ライフサイエンスコーパス: iodide

1 7% (decay-corrected to starting (11)C-methyl iodide).

2 ty reagent (organometallic reagents or alkyl iodides).

3 lactoferrin whilst iodine was only found as iodide.

4 selenides, using catalytic amounts of copper iodide.

5 nes without the involvement of free hydrogen iodide.

6 lk, 80-93% of the total iodine was inorganic iodide.

7 ymerization, yielding a well-defined polymer-iodide.

8 nd then an insoluble final product magnesium iodide.

9 concentration of more-reactive alkyl bromide/iodide.

10 d in the order bromide < nitrite < nitrate < iodide.

11 yroid uptake of iodide independently of free iodide.

12 (4:4) halogen bonding between I(4) Q(-.) and iodide.

13 oid drugs, surgical thyroidectomy, or (131)I-iodide.

14 cting the phenol precursor with (11)C-methyl iodide.

15 f its phenol precursor 25 with [(11)C]methyl iodide.

16 de elimination directly from the Pd(II)alkyl iodide.

17 le an alpha-quaternary aldehyde with a vinyl iodide.

18 th the complex Au(I)(PPh(3)) in place of the iodide.

19 of E-alkenes from terminal alkynes and alkyl iodides.

20 fluorinated halo-acetates and perfluoroalkyl iodides.

21 le-directed sp(3) C-H bond arylation by aryl iodides.

22 this reaction, along with select heteroaryl iodides.

23 m the corresponding alpha-substituted methyl iodides.

24 lyzed coupling of terminal alkynes with aryl iodides.

25 g, and the first Kumada coupling of tertiary iodides.

26 ilicon electrophiles, and primary alkyl zinc iodides.

27 d us to probe the effect of hole trapping at iodide (0.9 V) and bromide (1.15 V) in mixed halide pero

28 nes are catalyzed by the C(2)-symmetric aryl iodide 1 to provide access to enantioenriched 1,3-difluo

29 first time, 1,2-dimethyl-3-ethylimidazolium iodide (1a) catalyzes the ring opening of the bicyclic a

30 ovskites such as (2D)-phenethylammonium lead iodide (2D-PEPI) have layered structure that resembles m

31 (185 mg/l) or water supplemented with sodium iodide (500 mg/l) that contained (16 mice) or did not co

32 s methylcobalamin and is inhibited by propyl iodide, a specific inhibitor of cobalamin-dependent enzy

33 n the products and the cheap trifluoromethyl iodide acts as the oxidant in these C-C couplings.

34 Reduction of the aluminum iodide AlI(2)Ar(iPr8) (1; Ar(iPr8) = C(6)H-2,6-(C(6)H(2)

35 rain engineering of alpha-formamidinium lead iodide (alpha-FAPbI(3)) using both experimental techniqu

36 t 2-(alpha-naphthoyl) ethyltrimethylammonium iodide (alpha-NETA) that significantly suppressed diseas

37 new isostructural (TDMP)PbX(4) chloride and iodide analogues could be synthesized and structurally c

38 Nearly all of the iodine in cow milk is iodide and although fractional iodine absorption from mi

39 ation were measured using the dyes propidium iodide and bis-(1,3-dibutylbarbituric acid) trimethine o

40 Depending on the amount of copper iodide and diorganyl diselenide used in the reactions, m

41 ch as dicumyl peroxide, heptafluoroisopropyl iodide and diphenyl disulfide.

42 e, hydrogen peroxide, human serum, potassium iodide and doxorubicin/ oxaliplatin for both ex vivo and

43 1 - 2921 ) by reducing the amount of lithium iodide and exclusion of pivalic acid.

44 The nickel catalyst activates the alkyl iodide and promotes cross coupling with the alkenyl copp

45 the fragmentation of photoexcited iso-propyl iodide and tert-butyl iodide molecules (i-C(3)H(7)I and

46 e is based on the use of catalytic copper(I) iodide and trans- N, N'-dimethylcyclohexane-1,2-diamine

47 n in a nonpolar solvent to produce a polymer-iodide and was subsequently used as a substitution agent

48 action of alpha-heteroatom substituted alkyl iodides and -bromides with vinyl arenes/heteroarenes has

49 Readily available (hetero)aryl halides (39 iodides and 4 bromides) and inexpensive MeOTs or trimeth

50 A wide range of functional groups on alkyl iodides and alkenyl acetates are well tolerated, thus fu

51 alkyl radicals generated from perfluoroalkyl iodides and alkylpyridinium salts, respectively, with ho

52 n provides good yields using a range of aryl iodides and aryl bromides including functionalized examp

53 re competent in these couplings whereas aryl iodides and bromides cannot serve as the coupling partne

54 ayers of I(4) Q(-.) anion radicals linked by iodides and separated by Et(4) N(+) counter-ions.

55 re enabled by direct annulation between aryl iodides and unsaturated carboxylic acid anhydrides.

56 on donor of compound I, whereas thiocyanate, iodide, and bromide efficiently restore the ferric resti

57 oupling between non-conjugated alkenes, aryl iodides, and alkylzinc reagents is reported.

58 nes from readily available 1,3-dienes, alkyl iodides, and amines.

59 s-coupling of alkenyl carboxylic acids, aryl iodides, and aryl/alkenyl boronic esters is reported.

60 ng reaction between methyl, aryl, heteroaryl iodides, and sp(2) carbons both at beta- and gamma-posit

61 enzoquinone anion radicals (I(4) Q(-.) ) and iodide anions, was observed and characterized for the fi

62 Propidium iodide/annexin assays and caspase 3, caspase 7, and PARP

63 ,4-diene-based surrogate of gaseous hydrogen iodide are described.

64 en developed, wherein a beta amine and gamma iodide are incorporated onto an aliphatic alcohol in a s

65 A diverse range of aryl iodides are tolerated in this reaction, along with selec

66 ral functional groups including bromides and iodides are tolerated under the reaction conditions.

67 toxic iodine(III)-based oxidant and ammonium iodide as a cheap iodine atom source.

68 The results show how use of iodide as an electrochemical mediator, in combination wi

69 eported, achieved using simple primary alkyl iodides as initiators.

70 tioselective radical cyclization using alkyl iodides as precursors to unstabilized nucleophilic radic

71 lly, although the use of electron-rich alkyl iodides as radical precursors was found to be ineffectiv

72 ated halide levels from geogenic bromide and iodide, as well as enhanced formation of brominated and

73 brane interactions by performing a propidium iodide assay and fluorescence microscopy of supported MR

74 a unique Pd(I)-Pd(I) mechanism, involving an iodide-assisted binuclear step to release the product.

75 tivity-specifically the electro-oxidation of iodide at polycrystalline platinum-reveals unique (i.e.,

76 ons of arylmagnesium halides with cyclohexyl iodides at ambient temperature has been developed.

77 Here we use 5-ammonium valeric acid iodide (AVAI) to chemically stabilize the structure of a

78 a promising adjunctive therapy for restoring iodide avidity within the full spectrum from RAI-refract

79 report the use of quasi-3D azetidinium lead iodide (AzPbI(3)) as a secondary layer on top of the pri

80 stigating the behaviour of two types of lead-iodide based single crystals, we here highlight the extr

81 ar absorbers-including high-performance lead-iodide-based perovskites-and demonstrate simultaneous ac

82 ntal evidence for the WTI state in a bismuth iodide, beta-Bi(4)I(4).

83 compounds, BIX01294, CP-31398, and propidium iodide, bind directly to the repeat RNAs.

84 se segregation, resulting in a change in the iodide/bromide ratio compared with the precursor stoichi

85 th a variety of aryl and heteroaryl halides (iodides, bromides) is reported that overcomes the limita

86 es the synthesis of a broad range of alkenyl iodides, bromides, and chlorides under mild reaction con

87 In a comparative investigation, aryl iodides, bromides, and triflates were shown to be inferi

88 preparation of families of valuable organic iodides, bromides, chlorides, and fluorides.

89 step is the iodine abstraction from an alkyl iodide by (.) Mn(CO)5 .

90 sent in ICM formulations, in vitro uptake of iodide by NIS-expressing cells was not significantly aff

91 kenylcopper intermediate activates the alkyl iodide by single electron transfer to enable a radical c

92 iously unknown or difficult-to-prepare vinyl iodides can be accessed in stereocontrolled fashion.

93 athways are promoted by the same chiral aryl iodide catalyst with high enantioselectivity provides a

94 Coulomb explosion of fully deuterated methyl iodide, CD(3)I, irradiated with hard X-rays has been exa

95 ive surface of perovskite films with cadmium iodide (CdI(2)) effectively reduces the degree of surfac

96 n focuses principally on methylammonium lead iodide (CH(3)NH(3)PbI(3) or MAPbI(3)), which serves as a

97 brid perovskites such as methylammonium lead iodide (CH(3)NH(3)PbI(3)) are game-changing semiconducto

98 Formamidinium lead iodide (CH(NH(2))(2)PbI(3), FAPI) thin films have been d

99 lide perovskites such as methylammonium lead iodide (CH3NH3PbI3) are generating great excitement due

100 hot-carrier migration in methylammonium lead iodide (CH3NH3PbI3) thin films by ultrafast transient ab

101 ng reaction, leading to alkoxylation of aryl iodides complete at room temperature.

102 f tertiary amides by a sodium hydride/sodium iodide composite, in situ treatment of the resulting ani

103 hioates by a strong base and a primary alkyl iodide constitutes an alternate route to the formation o

104 ternized and subsequently ring-opened by the iodide counterion.

105 chiral copper catalyst, substituted allylic iodides couple with alpha-diazoesters to generate metal-

106 The emergence of cesium lead iodide (CsPbI(3) ) perovskite solar cells (PSCs) has gen

107 Cesium lead iodide (CsPbI(3)) perovskite has shown great potential a

108 ds were obtained when using simple copper(I) iodide (CuI) as the catalyst.

109 ngle crystal epitaxy of high quality cuprous iodide (CuI) film grown on Si and sapphire substrates by

110 (3) formation - this process is important in iodide deficiency and in Graves disease.

111 Selected thioantimonate iodides demonstrate good compatibility with Li metal, su

112 lling in hydrogen-bond rearrangements in the iodide-dihydrate complex and show that it can be control

113 ack to the presence of a free OH bond in the iodide-dihydrate complex, which effectively triggers the

114 demonstrate the first example of a 2D Ag-Bi iodide DP with a direct bandgap of 2.00(2) eV, templated

115 Using a live cell-based propidium iodide dye exclusion assay and flow cytometry, GB was fo

116 s the highest anion-transport activities for iodide (EC(50) =0.042 mum or 0.028 mol % relative to lip

117 becomes homogenized upon addition of cesium iodide, either alone or with rubidium iodide, for substo

118 opper-catalyzed coupling of uracil with aryl iodides, employing picolinamide 16 as the ligand, was di

119 hat hot holes stabilized by surface adsorbed iodide enable the site-selective oxidative etching of Au

120 It is found that lead iodide exhibits a very fast and intense scintillation re

121 nt absorption spectroscopy revealed that the iodide expulsion process leaves a defect-rich perovskite

122 th methylammonium iodide (MAI)/formamidinium iodide (FAI) (FAI is studied hereafter).

123 3) (MAPbI(3) ), 10.1% for formamidinium lead iodide (FAPbI(3) ), and 11.3% for formamidinium lead bro

124 (NHE) of high-quality formamidinium-lead-tri-iodide (FAPbI(3)) perovskite films.

125 g method for synthesizing formamidinium lead iodide (FAPbI3) perovskite solar absorbers.

126 dot and (ferrocenylmethyl) trimethylammonium iodide (Fc(+)), a photo-induced electron transfer (PET)

127 The polysulfide/iodide flow battery with the graphene felt-CoS(2)/CoS he

128 ylative coupling of the alkyne and the alkyl iodide, followed by reduction of the intermediate unsatu

129 a favorable energetics only for the loss of iodide following the oxidative addition of PhI on the Ni

130 mising protocol using visible light and aryl iodides for constructing valuable building blocks, inclu

131 cesium iodide, either alone or with rubidium iodide, for substoichiometric, stoichiometric, and overs

132 Moreover, they appear to work against iodide formation.

133 of the 2D passivation layers based on a lead iodide framework.

134 Abstraction of iodide from [(eta(5) -C(5) (i) Pr(5) )(2) UI] (1) produc

135 site in the MHP induces instability causing iodide from the lattice to move away toward grain bounda

136 EeAChE) and competitively displace propidium iodide from this site.

137 etical methods.Capturing radioactive organic iodides from nuclear waste is important for safe nuclear

138 These nucleoside analogs bearing an iodide functional group handle allow for rapid transform

139 gle crystals of perovskite-phase cesium lead iodide (gamma-CsPbI(3)) that are kinetically stable at r

140 data indicate that anodic oxidation of aryl iodides generates a transient I(II) intermediate that is

141 of the phenolic precursor with (11)C-methyl iodide, giving a radiochemical yield of 51.7% +/- 4.7% (

142 Upon trapping holes at the iodide site, the iodide gradually gets expelled from the mixed halide fil

143 ally enhances the recognition of bromide and iodide halide anions, with the chalcogen bonding heterod

144 g of terminal alkynes with unactivated alkyl iodides has been developed, enabling highly chemo- and r

145 ng of benzylamines, boronic esters, and aryl iodides has been investigated.

146 tron spectroscopic study on the archetypical iodide-hexafluorobenzene anion-pai bonded complex.

147 However, the propidium iodide/Hoechst assay gives morphological information abo

148 nation of the sulforhodamine B and propidium iodide/Hoechst assays would provide the most accurate qu

149 rtant roles in the immobilization of aqueous iodide (I(-)) and iodate (IO(3)(-)) in the environment,

150 Bromide (Br(-)) and iodide (I(-)) are common in many source waters, enhancin

151 ide effect is thought to be mediated by free iodide in ICM formulations, but this hypothesis has neve

152 own observed in the first hydration shell of iodide in solution, can be traced back to the presence o

153 her with terminal alkynes and perfluoroalkyl iodides in the presence of carbon monoxide.

154 oronates react with electron-deficient alkyl iodides in the presence of visible light to give boronic

155 ydes undergo coupling with a variety of aryl iodides, including less reactive iodo pyridine derivativ

156 monstrated that ICM reduce thyroid uptake of iodide independently of free iodide.

157 ein from DMPG/DMPC vesicles and by propidium iodide influx experiments on S. epidermidis.

158 ompeting roles for ion hydration and polymer-iodide interactions.

159 ups are involved in cation-cation and cation-iodide interactions.

160 Cys168 is proposed to attack the selenenyl iodide intermediate to regenerate Dio3 based upon struct

161 hat the QDs transfer energy to a Pd(II)alkyl iodide intermediate, pushing the reaction toward a Pd(I)

162 the absorption spectrum of a key Pd(II)alkyl iodide intermediate, the reaction proceeds with 82% yiel

163 starting material via formation of an allyl iodide intermediate.

164 ht-promoted iodination is used to form alkyl iodide intermediates from simple unreactive alcohols.

165 The titration of iodide into acetonitrile solutions of BiI3 resulted in t

166 We find that the iodide ion weakens the neighbouring water-water hydrogen

167 Here we show that iodide ions in the methylammonium lead iodide migrate vi

168 hing proceeding of AuNPLs by copper ions and iodide ions leads to the gradually blue-shifted LSPR sca

169 s, the analysis presented here suggests that iodide ions may accelerate hydrogen-bond rearrangements

170 netics of the redox reactions of polysulfide/iodide ions on graphite electrodes, which has become the

171 the electrolyte, which eliminates most free iodide ions, thus preventing the consequent dissolution

172 ~10(3) ) and to a lesser extent fluoride and iodide ions.

173 orhexidine gluconate (CHX), iodine-potassium iodide (IPI) and Sodium hypochlorite (NaOCl) both experi

174 rubicin (DOX) (an anticancer drug) and IR780 iodide (IR780) (an NIR-absorbing dye) into nanoparticles

175 Methyl iodide is a toxic halocarbon with diverse industrial and

176 Regeneration of the oxidized sensitizer by iodide is enhanced through halogen bonding, orbital path

177 a moderately strong Bronsted acid, hydrogen iodide is transferred from the surrogate onto C-C multip

178 yl)iodonium trifluoroacetate salts from aryl iodides is described.

179 ation of nitroalkanes with unactivated alkyl iodides is described.

180 oronic esters with carboxylic acids and aryl iodides is described.

181 oupling between alpha-chloro esters and aryl iodides is developed.

182 ss-coupling of styrenyl aziridines with aryl iodides is reported.

183 ines and commercially available (hetero)aryl iodides is reported.

184 ficial seawater (AS) than buffered potassium iodide (KI) solutions.

185 ative iodine, with the addition of potassium iodide (KI) to assess a potential matrix effect; and 3)

186 cyl-3,3,3',3'-tetramethylindotricarbocyanine iodide)-labeling showed improved retention of 3D CPCs.

187 ic or heteroaromatic and an alkyl bromide or iodide leads, in the presence of Zn and a catalytic amou

188 Rapid SYBR green I/propidium iodide live/dead microbial cellular discrimination assay

189 ansion and fast reaction with methylammonium iodide (MAI)/formamidinium iodide (FAI) (FAI is studied

190 ymers are doped into the methylammonium lead iodide (MAPbI(3) ) layer and/or inserted between the per

191 ted by QA, PSCs based on methylammonium lead iodide (MAPbI(3) ) showed significantly improved perform

192 m as capping layers onto methylammonium lead iodide (MAPbI(3)) films, age them under accelerated cond

193 potential of the hybrid Methylammonium lead iodide (MAPbI(3)) perovskite-based semiconductor detecto

194 ction (for example, from methylammonium lead iodide, MAPbI(3), to MAPb(0.5)Sn(0.5)I(3)).

195 trinsic doping surges in methylammonium lead iodide (MAPbI3) crystals as a response to environmental

196 he typical 3D perovskite methylammonium lead iodide (MAPI); direct evidence for the chemical source o

197 In this context, the role of iodide-mediated ozone (O3) deposition over seawater and

198 that iodide ions in the methylammonium lead iodide migrate via interstitial sites at temperatures ab

199 is challenge by creating radioactive organic iodide molecular traps through functionalization of meta

200 hotoexcited iso-propyl iodide and tert-butyl iodide molecules (i-C(3)H(7)I and t-C(4)H(9)I) through a

201 eport the effective synthesis of the highest iodide n-members yet, namely (CH(3)(CH(2))(2)NH(3))(2)(C

202 ermined KI compare to different alkali metal iodides: NaI, RbI, CsI; also investigation of different

203 ovskite, n-butylammonium methylammonium lead iodide (nBA-MAPI), compared to that of MAPI, and examine

204 ation of different potassium salts (acetate, iodide, nitrate, chloride, dihydrophosphate, perchlorate

205 ve addition of geometrically defined alkenyl iodides occurs readily, reversibly and stereospecificall

206 anions in solutions of p-benzoquinones with iodide or (for the strongest acceptor) bromide donors.

207 oss-coupling is the use of a small amount of iodide or bromide along with a recently reported ligand,

208 ction avoids precarious handling of hydrogen iodide or hydroiodic acid.

209 table salt is often fortified with potassium iodide or iodate.

210 chiometrically with I(2) to form either aryl iodides or beta-lactams within minutes at room temperatu

211 carbonylative coupling of cyanamide and aryl iodides or bromides.

212 blishing the different binding modes of aryl iodides, our results chart a path to actively controllin

213 rior scope for both ketones and (hetero)aryl iodides overcome the significant limitations of the prev

214 Conversely, reversible alkynyl iodide oxidative addition generates bimetallic complexes

215 rt a novel strontium-substitution along with iodide passivation strategy to stabilize the cubic phase

216 Excess/unreacted lead iodide (PbI(2) ) has been commonly used in perovskite fi

217 Lead Iodide (PbI(2)) is a large bandgap 2D layered material t

218 as cesium lead bromide (CsPbBr(3)), lead(II) iodide (PbI(2)), zinc oxide (ZnO), and sodium chloride (

219 e the surface of a formamidinium-cesium lead iodide perovskite (Cs(0.08) FA(0.92) PbI(3) ) and also r

220 d for the nanoscale thienylethylammonium tin iodide perovskite (TEA(2)SnI(4)).

221 LQY than the standard 3D methylammonium lead iodide perovskite although this is accompanied by increa

222 The best-performing tin iodide perovskite cells employing the novel mixed-cation

223 layer between TiO(2) and methylammonium lead iodide perovskite is probed to reduce the current-voltag

224 rent polymer films and a methylammonium lead iodide perovskite layer was used as basis for modelling

225 t and the photoluminescent properties of tin iodide perovskite nanodisks.

226 Herein, we report that cesium lead iodide perovskite quantum dots (CsPbI3 QDs) can be used

227 erlattice-like Ruddlesden-Popper hybrid lead iodide perovskite semiconductors, 2D (BA)(2)(MA)Pb(2)I(7

228 n compared to any other reported layered tin iodide perovskite.

229 the crystal structure of benzylammonium lead iodide perovskites (4-XC(6)H(4)CH(2)NH(3))(2)PbI(4) (X =

230 cation engineered 2D Ruddlesden-Popper lead iodide perovskites (BA)(2)(EA(x)MA(1-x))(2)Pb(3)I(10) (x

231 Lead iodide perovskites show an increase in band gap upon par

232 Here we present three new layered tin iodide perovskites templated by chiral (R/S-)methylbenzy

233 antum efficiency of nanoscale 2D layered tin iodide perovskites through fine-tuning the electronic pr

234 y responsible for photosensitization of aryl iodides (photoexcitation by 254 nm UV light) with blue L

235 on bromodeoxyuridine (BrdU) assay, propidium iodide (PI) staining and growth curves, and blocks cell

236 designed bifunctional molecule, piperazinium iodide (PI), containing both R(2)NH and R(2)NH(2)(+) gro

237 portant role, as it distorts the neighboring iodide positions from their centrosymmetric positions.

238 indicated by the reduced number of propidium iodide-positive cells and the cleavage of caspase-3 and

239 th was necrosis by trypan blue and propidium iodide positivity, absence of mitochondrial death pathwa

240 luding secondary alpha-amino acids, and aryl iodides provides efficient access to highly functionaliz

241 Kosower's salt, 1-methylpyridinium iodide, provides an early outer-sphere charge-transfer e

242 rming organic halide, phenyltriethylammonium iodide (PTEAI), successfully extends the MAPbI(3) stabil

243 Herein, a new reaction of an alkyl iodide (R-I) with an azide anion (N3(-)) to reversibly g

244 organolithium reagent derived from the alkyl iodides (R)- or (S)-30, which contain the C11-C13 atoms

245 ide symporter (hNIS) expression, radioactive iodide (RAI) therapy is ineffective.

246 l ionization mass spectrometer equipped with iodide reagent ion chemistry (I-HR-ToF-CIMS).

247 Aqueous polysulfide/iodide redox flow batteries are attractive for scalable

248 mination leads to localized surface sites of iodide-rich perovskite intermixed with passivating PbI(2

249 arges efficiently transfer to the passivated iodide-rich perovskite surface layer, leading to high lo

250 hese conditions are a result of nucleophilic iodide ring opening of the aziridine to generate an iodo

251 ntroduced as the N and O source and a simple iodide salt can be utilized as the catalyst.

252 compared to the conventional tracer [(123)I]iodide (sequential SPECT/CT).

253 Localization of holes on the iodide site in the MHP induces instability causing iodid

254 ollowing the hole trapping (oxidation of the iodide site) and its expulsion from the lattice in the f

255 Upon trapping holes at the iodide site, the iodide gradually gets expelled from the

256 performance is also achieved for cesium tin iodide solar cells with en loading, demonstrating the br

257 Inkjet cartridges were filled with potassium iodide solutions (600 mg/mL) and prints were realized on

258 rt for cooperative hydrogen-bond dynamics in iodide solutions, the analysis presented here suggests t

259 The selective mobility of iodide species provides insight into the photoinduced ph

260 ubstrates with a preference for forming aryl iodide species; this has potential implications for the

261 has been determined via Annexin V/Propidium iodide stain and flow cytometry.

262 th rRNA transcription, as shown by propidium iodide staining and BrUTP incorporation.

263 molytic cleavage of the C-I bond in the aryl iodide substrates.

264 ntiation, including the loss of human sodium iodide symporter (hNIS) expression, radioactive iodide (

265 Anion transport by the human sodium-iodide symporter (hNIS) is an established target for mol

266 PET radioligand for imaging the human sodium/iodide symporter (hNIS).

267 lymerase chain reaction for gal-3 and sodium-iodide symporter (NIS) expression.

268 The sodium iodide symporter (NIS) is required for iodide uptake, wh

269 l of hypothyroidism: mice lacking the sodium/iodide symporter (NIS), the plasma membrane protein that

270 n of TTF1 increased thyroglobulin and sodium/iodide symporter mRNA levels, cell migration, and prolif

271 tomography imaging of the hNIS (human sodium/iodide symporter) to noninvasively quantify adeno-associ

272 reagents that incorporate a photolabile aryl iodide that is selectively activated by laser irradiatio

273 h3 ]X, X=Cl and I showed that in the case of iodide, thermodynamics prevents the production of benzen

274 y PhI(OAc)(2)/I(2), gives rise to an acyclic iodide through which a pentavalent atom of phosphorus ca

275 s, which can be N-deprotected using samarium iodide to generate the free 1-arylisoindolinones.

276 iazabicyclooctane and tetra(n-butyl)ammonium iodide to halothane solutions, indicating that nitrogen

277 ar solvent, thereby transforming the polymer-iodide to polymer-N3 in one pot.

278 The confusion regarding the bonding of aryl iodides to Au electrodes is a case in point, with ambigu

279 ar oxidative addition of alkenyl and alkynyl iodides to Au(I) are reported.

280 n approaches, this method allows simple aryl iodides to be used as substrates with complete control o

281 An umpolung 1,4-addition of aryl iodides to enals promoted by cooperative (terpy)Pd/NHC c

282 work employed the oxidative addition of aryl iodides to Me-DalphosAu(+) for the formation of a Au(III

283 tably, even in cholesterol-rich environment, iodide transport activity remains high with an EC(50) of

284 thyroid hormone biosynthesis, including the iodide transporters Nis and Pds, both of which showed en

285 roxide in the presence of tetrabutylammonium iodide under microwave irradiation in the absence of a s

286 Treatment with an aryl iodide under palladium catalysis leads to rearomatizing

287 ectron deficient radicals derived from alkyl iodides under visible light irradiation add to the centr

288 fferentiation and concomitant restoration of iodide uptake in RAI-refractory papillary and follicular

289 plasma membrane protein that mediates active iodide uptake in the thyroid.

290 Perturbation of thyroid iodide uptake is a well-documented side effect of the us

291 odium iodide symporter (NIS) is required for iodide uptake, which facilitates thyroid hormone biosynt

292 bits high capacities for radioactive organic iodides uptake.

293 2) )(4-x) ](2-x) superhalide ions serving as iodide vehicles in the electrolyte, which eliminates mos

294 tho thiolation of common aryl and heteroaryl iodides via palladium-norbornene cooperative catalysis.

295 Although free iodide was present in ICM formulations, in vitro uptake

296 irconation/iodine quench afforded an alkenyl iodide which is employed in the NHK coupling with the C7

297 20%, normally employ methylammonium lead tri-iodide with a sub-optimal bandgap.

298 formate-mediated reductive coupling of aryl iodides with aldehydes occurs in a chemoselective fashio

299 ed for a series of linear and branched alkyl iodides with increasing structural complexity by means o

300 tage aminocarbonylation of unactivated alkyl iodides with stoichiometric amounts of carbon monoxide i

301 Translation of mixed-metal DPs to iodides, with their prospectively lower bandgaps, repres