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 Phase-transfer alkylation of diethyl 2-oxopropylphosphonate (9) with 2-iodoalkyl azid

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

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

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

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

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

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

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

22 -18 ((18)F) facilitated production of 2-(5,7-diethyl-2-(4-(2-[(18)F]fluoroethoxy)phenyl)pyrazolo[1,5-

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

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

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

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

27 rt that ethosuximide, trimethadione, and 3,3-diethyl-2-pyrrolidinone increase mean and maximum life-s

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

29 0 (manganese [III] 5,10,15,20-tetrakis [1,3,-diethyl-2imidazoyl] manganese-porphyrin pentachloride [T

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

31 tolylthio)ben zene(3-); L(O)-S(2)N(2) = N,N'-diethyl-3,7-diazanonane-1,9-dithiolate(2-); pdmt = pyrid

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

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

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

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

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

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

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 Azaspirane (N-N-diethyl-8,8-dipropyl-2-azaspiro [4.5] decane-2-propanami

46 f selective A2A antagonist (KW-6002 [(E)-1,3-diethyl-8-(3,4-dimethoxystyryl)-7-methyl-3,7-dihydro-1H-

47 5-c]pyrimidin-5-amine] and KW-6002 [(E)-1, 3-diethyl-8-(3,4-dimethoxystyryl)-7-methyl-3,7-dihydro-1H-

48 tiated by an A2A antagonist KW-6002 [(E)-1,3-diethyl-8-(3,4-dimethoxystyryl)-7-methylxanthine], both

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

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

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

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

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

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

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

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

57 alkynes has been expanded further to include diethyl acetamidomalonate.

58 2, which is prepared by a de novo route from diethyl acetamidomalonate.

59 synthesized from alpha-bromoacetophenone and diethyl acetamidomalonate.

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

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

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

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

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

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

66 The caging group 7-N,N-diethyl aminocoumarin (DECM) was used to cage the gamma-

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

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

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

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

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

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

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

74 imethyl-1-piperazinyl)-3-methoxybenzyl]-N,N -diethyl-benzamide (SNC80), on behavioral seizures and hi

75 und 7 from ethyl glyoxylate and dimethyl and diethyl beta-methylglutaconate is described along with i

76 entiated by the nucleotidase inhibitor 6-N,N-diethyl-beta-gamma-dibromomethylene-D-adenosine-5'-triph

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

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

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

80 endohedral compound was cyclopropanated with diethyl bromomalonate.

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

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

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

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

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

86 Diethyl chlorophosphate and lithium hexamethyldisilazide

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

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

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

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

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

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

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

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

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

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

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

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

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

100 the presence of dicyclohexyl-, diisobutyl-, diethyl-, diphenyl-, cyclohexyl-, and phenylphosphine.

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

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

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

104 Diethyl dithiocarbamate was used as chelating reagent.

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

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

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

108 The diethyl ester prodrug showed the best total absorption (

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

110 This trial compared EPA diethyl ester with placebo in cachectic cancer patients

111 CFTR; 3) a novel agent, S-nitrosoglutathione diethyl ester, bypasses the need for GSNO bioactivation

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

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

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

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

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

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

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

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

120 eir progress through subsequent washing with diethyl ether and reactions with measured amounts of wat

121 chieved with ethyl iodide in the presence of diethyl ether as cosolvent; the 1-ethoxyethyl adduct was

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

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

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

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

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

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

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

129 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) (

130 18-crown-6 at -45 degrees C under vacuum in diethyl ether react with CO at -78 degrees C to form col

131 to the Z-enolate in the poorly coordinating diethyl ether solvent.

132 In diethyl ether the E:Z ratio was 15:1 in favor of the E-e

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

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

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

136 netic isotope effects for the reactions with diethyl ether were measured.

137 two intermediates with ethyl vinyl ether and diethyl ether were monitored by single- and double-mixin

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

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

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

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

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

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

144 1,3-(SiMe3)2)Zr, with dialkyl ethers such as diethyl ether, CH3OR (R=Et, nBu, tBu), nBu2O, or iPr2O r

145 y mediates sedation by ethanol vapor but not diethyl ether, indicating that the observed NPF/NPFR1 ac

146 t-butylphenyl)lithium, which is slow in pure diethyl ether, is virtually quantitative in heptane cont

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

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

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

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

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

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

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

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

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

156 e unsaponifiable fraction was extracted with diethyl ether.

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

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

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

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

161 allyl ether by exposure to boron trifluoride diethyl etherate.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

176 e reaction were deprotected and coupled with diethyl-l-glutamate followed by saponification.

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

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

179 0-36, which were hydrolyzed and coupled with diethyl-L-glutamate, followed by saponification, to give

180 Diethyl labeling of amino groups of monoamines affords 2

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

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

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

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

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

186 mpared the actions of 2 other GSH depleters, diethyl maleate (DEM) and buthionine sulphoximine (BSO),

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

188 acute depletion by 1 hour pretreatment with diethyl maleate (DEM), which conjugates GSH by the GSH-S

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

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

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

192 Neither oxidants (sulforaphane and diethyl maleate) nor reducing compounds (N-acetyl-l-cyst

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

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

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

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

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

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

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

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

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

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

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

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

205 1,1,5,5,5-hexafluoro-2,4-pentanedionato)(N,N-diethyl-N',N'-dimethyl- ethylenediamine)cadmium(II), Cd(

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

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

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

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

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

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

212 prepared by treatment of chloroproguanil and diethyl oxalate, yielding a mixture of two closely relat

213 s of diethyl p-nitrophenyl phosphate (I) and diethyl p-chlorophenyl phosphate (II) demonstrated that

214 netic constants for the hydrolysis of II and diethyl p-chlorophenyl thiophosphate (IV) were determine

215 pH-rate profiles for the hydrolysis of diethyl p-nitrophenyl phosphate (I) and diethyl p-chloro

216 ophenyl phosphorothioate, and the triesters, diethyl p-nitrophenyl phosphate and diethyl p-nitropheny

217 activity is sensitive to the serine reagent diethyl p-nitrophenyl phosphate, indicating that RcOBL1

218 iesters, diethyl p-nitrophenyl phosphate and diethyl p-nitrophenyl phosphorothioate.

219 abeled methyl, ethyl, phenyl, p-nitrophenyl, diethyl p-nitrophenyl, triphenyl, and di-tert-butyl ethy

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

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

222 lobutyl triflate, the mesylate derivative of diethyl (phenylhydroxymethyl)-thiophosphonate, and Z-1-p

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

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

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

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

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

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

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

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

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

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

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

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

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

236 bromoalkyl porphyrin or use of a dimethyl or diethyl phosphonate substituted precursor in a porphyrin

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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 Reacting the 37-mer with diethyl pyrocarbamate incorporated into SUVs increased t

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

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

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

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

265 NEM and diethyl pyrocarbonate inhibition suggested that the cata

266 istidine-selective inactivation studies with diethyl pyrocarbonate provide further evidence regarding

267 Modification of histidine residues by diethyl pyrocarbonate specifically inhibited Zn(2+) bind

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

269 of EDTA or upon treatment of the enzyme with diethyl pyrocarbonate, it is proposed that Cu(2+) of L2

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

271 that Lit was susceptible to inactivation by diethyl pyrocarbonate, with about three histidines rever

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

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

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

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

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

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

278 Diethyl succinate can be hyperpolarized via parahydrogen

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

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

281 Diethyl succinate was the only volatile clearly influenc

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

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

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

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

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

287 sing this system, point mutations induced by diethyl sulfate were found in the all genes of the essen

288 6-bis(p-anizolyl)-2-carboranyl-pyridine, and diethyl sulfide (1), triphenylphosphine (2), and t-butyl

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

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

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

292 Using diethyl sulfone with alpha-tetralone lead to pure naphth

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

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.