosyl

86 nce of a stochiometric amount of BF3.OEt2 in dichloromethane at -78 degrees C.

87 r-O-acetyl or benzyl-protected KDO donors in dichloromethane at -78 degrees C.

88 ne and boron trifluoride diethyl etherate in dichloromethane at 0 degrees C rapidly affords a cyclic

89 uring the bromination of benzodiazocine 8 in dichloromethane at 0 degrees C, and the second during th

90 At 0.33 mM in dichloromethane at 25 degrees C the cyclic metalloporphy

91 While EPR spectra of monoradicals in dichloromethane at 295 K reveal the expected three-line

92 equiv) and iron(III) chloride (2.0 equiv) in dichloromethane at 40 degrees C for 30 min to be optimal

93 with 0.5 equiv of 1,3,5-trimethoxybenzene in dichloromethane at 40 degrees C.

94 ith a mixture of triphosgene and pyridine in dichloromethane at reflux.

95 tones via triphosgene-pyridine activation in dichloromethane at reflux.

96 ount of zinc chloride etherate (10 mol %) in dichloromethane at room temperature gave 2,5-di- and 2,3

97 late (8), and i-Pr2NEt and their coupling in dichloromethane at room temperature with alkene acceptor

98 On exposure to dichlorodicyanoquinone in wet dichloromethane at room temperature, equatorial 4-O-benz

99 initial pH 6.0 aqueous phase, an intervening dichloromethane barrier containing the calix[4]pyrrole c

100 as been studied in gas phase and in aqueous, dichloromethane, benzene, and cyclohexane solutions usin

101 , (8.4), (8.4), and (8.2) kcal/mol in water, dichloromethane, benzene, and cyclohexane, respectively,

102 Ethanol, dichloromethane, benzene, and heptane were selected as r

103 rtho substituent were treated with 1% TFA in dichloromethane, benzofurans were released from resin in

104 [NBu(4)][B(C(6)F(5))(4)] in tetrahydrofuran, dichloromethane, benzotrifluoride, and acetonitrile and

105 In acetonitrile and in dichloromethane BpCCO2CH3 has a singlet ground state.

106 nts, exhibiting narrow, sharp band shapes in dichloromethane but broad features in toluene; this chan

107 ttern was seen for SQ stored in the light in dichloromethane but with a slower formation of SQ-[OOH]

108 nteraction by solvent is large (about 70% in dichloromethane), but not complete, and that current sta

109 onjugants varied in their ability to grow on dichloromethane, but their fitness on dichloromethane di

110 be reduced considerably, especially for the dichloromethane (by a factor of 3).

111 trile, nitromethane, 1,2-dichloroethane, and dichloromethane, carried out using various chloride salt

112 elds were measured for all compounds in both dichloromethane (CH(2)Cl(2)) and dimethylacetamide (DMAc

113 Unregulated chlorocarbons, here defined as dichloromethane (CH(2)Cl(2)), perchloroethene (C(2)Cl(4)

114 However, the solvent dichloromethane (CH2Cl2) can be employed to form stable

115 ed-bed plasma reactor for the remediation of dichloromethane (CH2Cl2, DCM).

116 investigated in different solvents (toluene, dichloromethane, chlorobenzene, and benzyl alcohol).

117 d toluene but not with chlorinated solvents (dichloromethane, chloroform).

118 facile in such solvents as benzene, toluene, dichloromethane, chloroform, and pyridine; was unaffecte

119 complished by washing the aqueous phase with dichloromethane, chloroform, or hexane.

120 PAHs and dichloromethane co-permeate the membrane into the accept

121 e study indicate that the choice of solvent, dichloromethane compared to toluene and toluene/methanol

122 We have explored this issue using dichloromethane consumption in Methylobacterium strains.

123 fluoroisopropanol hydrogen bonded complex in dichloromethane-d2 were determined to be k1 > 10(5) M(-1

124 ethanol (E3), ethanol:HCl (100:1, v/v) (E4), dichloromethane (D5) and hexane (H6) were prepared.

125 arate, complementary extraction chemistries, dichloromethane (DCM) and a methyl tert-butyl ether/hexa

126 (EF) of chemicals extracted from the soil by dichloromethane (DCM) and air were found.

127 inct Dehalobacter strains that respire CF to dichloromethane (DCM) and ferment DCM to nonchlorinated

128 s components (using piperidine as a base and dichloromethane (DCM) and N,N-dimethylformamide (DMF) as

129 Pyridine derivatives and dichloromethane (DCM) are commonly used together in a va

130 By adding electrochemically "inert" dichloromethane (DCM) as a diluent in concentrated ethyl

131 The microbial mixed culture RM grows with dichloromethane (DCM) as the sole energy source generati

132 m (quaternary and primary) chloride salts in dichloromethane (DCM) solution and in the solid-state.

133 e permethylated and partitioned into a water-dichloromethane (DCM) solvent mixture.

134 dy, biotic degradation of chloroform (CF) to dichloromethane (DCM) was carried out by the Dehalobacte

135 e (DMF) compared with those in chloroform or dichloromethane (DCM).

136 ~17 nm) compared with that of 1a solution in dichloromethane (DCM).

137 In dichloromethane (DCM-d(2)), nonalkylated BINAM-derived b

138 s of DOC: (1) solid-phase extract (HLB); (2) dichloromethane (DCM-total) extract used in TPHd; and (3

139 ptive process and directly enabled effective dichloromethane degradation across diverse Methylobacter

140 a significant impact on trichloromethane and dichloromethane degradation and that compound-specific i

141 strating that effective use of an introduced dichloromethane degradation pathway required one of seve

142 to compare abiotic and biotic chloroform and dichloromethane degradation.

143 ing multiple mechanisms were contributing to dichloromethane degradation.

144 ns that independently evolved in two natural dichloromethane-degrading strains.

145 Methylobacterium extorquens DM4 expresses a dichloromethane dehalogenase (DcmA) that has been acquir

146 The glutathione (GSH)-dependent dichloromethane dehalogenase from Methylophilus sp. stra

147 In concentrated solutions of dichloromethane, Deoxofluor (1) efficiently fluorinates

148 In dichloromethane, DIBA(i)OPr behaves as a bulky reducing

149 row on dichloromethane, but their fitness on dichloromethane did not correlate with the phylogeny of

150 the same reactions in the molecular solvents dichloromethane, dimethylsulfoxide, and methanol.

151 f N-chlorodimethylamine with sodium azide in dichloromethane does not lead to N-azidodimethylamine, a

152 en organic molecules (acetone, acetonitrile, dichloromethane, ethanol, ethyl acetate, hexane, and tol

153 A solvent ratio of 50:50 dichloromethane/ethanol was found to be optimum for sele

154 nia, chlorine, tetrahydrothiophene, benzene, dichloromethane, ethylene oxide, and carbon monoxide.

155 -[di(4-methoxyphenyl)amino]styryl}benzene in dichloromethane exhibit five lines over a wide temperatu

156 The electrochemistry of these compounds in dichloromethane exhibits, besides several reversible red

157 nd evaluate the bioactive compounds from the dichloromethane extract of the fruits of Heracleum mante

158 of a semi-purified fraction, DW-F5, from the dichloromethane extract of W. tinctoria leaves against m

159 However, dichloromethane extract proved the utmost antioxidant ac

160 carbon constituted approximately 40% of the dichloromethane-extractable carbon (DeOC) in the soil.

161 LC/MS analysis of dichloromethane extracts of (ADSR-1), (ADSR-2) and (ADSR

162 nti-diabetic effects of methanol, hexane and dichloromethane extracts of the aerial parts of Ocimum b

163 The enrichment factor for dichloromethane fermentation was -15.5 +/- 1.5 per thous

164 The dichloromethane-fermenting culture transformed dichlorom

165 cai samples were extracted sequentially with dichloromethane followed by methanol.

166 (TIPS) propynal 1 with 3,4-diethylpyrrole in dichloromethane, followed by oxidation with 2,3-dichloro

167 the dialdehydes with the tetrapyrrole in TFA-dichloromethane, followed by oxidation with dilute aqueo

168 olvent to milk for protein precipitation and dichloromethane for lipid removal, was developed to dete

169 When stored as a solution in dichloromethane for one month, the PCO-isomer rearranges

170 Chloroform transformation and dichloromethane formation was up to 8-fold faster and 14

171 Geminal dichloromethane functionality was introduced by the addi

172 benzyltriethylammonium nitrite (BTEA-NO2) in dichloromethane gave the crystalline 2,6-dichloropurine

173 Although there are gaps in the database for dichloromethane genotoxicity (i.e., DNA adduct formation

174 old acetonitrile and the chlorosugar in cold dichloromethane gives essentially quantitative yields of

175 Dichloromethane, however, gives only C-Cl cleavage produ

176 completed an updated toxicological review of dichloromethane in November 2011.

177 nnosyl donor is achieved at -60 degrees C in dichloromethane in the presence of 2,4,6-tri-tert-butylp

178 The reaction occurs at room temperature in dichloromethane in the presence of 3 mol % [IPrAuCl]/AgB

179 hlorotrityl chloride resin (Barlos resin) in dichloromethane in the presence of diisopropylethylamine

180 , in a matter of minutes at -60 degrees C in dichloromethane, in the presence of 2,4,6-tri-tert-butyl

181 The (1)H NMR spectra recorded in deuterated dichloromethane indicated the presence of contact ion pa

182 lic activity, the key activation pathway for dichloromethane-induced cancer.

183 fluorine (F) atoms in d3-acetonitrile and d2-dichloromethane involve efficient energy flow to vibrati

184 the nitration of toluene by NO2(+)BF4(-) in dichloromethane is accurately predicted from trajectorie

185 Dichloromethane is better suited for generating the more

186 traction of caffeine with a minute amount of dichloromethane, isolating caffeine from the sample matr

187 The dichloromethane/isopropanol solvent has been identified

188 Reductive electrolysis of 1, 2 and 6 in dichloromethane leads to a different reaction, which we

189 Reductive electrolysis of 1 and 3-5 in dichloromethane leads to the removal of the addend and t

190 able pre-equilibrium for dissociation of the dichloromethane ligand in the trimethyl phosphite comple

191 s (SQUID) indicate that the diradical in the dichloromethane matrix predominantly adopts anticonforma

192 nate) and other small molecules (chloroform, dichloromethane, mercaptoethanol, and nitric oxide), we

193 The samples were dissolved in acetone-dichloromethane-methanol (3:2:1, v/v/v) and diluted with

194 -lock micro test tube, homogenized in 1.5 mL dichloromethane-methanol (8:2) and mixed in a mixer mill

195 lectively oxidized with silver(I) acetate in dichloromethane-methanol to give stable nonaromatic stru

196 rin with tert-butyl hydroperoxide and KOH in dichloromethane/methanol gave a benzocarbachlorin and tw

197 nd widths of 0.86 +/- 0.07/0.86 +/- 0.06 eV (dichloromethane/methanol).

198 - 20/590 +/- 20 and 710 +/- 20/680 +/- 20 K (dichloromethane/methanol).

199 water followed by an organic extraction with dichloromethane/methanol, with resuspension of the dried

200 sting of LiChrolut EN resins and eluted with dichloromethane/methanol.

201 ]CPP ring of the alpha form encapsulates two dichloromethane molecules, held through C-H...pai intera

202 flates but was successful when four solvent (dichloromethane) molecules were taken into account.

203 ed to a solution of cis-cyclooctene (COE) in dichloromethane/[NBu(4)][B(C(6)F(5))(4)] containing a ca

204 five diaryldisulfides have been studied in a dichloromethane/[NBu4][B(C6F5)4] electrolyte.

205 tandard Scholl reaction conditions (FeCl(3), dichloromethane) occurs for perylene-substituted porphyr

206 ssociations between the chlorinated solvents dichloromethane (odds ratio (OR) = 1.69, 95% confidence

207 s requiring a higher percentage (1.6% v/v in dichloromethane) of methanol to disassemble the capsules

208 tracted with NaOH/methanol, partitioned into dichloromethane on a ChemElut column and cleaned-up by s

209 hat although currently modest, the impact of dichloromethane on ozone has increased markedly in recen

210 inetic photoacidity when operating either in dichloromethane or acetonitrile solutions.

211 trifluoroacetic acid followed by addition of dichloromethane or dibromomethane to remove the lipids.

212 In dichloromethane or trifluoroacetic acid (TFA), the react

213 0673 in the cytochrome P4502E1 gene, CYP2E1 (dichloromethane: OR = 4.42, 95% CI: 2.03, 9.62; P(intera

214 by moderately polar (methanol) and nonpolar (dichloromethane) organic solvents, and is hypothesized t

215 of these intermediates with a Lewis acid in dichloromethane permits the regeneration of a reactive a

216 disperse LCOs and isotropic organic solvent (dichloromethane) phase-separate at the surface of oil-in

217 ymer films at the interface of the water and dichloromethane phases.

218 The 2011 IRIS assessment of dichloromethane provides insights into the toxicity of a

219 Dichloromethane reacts to give the corresponding 4-chlor

220 OSPW extracted using dichloromethane removed the potential for sample matrix

221 Cl) to the solutions of o-chloranil, oCA, in dichloromethane resulted in the transient formation of t

222 Cyclic voltammetry measurements of 1(Bz) in dichloromethane reveal separation of the first and secon

223 In dichloromethane, reversible chelation and partial displa

224 Recent epidemiologic studies of dichloromethane (seven studies of hematopoietic cancers

225 utations, using a continuum solvation model (dichloromethane), show that allostery contributes approx

226 llow fiber membrane directly immersed into a dichloromethane/soil slurry.

227 We identified a dichloromethane-soluble fraction (Qu Mai fraction AD [QM

228 oranes) have been studied photometrically in dichloromethane solution at 20 degrees C.

229 gle crystal X-ray diffraction methods and in dichloromethane solution by means of continuous variatio

230 e been prepared by adding diethyl ether to a dichloromethane solution containing equimolar amounts of

231 rearrangement reactions of five epoxides in dichloromethane solution have been studied at the M062X/

232 ndicate that the molecular capsules exist in dichloromethane solution in the absence of any cations.

233 ster-2,2'-bipyridine; bpz = 2,2'-bipyrazine) dichloromethane solution led to the formation of two con

234 eous solution of a polymer and Zn(2+) with a dichloromethane solution of ( S)- or ( R)-amino alcohols

235 d dextran particles were then suspended in a dichloromethane solution of polylatic-co-glyclic acids (

236 ninic acid and p-thiocresol react rapidly in dichloromethane solution to give the selenosulfide along

237 Evidence for anion binding in dichloromethane solution was obtained from static fluore

238 The procedure uses Bodipy FL in basic dichloromethane solution with Mukaiyama's reagent (2-chl

239 n-bound dimers, both in the gas phase and in dichloromethane solution, showing that attenuation of in

240 ated to phenol through hydrogen bonding in a dichloromethane solution, the rate of an H atom abstract

241 minescence upon addition of BQ to PbS QDs in dichloromethane solution.

242 different resorcinarenes was investigated in dichloromethane solution.

243 lpy change of DeltaHD = -9.5 kcal mol(-1) in dichloromethane solution.

244 s 2 and 3 by NMR line-broadening analysis in dichloromethane solution.

245 vior of pillar[5]quinone was investigated in dichloromethane solution.

246 Dichloromethane solutions of the cationic receptor compl

247 and 0.032 in 4.0 x 10(-5) and 4.0 x 10(-3) M dichloromethane solutions, respectively.

248 nd 0.013 for 5.0 x 10(-5) and 5.0 x 10(-3) M dichloromethane solutions, respectively.

249 radiation of 8.0 x 10(-5) and 8.0 x 10(-3) M dichloromethane solutions, respectively.

250 2*) affords only the long-bonded pi-dimer in dichloromethane solutions, under conditions in which the

251 e units was investigated in acetonitrile and dichloromethane solutions.

252 ction analysis of a photochemically inactive dichloromethane solvate was used to confirm the molecula

253 The O-O bond in 4 undergoes heterolysis in dichloromethane solvent and is postulated to produce nit

254 esence of a palladium Lewis acid catalyst in dichloromethane solvent at room temperature.

255 diethyl ether 1:2v/v (solvent A) as well as dichloromethane (solvent B).

256 actions of chloride from water into nonpolar dichloromethane solvents.

257 .6 min), chlorobenzene ( t(1/2) = 14.0 min), dichloromethane ( t(1/2) = 27.9 min), and benzyl alcohol

258 growth in the three surveyed solvent media (dichloromethane, tetrahydrofuran, and acetonitrile).

259 However, in dichloromethane the Ni(II) reaction product is interpret

260 In dichloromethane, the macrocycles prevail in wide-stretch

261 In dichloromethane, the reaction between radicals 1 and 2 i

262 matography and ranged from -5.9 kcal/mol for dichloromethane to -13.5 kcal/mol for toluene.

263 were condensed with dipyrrylmethanes in TFA/dichloromethane to afford good to excellent yields of di

264 in solvents of widely different polarities (dichloromethane to dimethyl sulfoxide).

265 ly reactive complexes abstract chloride from dichloromethane to generate U(NDipp)(2)Cl(R(2)bpy)(2) or

266 cal 1+ slowly abstracts a chlorine atom from dichloromethane to give the 18-electron complex [ReCp(CO

267 It reacts with dichloromethane to give the [Zr]Cl[OCH2CH2N(CH2Cl)(i)Pr2

268 te and trifluoromethanesulfonic anhydride in dichloromethane to provide a ready source of the nitroni

269 ing: On BDD, this pathway accounted for 40% (dichloromethane) to 100% (tetrachloromethane) and on TDI

270 butylhydrogen peroxide, trifluoroacetic acid-dichloromethane) to form mixtures of the chain isomer of

271 Recrystallization of O-PtC(2) from dichloromethane/toluene gave single crystals of PtC(2) x

272 rt-butyl-4-methylpyridine as the base, and a dichloromethane/toluene solvent mixture, ethyl 1-thio-be

273 BDD produced mainly short chained OCBPs (dichloromethane, trichloromethane, and tetrachloromethan

274 ate monoester anhydrides form efficiently in dichloromethane/triethylamine from 1 equiv of the alcoho

275 Thus, heating an aminobenzanilide in dichloromethane under reflux in the presence of 1 equiv

276 Solutions of (p-tosyl)CH(2)NCAuCl in dichloromethane undergo significant oligomerization lead

277 chloromethane-fermenting culture transformed dichloromethane up to three times faster with Fe(0) comp

278 cetoxy-2-butene as a chain transfer agent in dichloromethane using a Hoveyda-Grubbs second-generation

279 performed in toluene over those obtained in dichloromethane using the diastereomeric chiral cationic

280 rylene dyad (PDIPe) has been investigated in dichloromethane using ultrafast transient electronic abs

281 ent exposure of these crystals to acetone or dichloromethane vapor results in the reformation of crys

282 und that the type of the solvent used (e.g., dichloromethane vs acetonitrile) significantly affected

283 Dichloromethane was classified as likely to be carcinoge

284 ntional continuous overnight extraction with dichloromethane was used to remove NDMA from the aqueous

285 les and placed in a two-phase liquid such as dichloromethane/water, these materials will accumulate a

286 Crystals grown from benzene and dichloromethane were characterized by X-ray diffraction,

287 iquid, and compared to a similar reaction in dichloromethane, where these parameters were found for r

288 relatively stable mixed-valence state in the dichloromethane, whereas in the acetonitrile both the fi

289 are safer solvents than the previously used dichloromethane, which can form an explosive byproduct w

290 ained by fast precipitation from hexanes and dichloromethane, which displayed slower dynamics within

291 mol concentrations at 25 degrees C for 4h in dichloromethane with 200- to 5000-fold excess of BODIPY

292 ReL3 reduces acids to H2 in dichloromethane with an overpotential of 380 mV and a tu

293 th various aldehydes using 10 mol % InBr3 in dichloromethane with high selectivity.

294 udied as glucosyl donors at -60 degrees C in dichloromethane with preactivation by 1-benzenesulfinyl

295 ] capable of delivering dichloromethide from dichloromethane with subsequent transfer to nitrones und

296 sing a one-phase extraction method (methanol-dichloromethane) with appropriate internal standards.

297 n near lambda(max)700 nm (epsilon: 45 000 in dichloromethane) with singlet oxygen ((1)O2) production

298 er strains (UNSWDHB and CF) transform TCM to dichloromethane, with inconsistent carbon isotope effect

299 the regioselectivity of this reaction, as in dichloromethane without TBAF the 2,7-diamino isomer was

300 Sustained growth in dichloromethane would therefore offset some of the gains