ライフサイエンスコーパス: salt

1 -quality Si films from a CaCl2 -based molten salt.

2 and NHC generated from the chiral triazolium salt.

3 electrodes by electroreduction of diazonium salt.

4 stabilized with a quaternary ammonium halide salt.

5 g layer could be compressed upon addition of salt.

6 , but this was suppressed by the addition of salt.

7 rose and another context with less-desirable salt.

8 midine ions compared to the system with only salt.

9 organic compounds, and often, high levels of salts.

10 han the diameters of hydrated ions of common salts.

11 positive effects in OA induced by persulfate salts.

12 neri strain 2457T following exposure to bile salts.

13 compounds such as sugars, organic acids and salts.

14 rimidin-1,3-diium and pyrimidinium-2-ylidene salts.

15 an theory and the observed high rejection of salts.

16 2.0), temperature (5 to 75 degrees C), ionic salts (2.0 M LiCl, NaCl, and KCl), as well as in the pre

17 1,3,5-naphthalenetrisulfonic acid hexasodium salt), a structural analog of suramin, has an increased

18 ty of the epithelial Na(+) channel (ENaC) in salt-absorbing epithelia in the kidney, lung, and other

19 benzo-thiazoline-6-sulfonic acid) diammonium salt (ABTS(+)), Fe(III) reducing ability (FRAP) and lino

20 on the composition and concentration of the salt/acidic-methanol solutions.

21 on pressure, number of extraction cycles and salt addition.

22 degrees C using tri-distilled water without salt, adjusted pH of 5.4 and a flow rate of 0.36mL/min.

23 suggest that snow deposition, scavenging sea-salt aerosol bound PFAS, plays a role as a significant i

24 iffusion of Et2O into CH3CN solutions of the salts afforded X-ray quality crystals of five compounds

25 kyl halide precursors and simple borohydride salts, alkyl radicals can be generated in aqueous soluti

26 nitroxide free radicals and the oxoammonium salts, along with TEMPO and its oxoammonium salt, have b

27 CFA, calcium nanoparticles, and calcium salts also activated transient receptor potential vanill

28 membrane to be very efficient with up to 96% salt and 47% other dissolved solids removed while retain

29 role in the distal colon, which also absorbs salt and fluid and expresses ENaC, is unknown.

30 methylthioadenosine 5'-diphosphate trisodium salt and MRS2365 (5'-diphosphates) in some signaling eve

31 ved metabolomics measurements in yeast under salt and pheromone stimulation and developed a machine l

32 salT and salA were significantly elevated in PCOS compar

33 , spherical colloidal silica particles using salt and surfactant additives and that more pronounced o

34 ived aminophosphine ligand for the silver(I) salt and the 2-bis(aryl)methylpyrrolidine catalyst which

35 ine to phosphorus in DNA), are stable in low salt and up to tenfold more resistant to DNase I digesti

36 of PCR-inhibiting reagents (e.g., chaotropic salts and alcohol) and (ii) the washing and elution step

37 to various environmental cues, such as bile salts and alkaline pH, but how these factors influence T

38 , we define mechanisms of resistance to bile salts and build on previous research highlighting induce

39 e process uses commercially available cobalt salts and chiral ligands.

40 es are converted into heteroaryl phosphonium salts and coupled with aryl boronic acids.

41 tentially predicting sensitivity to platinum salts and PARP inhibitors, the data regarding somatic mu

42 promote HR and confer resistance to platinum salts and PARP inhibitors.

43 st the reaction is catalyzed by trace copper salts and that a Z- to E-hydrazone isomerization occurs

44 Three new homologous TEMPO oxoammonium salts and three homologous nitroxide radicals have been

45 dox equilibrium as shown between oxoammonium salts and trace amounts of corresponding nitroxide.

46 g., tetraalkylammonium cyanide and phenoxide salts) and fluorine-containing electrophiles (e.g., acid

47 unknown transducer elements underlying sour, salt, and other taste qualities, given the staged expres

48 heat treatment temperature, type of lithium salt, and physical state of the precursors (powder or pe

49 ess physically active and consume more fats, salt, and processed food than individuals of low socioec

50 table at varying pH and in various solvents, salts, and chemicals.

51 gene, SsMT2, was cloned from Suaeda salsa, a salt- and alkali-tolerant plant, which is dominant speci

52 Salt appetite, in which animals can immediately seek out

53 imidazolium, quinolinium, and isoquinolinium salts are accessible in 1-2 steps from the commercial ar

54 N-Methoxy imidazolium salts are accessible in three steps from commercial amin

55 Organic molecular salts are an emerging and highly tunable class of materi

56 secondary and tertiary radicals to pyidinium salts are documented: harder secondary radicals favor C-

57 The bromo- and chloroxenate salts are stable in the atmosphere at room temperature a

58 Aluminum hydroxide (AH) salts are the most widely used adjuvants in vaccine form

59 ilic substitution reaction between aryl-BF3K salts (aryl = mesityl, phenyl) and lithiated bromonaptha

60 The primary salt arylation products were dehydrohalogenated to obtai

61 azoesters using 5 mol% of a simple copper(I) salt as catalyst.

62 h oil marinade, emulsion marinade, seasoning salt as well as breadcrumbs, only very little effects of

63 combination of PEO-b-P2VP and Au, Ag, and Cu salts as a model three-component system to investigate t

64 e 1,2-hydrocarbation with N-methylacridinium salts as the carbon Lewis acid.

65 y from the reduced level of enzymes and bile salts, as well as the higher gastric pH in the infant mo

66 and inexpensive Si source soluble in molten salts, at a low temperature of 650 degrees C by using lo

67 ansforming once lush marshes into persistent salt barrens.

68 demonstrate that various solutions of copper salts, bases, and ancillary ligands can be utilized to e

69 P-like particles larger than 149 mum from 17 salt brands originating from 8 different countries follo

70 Instead, a labile salt bridge acts as an incessantly active "agitator" tha

71 ntacts for a network of hydrogen bonds and a salt bridge in the core of binding.

72 ing unless the mutated residue also formed a salt bridge with GpIbalpha, in which case the mutations

73 ic, competes for a lysine from a preexisting salt bridge, initiating a partial unfolding event and pr

74 erall, we propose interstrand separation and salt-bridge formation as key reaction coordinates descri

75 EXXX, where X is K or R) expected to promote salt-bridge formation between Glu and Lys/Arg.

76 orylation destabilizes this highly conserved salt-bridge in temporal and physical space.

77 m this turn, along with Arg12, which forms a salt-bridge with Asp8, are instrumental in modulating th

78 isease mutations all destabilize a D354-R375 salt-bridge, which normally acts as an electrostatic loc

79 Mutations aimed at disrupting any of these salt bridges activated binding unless the mutated residu

80 ding experiments, we identified a network of salt bridges between Asp(1261) and the rest of A1 that l

81 adjacent subunit's backbone alpha-helix form salt bridges in hexamers and pentamers.

82 Recently we showed that salt bridges located at the cytoplasmic domain subunit i

83 Understanding how salt bridges promote their stability is challenging as S

84 r both decarboxylations, while a lysine that salt bridges to propionate 4 is required solely for the

85 aM (Glu-11, Glu-14, Glu-84, and Glu-87) form salt bridges with key lysine residues in ER-alpha (Lys-2

86 attention compared to ion-ion interactions (salt bridges) and dipole-dipole interactions (hydrogen b

87 have examined the contributions of conserved salt-bridging residues in stabilizing the dimeric state

88 icity is evidently obscured in physiological salt by non-specific, predominantly electrostatic intera

89 C by using low-melting-point ternary molten salts CaCl2 -MgCl2 -NaCl, which still retains high CaSiO

90 ts of heating skim milk with soluble calcium salts, calcium chloride, calcium lactate, calcium glucon

91 High concentrations of monovalent salt can induce the solubilization or crystallization of

92 Both aryl components of diaryliodonium salts can be used in a domino one-pot reaction via in si

93 sing NMR and DSF, it was shown that the bile salts cholate and chenodeoxycholate interact with purifi

94 process is directly and sensitively tuned by salt concentration and temperature, implying it is modul

95 Given the relatively high salt concentration of urine, marine bacteria would be pa

96 Comparison of SAXS curves at high and low salt concentration shows that R10 self-associates, while

97 ned gate shape, sensitive response to pH and salt concentration, and selectivity in cargo transport c

98 ships between site diffusion coefficient and salt concentration, conditions were identified that allo

99 FERM domain of Ezrin is sensitive to buffer salt concentration, correlating with the excited nanosca

100 s solutions can be directed by modifying the salt concentration.

101 hrough denaturation induced by physiological salt concentrations and degradation mediated by nuclease

102 he electrolyte, NPs pairs at high monovalent salt concentrations interact via remarkably strong long-

103 to approximately 1.5 higher at low sugar and salt concentrations).

104 rved to start the G4 folding process in both salt conditions.

105 raction patterns with increasing addition of salt consistent with interactions between added ions and

106 DEC-medicated salt consistently reduced microfilaria (mf) prevalence f

107 A Western lifestyle with high salt consumption can lead to hypertension and cardiovasc

108 rengths and as long helical ribbons at lower salt content.

109 iently robust to analyze samples with a high salt content.

110 ace of typical dry SSA particles composed of salt cores and organic-rich coatings.

111 ts pristine condition by simply scraping off salt crystals from its surface and rinsing with water.

112 Ethers and chloride salts dampen or turn off reactivity, leading to three di

113 the interplay of chain backbone entropy and salt-dependent electrostatic repulsions.

114 s were water-deprived but not under food- or salt-depleted conditions, indicating that the hedonic va

115 ntake after fasting or salt intake following salt depletion; inactivation increased saline intake aft

116 re investigated, and the quaternary ammonium salts, derived from alkyl halides and tertiary amines, w

117 Rats fed a normal-salt diet (0.3% NaCl) served as controls (n=13).

118 After 7 weeks of a high-salt diet, 31 of 38 rats showed diastolic dysfunction an

119 To assess whether a high-salt diet, as measured by urinary sodium concentration,

120 On a normal salt diet, dKO and single-knockout mice exhibited simila

121 Additional studies showed that, on a high-salt diet, Tmem27(Y/-) mice had lower renal blood flow,

122 On a high-salt diet, WT mice with Tmem27(Y/-) kidneys had the high

123 model of colitis relative to mice fed a low salt diet.

124 ption of the afferent taste signal to sodium salts disrupts the normal age-dependent "pruning" of all

125 The projected effect of salt-driven hormone rhythm modulation corresponded well

126 sed in a dose-response manner with delays in SALT dysphagia assessment, with an absolute increase of

127 lar volume conservation and concentration of salt excreted into urine.

128 This water-conserving mechanism of dietary salt excretion relies on urea transporter-driven urea re

129 i-interlinked OOCOR molecules that host LiCl salt exhibit fast charge-transfer kinetics and as much a

130 rahepatic cholestasis-1 (FIC1), 18 with bile salt export pump (BSEP) disease, and 4 others with low g

131 ephrectomized, aldosterone-infused, and high salt-fed (ALDO) systemic GC-A KO mice with enhanced phos

132 (11)C-carbonylation of aryl(mesityl)iodonium salts followed by suitable quench provides a rapid room-

133 ely in plants, animals, fermented foods, and salted foods.

134 xpands the catalog and properties of organic salts for inexpensive, and stable NIR-selective molecula

135 e proper electrolyte, including solvents and salts, for LSBs strongly depends on its physical and che

136 The products, in their hydrobromide salt form, could be conveniently isolated and purified b

137 The first synthetic route to obtain salt-free intrinsic plutonium colloids by ultrasonic tre

138 re retained in the sample, and the resulting salt-free sample is then used for subsequent analysis.

139 6-trimethoxyphenyl)iodonium trifluoroacetate salts from aryl iodides is described.

140 f a solution containing hexose and a lithium salt generates [Hexose+Li](+).

141 ction are dynamically regulated by the renal salt gradient, we find that patients with urinary concen

142 -Kb/K2 is assumed to have a critical role in salt handling by the thick ascending limb.

143 salts, along with TEMPO and its oxoammonium salt, have been successfully measured with little peak b

144 lities as high as those in liquids or molten salts, have been employed as solid-state electrolytes in

145 erved within the physiological range of bile salts; however, growth was inhibited at higher concentra

146 -Bu)3PC14H7O2B(C6F5)2 (5) in addition to the salt [HP(t-Bu)3][C14H8O2B(C6F5)2] (6).

147 egulation during deoxycorticosterone acetate-salt hypertension occurs selectively on neurons, and neu

148 e in subsurface transport of mass, heat, and salt in the global ocean.

149 nthesis, indicating that elevated serum bile salts in Fut2(-/-)(high) mice were not explained by chol

150 dates the critical role of calcium chelating salts in modulating casein hydration and dispersion and

151 Application of road salts in regions with colder climates is leading to grou

152 F solution unless in the presence of lithium salts, in which case they are indefinitely stable at roo

153 crylamide gel route using different aluminum salts, including Al2(SO4)318H2O, AlCl3, and Al(NO3)39H2O

154 and the DeltaHvH/DeltaHcal ratio seen at low salt indicate the four-way junction exists as a mixture

155 grik1-2 grik2-1 mutant was sensitive to high salt, indicating that GRIKs are also involved in salinit

156 In summary, serelaxin reversed DOCA-salt induced cardiac and renal dysfunction.

157 tress, we have used a Y1H system to screen a salt induced rice cDNA expression library from Hasawi.

158 fGNPs) resulting in the inhibition of nfGNPs salt-induced aggregation and the stabilization of purifi

159 Salt-induced changes in RSA were associated with 100 gen

160 It has been suggested that sea-salt-induced chemical cycling of Hg (through 'atmospheri

161 /microtubule affinity-regulating kinases and salt-inducible kinases.

162 exhibited a dominant coarse mode due to sea salt influence, with substantially diminished concentrat

163 the mechanisms by which guanidinium (Gnd(+)) salts influence the stability of the collapsed versus un

164 Here we show that high salt intake affects the gut microbiome in mice, particul

165 We show that high dietary salt intake caused an increase in the expression and act

166 e unexpected observation that long-term high salt intake did not increase water consumption in humans

167 id not decrease food intake after fasting or salt intake following salt depletion; inactivation incre

168 High dietary salt intake for 7 days caused an increase in expression

169 ys' duration, we exposed 10 healthy men to 3 salt intake levels (12, 9, or 6 g/d).

170 nt study, we evaluated the effect of dietary salt intake on ENaC regulation and activity in VP neuron

171 data suggest that animals exposed to chronic salt intake to a level close to that reported for human'

172 nomer, tropoelastin, in response to heat and salt is a critical step in the assembly of elastic fiber

173 roteomics, dodecyl sulfate (DS(-)) as sodium salt is commonly used in protein solubilization prior to

174 zed halocyclization of sulfonate thioimidate salts is also described.

175 en allow us to conclude that the imidazolium salts is crucial for the oxidation.

176 ven-membered ring alkenes and aryl diazonium salts is presented.

177 multiplex PCR assay (Great Basin Scientific, Salt Lake City, UT) for the rapid and simultaneous ident

178 in two patients with a hypokalemic-alkalotic salt-losing nephropathy.

179 ndings were not in line with any other known salt-losing nephropathy.

180 GS autosomal recessive hypokalemic-alkalotic salt-losing phenotype.

181 Salt-losing tubulopathies can affect all tubular segment

182 low, biliary bile salt secretion, fecal bile salt loss, and expression of major hepatocellular bile s

183 r syndrome phenotype, characterized by renal salt loss, marked hypokalemia, and metabolic alkalosis.

184 positive influence on elevation, while other salt marsh species (e.g. Suaeda maritima) had no influen

185 where mangroves are expanding and replacing salt marsh, wetland capacity to respond to sea-level ris

186 Field experiments revealed that in protected salt marshes experiencing a severe drought, plant-eating

187 average reduction in annual flood losses by salt marshes with higher reductions at lower elevations.

188 High salt may additionally drive autoimmunity by inducing T h

189 This suggests that salT measurement by LC-MS/MS holds the promise of comple

190 cultured dendritic cells we found that high salt media potentiates cytokine expression downstream of

191 his requirement, we have developed a facile, salt-mediated synthesis of covalent organic frameworks (

192 (CTAB) Method, Alkaline Method, Urea Method, Salt Method, Guanidinium Isothiocyanate (GuSCN) Method,

193 -that are essential for accessing SM in bile salt micelles.

194 tions tended toward additivity for most bath salts mixtures, supra-additive (3 : 1 MDPV : caffeine, a

195 mponent of the biocrystals-the hydrochloride salt of CFZ (CFZ-HCl)-has a corrugated packing along the

196 a total residence time of 9 min, the sodium salt of ciprofloxacin was prepared from simple building

197 f cocaine, flutamide, flufenamic acid, the K salt of penicillin G, and form 4 of the drug 4-[4-(2-ada

198 cessing conditions like temperature, pH, and salting of hams.

199 The preparation of shelf-stable crystalline salts of tert-butylmethylphosphinous acid borane 1 is de

200 e(vbpy)2(CN)2 followed by surface binding of salts of the cations and electrochemical reduction gave

201 The influence of different aluminum salts on the phase purity, morphologies, thermal stabili

202 The combination of salT or FAI identified 100% of PCOS women.

203 nown carbohydrates, both KCl and NaCl act as salting-out agents towards trehalose, as seen in the ele

204 NP assembly and design rules to utilize the salting-out process to crystallize NPs.

205 y reduced the elevation in time spent in the salt-paired context.

206 epresent the hygroscopicity of inorganic sea salt particles in numerical models.

207 uct of the exchange, in both cases, was rock-salt PbSe nanocrystals, we show here that the crystal st

208 The findings suggest that although salt perception is stunted in samples containing a rando

209 substrate, the existence of Lix Fe3 O4 rock-salt phase during lithiation consequently restrains the

210 xpensive, and stable NIR-selective molecular salt photovoltaics.

211 The altered bile salt pool stimulated robust secretion of cholesterol int

212 e settings possible, we developed an imidate salt protecting strategy that employs methyl trifluorome

213 -diastereoselective halocyclization of these salts provides a variety of substituted alkyl- and arylt

214 After 4 weeks, the DOCA-salt rats were randomly selected and implanted with osmo

215 Treatment of DOCA-salt rats with serelaxin decreased renal inflammation, i

216 vented cardiac and renal dysfunction in DOCA-salt rats.

217 Claudin-2 expression in colon and that bile salt receptors VDR and Takeda G-protein coupled receptor

218 Differences due to salt reduction were perceptible in a faint decline of wa

219 applications, but their scalability and high salt rejection when in a strong cross flow for long peri

220 ycle so that energy discharge coincides with salt removal (1.96 kg-NaCl kWh(-1)).

221 easured partition coefficients for inorganic salts report values significantly higher than one ( appr

222 Since the salt represents around 4% of the final product, it will

223 Salt resistance assays, acridine-orange fluorescence deq

224 notations, and 936 and 220 genes involved in salt response in roots and leaves, respectively.

225 At pH 7.0, the divalent salts resulted in weaker gels formed by agglomerates, su

226 ategies employed by methanogens to thrive in salt-saturating conditions are not limited to the classi

227 Nevertheless, low-salt sausages were clearly preferred by panellists.

228 l serum liver tests, bile flow, biliary bile salt secretion, fecal bile salt loss, and expression of

229 eural circuitry necessary for context-driven salt-seeking behavior is unknown.

230 lls contribute to renal sodium retention and salt-sensitive hypertension is unknown.

231 t in sodium handling and the pathogenesis of salt-sensitive hypertension.

232 e OsBZ8 locus in salt-tolerant Nonabokra and salt-sensitive IR64 rice varieties.

233 notype of yeast strain CY162, suppressed the salt-sensitive phenotype of yeast strain G19, and comple

234 Vulnerable salt-sensitive populations may have in common underlying

235 fectors has provided important insights into salt sensitivity.

236 r challenging physiological conditions (high salts, serum, and acidic pH).

237 ly increased albuminuria in response to high salt; severe albuminuria, nephrinuria, FSGS, and podocyt

238 play key roles in P. euphratica response to salt shock.

239 nally, the prepared oxadiazolium perchlorate salts showed excellent moisture stability, an unusual fe

240 ts previously shown to function in chitin or salt signaling physically interact and intimately link t

241 wide range of commercially available uranyl salts, silyl halides, and alkylating reagents.

242 able means to form aoQMs, independent of the salt solubility and base strength.

243 ted overall paramagnetism in the oxoammonium salt solutions is explained by a redox equilibrium as sh

244 Supplementation with salt stabilized the DeltadacA mutant in rich medium and

245 new insights into the function of SlCBL10 in salt stress tolerance.

246 Under the salt stress, the T3 of RNAi plants showed significant hi

247 n, which is known to be highly induced under salt stress, we have used a Y1H system to screen a salt

248 Transcriptome analysis revealed that salt stress-induced genes are highly correlated with chi

249 o be upregulated by high light intensity and salt stress.

250 he downstream responses to fungal attack and salt stress.

251 differential expression of OsBZ8 gene during salt stress.

252 under multiple stress conditions, including salt stress; however, factors regulating this process ar

253 n the control wheat plants under drought and salt stresses.

254 Flavylium salts substituted at 4-position with hydroxyphenyl subst

255 o NaCl, no proliferation was detected in the salt-susceptible mutants fry1-6, sos1-14, and sos1-15.

256 tochrome P450 7a1, the key regulator of bile salt synthesis, indicating that elevated serum bile salt

257 temperatures can be applied to other molten salt systems and is also promising for waste glass and c

258 health problems, it could be useful to have salt taste enhancers that are not sodium based.

259 ompounds, such as lithium chloride (LiCl), a salt that creates gastric discomfort, and lipopolysaccha

260 on a non-hygroscopic dilithium nitrogen-rich salt that serves as both oxidizer and red colorant.

261 give black precipitates of Sb@Ni12@Sb20(n-) salts that give similar Sb@Ni12@Sb20(-/+) parent ions an

262 enerator composed of crystalline radical ion salts: The unipolar charge transport along the molecular

263 In the absence of calcium chelating salts, these concentrations were significantly lower at

264 gement practices affect the movement of road salt through urban watersheds.

265 al polypyridyl complexes and a palladium(II) salt to form electrochemically addressable films with a

266 The effect of adding salt to the charged phase changes the structure from the

267 Addition of Tb(3+) salts to a solution of a (YbLD) complex in D2O resulted

268 g elution of histones using intercalators or salt, to assess stability features dependent on DNA supe

269 iolylium, activated pyridines, Eschenmoser's salt, Togni's reagent, Selectfluor, diisopropyl azodicar

270 Thus, it is proposed that SlCBL10 mediates salt tolerance by regulating Na(+) and Ca(2+) fluxes in

271 Identification of major salt tolerance genes and marker assisted selection (MAS)

272 resulted in Arabidopsis lines with enhanced salt tolerance than wild type plants, as indicated by re

273 -associated molecular pattern) have improved salt tolerance, was observed in Arabidopsis, but is not

274 with AtPMT1 essential for normal growth and salt tolerance, whereas AtPMT2 and AtPMT3 overlap functi

275 hromatin modifications at the OsBZ8 locus in salt-tolerant Nonabokra and salt-sensitive IR64 rice var

276 ined in the aerogel guarantees its excellent salt-tolerant property.

277 In this study, we report a low-cost and salt-tolerant superoleophobic aerogel for efficient oil/

278 nd unusual reactivity of 2-methylimidazolium salts toward aryl-N-sulfonylimines and aryl aldehydes is

279 and expression of major hepatocellular bile salt transporters and cytochrome P450 7a1, the key regul

280 and lipid accumulation were studied in DOCA-salt treated rats.

281 the poorly soluble potassium (pseudo)halide salts), typically higher conversions and higher molecula

282 ion was promoted by the inexpensive Cu(OTf)2 salt under mild reaction conditions.

283 computational models that can better predict salt up-regulated genes in the root and shoot compared w

284 RE combinations led to better performance in salt up-regulation prediction in the root and shoot.

285 Bath salts use is associated with high rates of abuse, toxici

286 ynthesis of S-allyl thioimidate hydrobromide salts via coupling of thioamides with allyl bromide deri

287 Substitution of ammonia in ammonium salts was observed not only in aerosol but also in parti

288 gly correlated quantum material is stable in salt water, does not corrode, and allows exchange of pro

289 ion, and in the absence of either sucrose or salt, we found that inhibiting the VP selectively reduce

290 O-Arylations with these TMP salts were demonstrated to be highly chemoselective.

291 essments by a speech and language therapist (SALT) were associated with patients' risk of SAP.

292 e, in which animals can immediately seek out salt when under a novel state of sodium deprivation, is

293 nerated from its sulfite/sulfate heat stable salt, which enables the simultaneous absorption of CO2 a

294 k reaction) of electron rich arene diazonium salts with electron deficient olefins has been exploited

295 reagent followed by reaction of the ensuing salts with pyrrole, results in the formation of 5-alkoxy

296 The methodology provides diaryliodonium salts with the trimethoxyphenyl (TMP) moiety as dummy gr

297 ized by the direct reaction of aryldiazonium salts with two equivalent of nitriles.

298 activated by halide abstraction with sodium salts, with the resulting catalyst [kappa(5) -((15c5) NC

299 of the matrices containing calcium chelating salts; with approximately 23% of total calcium solubilis

300 ice on an HSD, suggesting a direct effect of salt within the colon.