ライフサイエンスコーパス: dimethyl

1 ecifically demethylates histone H3 lysine 27 dimethyl.

2 on complex [Fe(btz)3](3+) (where btz is 3,3'-dimethyl-1,1'-bis(p-tolyl)-4,4'-bis(1,2,3-triazol-5-ylid

3 boxylate (11), 1,10-phenanthroline (12), 2,9-dimethyl-1,10-phenanthroline (13), or 4,7-diphenyl-1,10-

4 (3) (dmphen)(ptolICN)](+) , where dmphen=2,9-dimethyl-1,10-phenanthroline and ptolICN=para-tolyl ison

5 r, details of the mechanism by which the 5,6-dimethyl-1,10-phenanthroline ligand contributes to the c

6 avepacket dynamics of a prototypical [Cu(2,9-dimethyl-1,10-phenanthroline)(2)](+) complex using TR-XA

7 um agent [Pt(1 S,2 S-diaminocyclohexane)(5,6-dimethyl-1,10-phenanthroline)](2+) (56MeSS, 5) is a pote

8 lete conversion of the side chain to the N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl moiety by NM

9 ock, poly(2-methyl-2-oxazoline)-b-poly(2-N,N-dimethyl-1,3,5-triazine-2,4-diamine-6-ethyl-2-oxazoline)

10 ng smoking, of which 3-methyl-1-butanol, 3,7-dimethyl-1,3,6-octatriene, hydroxy butanone, and 1-octen

11 s shown to proceed efficiently from 1 to 2,3-dimethyl-1,3-butadiene to form Diels-Alder product 3 wit

12 = N,N'-bis(2,6-dialkylphenyl)-1,4-diaza-2,3-dimethyl-1,3-butadiene) carrying nearly unperturbed nitr

13 ytacn)](2+) (Pytacn=1-(2'-pyridylmethyl)-4,7-dimethyl-1,4,7-triazacyclononane) (2) generated during c

14 Tf)(2)] (1) (L(N4) = 1-[2-pyridylmethyl]-4,7-dimethyl-1,4,7-triazacyclononane) such as a highly react

15 ) [(Fl)DAB = N,N'-bis(pentafluorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene; TFA = trifluoroacetate

16 ne; isopropyl 2-methylbutanoate; cymene; 2,6-dimethyl-1,6-octadiene; 3-methyloctane; 1-(1,4-dimethyl-

17 cyclizations which furnished a series of 2,5-dimethyl-1-((3R,4'S)-2H-spiro[benzofuran-3,1'-cyclopenta

18 tionic polymer dots (Pdots) made of poly[1,4-dimethyl-1-(3-((2,4,5-trimethylthiophen-3-yl)oxy)propyl)

19 l-1 levels and 4-(4-{[2-(4-chlorophenyl)-5,5-dimethyl-1-cyclohexen-1-yl]methyl}-1-piperazinyl)-N-[(4-

20 ylindolin-2-ylidene)penta-1,3-dien-1-yl)-3,3-dimethyl-1-octadecyl-3H-indol-1-ium perchlorate.

21 rescently labeled with 2-((1E,3E)-5-((Z)-3,3-dimethyl-1-octadecylindolin-2-ylidene)penta-1,3-dien-1-y

22 (mu(4) -N)(2) S(6) L(4) ](2-) (Tp*=tris(3,5-dimethyl-1-pyrazolyl)hydroborate(1-), L=Cl(-) or Br(-) )

23 Using the spin trap, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO), hydroxyl radical ((

24 ule (E)-(5-(3-anthracen-9-yl-allylidene)-2,2-dimethyl-[1,3] dioxane-4,6-dione) (E-AYAD) undergoes E->

25 Here we used [(13)C]itaconate and dimethyl [(13)C]itaconate (DMI) to probe itaconate metab

26 ng process when employing 4-(2,3-dihydro-1,3-dimethyl-1H-benzimidazol-2-yl)-N,N-dimethylbenzenamine (

27 l hit compound (Z)-5-((1-(4-bromophenyl)-2,5-dimethyl-1H-pyrrol-3-yl)methylene)thiazolidine-2,4- dion

28 ne (9), 4,4'-dimethoxy-2,2'-bipyridine (10), dimethyl 2,2'-bipyridine-4,4'-dicarboxylate (11), 1,10-p

29 H2)](+) where NN = 2,2'-bipyridine (8), 4,4'-dimethyl-2,2'-bipyridine (9), 4,4'-dimethoxy-2,2'-bipyri

30 t of [B{3,5-(CF3)2C6H3}4]AgFe(CO)5 with 4,4'-dimethyl-2,2'-bipyridine (Me2Bipy) and Fe(CO)5 afforded

31 A series of 4,4'-dimethyl-2,2'-bipyridyl ruthenium complexes with carbony

32 -propane (DSTAP) and N-(4-carboxybenzyl)-N,N-dimethyl-2,3-bis(oleoyloxy)propan-1-aminium (DOBAQ).

33 adding n-type dopant 2-(2-methoxyphenyl)-1,3-dimethyl-2,3-dihydro-1H-benzoimidazole.

34 ure the test-retest reliability of (11)C-N,N-dimethyl-2-(2'-amino-4'-hydroxymethylphenylthio)benzylam

35 droxy-3-(2-cyano-3-chlorophenoxy)propyl)-1,1-dimethyl-2-(2-nephthyl)ethylamine] or Ca(2+) (o) removal

36 f [BO(2) ](-) produced by elimination of 2,3-dimethyl-2-butene from a pinacolatoboryl anion.

37 3',6'-bis(diethylamino)-2-{[(1E)-(4,5-dimethyl-2-furyl)methylene]amino}spiro[isoindole-1,9'-xa

38 = 7 +/- 1%) in acetonitrile (MeCN) with 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole (BIH)

39 or to ensure the sacrificial behavior of 1,3-dimethyl-2-phenyl-2,3-dihydro-1H-benzo[d]imidazole as an

40 ine (MAH), 9,10-dimethylacridine (DMAH), 1,3-dimethyl-2-phenylbenzimidazoline (DMPBIH) and on the oxi

41 cule 3-amino-5-[(p-hydroxyphenyl)methyl]-4,4-dimethyl-2-pyrrolidinone (AHDP), no activity has been sh

42 M to 1.73 muM; selective index SI for 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromid

43 amely (4Tm)(2)SnI(4), where 4Tm is 2-(3"',4'-dimethyl-[2,2':5',2":5",2"'-quaterthiophen]-5-yl)ethan-1

44 se of integrated 5-(3-chlorobenzylidene)-2,3-dimethyl-3,5-dihydro-4H-imidazol-4-one (Cl-BI) chromopho

45 oHBI = 5-(5-chloro-2-hydroxybenzylidene)-2,3-dimethyl-3,5-dihydro-4H-imidazol-4-one, chromophore) sys

46 mixture of surfactants (Brij-30/N-decyl-N,N-dimethyl-3-ammonio-1-propanesulfonate).

47 methyl-1,6-octadiene; 3-methyloctane; 1-(1,4-dimethyl-3-cyclohexen-1-yl)ethanone; terpinolene; ethyl

48 For the first time, 1,2-dimethyl-3-ethylimidazolium iodide (1a) catalyzes the ri

49 nopyrazine-2-carboxylate (przNH(2)), and 1,2-dimethyl-3-hydroxy-4(1 H)-pyridinonate (dhp), was studie

50 Herein, 1,3-dimethyl-3-imidazolium hexafluorophosphate (DMIMPF(6) )

51 ivity of 2,6-dimethylphenol with that of 2,6-dimethyl-3-methoxyphenol in HAT promoted by a series of

52 uding an azocine ring and an unprecedented 2-dimethyl-3-methyl-azetidine ring.

53 ylated derivative of kavain, Kava-205Me (5,5-dimethyl-3-oxocyclohex-1-en-1-yl 4-methylbenzoate.) In a

54 sly undisclosed] and AZ12799734 [4-({4-[(2,6-dimethyl-3-pyridinyl)oxy]-2-pyridinyl}amino)benzenesulfo

55 By using methyl viologen (N,N'-dimethyl-4,4'-bipyridinium) to shuttle electrons to nitr

56 *) (MV refers to methyl viologen, i.e., N,N'-dimethyl-4,4'-bipyridinum) engage in weak radical-radica

57 P(i)Pr(2))(2)]} (1; xant(P(i)Pr(2))(2) = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene) coordina

58 nt(P(i)Pr(2))(2)]} (xant(P(i)Pr(2))(2) = 9,9-dimethyl-4,5-bis(diisopropylphosphino)xanthene).

59 e describes a new class of EDLs for QDs, 1,3-dimethyl-4,5-disubstituted imidazolylidene N-heterocycli

60 er single crystals of an azo compound, 3',4'-dimethyl-4-(dimethylamino)azobenzene that can be used as

61 astereoselective cyclization promoted by N,N-dimethyl-4-aminopyridine.

62 ne, MAC = 1,3-bis(2,6-diisopropylphenyl)-5,5-dimethyl-4-keto-tetrahydropyridylidene).

63 reaction of (TPA*)Fe(II) (1) (TPA*=tris(3,5-dimethyl-4-methoxypyridyl-2-methyl)amine) in CH(3) CN wi

64 In this work, the first application of 3,5-dimethyl-4-nitroisoxazole as a vinylogous pronucleophile

65 against the chemical warfare agent simulant dimethyl-4-nitrophenyl phosphate (DMNP) compared to UiO-

66 he breakdown of a chemical warfare simulant (dimethyl-4-nitrophenyl phosphate, DMNP) compared to MOFs

67 tic parameters of the S(N)2 reaction between dimethyl-4-nitrophenylsulfonium trifluoromethanesulfonat

68 cific compound, identified as (2 S, 5E)-6,10-dimethyl-5,9-undecadien-2-ol (common name (S)-fuscumol),

69 S)-fuscumol), and a minor component (E)-6,10-dimethyl-5,9-undecadien-2-one (geranylacetone).

70 and its dimethyl counterpart, methyl 9-(3,4-dimethyl-5-pentylfuran-2-yl) nonanoate (9D5-FuFA), in tw

71 responding tetrazene species to generate 2,2-dimethyl-5-phenylpyrrolidine in a catalytic fashion with

72 I (Ks) blocker (3R,4S)-(+)-N-[3-hydroxy-2,2-dimethyl-6-(4,4,4-trifluorobutoxy) chroman-4-yl]-N-methy

73 reaction of vinyl magnesium bromide with 2,2-dimethyl-6-t-butyl-dimethyl-silyoxy-methyl-1-cyclo-hexan

74 ldehyde is obtained as dimethoxymethane, its dimethyl acetal, by selective reduction of carbon dioxid

75 olves an Ugi reaction with aminoacetaldehyde dimethyl acetal, followed by acid-mediated cyclization t

76 Following protection as the corresponding dimethyl acetals, the iodofulvenes were metalated with B

77 s-Alder reaction and reacts with dienophiles dimethyl acetylenedicarboxylate (DPF.DMAD, 68%), norborn

78 propylphenyl)-imidazol-2-ylidene borane with dimethyl acetylenedicarboxylate gives 80% yield of a sta

79 We show the two-step hydrogenation of dimethyl acetylenedicarboxylate with para-enriched hydro

80 Branched alkylation with N,N-dimethyl acrylamide was successfully applied to the alky

81 trates with the exception of the alpha,alpha-dimethyl allyl ester, which required more forcing condit

82 a supplemented with glutamine, glutamate, or dimethyl-alphaKG increased palmitate lipotoxicity compar

83 dissociation path out of the 3p state to the dimethyl amine radical (16.6+/-1.2 %) and a slower disso

84 Additionally, it is found that the transient dimethyl amine radical has a N-C bond length of 1.45+/-0

85 f ketones using a commercially available 2,2-dimethyl aminooxyacetic acid auxiliary.

86 raarsenic marine metabolite arsenicin A, the dimethyl analogue 2 and four isomeric methylene homologu

87 We found that two phthalates, dimethyl and diethyl phthalates, penetrate deeper into s

88 The dioctyl, dimethyl, and dibenzyl derivatives also show distinctive

89 fluorine, chlorine, bromine, NO(2), methyl, dimethyl, and methoxy, as well as 2-pyridone-N-bearing m

90 Ph), thiophene (Th), bithiophene (biTh), and dimethyl aniline (PhNMe(2)), and Au(I)-azide PPh(3)AuN(3

91 synthesized a push-pull molecule named DAF (Dimethyl Aniline Furaldehyde) that possesses a strong po

92 reaction between nitrostyrene and 3-methoxy-dimethyl aniline was modulated in situ by visible light

93 rsenosugars and their metabolites (including dimethyl arsenate (DMA), thio-dimethylarsinoylethanol (t

94 ation producing monomethyl arsenic (MMA) and dimethyl arsenic (DMA).

95 Cadmium, inorganic arsenic and, potentially, dimethyl arsenic acid are carcinogens widely elevated in

96 d to monomethyl-arsenical species (MMAs) and dimethyl-arsenical species (DMAs), facilitating urinary

97 inary arsenic (As) (inorganic + monomethyl + dimethyl As) was measured by high-performance liquid chr

98 Pd(PPh)3)4 and dimethyl barbituric acid.

99 s and 2,3-dimethylphenol yielded methyl- and dimethyl-BDA species.

100 he tumor incidence of mice treated with 7,12-dimethyl benzanthracene when applied before phorbol myri

101 SAMs of NO(2)-functionalized NHCs and dimethyl-benzimidazole were electrochemically deposited

102 venagel condensation of the latter and a gem-dimethyl, beta-ketoester-substituted BC dihydrodipyrrin

103 , BDI = N, N'-bis(2,6-diisopropylphenyl)-3,5-dimethyl-beta-diketiminate) and initial investigations o

104 1; BDI = N,N'-bis(2,6-diisopropylphenyl)-3,5-dimethyl-beta-diketiminate) have revealed that this spec

105 (BDI = N, N'-bis(2,6-diisopropylphenyl)-3,5-dimethyl-beta-diketiminate), and the uranium(III) salt,

106 as been designed for the direct synthesis of dimethyl carbonate (DMC) from methanol and carbon dioxid

107 ing a 1 M LiAsF(6) in 1:1 ethylene carbonate/dimethyl carbonate (EC/DMC) electrolyte under galvanosta

108 It was observed that the dimethyl carbonate is only formed when the electrode is

109 lives of LMBs with ethylene carbonate (EC), dimethyl carbonate, ethylene sulfite (ES), and their com

110 oxy groups that can further react with CO to dimethyl carbonate.

111 tylfuran-2-yl) nonanoate (9M5-FuFA), and its dimethyl counterpart, methyl 9-(3,4-dimethyl-5-pentylfur

112 ivity, was synthesized from myo-inositol and dimethyl d-camphor acetal in 14 steps.

113 Dimethyl dihydroacridines are presented here as a new fa

114 s to be triggered by a single chemical cue - dimethyl disulfide (DMDS) - emitted from carcasses consu

115 centered) mono-, bi-, and triradicals toward dimethyl disulfide (DMDS) were studied by using a linear

116 some volatile compounds, such as methional, dimethyl disulfide and 1-octen-3-one, which imparted sli

117 Dimethyl disulfide and methyl thioacetate were important

118 Degradation of dimethyl disulfide by direct photolysis caused a small b

119 ion, and the release of dimethyl sulfide and dimethyl disulfide was related to the total aerobic bact

120 unds, such as methanethiol, diethyl sulfide, dimethyl disulfide, methional and dimethyl trisulfide, i

121 atile sulfur compounds, namely methanethiol, dimethyl disulphide and dimethyl trisulphide.

122 hosphate-benzene and dimethyl phosphate- and dimethyl dithiophosphate-benzene model systems.

123 Discrete endo,exo-norbornenyl dialkylesters (dimethyl DME, diethyl DEE, di-n-butyl DBE) were strategi

124 Starting from dimethyl (E)-2-{[(1-tert-butoxycarbonyl)-1H-indol-3-yl]m

125 fter the evaluation of the reactivity of the dimethyl ester derivative with various primary amines, t

126 le-1,2,5-tricarboxylic acid tert-butyl ester dimethyl ester with electrophiles such as methyl chlorof

127 pattern for 3,8-diphenyldeuteroporphyrin IX dimethyl ester, most likely due to the presence of addit

128 tion of the vinyl groups of protoporphyin IX dimethyl ester.

129 d out on both deutero- and protoporphyrin IX dimethyl esters.

130 -positions of deutero- and protoporphyrin IX dimethyl esters.

131 the direct selective oxidation of methane to dimethyl ether (DME) over Pt/Y(2) O(3) .

132 for one-step conversion of synthesis gas to dimethyl ether (DME) was imaged simultaneously and in si

133 of CO2 to formate/formic acid, methanol, and dimethyl ether are thoroughly reviewed, with special emp

134 angren B trimethyl ether and palodesangren D dimethyl ether could be synthesized in 29 and 18% overal

135 -O(2) batteries with a tetra(ethylene)glycol dimethyl ether electrolyte.

136 O(2) (formed at >10 wt %) were selective for dimethyl ether formation, while atomically dispersed ReO

137 t and outlook in synthesis of light olefins, dimethyl ether, liquid fuels, and alcohols through two l

138 rmolecular interactions with systems such as dimethyl ether, trimethylamine, trimethylphosphine, and

139 to fuel conversion with 79% selectivity for dimethyl ether.

140 The synthesis of 14,15-dimethyl-FDP, 12-methyl-FDP, 12-hydroxy-FDP, homo-FDP, a

141 N,N-dimethyl formamide (DMF) is an extensively used organic

142 itrophenol and [DMF.H(+)](CF3SO3(-))) (DMF = dimethyl-formamide) or electron (decamethylferrocene (Fc

143 issect the biosynthetic pathway of mono- and dimethyl FuFAs and their intermediates in two related ba

144 mulation of fumarate by the therapeutic drug dimethyl fumarate (DMF) also promotes ULBP2/5 surface ex

145 daily, or 75 mg twice daily), or open-label dimethyl fumarate (DMF) as a reference.

146 We found that dimethyl fumarate (DMF) delivered to cells or endogenous

147 We show here that dimethyl fumarate (DMF) dose-dependently induces mitocho

148 of this study was to explore the efficacy of dimethyl fumarate (DMF) in preventing disease reactivati

149 itaconate (4-OI) and the clinically approved dimethyl fumarate (DMF) induce a cellular antiviral prog

150 Dimethyl fumarate (DMF) is a prescribed treatment for mu

151 modifiers, including sulforaphane (SFN) and dimethyl fumarate (DMF), are unable to induce a similar

152 se IV trial of the first-line oral treatment dimethyl fumarate (DMF), we examined dynamics of neurofi

153 Dimethyl fumarate (DMF; trade name Tecfidera) is an oral

154 and structurally similar EDO ligands such as dimethyl fumarate and electron-deficient styrenes afford

155 We used an oral treatment with dimethyl fumarate and the HCAR2 endogenous ligand beta-h

156 However, it is no more effective than dimethyl fumarate at reducing the barrier to Csp(3)-Csp(

157 Treatment of HLRCC cells with dimethyl fumarate or PKM2 activators altered PKM2 oxidat

158 ls and anti-inflammatory mediators, that is, dimethyl fumarate, phosphodiesterase 4, and leukotriene

159 onomethyl fumarate, the active metabolite of dimethyl fumarate, reduces circulating lymphocytes and m

160 ed oral compounds now available: fingolimod, dimethyl fumarate, teriflunomide, and cladribine.

161 ived initial therapy with newer (fingolimod, dimethyl fumarate, teriflunomide, natalizumab, rituximab

162 In this respect, we have recently shown that dimethyl fumerate (DMF) inhibits NF-kappaB acting as a s

163 l furfural (5-HMF) to the fuel precursor 2,5-dimethyl furan (2,5-DMF).

164 that the fish oil was rich in monomethyl and dimethyl furan fatty acids (c = 1.3 g/100 g lipids).

165 Upon oxidation of the fish oil, the dimethyl furan fatty acids degraded faster than the mono

166 e by incorporation of a symmetrizing geminal dimethyl group at C5.

167 te to a model bacteriochlorophyll with a gem-dimethyl group in each pyrroline ring has been probed fo

168 ns a trans-dialkyl group in ring D and a gem-dimethyl group in ring B.

169 nal chemists have elegantly employed the gem-dimethyl group to obtain clinically useful drugs and to

170 With the strategic implementation of a gem-dimethyl group to promote both stability and cyclization

171 d (C-C and C-H) cleavages convert the C5 gem-dimethyl group to the C15 lactone of PXN.

172 d to be sensitive to the location of the gem-dimethyl group.

173 o provide synthetic methods to install a gem-dimethyl group.

174 N, N-dimethyl groups are, however, oxidized when exposed to a

175 rtiary amines with catalytically active N, N-dimethyl groups as the base catalyst and a longer alkyl

176 ture of tertiary amine catalysts having N, N-dimethyl groups can be modified to avoid this source of

177 ystal structure shows that the squaraine gem-dimethyl groups force a relatively wide separation betwe

178 AM1710 (3-(1,1-dimethyl-heptyl)-1-hydroxy-9-methoxy-benzo(c) chromen-6-

179 Using this approach, dimethyl-histone H3 and p53 proteins have been synthesiz

180 n treat Ndufs4-KO mice, a cell-permeable KG, dimethyl ketoglutarate (DMKG) was administered.

181 An analogue of MACE2 containing 2,6-dimethyl-l-tyrosine (MACE4) showed the best potency and

182 ty of different endoglycosidases and isotope dimethyl labeling, six N-glycan types of structures link

183 ification by DIA using mass defect-based N,N-dimethyl leucine (mdDiLeu) tags and high-resolution tand

184 loped cost-effective 5-plex mass defect N, N-dimethyl leucine (mdDiLeu) tags for quantification of va

185 to different Mg centers and the mononuclear dimethyl magnesium.

186 phthoquinones, such as menaquinone (MK), and dimethyl-menaquinone (DMK).

187 In nitrogen, protonated forms of dimethyl methyl phosphonate (DMMP) and methyl phosphonic

188 ene Blue (MB), New Methylene Blue (NMB), 1,9-Dimethyl Methylene Blue (DMMB) and Toluidine Blue O (TBO

189 Combination of Methylene Blue + 1,9-Dimethyl Methylene Blue demonstrated superior efficacy c

190 t Methylene Blue, New Methylene Blue and 1,9-Dimethyl Methylene Blue increased by 5000% the reactive

191 o 172% and 1300% for six analytes, including dimethyl methylphosphonate (DMMP), 3-octanone, and perfl

192 and decomposition of a nerve-agent simulant, dimethyl methylphosphonate (DMMP), on UiO-66, UiO-67, MO

193 or and limits of detection for acetonitrile, dimethyl methylphosphonate, diisopropyl methyl phosphona

194 s described herein entail the use of the gem-dimethyl moiety as a means of improving the pharmacologi

195 alpha-[Fe(OTf)(2)(mcp)] (1alpha; mcp = N, N'-dimethyl- N, N'-bis(pyridin-2-ylmethyl)cyclohexane-1,2-d

196 ith 1.8 x 10(-4)% quantum yield (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-ylpyridine-2,6-diamine).

197 ns of nitramine, N-methyl nitramine, and N,N-dimethyl nitramine with anhydrous HF and the superacids

198 omimetic route to farnesyl pyrophosphate and dimethyl orsellinic acid (DMOA)-derived meroterpenoid sc

199 jection led us to test the effect of the PHI dimethyl oxalyl glycine (DMOG) in the pathophysiology of

200 MS, of dopamine (DA), tyrosine (Tyr) and N,N-dimethyl-p-phenylenediamine (DMPA), were evaluated using

201 vo in splenic DC following administration of dimethyl PGE2 in conjunction with LPS.

202 GDH inhibitor + PGE2 or metabolism-resistant dimethyl-PGE2 resulted in preterm cervical ripening and

203 h phosphate- and dithiophosphate-benzene and dimethyl phosphate- and dimethyl dithiophosphate-benzene

204 Furthermore, dimethyl phthalate (DMP) and diethyl phthalate (DEP) wer

205 eto intermediate to yield an alpha,alpha-gem-dimethyl product, a new programing feature among HRPKSs.

206 nges to a two-step one for the reaction with dimethyl propynamine.

207 cholerae, the quorum-sensing autoinducer 3,5-dimethyl-pyrazin-2-ol (DPO) binds the receptor and trans

208 ine-reactive mass defect-based chemical tag, dimethyl pyrimidinyl ornithine (DiPyrO), that is compact

209 bene (2,6-diisopropylphenyl)-4,4-diethyl-2,2-dimethyl-pyrrolidin-5-ylidene ((Et)CAAC) were discovered

210 Dimethyl selenide (DMSe) is one of the major volatile or

211 agnesium bromide with 2,2-dimethyl-6-t-butyl-dimethyl-silyoxy-methyl-1-cyclo-hexanone to give a vinyl

212 Meanwhile, in the presence of dimethyl substituent 1(Me), regioselective gamma-arylati

213 (3))-H bonds in substrates that bear geminal dimethyl substituents furnished chiral amines that featu

214 The library contained cyclohexenones (5,5-dimethyl substituted cyclohexenones) substituted with a

215 omplementary route employs reaction of a gem-dimethyl-substituted dihydrodipyrrin-carboxaldehyde (AD

216 Here we present dimethyl sulfate (DMS) mutational profiling with sequenc

217 otides and then detects these events through dimethyl sulfate (DMS) probing and mutational profiling.

218 sceptibility of adenine-N1 to methylation by dimethyl sulfate (DMS) when in an A-T Watson-Crick versu

219 Here we convert the common reagent dimethyl sulfate into a useful probe of all 4 RNA nucleo

220 le-cycle reverse transcription of long RNAs, dimethyl sulfate mutational profiling (DMS-MaP), selecti

221 We additionally performed dimethyl sulfate mutational profiling with sequencing (D

222 Here we use dimethyl sulfate mutational profiling with sequencing (D

223 sulfoniopropionate (DMSP) cleavage, yielding dimethyl sulfide (DMS) and acrylate, provides vital carb

224 ination with the algal-derived infochemicals dimethyl sulfide (DMS) and dimethylsulfoniopropionate (D

225 sulfoniopropionate (DMSP) and its catabolite dimethyl sulfide (DMS) are key marine nutrients(1,2) tha

226 As dimethyl sulfide (DMS) is a reliable marker for meat fre

227 Marine emissions of dimethyl sulfide (DMS) to the atmosphere play a fundamen

228 methanethiol (MeSH), ethanethiol (EtSH), and dimethyl sulfide (DMS) were assessed in wines post-bottl

229 Dimethyl sulfide (DMS), emitted from the oceans, is the

230 BlMGL) produced the sulfur volatile compound dimethyl sulfide (DMS).

231 Dimethyl sulfide (DMS; CH(3)SCH(3)), a biogenically prod

232 le volatile organic sulfur compounds such as dimethyl sulfide and (2-methylthio)ethanol.

233 of tissue disintegration, and the release of dimethyl sulfide and dimethyl disulfide was related to t

234 The AuNPs enable the detection of dimethyl sulfide and histamine at limits of 0.5 and 0.03

235 o important volatile biogenic markers, i.e., dimethyl sulfide and histamine, is developed to monitor

236 hanol with H(3)O(+), acetone with NO(+), and dimethyl sulfide with O(2)(+*) reagent ions in single br

237 s affected by time include 2-methylpropanal, dimethyl sulfide, and benzaldehyde.

238 terised by a high level of sulfur compounds (dimethyl sulfide, ethanethiol), and ester and alcohol co

239 te with levels of isoprene, monoterpenes, or dimethyl sulfide.

240 g isoprene, monoterpenes, and very recently, dimethyl sulfide.

241 ), while the subsequent oxidation of DMSO to dimethyl sulfone (DMSO(2)) is much slower (0.4 M(-1) s(-

242 idney bean' aroma, while dimethyl sulfoxide, dimethyl sulfone and ethyl methyl sulfone were responsib

243 of room temperature solution calorimetry in dimethyl sulfoxide (DMSO) and differential scanning calo

244 tal by dissolving 4m concentrated LiNO(3) in dimethyl sulfoxide (DMSO) as an additive for a fluoroeth

245 le transfer to ever higher concentrations of dimethyl sulfoxide (DMSO) as the temperature was reduced

246 sphate buffer saline solution containing 10% dimethyl sulfoxide (DMSO) at 21 degrees C.

247 od to excellent yields using only KO(t)Bu in dimethyl sulfoxide (DMSO) at rt.

248 perfluorooctanesulfonic acid (PFOS), or 0.4% dimethyl sulfoxide (DMSO) daily from 0-5 d post fertiliz

249 The method involves mixing volatile additive dimethyl sulfoxide (DMSO) into aqueous PEDOT:PSS solutio

250 owth in dilute aqueous electrolyte by adding dimethyl sulfoxide (DMSO) into ZnCl(2)-H(2)O, in which D

251 Dimethyl sulfoxide (DMSO) is widely used in a number of

252 Compound 7 in dimethyl sulfoxide (DMSO) or ethanol solutions exists in

253 hetarylacetylenes in the presence of KOBu(t)/dimethyl sulfoxide (DMSO) or NaOBu(t)/DMSO systems under

254 esis from ketoximes and acetylene in the KOH/dimethyl sulfoxide (DMSO) superbase medium (here abbrevi

255 Three solvents: water, methanol, and dimethyl sulfoxide (DMSO) were investigated at varying c

256 Dimethyl sulfoxide (DMSO), but not pyrenebutyrate (PB),

257 ethylene glycol (EG), propylene glycol (PG), dimethyl sulfoxide (DMSO), glycerol (GLY), and methanol

258 r, when the media contains a small amount of dimethyl sulfoxide (DMSO), the adduct is able to move to

259 found that HOBr reacts very fast with DMS to dimethyl sulfoxide (DMSO), with a second-order rate cons

260 orm-compatible poly(methyl methacrylate) and dimethyl sulfoxide (DMSO)-compatible poly(2-hydroxyethyl

261 re exposed to K(2)CrO(4), HgSO(4) salts, and dimethyl sulfoxide (DMSO).

262 nsitized with 5% ammonium persulfate (AP) or dimethyl sulfoxide (DMSO).

263 er lowering on the order of 30 kJ mol(-1) in dimethyl sulfoxide and acetonitrile.

264 ize-selective etching agent and a mixture of dimethyl sulfoxide and methanol as a dilute solvent.

265 hat drug release can be influenced by adding dimethyl sulfoxide as a co-solvent for electrospinning.

266 ed using iodine as a catalyst (30 mol %) and dimethyl sulfoxide as an oxidant under metal-free reacti

267 developed employing iodine as a catalyst and dimethyl sulfoxide as an oxidant.

268 was generated in situ from CS(2) and KOH in dimethyl sulfoxide by a simple method and used as a nove

269 hiafulvalene (TTF) in 1.0 m LiClO4 dissolved dimethyl sulfoxide electrolyte are reported.

270 thode catalyst combined with an ionic liquid/dimethyl sulfoxide electrolyte.

271 , or butanol, but activity was observed with dimethyl sulfoxide extracts.

272 cules and surface bound red blood cells from dimethyl sulfoxide for antigen typing.

273 The system I(2)/dimethyl sulfoxide mediates the one-step transformation

274 Enzymes of the dimethyl sulfoxide reductase (DMSOR) family catalyse two

275 Mononuclear molybdoenzymes of the dimethyl sulfoxide reductase (DMSOR) family catalyze a n

276 ions and equilibria of LMC, LEMC and LEDC in dimethyl sulfoxide solutions are also investigated.

277 as used to predict the stability trends in a dimethyl sulfoxide solvent from the gas-phase binding en

278 n affinities, particularly when solvation by dimethyl sulfoxide was taken into account by applying th

279 ts, we have utilized the chemical denaturant dimethyl sulfoxide which, in conjunction with a short th

280 )], Tp(-), hydrotris(pyrazolyl)borate; DMSO, dimethyl sulfoxide), which has a fluctuating valence due

281 ibuting to 'cooked kidney bean' aroma, while dimethyl sulfoxide, dimethyl sulfone and ethyl methyl su

282 Molecular inks based on dimethyl sulfoxide, thiourea (TU), and metal salts have

283 l, and acetonitrile, pure or as mixture with dimethyl sulfoxide, which were added postcolumn to the e

284 did not alter cell viability in untreated or dimethyl sulfoxide-treated cells; however, it did increa

285 njugated to CRM197 by reductive amination in dimethyl sulfoxide.

286 (xDP and xFP) were prepared and dissolved in dimethyl sulfoxide.

287 s similar behavior to drugs pre-dissolved in dimethyl sulfoxide.

288 , which were compared with dissolved PhIP in dimethyl sulfoxide.

289 CPAs such as dimethyl-sulfoxide (DMSO), propylene glycol (PG), and fo

290 st one, fragment C1-C12 that has an anti-1,3-dimethyl system and a terminal diene unit, was accomplis

291 e set of compounds, namely, small molecules (dimethyl terephthalate and zearalenone), a (13)C-labeled

292 decreases the fragmentation half-life of 2,5-dimethyl-tetrazole in refluxing o-xylene from 300,000 ye

293 For 2,5-dimethyl-tetrazole, a positive CFG on the N-methyl (2-po

294 Here, we have shown that the histone dimethyl transferase WHSC1 critically drives indolent PT

295 e: dipropyl disulfide, S-propyl thioacetate, dimethyl trisulfide, 1-octen-3-one, methional, dipropyl

296 l sulfide, dimethyl disulfide, methional and dimethyl trisulfide, in contributing to 'cooked kidney b

297 namely methanethiol, dimethyl disulphide and dimethyl trisulphide.

298 nd, [Si(II)(Xant)Si(II)]Si(0) (4, Xant = 9,9-dimethyl-xanthene-4,5-diyl), has been synthesized via th

299 n utilizing the (LSi:)(2)Xant 1a [Xant = 9,9-dimethyl-xanthene-4,5-diyl; PhC(N (t)Bu)2] and (LSi:)(2)

300 ,6-diisopropylanilido)-2,7-di-tert-butyl-9,9-dimethyl-xanthene; Dipp=2,6-diisopropylphenyl) structura