ライフサイエンスコーパス: diethyl

1 % of commercially available Ru(bpy)3(PF6)2, diethyl 1,4-dihydro-2,6-dimethylpyridine-3,5-dicarboxyla

2 Diethyl 1-fluoro-1-phenylsulfonylmethanephosphonate (1)

3 ere weak for the nonactivated alkoxyamine 1 (diethyl (1-(tert-butyl(1-(pyridin-4-yl)ethoxy)amino)-2,2

4 oro-3-octenoate (4a and 17) and (E)- and (Z)-diethyl (1-cyano-2-heptenyl)phosphate (21a and 21b) with

5 microarray analysis of livers from mice fed diethyl-1,4-dihydro-2,4,6-trimethyl-3,5-pyridine decarbo

6 )-(7-trifluoromethyl-4-quinolinyl)-N(1),N(1)-diethyl-1,4-pentanediamin e (CQ7a) shows expression effi

7 es lower, while N(4)-(4-pyridinyl)-N(1),N(1)-diethyl-1,4-pentanediamine (CP), a CQ analogue that has

8 he presence of N(4)-(4-quinolinyl)-N(1),N(1)-diethyl-1,4-pentanediamine (CQ7b) does not reveal any en

9 extraordinary reactivity toward the triester diethyl 2,4-dinitrophenyl phosphate (DEDNPP) and the die

10 mixtures for (i) the hydrolysis reaction of diethyl 2,4-dinitrophenylphosphate (DEDNPP) and (ii) the

11 e form on the Au electrode at 0.6 V, whereas diethyl 2,5-dioxahexane dicarboxylate and lithium propio

12 oline-3-carboxylate (5Me-HQE), obtained from diethyl 2-[((3-methylphenyl)amino)methylene]malonate.

13 re of the substrate (ethene, cyclohexene, or diethyl 2-benzylidenesuccinate) and the character of the

14 l)(amino)carbene (2,6-diisopropylphenyl)-4,4-diethyl-2,2-dimethyl-pyrrolidin-5-ylidene ((Et)CAAC) wer

15 es of aromatic-aliphatic polyesters based on diethyl-2,5-furandicarboxylate and of the petroleum-base

16 ere imaged at 7 wk after induction using N,N-diethyl-2-(2-(3-(125)I-iodo-4-methoxyphenyl)-5,7-dimethy

17 translocator protein (TSPO) radioligand N,N-diethyl-2-(2-(4-(2-(18)F-fluoroethoxy)phenyl)-5,7-dimeth

18 lopyrimidinyl-based TSPO imaging ligand, N,N-diethyl-2-(2-(4-(2-(18)F-fluoroethoxy)phenyl)-5,7-dimeth

19 Two TSPO radioligands, [(18)F]DPA-714 [N,N-diethyl-2-(2-(4-(2-[(18)F]fluoroethoxy)phenyl)-5,7-dimet

20 g the TSPO radioligand [(1)(8)F]DPA-714 [N,N-diethyl-2-(2-(4-(2-fluoroethoxy)phenyl)-5,7-dimethylpyra

21 lo[1,5-a]pyrimidines, closely related to N,N-diethyl-2-(2-(4-(2-fluoroethoxy)phenyl)-5,7-dimethylpyra

22 (18)F-labeled N,N-diethyl-2-(2-[4-(2-fluoroethoxy)phenyl]-5,7-dimethylpyra

23 -18 ((18)F) facilitated production of 2-(5,7-diethyl-2-(4-(2-[(18)F]fluoroethoxy)phenyl)pyrazolo[1,5-

24 lopyrimidines led to the discovery of 2-(5,7-diethyl-2-(4-(2-fluoroethoxy)phenyl)pyrazolo[1,5-a]pyrim

25 Recently, a novel radioligand, (11)C-N,N-diethyl-2-[2-(4-methoxyphenyl)-5,7-dimethyl-pyrazolo[1,5

26 the known high-affinity TSPO ligand (l)-N,N-diethyl-2-methyl-3-(2-phenylquinolin-4-yl)propanamide in

27 Hstar, catalyzes the cyclopropanation of N,N-diethyl-2-phenylacrylamide with an estimated initial rat

28 ethylbarbiturate, 2-thiobarbiturate, and 1,3-diethyl-2-thiobarbiturate with diarylcarbenium ions and

29 atives with L = 4-pyridyl phosphonic acid or diethyl 3-(pyridin-4-yloxy)decyl-phosphonic acid, leads

30 ussin is described starting from decanal and diethyl 3-diazo-2-oxopropylphosphonate.

31 d the degradation of two such chemicals, N,N-diethyl-3-methylbenzamide (DEET) and caffeine, by low pr

32 N,N-diethyl-3-methylbenzamide (DEET) is popular insect repel

33 inue to have practices of applying DEET (N,N-diethyl-3-methylbenzamide) based repellents that may lea

34 DEET (N,N-diethyl-3-methylbenzamide) is a 6-decade-old synthetic r

35 ary side chain length for both monoethyl and diethyl 4-N CQ derivatives.

36 ivity and selectivity of the reaction of O,O-diethyl 4-nitrophenyl phosphate triester (Paraxon, 1) wi

37 The compound 1,1-diethyl-4(naphthalene-2-yl)piperazin-1-ium (2NDEP) a wea

38 2,2'-diylidene (L2), and 1,1'-methylene-3,3'-diethyl-4,4'-diimidazoline-2,2'-diylidene (L3) in THF.

39 Bis[1,3-diethyl-4,5-bis(4-fluorophenyl)imidazol-2-ylidene]gold(I

40 Cationic bis[1,3-diethyl-4,5-diarylimidazol-2-ylidene]gold(I) complexes w

41 Six different 2,6-diethyl-4,8-diarylbenzo[1,2-d:4,5-d']bis(oxazoles) and f

42 nt dyes-4,4-difluoro-1,3,5,7-tetramethyl-2,6-diethyl-4-bora-3a,4a-diaza-s-indacene (Bodipy) and a Ru(

43 The reactions of nitrosobenzene and N,N'-diethyl-4-nitrosoaniline with [Cu(CH3CN)4]PF6 provide no

44 Diethyl (7, MRS4084) and diisopropyl (8, MRS4074) phosph

45 5-c]pyrimidin-5-amine] and KW-6002 [(E)-1, 3-diethyl-8-(3,4-dimethoxystyryl)-7-methyl-3,7-dihydro-1H-

46 Herein we utilize cyanine dye 3,3'-diethyl-9-methyl-thiacarbocyanine iodide (C11) to modula

47 One potent member of the series, 3,3'-diethyl-9-methylthiacarbocyanine iodide (compound 11), r

48 elet reaction of bromomethylated 2-bromo-9,9-diethyl-9H-fluorene produced the key precursor 7-bromo-9

49 orene produced the key precursor 7-bromo-9,9-diethyl-9H-fluorene-2,4-dicarbaldehyde required for the

50 enzyme-like catalyst for substrate selective diethyl acetal hydrolysis.

51 talyzed reaction between tropones and ketene diethyl acetal to give bicyclo[3.2.2] ring structures, w

52 phenyl thioethers, alkyl chlorides, acrolein diethyl acetal, and isochroman.

53 ailable propargyl alcohol, bromoacetaldehyde diethyl acetal, and OEGs or PEGs was developed as a conv

54 cetate and vanillin for MPX and acetaldehyde diethyl acetal, isobutyl acetate, ethyl isovalerate and

55 alkynes has been expanded further to include diethyl acetamidomalonate.

56 Nucleophilic addition of thiolates to diethyl acetylenedicarboxylate in chloroform at room tem

57 undergoes a clean Diels-Alder reaction with diethyl acetylenedicarboxylate to give a rearomatized 1:

58 hat quantitatively cycloadded to dimethyl or diethyl acetylenedicarboxylate to give stable thioacid c

59 one-step procedure consisting of reaction of diethyl acetylphosphonate with prochiral aldehydes in th

60 ethyl ester (PME), dimethyl carbonate (DMC), diethyl adipate (DEA), and butanol (Bu)) with ultralow s

61 in nonaqueous media is observed for the N,N-diethyl amides 5a than the N,N-diisopropyl amides 5b.

62 mall cationic molecule EtNBS (5-ethylamino-9-diethyl-aminobenzo[a]phenothiazinium chloride) have prov

63 s (derived from various salicylaldehydes and diethyl aminomalonate).

64 Crystals of the diethyl and bistetradecyl derivatives, containing no sol

65 ilm of 7 to vapor samples of butyl-, hexyl-, diethyl-, and diisopropylamine resulted in a rapid and r

66 ied the [2sigma+2sigma+2pi] cycloaddition of diethyl azodicarboxylate (DEAD) and quadricyclane and re

67 Addition of a small molecule (diethyl azodicarboxylate) promotes rapid network formati

68 the original Mitsunobu reagents, Ph(3)P and diethyl azodicarboxylate, but not with Ph(3)P and di-ter

69 and (1)H NMR titrations were performed with diethyl barbital.

70 he inexpensive, environmentally benign agent diethyl (bromodifluoromethyl) phosphonate (DBDFP) as a d

71 re ethyl/methyl 2-bromo-2,2-difluoroacetate, diethyl (bromodifluoromethyl)phosphonate, [(bromodifluor

72 onic acids and the difluorocarbene precursor diethyl bromodifluoromethylphosphonate (BrCF(2)PO(OEt)(2

73 ifluoromethylation of tertiary amines, using diethyl bromodifluoromethylphosphonate and fluoride, is

74 nally, we report the first EHF derivative, a diethyl bromomalonate monoadduct of Gd(2)@C(79)N, which

75 The palladium-catalyzed ortho-arylation of diethyl carbamate-protected estrone and estriol with ary

76 trolyte, 1.0 M LiPF6/ethylene carbonate (EC)/diethyl carbonate (DEC), reduction products on crystalli

77 BF(4).EC.DEC (EC = ethylene carbonate; DEC = diethyl carbonate).

78 generated upon anodic oxidation of ethyl and diethyl carbonates at Li(x)Ni(0.5)Mn(1.5)O(4-delta), for

79 talation and cross-coupling of chrysenyl N,N-diethyl carboxamides with o-tolyl and methylnaphthalenyl

80 cence response within seconds of exposure to diethyl chlorophosphate (DCP) vapor.

81 gradation of selective organophosphates (i.e diethyl chlorophosphate, diethyl cyanophosphonate, tris

82 F3)2C6H3) was prepared by protonation of the diethyl complex (N/\N)PtEt2 with [H(OEt2)2][BAr'4].

83 both hydrolysis of the nerve agent simulant, diethyl cyanophosphonate (DECP) and selective oxidation

84 ganophosphates (i.e diethyl chlorophosphate, diethyl cyanophosphonate, tris (2-chloroethyl) phosphate

85 enced with a C2-symmetric starting material, diethyl D-tartrate, and took advantage of a relay of dia

86 e ectonucleotidase inhibitor ARL67156 (6-N,N-diethyl-D-beta,gamma-dibromomethyleneATP) (100 microM).

87 ) metabolites of OP pesticides, specifically diethyl (DE) and dimethyl (DM) phosphate metabolites, we

88 exo-norbornenyl dialkylesters (dimethyl DME, diethyl DEE, di-n-butyl DBE) were strategically designed

89 methyl-12-ethyl, 7-ethyl-12-methyl, and 7,12-diethyl derivatives (16, 17, and 18), two ipso-protonate

90 n kinetics of complexes 1-3 with the olefins diethyl diallyl malonate (DEDAM), butyl vinyl ether (BuV

91 d ring closing metathesis (RCM) reactions of diethyl diallylmalonate (DEDAM) were conducted containin

92 ve and nonproductive metathesis reactions of diethyl diallylmalonate are compared for eight different

93 conversion in the ring-closing metathesis of diethyl diallylmalonate.

94 on products (in case of N,N-dimethyl and N,N-diethyl diazoamides) or almost exclusive Wolff rearrange

95 For the metabolites of diethyl-, dibutyl-, and butylbenzyl-phthalates moderate

96 ent with the absorption spectra of analogous diethyl dipropargylmalonate polymers (1/N approximately

97 y a succinate ester prodrug of Cur, curcumin diethyl disuccinate (CurDD) with better chemical stabili

98 VSCs - ethanethiol, S-ethyl thioacetate and diethyl disulfide - increased proportionally to H2S.

99 tidine (His), cysteine (Cys), and lipophilic diethyl dithiocarbamate (DDC) at different concentration

100 Diethyl dithiocarbamate was used as chelating reagent.

101 hoxysilane, followed by an iniferter (sodium diethyl dithiocarbamate) initiated photopolymerization o

102 or diethyl phosphate, diethyl thiophosphate, diethyl dithiophosphate, dimethyl phosphate, dimethyl th

103 Coupling 8 with L-glutamic acid diethyl ester and saponification afforded 2.

104 The diethyl ester prodrug showed the best total absorption (

105 constitutively active S-nitroso-glutathione diethyl ester stimulate CFTR transcription through SP1 a

106 iophene-2-carbonyl)-amino]-pentanedioic acid diethyl ester, followed by hydrogenation and saponificat

107 on in contrast to the commonly used Hantzsch diethyl ester.

108 traction applying the mixture of pentane and diethyl ether 1:2v/v (solvent A) as well as dichlorometh

109 be the unusual reactivity of a highly labile diethyl ether adduct of an asymmetric niobium(V) bis(imi

110 ethoxide with [H(OEt2)2][H2N{B(C6F5)3}2] in diethyl ether afforded [Tl(OEt2)3][H2N{B(C6F5)3}2] (2a),

111 IR spectra of diethyl ether and diethyl sulfide reveal that both molec

112 ithium exists as a tetrasolvated tetramer in diethyl ether and exclusively as bis-solvated dimers wit

113 etypal volatile anesthetic molecules such as diethyl ether and halothane.

114 eduction of molecular nitrogen to ammonia in diethyl ether between -78 and 22 degrees C in a batchwis

115 action with a mixture of dichloromethane and diethyl ether containing lipases and a subsequent concen

116 By contrast, nonhalogenated diethyl ether does not interact with entangled photons.

117 st to Z-5F-Li, the E isomer is tetrameric in diethyl ether even in the presence of excess HMPA.

118 Subsequent treatment with diethyl ether fails to remove any surface species, but i

119 obtained by performing the same reaction in diethyl ether followed by lyphilization of 2 from benzen

120 similar propyl carbamate; (2) extraction by diethyl ether instead of more toxic dichloromethane, and

121 hetics, demonstrating that short exposure to diethyl ether is the most effective for long-term immobi

122 tone, or choloroform (1b); toluene (1c); and diethyl ether or ethyl acetate (1d), demonstrate differe

123 esults have been obtained considering either diethyl ether or toluene as a solvent, in both cases in

124 C-t-Bu(2) to CrCl(3), MoCl(5), and WCl(6) in diethyl ether produced the complexes M(N=C-t-Bu(2))(4) (

125 18-crown-6 at -45 degrees C under vacuum in diethyl ether react with CO at -78 degrees C to form col

126 onditions permitted the elusive synthesis of diethyl ether through reductive elimination, a remarkabl

127 )(AsF(6))(0.50) have been prepared by adding diethyl ether to a dichloromethane solution containing e

128 procedure, the crude solids are washed with diethyl ether to afford the pure products, as revealed b

129 ed silica gel column eluted with pentane and diethyl ether to separate minor compounds.

130 Liquid-liquid extraction with diethyl ether was followed by GC-MS for TCE quantificati

131 nic solvents (methanol, ethanol, acetone and diethyl ether) in isolation of these compounds to gain i

132 Li or t-BuLi) and/or the solvent (pentane or diethyl ether); the 3-deuterated substrate, 3-Ddman, was

133 c molecules, including ethanol, ethanethiol, diethyl ether, and diethyl sulfide, at the Ge(100)-2 x 1

134 The Z isomer is completely dimeric in pure diethyl ether, and mostly dimeric in 3:2 THF/ether, wher

135 anic solvents such as tetrahydrofuran (THF), diethyl ether, and toluene.

136 During the catalytic reduction of diethyl ether, cationic iridium silane complex, [(POCOP)

137 s found when 4 L were extracted with hexane, diethyl ether, methanol, or butanol, but activity was ob

138 with ethereal and ester donor ligands (THF, diethyl ether, MTBE, THP, tert-butyl acetate) are charac

139 In diethyl ether, N-Boc-2-lithio-2-arylpiperidines have bee

140 trahydrofuran, tetrahydropyran, 1,4-dioxane, diethyl ether, tetrahydrothiophene, and 1,3-dithiolane.

141 fferentiate between common solvents, such as diethyl ether, THF, ethyl acetate, acetone, alcohol, ace

142 anesthetics, such as chloroform, isoflurane, diethyl ether, xenon, and propofol, disrupt lipid rafts

143 ds invert faster in THF-d(10) compared to in diethyl ether-d(10) as solvent.

144 ive DeltaS(double dagger) values, whereas in diethyl ether-d(10) DeltaS(double dagger) values for inv

145 ounds 6, 7, and 9 are monomeric in THF-d8 or diethyl ether-d10 solution and exhibit one bond 13C1, 6L

146 action method was applied using a mixture of diethyl ether-pentane (1:1,w/w) as solvent.

147 ed with n-butyllithium in tetrahydrofuran or diethyl ether.

148 in a suspension of SnCl4.(Et2O)2 complex in diethyl ether.

149 e unsaponifiable fraction was extracted with diethyl ether.

150 rude protein, Ara h 1, and Ara h 2 than with diethyl ether.

151 ent polarities (dipole moment - hexane: 0.0, diethyl ether: 2.80, ethyl acetate: 4.40, methanol: 5.10

152 he partial release of the surface-associated diethyl ether; Si-CH3 moieties remain.

153 allyl ether by exposure to boron trifluoride diethyl etherate.

154 ar cyclocarbonylation of 2-iodoanilines with diethyl ethoxycarbonylbutendienoate produces 2,3,3-triet

155 An HPLC-UV method involving diethyl ethoxymethylenemalonate (DEEMM) was adapted and

156 Derivatisation treatment with diethyl ethoxymethylenemalonate followed by ultra-HPLC a

157 rticles each of dimethyl methyl phosphonate, diethyl ethyl phosphonate, diethyl phosphoramidate, and

158 g porous gold IDEs featured a sensitivity to diethyl ethylphosphonate (DEEP, a simulant of the nerve

159 Terminal alkyne diethyl ethynylphosphonate reacted with ketones to give

160 ne fumarate) (PPF) by a two-step reaction of diethyl fumarate and propylene glycol through a bis(hydr

161 yield, using inexpensive cyclopentadiene and diethyl fumarate as starting materials.

162 re detected in 5.6% of the data values, with diethyl hexyl phthalate and bisphenol A being the most u

163 and 6-chloro-2-(4'-(123)I-iodophenyl)-3-(N,N-diethyl)-imidazo[1,2-a]pyridine-3-acetam ide ((123)I-CLI

164 ing 6-chloro-2-(4'-(123)I-iodophenyl)-3-(N,N-diethyl)-imidazo[1,2-a]pyridine-3-acetam ide SPECT ((123

165 etween 2,4-diethyl pyridinedicarboxylate and diethyl isophthalate (amorphous polymers) and between 2,

166 he petroleum-based diethyl terephthalate and diethyl isophthalate were also synthesized.

167 DTbuK), and a series of partially deuterated diethyl ketones (DEK) is studied in the gas phase at 8 T

168 Hydrolysis and subsequent coupling with diethyl l-glutamate and saponification afforded target c

169 coupling the benzoic acid derivative 19 with diethyl L-glutamate and saponification.

170 on reaction was deprotected and coupled with diethyl l-glutamate followed by saponification.

171 he reaction was deprotected and coupled with diethyl L-glutamate followed by saponification.

172 e with the alpha-bromoketones, coupling with diethyl-L-glutamate, and saponification afforded 2-5.

173 er precursors were deprotected, coupled with diethyl-L-glutamate, and saponified.

174 0-36, which were hydrolyzed and coupled with diethyl-L-glutamate, followed by saponification, to give

175 Diethyl labeling of amino groups of monoamines affords 2

176 ethod for NE, DA, 5-HT/ and NM, with/without diethyl labeling of monoamines, are 0.005/0.4 (30/2367 p

177 , a UPLC/ MS/MS-based method combined with a diethyl labeling technique was developed for simultaneou

178 N,N-Diethyl-m-toluamide (DEET) is one of the most effective

179 pyridostigmine (PB), permetrim (PM) and N,N-diethyl-m-toluamide (DEET) used as protectants against i

180 itoes as much as three times longer than N,N-diethyl-m-toluamide (DEET), the most widely used repelle

181 The insect repellent DEET (N,N-diethyl-m-toluamide), which attenuates odor responses of

182 as S,S,S-tributyl phosphorotrithioate (DEF), diethyl maleate (DEM), piperonyl butoxide (PBO) and cycl

183 Reactive oxygen species-inducing diethyl maleate increased glutathione levels and (18)F-F

184 Results: Reactive oxygen species-inducing diethyl maleate increased glutathione levels and (18)F-F

185 in hepatocyte function, and GSH depletion by diethyl maleate was shown previously to inhibit expressi

186 ted by provision of either exogenous H2O2 or diethyl maleate, which raises intracellular H2O2 levels.

187 say, cellular uptake after OS induction with diethyl maleate, with and without anti-xCT small interfe

188 nted disruption of tubular morphology during diethyl maleate-induced oxidative stress in an organotyp

189 NT EMFs) with carbon radicals generated from diethyl malonate catalyzed by manganese(III) acetate are

190 lonamides derived from amines and diazidated diethyl malonate react with lithiated alcohols through n

191 x catalyzes the enantioselective addition of diethyl malonate to trans-beta-nitrostyrene.

192 The synthetic repellents N,N-diethyl-meta-toluamide (DEET) and IR3535 did not activat

193 thalates, insecticides, pyrethroids, and N,N-diethyl-meta-toluamide (DEET)) and some of their metabol

194 the AM2 glomerulus is also sensitive to N,N-diethyl-meta-toluamide (DEET), a mosquito repellent.

195 nts, including the widely used repellent N,N-diethyl-meta-toluamide (DEET), on the function of specif

196 Insect repellents containing DEET (N,N-diethyl-meta-toluamide) are highly effective, but the me

197 DEET (N, N-diethyl-meta-toluamide) is the most effective and widely

198 DEET (N,N-diethyl-meta-toluamide) is the world's most widely used

199 ensitivity to the insect repellent DEET (N,N-diethyl-meta-toluamide).

200 tic NMR line width simulations) for the OIPC diethyl(methyl)(isobutyl)phosphonium hexafluorophosphate

201 A computational study on a VX-model, O,S-diethyl methylphosphonothioate (1), clarifies the distin

202 amine (triethylamine) and organophosphonate (diethyl methythiomethylphosphonate (DEMTMP)) portions of

203 We had previously characterized N,N-diethyl-N'-phenylpiperazine analogs with various functio

204 umors in response to the chemical carcinogen diethyl nitrosamine (DEN) than wild-type animals.

205 es in AH and become tumor cells in mice with diethyl nitrosamine (DEN)-initiated, Western alcohol die

206 hepatobiliary carcinoma after initiation by diethyl-nitrosamine (DEN).

207 ith decreased proliferation and delay in the diethyl-nitrosamine-induced inflammatory process.

208 GFR mice showed a delay in the appearance of diethyl-nitrosamine-induced tumors, which correlated wit

209 We found that the gem-diethyl nitroxide-labeled Bax variants were reasonably s

210 ytical method to determine chlorpyrifos (O,O-diethyl O-3,5,6-trichloro-2-pyridyl phosphorothioate) (C

211 xes bearing CNN- and PNN-pincer ligands with diethyl- or diisopropylamino side groups, which have pre

212 arboxylase competitive inhibitors malate and diethyl oxalacetate (DOA) in the strong isoprene emitter

213 iselectrophiles such as ethyl glyoxalate and diethyl oxalate in aqueous medium leads to the formation

214 Submicrometer particles of diethyl p-phenylenediacrylate (EPA) with tunable molecul

215 A modified acid-quenched N,N-diethyl-p-phenylenediamine (DPD) assay was used to measu

216 Isotopically enriched diethyl phenylphosphonates (P horizontal line(17)O or P

217 nantiopure) epoxides with the sodium salt of diethyl (phenylsulfonyl)methylphosphonate in DME at 140

218 diethyl piperidinophosphate diester (2), O,O-diethyl phosphate (3), and O-ethyl 4-nitrophenyl phospha

219 d in the presence of the hydrolysis product, diethyl phosphate (DEP), and a product analogue, cacodyl

220 Concentrations of three diethyl phosphate (SigmaDEP) and three dimethyl phosphat

221 e presence of phosphate esters, as shown for diethyl phosphate and methyl phosphate, which form outer

222 In the structure of the PTE-diethyl phosphate complex, the DEP product is found symm

223 perimentally determined structure of the PTE-diethyl phosphate product complex is inconsistent with a

224 Three derivatives of 1 (diethyl phosphate, acetate, and bromide) were isolated a

225 li to utilize alkyl phosphodiesters, such as diethyl phosphate, as the sole phosphorus source.

226 Urine samples were analyzed for diethyl phosphate, diethyl thiophosphate, diethyl dithio

227 yl phosphate, and the product of hydrolysis, diethyl phosphate.

228 For example, after the diethyl phosphonate derivative of gamma-butyrolactone wa

229 nt HIV protease inhibitor (PI) with a unique diethyl-phosphonate moiety.

230 is described on the basis of the addition of diethyl phosphonite-borane to a glucal-derived aldehyde,

231 thyl phosphonate, diethyl ethyl phosphonate, diethyl phosphoramidate, and diethyl phthalate using las

232 The resulting diethyl phosphoryl complex was used to model the tetrahe

233 in urinary concentrations of metabolites of diethyl phthalate (DEP) and butylbenzyl phthalate (BBzP)

234 ed transdermal uptake, directly from air, of diethyl phthalate (DEP) and di(n-butyl) phthalate (DnBP)

235 ) based on NAS recommendations, and included diethyl phthalate (DEP) and diisononyl phthalate (DiNP)

236 Biomarker concentrations of diethyl phthalate (DEP) and three phthalates with known

237 Diethyl phthalate (DEP) has been found to be anti-androg

238 Furthermore, dimethyl phthalate (DMP) and diethyl phthalate (DEP) were the main PAEs released from

239 respectively), and dibutyl phthalate (DBP), diethyl phthalate (DEP), and diisobutyl phthalate (DIBP)

240 an archetypal adult and toddler over 24 h to diethyl phthalate (DEP), butyl benzyl phthalate (BBzP),

241 ontaining no target analytes, was mixed with diethyl phthalate (DEP), di-n-butyl phthalate (DnBP), an

242 re measured for diisobutyl phthalate (DiBP), diethyl phthalate (DEP), dibutyl phthalate (DBP), and sy

243 dely used personal care product ingredients [diethyl phthalate (DEP), methyl paraben (MPB), and tricl

244 With the exception of diethyl phthalate (DEP), phthalates had over 50% detecti

245 nBP), di(2-ethylhexyl) phthalate (DEHP), and diethyl phthalate (DEP).

246 as an excipient, and 45 specified the use of diethyl phthalate (DEP).

247 in perfumes (detection frequency of 100% for diethyl phthalate [DEP], 67% for dibutyl phthalate [DBP]

248 ome personal care products may be sources of diethyl phthalate exposure.

249 ntial liquid-solid adsorption properties for diethyl phthalate in front of other commercial phthalate

250 al study indicate that low level exposure to diethyl phthalate results in measurable genomic changes

251 three main sources: PEs-BPA to plastic, PBs-diethyl phthalate to personal hygiene products, and OPs

252 yl phosphonate, diethyl phosphoramidate, and diethyl phthalate using laser fluences between 0.58 and

253 pm for di(isobutyl) phthalate, 7,700 ppm for diethyl phthalate, and 8,000-24,000 ppm (range) for tric

254 ve compounds are analyzed in these sections: diethyl phthalate, caffeine and nicotine.

255 um and urine concentrations of biomarkers of diethyl phthalate, methyl paraben, and triclosan in rats

256 We found that two phthalates, dimethyl and diethyl phthalates, penetrate deeper into skin with simi

257 i-iso-butyl-, di-n-butyl-, butylbenzyl-, and diethyl phthalates-were measured in spot urine samples c

258 ated products are identified as follows: O,O-diethyl piperidinophosphate diester (2), O,O-diethyl pho

259 trodeposited poly(thiophene) films (i) poly((diethyl)propylenedixoythiophene), P(Et)(2)ProDOT; (ii) p

260 milarity in the thermal behavior between 2,4-diethyl pyridinedicarboxylate and diethyl isophthalate (

261 thalate (amorphous polymers) and between 2,5-diethyl pyridinedicarboxylate and diethyl terephthalate

262 at the enzymatic synthesis starting from 2,4-diethyl pyridinedicarboxylate leads to the best polymers

263 thermophilus Rieske protein was reacted with diethyl pyrocarbonate (DEPC) over a range of pH values.

264 lity of histidyl residues to modification by diethyl pyrocarbonate and observed that more than 50% pr

265 ss spectrometry of the peptide modified with diethyl pyrocarbonate before and after Cu binding sugges

266 Modification of His residues with diethyl pyrocarbonate completely inhibited Zn2+ binding

267 n the protection of His from modification by diethyl pyrocarbonate when this residue binds Cu(II) in

268 Cys and His residues using iodoacetamide and diethyl pyrocarbonate, respectively.

269 ions inactivate LpxE, as does treatment with diethyl pyrocarbonate.

270 Calculations on diethyl selenide show that the Se-Ge dative bond is slig

271 the association of total dialkyl (SigmaDAP), diethyl (SigmaDEP), and dimethylphosphate (SigmaDMP) met

272 unctional thioimidate cross-linking reagent (diethyl suberthioimidate) that modifies amines without s

273 On the basis of our results, hyperpolarized diethyl succinate allows for real-time in vivo MRI and M

274 s were identified, with phenylethyl alcohol, diethyl succinate and ethyl lactate having the highest f

275 te, ethyl isovalerate, ethyl monosuccionate, diethyl succinate and gamma-butyrolactone production.

276 Hyperpolarization of diethyl succinate and its in vivo applications may revea

277 Diethyl succinate can be hyperpolarized via parahydrogen

278 r injection of 10-20 mumol of hyperpolarized diethyl succinate into normal mice.

279 The metabolism of diethyl succinate was altered after exposing the animal

280 Diethyl succinate was the only volatile clearly influenc

281 The downstream metabolites of hyperpolarized diethyl succinate were identified in vivo as malate, suc

282 the final concentrations of anthocyanins and diethyl succinate were the major compounds influenced by

283 s of 2-phenylethanol, 3-methyl-1-butanol and diethyl succinate, and lower concentrations of ethyl dec

284 d most influenced by these fungicides, while diethyl succinate, decanoic acid, beta-ionone, and citro

285 tion of ethyl decanoate and ethyl octanoate, diethyl succinate, hydroxylinalool, and 2-phenyl ethanol

286 new metabolic imaging agent, hyperpolarized diethyl succinate-1-(13)C-2,3-d(2) , that allows for rea

287 6-bis(p-anizolyl)-2-carboranyl-pyridine, and diethyl sulfide (1), triphenylphosphine (2), and t-butyl

288 IR spectra of diethyl ether and diethyl sulfide reveal that both molecules adsorb via da

289 ing ethanol, ethanethiol, diethyl ether, and diethyl sulfide, at the Ge(100)-2 x 1 surface was invest

290 the role of compounds, such as methanethiol, diethyl sulfide, dimethyl disulfide, methional and dimet

291 salen complexes with chiral ((R)/(S)-BINOL, diethyl tartrate) and achiral (piperazine and trigol) li

292 etween 2,5-diethyl pyridinedicarboxylate and diethyl terephthalate (crystalline polymers).

293 urandicarboxylate and of the petroleum-based diethyl terephthalate and diethyl isophthalate were also

294 samples were analyzed for diethyl phosphate, diethyl thiophosphate, diethyl dithiophosphate, dimethyl

295 1,7-Diene 5 reacts with diethyl thiophosphite in an efficient and diastereoselec

296 h neutral dihydride, (POCOP)Ir(H)(2) (5) and diethyl(triethylsilyl)oxonium ion, [Et(3)SiOEt(2)](+)[B(

297 rticular, exposure of epoxidized graphene to diethyl zinc abstracts oxygen, creating mobile species t

298 prepared through the reaction of ICF2H with diethyl zinc and DMPU.

299 e synthesized using a nonthermal plasma from diethyl zinc and oxygen and deposited by inertial impact

300 using the atomic layer deposition precursor diethyl zinc.