ライフサイエンスコーパス: ether

1 solvents (tetrahydrofuran, methyl tert-butyl ether).

2 of degradable and depolymerizable poly(enol ether).

3 ly analyse the dimers (3beta,3'beta-disteryl ethers).

4 ction or all of Na(+) is chelated by a crown ether.

5 conversion with 79% selectivity for dimethyl ether.

6 methyl sulfenate and the aryl or heteroaryl ether.

7 sponding salts in the presence of 18-crown-6 ether.

8 wo EOM and two (+)-catechin-4-O-methyl (COM) ethers.

9 eoselective cationic polymerization of vinyl ethers.

10 amline the synthesis of methylsulfoxylmethyl ethers.

11 bic TEMPO oxidations of alcohols, diols, and ethers.

12 s sorption capacity compared with pure crown ethers.

13 nd alcohols to afford alkyl aryl(heteroaryl) ethers.

14 sponding isomeric ketones from aromatic enol ethers.

15 ium transference numbers compared to typical ethers.

16 in situ-generated beta-pyridinium silyl enol ethers.

17 rganophosphates, and polybrominated diphenyl ethers.

18 alcohols, affording synthetically important ethers.

19 s-1-Bromo-2-methoxycyclohexane provides enol ether 1-methoxycyclohexene, while trans-1-bromo-2-methox

20 Exhaustive demethylation of both permethyl ethers 6 and 7 gave the polyphenolic natural lamellarins

21 nstrates that heterologously expressed human ether a-go-go-related gene (hERG) 1a/1b channels, which

22 rs are combined with low-strain cyclic vinyl ethers, a controlled chain-growth copolymerization occur

23 Ether-a-go-go (EAG) potassium selective channels are maj

24 We also identify body cavity neurons and an ether-a-go-go (EAG)-related potassium channel that funct

25 The KCNH2-encoded Kv11.1 hERG (human ether-a-go-go related gene) potassium channel is a criti

26 The EAG (ether-a-go-go) family of voltage-gated K(+) channels are

27 We focus on the human Ether-a-go-go-Related Gene (hERG) channel, which is impo

28 The human ether-a-go-go-related gene (hERG) encodes the channel th

29 The human ether-a-go-go-related gene (hERG) encodes the pore-formi

30 Human ether-a-go-go-related gene (hERG) encodes the pore-formi

31 played a low propensity to inhibit the human ether-a-go-go-related gene (hERG) potassium ion channel

32 The human ether-a-go-go-related gene (hERG1) channel conducts smal

33 d block of the promiscuous drug target human ether-a-go-go-related gene (hERG1), the pore-forming dom

34 The human ether-a-go-go-related gene1 (hERG) ion channel has been

35 nergic combination of bulky diols with crown ethers able to accelerate this kind of reaction.

36 utilizes glycosyl fluoride donors and silyl ether acceptors while tolerating the Lewis basic environ

37 ic PFAS (PFEtCHxS), per- and polyfluoroalkyl ether acids (GenX, ADONA, 9Cl-PF3ONS), and three aqueous

38 PEG diacrylate (PEGDA, M(n) 700), PEG methyl ether acrylate (PEGMEA, M(n) 480), and acrylate-PEG(2000

39 A 5 x 5 cm(2) pouch cell with LAGP/poly(ether-acrylate) NCPE exhibits stable cycling with a capa

40 Perfluoro-15-crown-5-ether alginate capsules were infused intraperitoneally i

41 rformed the polymerization from a variety of ethers, alkanes, unactivated C-H bonds, and alcohols.

42 linic (Lev) ester, thexyldimethylsilyl (TDS) ether, allyloxycarbonate (Alloc), and 9-fluorenylmethyl

43 ere tolerated, including those with halides, ethers, amines, and pyridyl groups.

44 enative cross-couplings of heteroarenes with ethers, amines, and unactivated alkanes with turnover nu

45 404) is a novel antitumor alkyl phospholipid ether analog that broadly targets cancer cells.

46 ylative lactonization between an aryl methyl ether and a neighboring carboxylic acid was developed fo

47 factor associated with accumulation of dill ether and alpha-phellandrene, volatile compounds associa

48 with various directing groups, such as oxime ether and benzothiazole.

49 ).6H(2)O/NaBH(4) reduction of a chiral oxime ether and chemoselective amidation of the resulting unpr

50 e CNMe ether group in the presence of benzyl ether and isopropylidene acetal protection have also bee

51 he tricyclic core, palodesangren B trimethyl ether and palodesangren D dimethyl ether could be synthe

52 three remaining Rb(+) ions wrapped by crown ether and THF molecules.

53 the activation of the intermediate dibenzyl ether and to identify the rate-determining step.

54 axle selectivity, from primary amines, crown ethers and a range of C=O, C=S, S(=O)(2) and P=O electro

55 mance for ketones, and worst performance for ethers and aldehydes.

56 isting of double bond isomerization of allyl ethers and amines and subsequent intramolecular reaction

57 te the catalyst following metathesis of enol ethers and cleave the catalyst off the resulting polymer

58 We report the conversion of aryl methyl ethers and phenols into six fluoroalkyl analogues throug

59 Since aryl ethers and phenols represent the main linkages or units

60 , aromatics, mono-and sesquiterpenes, oxides/ethers and pyrans/furans.

61 cyclopentylmethyl ether); and (5) the reaction is largely insensitive with

62 iketene acetal monomers from diols and vinyl ether, and their polymerization with a diol to first syn

63 oxyphenyl, unprotected benzyl alcohol, silyl ether, and thiophene groups are tolerated.

64 overall wide substrate scope (e.g., halides, ethers, and amines).

65 ot observed, or seen weakly, with aldehydes, ethers, and ketones due to their strained four-member ri

66 urated phosphatidylcholines and phospholipid ethers, and lower sphingomyelins was protective for mAb+

67 c.), aryl carbamates and carbonates, to aryl ethers (anisoles, diaryl ethers, aryl pyridyl ethers, ar

68 ofuranosides, and even simple 5-O-aminoalkyl ethers are effective in this respect through the use of

69 Enol ethers are widely used as quenching reagents for Grubbs

70 ferent substrates, viz., cyclohexane, cyclic ethers, arenes, alkyl aromatic systems, and aldehydes/ke

71 carbonates, to aryl ethers (anisoles, diaryl ethers, aryl pyridyl ethers, aryl silyl ethers), to phen

72 thers (anisoles, diaryl ethers, aryl pyridyl ethers, aryl silyl ethers), to phenolate salts, and ulti

73 Herein, we report cyanomethyl (CNMe) ether as an efficient and effective participating orthog

74 s initiators or by the use of a linear vinyl ether as the chain transfer agent.

75 wards alkylarenes for hydrogenolysis of aryl ethers as model bio-oxygenates without over-hydrogenerat

76 een tea tissues revealed two EOM and two COM ethers associated with PA biosynthesis.

77 yl group and the second has a carboxymethoxy ether at the C-3 position.

78 nd benzylic C-H bonds and alpha-C-H bonds of ethers at room temperature.

79 tering compared to those with the more polar ether backbone.

80 -metal-free arylation of difluoro enol silyl ethers based on hypervalent iodines.

81 lass of readily available bifunctional silyl ether-based cyclic olefins that copolymerize efficiently

82 the limited dispersibility of protein in the ether-based electrolyte and achieve a remarkably enhance

83 Here, ether-based electrolytes are in situ polymerized by a ri

84 For example, ether-based electrolytes have high ionic conductivity bu

85 es using mixtures of a hydrolytically stable ether-based monomer, triethylene glycol divinylbenzyl et

86 adhesives were composed of equimolar ester-/ether-based vinyl functional groups.

87 athesis polymerization (ROMP) of cyclic enol ethers, because the resulting electron-rich ruthenium al

88 estigations reveal sodium cation-benzo-crown ether binding dramatically enhances the recognition of b

89 showed that the formation of the alk-1-enyl ether bond involves an aerobic process in animal cells a

90 at different cleavage mechanisms for the C-O ether bonds in alpha-keto and alpha-hydroxy beta-O-4 typ

91 hemical degradative method that cleaves beta-ether bonds in lignin, indicating that the hydroxystilbe

92 No NMR signals indicating ether bonds were observed.

93 rated into the lignin structure through beta-ether bonds.

94 erization by acid-catalyzed cleavage of aryl-ether bonds.

95 The polymer systems considered here comprise ether, butadiene, and siloxane backbones with grafted im

96 dvertent formation of a methylsulfoxylmethyl ether byproduct.

97 Instead, the cleavage of ether C-O bonds generates unstable perfluoroalcohols and

98 measurements for octaethylene glycol dodecyl ether (C(12)EO(8)), octyl glucoside (OG), and dodecyl ma

99 luoromethylthiolation of difluoro enol silyl ethers can be used for the construction of a novel trifl

100 Perfluoro-15-crown-5-ether capsules retrieved on day 7 were intact and free-f

101 r the degradation of emerging perfluoroalkyl ether carboxylic acid (PFECA) pollutants with ultraviole

102 2; range: 1-110 ng/g) and two perfluorinated ether carboxylic acids (PFO(4)DA and PFO(5)DoDA; PFO(5)D

103 functional group tolerance (phenols, amides, ethers, carboxylic acids, ketones, and acrylic esters).

104 se in the reaction rate in relation to crown ether catalysis only.

105 stic studies with peptide and prolinol silyl ether catalysts showed the generality of this so-far und

106 rogenolysis of the aromatic C-O bond in aryl ethers catalyzed by Ni was studied in decalin and water.

107 not ACOT was stimulated by non-cleavable C14 ether-CoA.

108 enyltrichloroethane, and brominated diphenyl ether congeners, in higher trophic level (TL) organisms

109 rysophaentin A features a macrocyclic biaryl ether core incorporating two trisubstituted chloroalkene

110 trimethyl ether and palodesangren D dimethyl ether could be synthesized in 29 and 18% overall yields,

111 ations across a broad range of beta-O-4 type ethers create a hierarchy of cleavage rates that support

112 s followed by cross-linking with a bis-silyl ether cross-linker.

113 Decabromodiphenyl ether (decaBDE) and five proposed alternatives were sele

114 Crown ether derivatives exhibit selectivity to Na(+) and K(+)

115 The reaction of acyclic vinyl ethers, dihydrofuran, and norbornenes with a variety of

116 the presence of Lewis acid salts, the cyclic ether, dioxolane (DOL), is known to undergo ring-opening

117 tution on the PP scaffold included 2-pyridyl ethers directed into the hydrophobic pocket and small ca

118 t selective oxidation of methane to dimethyl ether (DME) over Pt/Y(2) O(3) .

119 better known as plasmalogens, harbor a vinyl ether double bond conferring special chemical and physic

120 e enzyme introducing the crucial alk-1'-enyl ether double bond.

121 characteristic 1-O-alk-1'-enyl ether (vinyl ether) double bond that confers special biophysical, bio

122 Moreover, in contrast to conventional ether electrolyte with a low flash point (ca. 2 degrees

123 teries with a tetra(ethylene)glycol dimethyl ether electrolyte.

124 shell hollow host structure, and fluorinated ether electrolytes enables ultrastable Li stripping/plat

125 rk, we synthesize a new class of fluorinated ether electrolytes that combine the oxidative stability

126 formation are here compared in carbonate and ether-electrolytes.

127 nomer scope to include enantioenriched vinyl ethers enabled the preparation of an isotactic poly(viny

128 lic C-H bonds with alcohols to afford benzyl ethers, enabled by a redox-buffering strategy that maint

129 a wide range of functional groups, including ether, ester, amide, carbamate, and halide.

130 oethylene) (PTFE) tube is worse than in poly(ether ether ketone) (PEEK) tubing.

131 inearly (P < 0.01) greater protein and lower ether extract.

132 P-G) in human urine after a simple acidified ether extraction procedure when using multisegment injec

133 ro-Diels-Alder reaction of enones with vinyl ethers followed by a modified Knoevenagel-Stobbe reactio

134 ntify the mechanism of 3beta,3'beta-disteryl ether formation at high temperatures, an attempt was mad

135 nvestigated the I(2)-promoted cyclic dialkyl ether formation from 6-membered oxanickelacycles origina

136 med at >10 wt %) were selective for dimethyl ether formation, while atomically dispersed ReO(4) on Si

137 cation 16 via O-alkylation or by reversible ether formation.

138 y two electrons and in the presence of crown-ether forms the tetraanionic N(2) complex [K(2)][K(18-cr

139 o homophthalimides in the presence of cyclic ethers gave spirocyclic products of Stevens-type [1,2]-a

140 hiphilic guanidinocalix[5]arene pentadodecyl ether (GC5A-12C) and negatively charged oleic acid (OA),

141 orporation and selective removal of the CNMe ether group in the presence of benzyl ether and isopropy

142 UV-vis analysis revealed the pendant oligo-ether group of the catalyst strongly binds to the potass

143 a halide, trifluoromethyl, ester, amide, or ether group, a heterocycle, or an unprotected alcohol or

144 ernal aliphatic alkyne bearing a propargylic ether group, different P411 variants can selectively cat

145 omethyl, ester, nitro, acetate, cyanide, and ether groups.

146 e range of functional group tolerance (e.g., ethers, halides, thioetheres, esters, etc.).

147 yielding synthesis of lamellarin G trimethyl ether has been achieved from precursors and solvents tha

148 boxylic acids with liquid ketones and cyclic ethers has been accomplished in minutes using t-butyl hy

149 Crown ethers have been used for increasing the solubilization

150 Recently, tri- and difluoromethyl ethers have received increasing attention and several in

151 The crown ether hosts induce the formation of host-guest complexes

152 In these assays, hydroxytyrosyl hexyl ether (HT C6) exhibited the most potent inhibitory activ

153 ential of six synthetic hydroxytyrosyl alkyl ethers (HT C1, C2, C4, C6, C8 and C12).

154 ciated with isoflurane, a potent halogenated ether in common clinical use.

155 tical studies reveal the involvement of CNMe ether in the formation of a six-membered imine-type cycl

156 ility of HFEs with the ionic conductivity of ethers in a single compound.

157 chlorine pesticides, polybrominated diphenyl ethers in fat, and perfluoroalkyl substances in plasma i

158 oimides leads to the synthesis of hemiaminal ethers in good to excellent yields at room temperature.

159 rine pesticides, and polybrominated diphenyl ethers in mothers ranged from 897 to 13620 ng/g wet weig

160 atural products such as naringenin trimethyl ether, in yields up to 92%.

161 mple route towards the synthesis of hindered ethers, in which electrochemical oxidation is used to li

162 rom 2-azaallyl anions to 2-iodo aryl allenyl ethers initiates a radical cyclization that is followed

163 t uses an organic redox mediator and a vinyl ether initiator, in contrast to metal-based initiators t

164 demonstrating that short exposure to diethyl ether is the most effective for long-term immobilization

165 lene skeletons from suitable propargyl vinyl ethers is based on a one-pot, multistep process entailin

166 ethodology for the synthesis of 4-quinolinyl ethers is demonstrated via a highly reactive S(N)Ar reac

167 ectrophotocatalytic C-H functionalization of ethers is described.

168 terogeneous catalytic hydrogenolysis of aryl ethers is important both in hydrodeoxygenation of fossil

169 ermodynamically less stable than its acyclic ether isomer (O-CF(3)).

170 ts showed an absence or reduction of two EOM ether isomers in seeds.

171 le total syntheses of lamellarin G trimethyl ether, lamellarin D trimethyl ether, lamellarin H, lamel

172 in G trimethyl ether, lamellarin D trimethyl ether, lamellarin H, lamellarin eta, dihydrolamellarin e

173 e outer hydrogel layer to acidic pH or crown ether leads to the triggered separation of the bridging

174 electivities observed with diether and amino ether ligands arise from favorable weak interactions bet

175 ion for the most efficient diether and amino ether ligands prove to be foreseeable by modeling the re

176 -catalyzed oxidative hydrolysis of the vinyl ether linkage of arachidonoyl-plasmalogens.

177 The ether linkage of C4-C5 in the morphinan ring leads to a

178 ha-keto and alpha-hydroxy beta-O-4 type aryl ether linkages of lignin.

179 uring lignin biosynthesis, resulting in less ether linkages that generate monomers.

180 zene and catechol building units, which form ether linkages.

181 henols upon irradiation via photocleavage of ether linkages.

182 mprovements were realized upon replacing the ether-linked amines with carbon-linked morpholines, a mo

183 The ether-linked diarylamine phenoxazine, one of the most po

184 Deficient ether lipid biosynthesis in rhizomelic chondrodysplasia

185 egrated technology enabled identification of ether lipid species preferentially enriched in germinal

186 rafficking and lipid biosynthesis, including ether lipid synthesis.

187 In both C. elegans and human cancer cells, ether-lipid synthesis protects against ferroptosis.

188 by dietary fats and indicate that endogenous ether lipids act to prevent this nonapoptotic cell fate.

189 scrimination between plasmanyl and plasmenyl ether lipids is a major analytical challenge, especially

190 c analysis showed a coordinate regulation of ether lipids with sphingolipids, suggesting an adaptatio

191 nt AD arising from lipid pathways including; ether lipids, sphingolipids (notably GM(3) gangliosides)

192 attributed to lack of plasmanyl or plasmenyl ether lipids.

193 saturase and therefore cannot form plasmenyl ether lipids.

194 look in synthesis of light olefins, dimethyl ether, liquid fuels, and alcohols through two leading hy

195 ng diads) and produces degradable poly(vinyl ether) materials with low dispersities and targetable mo

196 In this work, we discovered a new silyl ether metathesis reaction and used it for the preparatio

197 double bonds, side chains, glucose moiety or ether moiety in molecules influence the efficiency of po

198 the chelation of a readily removable benzyl ether moiety to direct gamma- or delta-C-H carbonylation

199 In the aryl ether moiety, substituents para to the nitrile demonstra

200 the cationic RAFT polymerization of a vinyl ether monomer bearing a secondary dormant RAFT agent, wh

201 ucture covalently linked to benzo-15-crown-5 ether motifs exhibit remarkable cooperative recognition

202 The addition of methyl tert-butyl ether (MTBE) as an organic phase not only increased the

203 rd EME system comprising 2-nitrophenyl octyl ether (NPOE) as SLM and 10 mM HCl as sample/acceptor sol

204 The addition of silyl enol ethers obtained from ynones to sulfinimines furnished th

205 Trimethylsilyl ethers of 1,5-diaryl-3-(trifluoromethyl)-pent-1-en-4-yn-

206 odular gram-scale syntheses of the trimethyl ethers of lamellarins G (6) and D (7) were achieved from

207 Poly(vinyl ethers) of molar masses exceeding 50 kg mol(-1) can be p

208 udies with synthetized 3beta,3'beta-disteryl ethers on endothelial cells were conducted.

209 solvents (carbonate, sulfone, phosphate, and ether) on the stability of high-voltage LMBs are systema

210 to borylate the C-H bond alpha to a benzylic ether or amine resulted in C-O and C-N borylation, follo

211 mbranoids, were proposed to contain a C3-C14 ether or lactone bridge, similar to asbestinins.

212 on of the photocaged diene (o-quinodimethane ether or thioether) with electron-deficient alkynes is i

213 The diene methyl ethers or acetates, constructed from the Li-Br exchange/

214 The ether oxygen atoms increase the bond dissociation energy

215 in-derived nanotracer with a perfluoro-crown ether payload ((19)F-HDL) to allow myeloid cell tracking

216 Prenatal polybrominated diphenyl ether (PBDE) exposures are a public health concern due t

217 d biphenyl (PCB) and polybrominated diphenyl ether (PBDE) residues and gene expression in embryonic l

218 ted biphenyl (PCBs), polybrominated diphenyl ethers (PBDEs) and induction of cytochrome's P450 (CYP1A

219 Polybrominated diphenyl ethers (PBDEs) are a type of flame retardants which are

220 Polybrominated diphenyl ethers (PBDEs) are brominated flame retardant chemicals

221 alkyl acids (PFAAs), polybrominated diphenyl ethers (PBDEs), and "novel" brominated flame retardants

222 l ethane (DBDPE), 13 polybrominated diphenyl ethers (PBDEs), and hexabromocyclododecane (HBCDD) were

223 ed biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and organochlorine pesticides (OCPs).

224 ed biphenyls (PCBs), polybrominated diphenyl ethers (PBDEs), and organochlorine pesticides) to compre

225 FR groups, including polybrominated diphenyl ethers (PBDEs), organophosphate FRs (OPFRs), and novel b

226 e of POPs, including polybrominated diphenyl ethers (PBDEs), polychlorinated biphenyls (PCBs), polych

227 e pesticides (OCPs), polybrominated diphenyl-ethers (PBDEs), polycyclic aromatic hydrocarbons (PAHs),

228 For polybrominated diphenyl ethers (PBDEs), this within-age temporal trend has been

229 tive toxins, such as polybrominated diphenyl ethers (PBDEs).

230 s simulations show a selective enrichment of ether phosphatidylcholine around p24 proteins, which are

231 r, our work reveals roles for the peroxisome-ether-phospholipid axis in driving susceptibility to and

232 ferroptosis by synthesizing polyunsaturated ether phospholipids (PUFA-ePLs), which act as substrates

233 cts who became psychotic had lower levels of ether phospholipids than CHR individuals who did not (p

234 For trans allylic olefins, the Z- and E-enol ethers proceed through chair and boat transition states,

235 on of unactivated alkenols to furnish cyclic ether products.

236 Unexpectedly, also benzyl ether protecting groups can engage in remote participati

237 complex heterocycles through oxime and oxime ether radical cation intermediates produced via PET.

238 predictions as to how the formation of oxime ether radical cations can be tuned by substituents.

239 ylbenzaldehyde and 2'-arylacetophenone oxime ether radical cations.

240 h electron-rich moieties (i.e., phenylene or ether) red-shifts both the SubPz absorption and emission

241 A single enzyme (benzyl ether reductase, encoded by the gene ber) was sufficient

242 C-O bond cleavage among functionalized aryl ethers relevant to energy science.

243 ulky cyclopropylmethyl-derived acetoxymethyl ether renders carboVF weakly fluorescent; we show that f

244 n methods to synthesize aryl trifluoromethyl ethers require harsh reagents and highly controlled reac

245 for the translation of isotactic poly(vinyl ether)s to applied areas.

246 ng access to a range of isotactic poly(vinyl ether)s with high degrees of isotacticity.

247 nzofuran-amide scaffold yielded a simplified ether series of inhibitors, utilizing acyclic conformati

248 regularity was found for analogous PGCs with ether side-chain substituents.

249 DFT calculations suggest crown ether sodium cation complexation induces a polarisation

250 tional theory indices characterize the crown ether solvated complex benzene-lithium Bz-Li-Cro as a su

251 on behavior of PFECAs is attributed to their ether structures.

252 orders of magnitude, depending on the silyl ether substituents.

253 -donating methyl, methoxy, dimethoxy, benzyl ether-substituted iodo-benzenes, other iodoarenes, such

254 nstrate that this method is general to vinyl ether substrates, providing access to a range of isotact

255 fluorosulfonic acids and homologues of alkyl ether sulfates (C(8)- and C(10)/EO(n), C(8)H(17)(C(2)H(4

256 l ethoxylates, ethoxylated cocoamines, alkyl ether sulfates, alkyl amido dipropionates, linear alkyl

257 red coating fetal bovine serum onto the poly(ether sulfone) microdialysis membrane.

258 eaction and streamlined syntheses of complex ether, sulfone, and tertiary amine products, some of whi

259 roduction site in the CFRE: a perfluorinated ether sulfonic acid (Nafion byproduct 2; range: 1-110 ng

260 ent strategies: (i) ester condensation, (ii) ether synthesis, and (iii) ring closing metathesis.

261 ed monomer, triethylene glycol divinylbenzyl ether (TEG-DVBE), with urethane dimethacrylate (UDMA) or

262 (6) and 10(9) (e.g., polybrominated diphenyl ethers), the relative importance of near- and far-field

263 oids, a mild and general method of preparing ether, thioether, and amine analogues of galiellalactone

264 nal- and internal alkynes, ynamides, alkynyl ethers/thioethers, and even unsubstituted acetylene (40

265 s permitted the elusive synthesis of diethyl ether through reductive elimination, a remarkable featur

266 the protecting group strategy, from an alkyl ether to a bidentate ketal at the carbohydrate backbone

267 )(0.50) have been prepared by adding diethyl ether to a dichloromethane solution containing equimolar

268 ere oxidized to aldehydes or ketones, cyclic ethers to esters, and terminal diols to lactones.

269 Herein, we employ crown ethers to modulate perovskite films, affording passivati

270 aryl ethers, aryl pyridyl ethers, aryl silyl ethers), to phenolate salts, and ultimately to simply un

271 , by using a mixture of sodium powder, crown ether, trimethylsilyl bromide and N(2) as the nitrogen s

272 ent (I-CF(3), I-SCF(3)) to the corresponding ether-type form (O-CF(3), O-SCF(3)).

273 H) /k(D) =5.7) for the reactions of diphenyl ether under H(2) and D(2) atmosphere and a positive depe

274 controlled cationic polymerization of vinyl ethers under ambient conditions with excellent monomer c

275 ynthesis of high-molecular-weight poly(vinyl ethers) under mild conditions is a significant challenge

276 s from ECH reactions confirm that these aryl ethers undergo C-O cleavage via distinct paths.

277 Azidoalkyl enol ethers undergo intramolecular 1,3-dipolar cycloaddition

278 Ethers undergo oxidant-free coupling with isoquinolines,

279 them in tubing composed of hydrophilic poly(ether-urethane) -.

280 intramolecular hydroarylation of allyl aryl ethers using an amide directing group for the preparatio

281 ate the first example of ROMP of cyclic enol ethers, using 2,3-dihydrofuran as the monomer, producing

282 ens contain a characteristic 1-O-alk-1'-enyl ether (vinyl ether) double bond that confers special bio

283 The EOM ether was remarkably increased in CsANRa and CsMYB5b tra

284 functionalization of allyl and benzyl silyl ethers was achieved using rhodium(II) carbenes derived f

285 While attempting to synthesize biaryl ethers we discovered the inadvertent formation of a meth

286 1,2-Cyclohexanediamine, -diether, and -amino ether were compared as chiral inducers in the asymmetric

287 tative analyses of the 3beta,3'beta-disteryl ethers were conducted using liquid extraction, solid-pha

288 inal structures of briarellin and asbestinin ethers were confirmed.

289 ates with allyltrimethylsilane or silyl enol ethers were developed.

290 Both kaempferols and carboxymethoxy ethers were evaluated for their ability to inhibit ribos

291 Ethylene glycol-derived, oligomeric ethers were found to function as the formylating agent,

292 Aliphatic ethers were oxidized by this method, as demonstrated by

293 alcohols, acetates, aldehydes, ketones, and ethers were produced in the reactive stage using a 3.3 M

294 pound as an (-)-epicatechin-4-O-methyl (EOM) ether, which resulted from (-)-epicatechin carbocation a

295 new application area of difluoro enol silyl ethers, which can be easily obtained from trifluoromethy

296 d annulation of alpha,beta-unsaturated oxime ether with alkyne has been reported.

297 variety of delta-functionalized allyl silyl ethers with high diastereo- and enantioselectivity.

298 e strategy enables 1:1 interactions of crown ethers with various functional groups to be characterize

299 d the preparation of an isotactic poly(vinyl ether) with the highest stereoselectivity (95.1% +/- 0.1

300 ics, such as chloroform, isoflurane, diethyl ether, xenon, and propofol, disrupt lipid rafts and acti