ライフサイエンスコーパス: epoxy

1 omerisation of its 5,6-epoxy groups into 5,8-epoxy.

2 ing to be substantially higher than the pure epoxy.

3 dialyzer and (iii) sealing the dialyzer with epoxy.

4 ecific alpha-arylation of optically pure 2,3-epoxy-1,1,1-trifluoropropane (TFPO).

5 R-HPODE to an unstable allene oxide, 9(R),10-epoxy-10,12(Z)-octadecadienoic acid.

6 were confirmed by chemical synthesis: ct-8,9-epoxy-11-hydroxy-eicosatrienoic acid (ct-8,9-E-11-HET) a

7 19 carbon furan-containing fatty acid, 10,13-epoxy-11-methyl-octadecadienoate (9-(3-methyl-5-pentylfu

8 de; an epoxy-ketone derivative (9R,10R-trans-epoxy-11E-13-keto) is the most prominent oxidized cerami

9 eLOX3 to specific epoxyalcohol (9R,10R-trans-epoxy-11E-13R-hydroxy) and 9-keto-10E,12Z esters of the

10 f 8R-HPODE with formation of 10-hydroxy-8(9)-epoxy-12(Z)-octadecenoic acid (erythro/threo, 1-4:1) and

11 ts linoleic acid metabolite 9,10-EpOME (9,10-epoxy-12Z-octadecenoic acid) in dorsal root ganglia (DRG

12 e gonad samples, including less common 12,15-epoxy-13,14-dimethylnonadeca-12,14-dienoic acid with eve

13 sible triols arising from hydrolysis of 9,10-epoxy-13-hydroxy-octadecenoates, using LC-MS and chiral

14 ol is formed by SN2 hydrolysis of the 9R,10R-epoxy-13R-hydroxy-octadecenoate product of the LOX enzym

15 opically and by chemical synthesis as 9R,10S-epoxy-13S-hydroxyoctadeca-11E-enoic acid and only approx

16 satrienoic acid (ct-8,9-E-11-HET) and ct-8,9-epoxy-15-hydroxy-eicosatrienoic acid (ct-8,9-E-15-HET).

17 y-3beta,16beta-dihydroxy-oleanane (12,13beta-epoxy-16beta-hydroxy-beta-amyrin).

18 ycarbonyl-8-methyl-2,3,9,10-tetrahydr o-8,11-epoxy-1H,8H,11H-2,7b,11a-triazadibenzo(a,g)cyclocta9(cde

19 ,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-di indolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1

20 ,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-di indolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1

21 ,12-hexahydro-10-hydroxy-9-methyl-1-oxo-9,12-epoxy-1H-di indolo[1,2,3-fg:3',2',1'-kl]pyrrolo[3,4-i][1

22 12-hexahydro-10-hydroxy-9-methyl-1-oxo-9, 12-epoxy-1H-diindolo(1,2,3-fg:3',2',1'-kl)pyrrolo(3,4-i)(1,

23 operoxides, 2,4-alkadienals, 2-alkenals, 4,5-epoxy-2-alkenals, 4-oxo-2-alkenals, and 4-hydroxy-2-none

24 these are toxic, such as 4-hydroxy- and 4,5-epoxy-2-alkenals.

25 exenal, acrolein, 2-heptenal, 2-octenal, 4,5-epoxy-2-decadal, 2-decenal, and 2-undecenal, with the fi

26 oxo-2-pentenal, 4,5-epoxy-2-heptenal, or 4,5-epoxy-2-decenal in the presence of phenolic compounds wa

27 glycine was incubated in the presence of 4,5-epoxy-2-decenal, the amino acid was converted into glyox

28 oxy-2-hexenal, 4,5-epoxy-2-heptenal, and 4,5-epoxy-2-decenal, with 2-methylresorcinol and 2,5-dimethy

29 inverts the 3R-configuration of the (3R)-2,3-epoxy-2-fluoroprenyl acetate intermediate and installs t

30 p, the reactions of 4,5-epoxy-2-hexenal, 4,5-epoxy-2-heptenal, and 4,5-epoxy-2-decenal, with 2-methyl

31 enal, 2,4-heptadienal, 4-oxo-2-pentenal, 4,5-epoxy-2-heptenal, or 4,5-epoxy-2-decenal in the presence

32 tempt to fill this gap, the reactions of 4,5-epoxy-2-hexenal, 4,5-epoxy-2-heptenal, and 4,5-epoxy-2-d

33 Ethyl (E)-4,5-epoxy-2-hexenoate affords excellent S(N)2':S(N)2 regiose

34 ed to study the adsorption and reaction of 1-epoxy-3-butene (EpB) on Pt(111).

35 electivity of 1-epoxybutane formation from 1-epoxy-3-butene on palladium catalysts from 11 to 94% at

36 cyclic triterpene scaffold to give 12,13beta-epoxy-3beta,16beta-dihydroxy-oleanane (12,13beta-epoxy-1

37 (E)-1-(tert-Butyldimethylsilyloxy)-2,3-epoxy-4-hexenonate gives excellent S(N)2':S(N)2 regiosel

38 n alternative route to (1RS,2RS,3SR,4SR)-2,3-epoxy-4-N,N-dibenzylaminocyclohexan-1-ol, respectively.

39 (1RS,2SR,3RS,4RS)- or (1RS,2RS,3SR,4SR)-2,3-epoxy-4-N,N-dibenzylaminocyclohexan-1-ol, respectively.

40 quantities of 5,6-epoxy-beta-ionone and 5,6-epoxy-4-oxo-beta-apo-11-carotenal, no other epoxides wer

41 n epoxide intermediate 13S,14S-eMaR (13S,14S-epoxy- 4Z,7Z,9E,11E,16Z,19Z-docosahexaenoic acid) was co

42 ms arachidonic acid to the allene oxide 8R,9-epoxy-5,9,11,14-eicosatetraenoic acid from which arise c

43 pathway, the intramolecular reaction of 1,2-epoxy-5-hexene follows either the carbometalation or a c

44 In the case of 1,2-epoxy-5-hexene, consideration of competing reaction path

45 opioid receptor (OR) agonist (20R)-4,5-alpha-epoxy-6-(2-(18)F-fluoroethoxy)-3-hydroxy-alpha,17-dimeth

46 xide, (+/-)-anti-7,8-dihydroxy-9alpha,10beta-epoxy-7,8,9,10-tetrahydro-B[a]P.

47 (+/-)-7beta,8alpha-dihydroxy-9alpha,10alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyre ne (B[a]P DE-2) at

48 of (+/-)-7beta,8alpha-dihydroxy-9beta,10beta-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (B[a]P DE-1) and

49 )-7 beta, 8 alpha-dihydroxy-9 alpha,10 alpha-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BaP DE-2) by 2'

50 The carcinogen (+)-anti-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene (BPDE) is strong

51 binding of (+/-)-anti-7r,8t-dihydroxy-9t,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene [(+/-)-anti-BPDE

52 (BP), (+)-(7R,8S,9S,10R)-7,8-dihydroxy-9,10-epoxy-7,8,9,10-tetrahydrobenzo[a]pyrene, with the exocyc

53 Mean relative abundances of epoxy-, 7-keto-, 7-hydroxy- and triol-PS derived from si

54 epoxide containing a cyclopropyl ring, 14,15-epoxy-[9,10,11-cyclopropyl]-eicosa-5Z,7E,13E-trienoic ac

55 ted, the substrate dihydro analog cis-12,13S-epoxy-9Z,15Z-octadecadienoic acid did not cyclize in the

56 ity at high temperatures is demonstrated for epoxy-acid and epoxy-anhydride thermoset networks in the

57 t POXA1b laccase from Pleurotus ostreatus on epoxy activated poly(methacrylate) beads was optimized t

58 ple hydrothermal method, were deposited onto epoxy-activated standard glass slides, followed by immob

59 etric epoxidation and opening of propargylic epoxy alcohol anti-5 with NaN(3)/NH(4)Cl.

60 of mechanistic experiments carried out on an epoxy alcohol containing a tetrahydropyran ring (1a) and

61 A regioselective epoxy alcohol cyclization promoted by the combination of

62 ional functionalization of readily available epoxy alcohol derivatives).

63 le more than what is required to solvate the epoxy alcohol.

64 mploying a semipinacol-type rearrangement of epoxy-alcohol 33 gave aldehyde 34 with the desired stere

65 ated with titanium(IV) alkoxides to give the epoxy alcohols 26 and 27.

66 stereosepecific ring-opening reaction of 2,3-epoxy alcohols and 2,3-epoxy sulfonamides has been accom

67 Cyclic peroxides, hydroperoxides, and epoxy alcohols are major products formed from peroxidati

68 tic enantioselective aminolysis of trans-2,3-epoxy alcohols has been accomplished.

69 allylic alcohols, the reaction could provide epoxy alcohols in up to 83% yield and up to 98% ee, whil

70 ermination of absolute configurations of 2,3-epoxy alcohols is described.

71 orinic acid-catalyzed chloroacylation of 2,3-epoxy alcohols is presented.

72 ylic alcohols, up to 79% yield and 99% ee of epoxy alcohols rather than cyclized tetrahydrofuran comp

73 2,3-trisubstituted, and 2,3,3-trisubstituted epoxy alcohols rendered prominent ECCD signals upon comp

74 y diastereoselective epoxidations to provide epoxy alcohols with high enantio- and diastereoselectivi

75 straightforward assignment of chirality for epoxy alcohols.

76 ring system: (a) a reductive amination of an epoxy aldehyde with N-methylamine with subsequent intram

77 roups resident upon either thioester bearing epoxy-aldehyde or the tetrapeptide.

78 xploiting gamma,delta-unsaturated-alpha,beta-epoxy-aldehydes and a thiazole-thiazoline containing ome

79 in and converted to the corresponding 12R,13-epoxy allene oxide by the catalase-related domain.

80 acid and only approximately 30% to the 9R,10-epoxy allene oxide.

81 (and the equivalent NOE experiment in 12,13-epoxy allene oxides) allowed assignment at the isomeric

82 gioselective ring-opening reaction of chiral epoxy-allyl alcohols (Sharpless conditions as the key st

83 oramidates are precursors to enantioenriched epoxy allylamines.

84 inding that points to an ionic intermediate (epoxy allylic carbocation) during catalysis.

85 The existence of epoxy allylic carbocations in fatty acid transformations

86 ng closure (MIRC) reactions with gamma,delta-epoxy-alpha,beta-enoates, enones, enesulfones, and enami

87 ed and identified, including epoxy-epoxy and epoxy-alpha-glycol functional oligomers, and their indiv

88 s have in common that they originate from an epoxy amide derived from uridine, obtained via reaction

89 order to access 2-epi-bengamide E from these epoxy amides, a synthetic methodology, developed by Miya

90 ed with a dual-microcapsule system utilizing epoxy-amine chemistry in a high temperature cured thermo

91 ent stereoselectivity via the cyclization of epoxy amines derived from alpha-amino acids.

92 Treatment of a range of 2,3- and 3,4-epoxy amines with HBF(4).OEt(2) at room temperature resu

93 omplexes affords epoxy-diols and N-protected epoxy-amino alcohols with excellent enantio- and diaster

94 observed with the naturally occurring C6,C7-epoxy analogs of WA (withanone and withanolide A).

95 rning of platinum microelectrodes as well as epoxy and dry-film-resist insulation in a cost-effective

96 legans CYP-33E2 activity produces a range of epoxy and hydroxy metabolites from dietary DGLA.

97 as a degrading effect on the bonding between epoxy and silica, a technologically important interface.

98 ces between the solution composition and the epoxy and theoretic (68)Ge-to-(18)F response ratios were

99 s a pore-filling conductive adhesive (silver epoxy) and achieves significant reductions in contact re

100 d 7-keto) and campesterol oxides (beta/alpha-epoxy, and 7-keto) were detected in all beverages and at

101 ted surfaces are attributed to the hydroxyl, epoxy, and carboxyl functional groups of GO; higher depo

102 ve decay time, on the order of 100 ns, while epoxy- and hydroxy-graphanes lose electronic excitation

103 e), and of nanostructures in polyurethane or epoxy; and (iii) solvent-assisted micromolding of nanost

104 peratures is demonstrated for epoxy-acid and epoxy-anhydride thermoset networks in the presence of tr

105 fer prior to casting and PDMS casting of the epoxy are discussed to preserve the silicon wafer for fu

106 tial structure of an anticorrosive aluminium epoxy barrier marine coating obtained by serial block-fa

107 the construction of a commercially available epoxy-based (68)Ge calibration source.

108 These sources and several NIST-constructed epoxy-based (68)Ge mock syringes were then used as artif

109 lymerization like BADGE are extractable from epoxy-based coatings of commercially available tubes and

110 A new epoxy-based ink is reported, which enables 3D printing o

111 oped in this study enabled NIST to calibrate epoxy-based mock syringe sources with a relative combine

112 The ability for NIST to calibrate these epoxy-based mock syringes enabled, for the first time to

113 he three-dimensional covalent network of the epoxy-based polymer may directly influence water accumul

114 column consists of a hydrolyzed macroporous epoxy-based polymer.

115 age of oxidation and minor quantities of 5,6-epoxy-beta-ionone and 5,6-epoxy-4-oxo-beta-apo-11-carote

116 Monolithic glass plates were epoxy-bonded to polycarbonate substrates as a transparen

117 ormyl derivative which reacts further via an epoxy-borate intermediate to capture CO, affording a het

118 plained by Lewis acid induced opening of the epoxy bridge with transfer of one alkyl group to the int

119 s, identical in geometry to the solid (68)Ge epoxy calibration source currently on the market, were p

120 contrast, with canthaxanthin, apart from 5,6-epoxy-canthaxanthin, which was detected at the early sta

121 carbamazepine was only transformed to 10,11-epoxy carbamazepine and 10,11-dihydroxy carbamazepine as

122 r solid-state-fermentation conditions, 10,11-epoxy carbamazepine was further metabolized via acridine

123 ways were validated using metabolites (10,11-epoxy carbamazepine, 10,11-dihydroxy carbamazepine, and

124 The abrasion behavior of an epoxy/carbon nanotube (CNT) nanocomposite was investigat

125 ynthesis is the cleavage reaction of a 9-cis-epoxy-carotenoid catalyzed by the 9-cis-epoxy-carotenoid

126 -cis-epoxy-carotenoid catalyzed by the 9-cis-epoxy-carotenoid dioxygenases (NCEDs).

127 In comparison, the epoxy carotenoids cis-violaxanthin and cis-antheraxanthi

128 iquid-crystal monomers within micropatterned epoxy channels, followed by photopolymerization.

129 E, such as keto, hydroperoxide, hydroxy, and epoxy cholesteryl ester derivatives from cholesteryl lin

130 (intra- and inter-spot CVs 36% and 18%) and epoxy-coated glass (intra- and inter-spot CVs 26% and 20

131 by covalent bonding of the proteins with an epoxy-coated glass substrate while they are diffusing in

132 d fluoric residues and for immobilization on epoxy-coated solid surfaces.

133 an markets, were tested for migration of BPA epoxy-coating cans.

134 mbin was immobilized onto an avidin-graphite epoxy composite (AvGEC) electrode surface by affinity in

135 , the highest thermal conductivity of AlN@PI/epoxy composite reached 2.03 W/mK.

136 Fitting the measured thermal conductivity of epoxy composite with one physical model indicates that t

137 roved after adding kenaf fibers into the hBN/epoxy composite, potentially benefiting the composite's

138 00 W m(-1) K(-1)) of the 69.0% hBN and 31.0% epoxy composite.

139 Strong and tough epoxy composites are developed using a less-studied fibr

140 hat of untreated AlN composite, these AlN@PI/epoxy composites exhibit better thermal and dielectric p

141 The fabricated graphene/epoxy composites exhibit simultaneously remarkable incre

142 esins and be fabricated as transparent CDots/epoxy composites for multiple-color- and white-light-emi

143 ked toughening and strengthening effects for epoxy composites from natural silk reinforcements, which

144 We show that the toughening effects on silk-epoxy composites or SFRPs are dependent on the silk spec

145 xhibiting the thermal conductivity of AlN@PI/epoxy composites were in good agreement with the values

146 ral fiber into hexagonal boron nitride (hBN)/epoxy composites.

147 For tungsten carbide - epoxy crystals we identify all angle all mode normalized

148 approximately 1.5 h, not including overnight epoxy curing.

149 ADON), 15-acetyldeoxynivalenol (15-ADON), de-epoxy-deoxynivalenol (DOM-1) and ochratoxin A (OTA) duri

150 Epoxy derivatives exhibited a maximum after 6weeks of st

151 13S,14S-epoxy-DHA also reduced ( approximately 60%; P<0.05) arac

152 4Z,7Z,9E,11E,16Z,19Z-hexaenoic acid (13S,14S-epoxy-DHA) was prepared, and its stereochemistry was con

153 Epoxy, diene, and fluorinated substrate analogues, irrev

154 atalyzed by (salen)Co(III) complexes affords epoxy-diols and N-protected epoxy-amino alcohols with ex

155 led synthesis, enantiomerically pure 13S,14S-epoxy-docosa-4Z,7Z,9E,11E,16Z,19Z-hexaenoic acid (13S,14

156 stereochemistry, and precursor role of 13,14-epoxy-docosahexaenoic acid, an intermediate in MaR1 bios

157 lamide (10,17-diHDHEA) and 15-hydroxy-16(17)-epoxy-docosapentaenoyl ethanolamide (15-HEDPEA), each of

158 he sensory experiment indicated that (E)-4,5-epoxy-(E)-2-decenal, (E,E)-2,4-octadienal, and 1-octen-3

159 thers, (E,Z,Z)-2,4,7-tridecatrienal, (E)-4,5-epoxy-(E)-2-decenal, 4-ethyloctanoic acid, 3-methylindol

160 3(2H)-furanone (furaneol), vanillin, (E)-4,5-epoxy-(E)-2-decenal, 4-ethyloctanoic acid, 3-methylindol

161 endo-selective cyclizations and cascades of epoxy-(E)-enoate alcohols, thus enabling the synthesis o

162 double bond to form 8R-hydroxy-9R,10R-trans-epoxy-eicosa-5Z,11Z,14Z-trienoic acid as the predominant

163 n of hepoxilin A(3) (HXA(3); 8-hydroxy-11,12-epoxy-eicosatetraenoic acid), a potent neutrophil chemoa

164 tudy, the acid-stable 13-hydroxy-trans-14,15-epoxy-eicosatrienoic acid (13-H-14,15-EETA) was identifi

165 ants and sEHIs significantly increased 14,15-epoxy-eicosatrienoic acid and 15-epi-LXA4 generation by

166 The formation of alkynyl 11-hydroxy-8,9-epoxy-eicosatrienoic acid compared to alkynyl prostaglan

167 icosatetraenoic acid, alkynyl 11-hydroxy-8,9-epoxy-eicosatrienoic acid, and alkynyl prostaglandins.

168 roxide vapor fixation, followed by immediate epoxy embedment, an artifact-free protocol, which, to ou

169 ides) allowed assignment at the isomeric C10 epoxy-ene carbon as Z in the new isomer and the E config

170 diastereoselectivity can be achieved for the epoxy enoates, enones, and ensulfones, while the enamide

171 nt for alkyl Grignard reagents reacting with epoxy enoates, ensulfones, and enamides but solvent inde

172 Epoxy enolsilanes containing a terminal enolsilane and a

173 l-triflate-catalyzed (4+3) cycloadditions of epoxy enolsilanes with dienes provide a mild and chemose

174 nds were separated and identified, including epoxy-epoxy and epoxy-alpha-glycol functional oligomers,

175 degrades natural analgesic lipid mediators, epoxy fatty acids (EpFAs), therefore its inhibition stab

176 ydrophobic polyester of glycerol and hydroxy/epoxy fatty acids has not been fully resolved.

177 utin, a polyester of glycerol, hydroxyl, and epoxy fatty acids, covered and filled by waxes.

178 atalyzes the hydrolysis of anti-inflammatory epoxy fatty acids, including epoxyeicosatrienoic acids f

179 advances in therapy by omega-3, omega-6, and epoxy fatty acids; specialized proresolving mediators; a

180 Stabilization of natural epoxy-fatty acids (EFAs) through inhibition of the solub

181 Recently, the elevation of epoxy-fatty acids through inhibition of soluble epoxide

182 o manufacture thin, flexible and transparent epoxy films containing zirconium phosphate nanoplatelets

183 h carbon deposited array tip was filled with epoxy, followed by beveling of the tip of the array to f

184 plexes containing amine functional groups to epoxy-functionalised polymers of variable composition pr

185 rahigh-vacuum oxidization results in uniform epoxy functionalization.

186 d subsequently immobilized the conjugates on epoxy-functionalized glass slides through reaction of fr

187 ion of the extract by microfiltration led to epoxy-furanoxy rearrangement of violaxanthin and anthera

188 vative of this mimotope was immobilized onto epoxy-glass slides, and fumonisin B1 was detected in a c

189 Unexpectedly, we find that the epoxy group contributes only modestly to PB potency and

190 dation of the C-22,23 double bond in A to an epoxy group in AF.

191 earrangement and subsequent sulfation of the epoxy group in the particle phase.

192 Fungal bioassays show that the C12,13 epoxy group is an important determinant of antifungal ac

193 (QD@SiO2), modified with amino, carboxyl and epoxy groups and stabilized with polyethylene glycol fra

194 ) are examined to provide excess hydroxyl or epoxy groups for aminoferrocene coupling.

195 Monoliths with epoxy groups for antibody immobilization were prepared b

196 crylate (GMA) was examined to provide excess epoxy groups for HRP coupling.

197 hy immersion in a NaOH solution, most of the epoxy groups in the graphene oxide were destroyed, and m

198 We also introduced epoxy groups in the prenylation sites of the proteins to

199 ared because of the isomerisation of its 5,6-epoxy groups into 5,8-epoxy.

200 Epoxy groups on the surface can be activated by air plas

201 of amino groups present in the receptor with epoxy groups present in the co-polymer.

202 Then, a silane layer with terminal epoxy groups was created using 3-glycidyloxypropyltrimet

203 Epoxy groups were used to bind a layer of diamino-poly(e

204 nfrared region (e.g., acrylate double bonds, epoxy groups) or the MIR region (e.g., thiol signal).

205 s or pyridine, amine, hydroxyl, carboxyl, or epoxy groups) to understand the adsorption process of Bn

206 e residues on BSA and PVA with surface-bound epoxy groups.

207 using a polyacrylic support containing polar epoxy groups.

208 droxy-3-methyl-2,3-epoxybutanyl diphosphate (Epoxy-HMBPP), a proposed intermediate in one of the freq

209 rolase (LTA4H) is a bifunctional enzyme with epoxy hydrolase and aminopeptidase activities.

210 cedented cyclization cascade of a chiral bis(epoxy)hydroperoxide.

211 layer structures consisting of glass veneers epoxy-joined onto alumina or zirconia cores, all bonded

212 Monolithic glass plates were epoxy-joined to polycarbonate substrates as a transparen

213 nd 9-keto-10E,12Z esters of the ceramide; an epoxy-ketone derivative (9R,10R-trans-epoxy-11E-13-keto)

214 ared by the metal-catalyzed rearrangement of epoxy ketones.

215 unctionalized cyclopropanes from gamma,delta-epoxy malonates and amines mediated by LiCl under mild c

216 a intramolecular ring-opening of gamma,delta-epoxy malonates through the cooperative catalysis of LiC

217 osynthesis, this epoxide is now termed 13,14-epoxy-maresin (13,14-eMaR) and exhibits new mechanisms i

218 erted by platelet 12-lipoxygenase to 13S,14S-epoxy-maresin, which was further transformed by neutroph

219 enhanced by 10.6 times than that of the used epoxy matrix.

220 levels of inflammation-resolving DHA-derived epoxy metabolites compared to healthy colon tissues or t

221 These employ either epoxy-methoximes, vinyl-substituted oxiranes, or hydroxy

222 relative response ratios for a (68)Ge solid epoxy mock syringe source used in activity calibrators a

223 This aluminum-based epoxy mold, serving as the positive master mold for embo

224 ic techniques were adapted to fabricate bulk epoxy molds capable of resisting high temperatures and p

225 s the addition of Grignard reagents to alpha-epoxy N-sulfonyl hydrazones-directed by the alkoxide of

226 e fraction of particles abraded from a MWCNT-epoxy nanocomposite.

227 Three-point bending tests of the MWCNT/epoxy nanocomposites revealed a remarkable increase in e

228 Novel papers based on epoxy nanocomposites with magnetite and carbon nanofiber

229 toresistance (MR) is observed in synthesized epoxy nanohybrid papers for the first time.

230 cross-links into a dry, loosely cross-linked epoxy network.

231 )-promoted tandem cyclization of unsaturated epoxy nitrile.

232 The effect of trehalose and SU-8 epoxy novolac resin (SU-8) on the stability of horseradi

233 ax 236 nm) and NMR spectrum (defining a 9,10-epoxy-octadec-10,12Z-dienoate).

234 ) were synthesized from newly designed alpha-epoxy-omega-hydroxyl-functionalized AB(2)-type ketal mon

235 Individual plates were then embedded in epoxy or cemented to dental composites and subjected to

236 abricated using off-stoichiometric thiol-ene-epoxy (OSTEMER) polymer resulting in hard-polymer device

237 donic acid- and linoleic acid-derived CYP450-epoxy-oxlipins and resulted in a dramatic influx in mono

238 These findings demonstrate that epoxy-oxylipins have a critical role in monocyte lineage

239 d the roles of cytochrome P450 (CYP)-derived epoxy-oxylipins in a well-characterized model of sterile

240 Epoxy-oxylipins were produced in a biphasic manner durin

241 sEH (Ephx2)(-/-) mice, which have elevated epoxy-oxylipins, demonstrated opposing effects to epoxI-

242 C double bond peak in thiol-ene systems, C-O epoxy peak for epoxy resins).

243 graphy of a chemically functional commercial epoxy photoresist (SU-8).

244 When the native surface of the epoxy pillars is masked by a thin gold layer and modifie

245 ry in a high temperature cured thermosetting epoxy polymer.

246 ium phosphate nanoplatelets is stabilized by epoxy pre-polymer and exhibits rheology favourable towar

247 direct exposure of two specific DGLA-derived epoxy products, 8,9- and 14,15-epoxyeicosadienoic acids,

248 Comparison of NOE interactions of the epoxy proton at C9 in the two allene oxides (and the equ

249 portion of the transducer material (graphite-epoxy ratio) was chosen using constant amount of RIgG.

250 ining 43.6% hBN, 26.3% kenaf fiber and 30.1% epoxy reached 6.418 W m(-1) K(-1), which was 72.3% highe

251 of the E. coli RS2-GFP transport through the epoxy replica fracture, which capture for the first time

252 in a natural rock fracture and a transparent epoxy replica of that same fracture.

253 the diffractive optical effects produced by epoxy replicas of petals with folded cuticles persist an

254 Trend analyses on chromate (decreasing), epoxy resin (increasing) and nickel (heterogeneous) serv

255 d characterization and quantitation of solid epoxy resin components.

256 icropultruded glass and/or aramid fibers and epoxy resin with diameters of 0.89 mm (0.035 inch) for s

257 for fluorescence microscopy and embedding in epoxy resin with serial sectioning for transmission elec

258 2C-R(-/-), and C57BL/6 mice were embedded in epoxy resin, and semithin sections were stained with tol

259 e and flexural strength, as compared to pure epoxy resin, with an order of magnitude higher breaking

260 n nanotubes (MWCNTs) in ethanol solution and epoxy resin.

261 (w/w) as plasticizer casted on a conductive epoxy resin.

262 mpact strength some eight times that of pure epoxy resin.

263 maceutical use are internally lacquered with epoxy resins (ER) based on bisphenol A diglycidyl ether

264 at the CDots can be uniformly dispersed into epoxy resins and be fabricated as transparent CDots/epox

265 dely used in the manufacture of plastics and epoxy resins and is prevalent in the aquatic environment

266 (BPA) is found in polycarbonate plastic and epoxy resins and is used in a variety of commercial and

267 the production of polycarbonate plastic and epoxy resins found in numerous consumer products.

268 d bisphenol F diglycidyl ether (BFDGE)-based epoxy resins have a broad range of applications, includi

269 Epoxy resins incorporating bisphenol A diglycidyl ether

270 Bisphenol A (BPA) is widely used in epoxy resins lining food and beverage containers.

271 Different components present in the solid epoxy resins were separated and quantitated for the firs

272 eak in thiol-ene systems, C-O epoxy peak for epoxy resins).

273 he manufacture of polycarbonate plastics and epoxy resins, and > 93% of U.S. adults have detectable l

274 widely used in the manufacture of plastics, epoxy resins, and certain paper products.

275 ryday consumer products, including plastics, epoxy resins, and cosmetics.

276 cts made from BPA, polycarbonate plastic and epoxy resins, BPA has entered terrestrial and aquatic en

277 er used to produce polycarbonate plastic and epoxy resins, is weakly estrogenic and therefore of envi

278 Other occupational agents, such as epoxy resins, welding fumes and hand-arm vibration, have

279 the production of polycarbonate plastics and epoxy resins.

280 ing gold nanorods on a flexible, conformable epoxy resist membrane to realize a Pancharatnam-Berry ph

281 ng ~18% of the surface with a non-conductive epoxy results in a greater than 5x increase in heat tran

282 by PCM quantum-chemical method) of the model epoxy ring formation.

283 Ti (III) mediated ring opening of a terminal epoxy ring tethered to a butenolide to produce stereosel

284 ing an asymmetric epoxidation-intramolecular epoxy-ring-opening Friedel-Crafts reaction sequence was

285 oxane (PDMS) hybrid microchip using a simple epoxy silica sol-gel coating/bonding method and employed

286 Lectins were printed on epoxy slides in duplicate sets to generate lectin super-

287 t midrange fatty acids (C12:0 and C14:0) and epoxy stearic acid, 4-8-fold lower activity against C16:

288 Withaferin A (WA), a C5,C6-epoxy steroidal lactone derived from a medicinal plant (

289 dy-functionalized bead surface, highest with epoxy-/sulfate beads (85-86%), followed by carboxylate-m

290 ere synthesized by conjugating antibodies to epoxy-/sulfate, aldehyde-/sulfate, or carboxylate-modifi

291 ioselective aminolysis of aromatic trans-2,3-epoxy sulfonamides has been accomplished, which was effi

292 ening reaction of 2,3-epoxy alcohols and 2,3-epoxy sulfonamides has been accomplished.

293 and flexibility of welding and assembling of epoxy thermosets that do not exist for thermoplastics.

294 d the materials have properties of classical epoxy thermosets.

295 P profile characterized by a higher ratio of epoxy- to 7-keto-derivatives.

296 rol oxides (7alpha/7beta-hydroxy, beta/alpha-epoxy, triol, and 7-keto) and campesterol oxides (beta/a

297 selectively to both enantiomeric forms of an epoxy vinyl stannane, and a series of coupling reactions

298 intramolecular radical addition of different epoxy vinyl- and allylsulfones has been achieved.

299 struction of immunosensors based on graphite-epoxy which incorporate RIgG to the composite matrix.

300 By contrast, in neutral medium, free epoxy-xanthophylls were about 2-fold more stable than we