ライフサイエンスコーパス: exchange reaction

1 ould suggest the possibility of a facile ion-exchange reaction.

2 achieved using a nickel(0)-mediated halogen-exchange reaction.

3 crowave assistance mediate the silyl/acetate exchange reaction.

4 ramework for understanding the complex dimer-exchange reaction.

5 e preparation of 4-bromoisoxazoles via Br/Se exchange reaction.

6 reacting with thiols through a sulfide-thiol exchange reaction.

7 ate antiporter, is consistent with a classic exchange reaction.

8 e initial fast kinetics in a 5 min timescale exchange reaction.

9 ring in the linker, thereby preventing this exchange reaction.

10 ocking the formation of intermediates of the exchange reaction.

11 .2), is observed for the unidirectional self-exchange reaction.

12 " Au...Cu interactions induced by the ligand exchange reaction.

13 the action of the small complex in the H2A.Z exchange reaction.

14 aking these interfaces stable throughout the exchange reaction.

15 erned primarily by the O((1)D)+CO(2) isotope exchange reaction.

16 erials is controlled through an intermediate exchange reaction.

17 the transition state of the thiol/disulfide exchange reaction.

18 different exchange pathways for the sulfide exchange reaction.

19 n state geometry of the phenoxyl-phenol self-exchange reaction.

20 w focusing primarily on GEF distribution and exchange reaction.

21 g that it is oxidized by a similar disulfide exchange reaction.

22 Cu into CdSe/ZnS core/shell QDs via a cation-exchange reaction.

23 rt at quantifying individual thiol/disulfide exchange reactions.

24 tant consequences on the chemistry of ligand exchange reactions.

25 istine C(60) in the gas-phase by facile atom exchange reactions.

26 ccurs either by proton transfer or by charge exchange reactions.

27 alyst with reduced activity for isotopic H/D exchange reactions.

28 directional fluxes associated with metabolic exchange reactions.

29 stringent steric requirements for disulfide exchange reactions.

30 uld be induced to dissociate via competitive exchange reactions.

31 common to the decarboxylation and deuterium exchange reactions.

32 on mechanisms of biphasic nanocrystal ligand-exchange reactions.

33 the NC composition through successive cation exchange reactions.

34 rotein-protein cross-links through disulfide-exchange reactions.

35 kcal mol(-1) and therefore are close to self-exchange reactions.

36 on on DNA substrates and catalysis of strand-exchange reactions.

37 activated to catalyze ATPase and DNA strand-exchange reactions.

38 ation of the mechanism of thiolate-disulfide exchange reactions.

39 minescent quantum dots through direct ligand-exchange reactions.

40 generation of active OhrR by thiol-disulfide exchange reactions.

41 tor their postsynthesis peptide ligand place-exchange reactions.

42 boronates allowed their use in metal-halogen exchange reactions.

43 lease monomeric RRM2 through thiol-disulfide exchange reactions.

44 and carry out two pairs of sequential strand exchange reactions.

45 C (68% RH) through thiol (SH)/disulfide (SS) exchange reactions.

46 an be independently controlled through anion-exchange reactions.

47 on circuits based on toehold-mediated strand exchange reactions.

48 rs were radiolabeled via (18)F-(19)F isotope exchange reactions.

49 cope probe can be used to induce these place-exchange reactions.

50 went efficient Ir-catalyzed hydrogen isotope exchange reactions.

51 p, independent of the initial anionic ligand-exchange reactions.

52 PS)2(Ln)] complexes were inert toward ligand exchange reactions.

53 ispensible particularly for lithiation (Li-H exchange) reactions.

54 ree-energy barrier at 298 K for the hydrogen exchange reaction 3H(2) --> 3H(2) is reduced from 88.8 k

55 The ion exchange reactions affected bump, bulge, and crack forma

56 transition-state stabilization of the S(VI) exchange reaction all seem to be critical for conjugate

57 OhrR can be reactivated by thiol-disulphide exchange reactions allowing restoration of repression.

58 e dissolved on-demand, via a thiol-thioester exchange reaction, allowing for a facile burn dressing r

59 case UvsW completes the UvsX-promoted strand-exchange reaction, allowing the generation of a simple n

60 A simple exchange reaction allows extension of nanochemistry to a

61 amide can also be reduced by thiol-disulfide exchange reactions, although this process is much slower

62 demonstrated: a localized heat-mediated DNA exchange reaction and a method for dense selective funct

63 s of carbene/alkene additions, the diazirine exchange reaction and derived carbenes, carbene equilibr

64 tein is capable of catalyzing the DNA strand exchange reaction and is insensitive to inhibition by th

65 Addition of a proteolysis step between the exchange reaction and mass analysis can be used to local

66 mechanisms for the unidirectional PCET self-exchange reaction and the corresponding bidirectional PC

67 ive C-C bond formation via halogen/magnesium exchange reaction and/or palladium-catalyzed reactions.

68 ositions on nanoparticles prepared by ligand exchange reactions and by synthesis using thiol mixtures

69 for the surface functionalization via ligand-exchange reactions and the effect on the optical propert

70 ability to promote LexA cleavage and strand exchange reaction, and are believed to modulate its acti

71 ere we further clarify the mechanism of this exchange reaction, and we demonstrate that the CP:CARMIL

72 e proteins, to probe the dynamics of subunit exchange reactions, and to characterize polydispersity i

73 00-fold, and promoting the subsequent strand exchange reaction approximately 10 to 20-fold.

74 ely 10(4)-fold) and promoting the subsequent exchange reaction ( approximately 10-fold).

75 ubstrate and the efficiency of the magnesium exchange reaction are also described.

76 Intermediate steps in this exchange reaction are represented by Janus-type Cu(2-x)S

77 phenoxyl/phenol and the benzyl/toluene self-exchange reactions are calculated with a semiclassical a

78 The exchange reactions are driven by disparate solubilites b

79 quantum rods by successive complete cationic exchange reactions are partially re-exchanged for Cd cat

80 and thermogravimetric measurements, and ion-exchange reactions are reported.

81 At lower temperatures, the exchange reactions are very sluggish, and the materials

82 Both of these self-exchange reactions are vibronically nonadiabatic with re

83 Ligand exchange reactions are widely used for imparting new fun

84 tein filaments on DNA that catalyze a strand exchange reaction as part of homologous genetic recombin

85 delta-MoN and cubic gamma-MoN through an ion-exchange reaction at 3.5 GPa.

86 Finally, we mimicked the exchange reaction at 5% [CO2], 5 per thousand [H2(18)O],

87 Furthermore, a steady-state isotopic exchange reaction between 12CO and 13CO2 in solution was

88 A ligand exchange reaction between [Ni@(Ge9Ni-CO)]2- and potassiu

89 (N3)3] was prepared through a fluoride-azide exchange reaction between [VOF3] and Me3SiN3 in acetonit

90 This is illustrated by the exchange reaction between amyloid-beta (Abeta) monomers

91 clic alpha-amino aldehydes enabled by a B/Zn exchange reaction between arylboronic acids and Et2Zn is

92 y complex formation went along with a ligand exchange reaction between As(III) and hydroxylic/phenoli

93 sight into the mechanism of the axial ligand exchange reaction between chlorosubphthalocyanines and p

94 demonstrating a CODH-catalyzed steady-state exchange reaction between CO and CO2 in the absence of e

95 competitive inhibitor of the thiol-disulfide exchange reaction between glutathione and ESSG, a covale

96 This exchange reaction between labeled and unlabeled Fdx is c

97 tex sites occurs by performing a thiol place-exchange reaction between mercaptoethanol (ME) attached

98 We present evidence for a gas-phase O-atom exchange reaction between neutral O(2) and CO(2) at elev

99 s interaction is consistent with a disulfide exchange reaction between oxidized Txnip and reduced thi

100 The ligand exchange reaction between racemic Au(38)(2-PET)(24) (2-P

101 on mechanisms: a second-order intermolecular exchange reaction between specific sites located on diff

102 nealing function to actively catalyze strand-exchange reaction between the unwinding substrate and a

103 valuate the optimality of putative metabolic exchange reactions between heterocysts and vegetative ce

104 Mo, W), were prepared through fluoride-azide exchange reactions between MO2F2 and Me3SiN3 in SO2 solu

105 To test the idea that dithio-disulfide exchange reactions between p53 and thioredoxin were resp

106 o-called IDipp, catalyzes hydrogen/deuterium exchange reactions between pseudoacids and chloroform-d1

107 , we determined the rates of thiol-disulfide exchange reactions between selected pairs of Cys residue

108 pon the completion of the native GDP --> GTP exchange reaction, but also explains measurable GTP -->

109 SWR complex that is required for the histone exchange reaction, but its molecular role is unknown.

110 UvsX and RecA catalyze similar strand-exchange reactions, but differ in other properties.

111 propargyl, and acetonitrile halide identity exchange reactions, but does so to nearly the same exten

112 ry thus shares some similarities with cation-exchange reactions, but proceeds without the loss of hos

113 e found to undergo further chlorine-fluorine exchange reactions by treatment with silver(I) fluoride

114 ce phases and compositions resulting from an exchange reaction can be kinetically controlled, rather

115 taining segments of different materials, the exchange reaction can be made highly selective for just

116 The ligand exchange reaction can be terminated prior to complete cr

117 It is now shown that anion and cation exchange reactions can be coupled together and applied s

118 the only known system where cation and anion exchange reactions can be sequentially combined while pr

119 Strand exchange reactions catalyzed by phosphorylated versus un

120 structural information extracted from ligand-exchange reactions, circular dichroism and transmission

121 rgy of the [NiII(SODM2)]/[NiIII(SODM2)] self-exchange reaction combined with the experimentally deter

122 catalyze oxidation, reduction, or disulfide exchange reactions depending on their redox properties.

123 This exchange reaction depends mainly on DNA concentration wi

124 basic step with a redox-mediated, disulfide-exchange reaction directionally transports the bipedal m

125 ely modest inhibition of the thiol-disulfide exchange reaction does not affect the overall rate of tu

126 ope fractionation is pH-dependent in that H+ exchange reactions dominate below and N atom oxidation p

127 s been challenging because of undesired back-exchange reactions during analysis.

128 In PEt(4)(+) for NEt(4)(+) exchange reactions, egress of the initial guest (G1) is

129 Catalytic control of bond exchange reactions enables healing of cross-linked polym

130 H(2)O((g))/K(2)((2,1)H(2)O)(2)B(12)F(12 (s)) exchange reactions fit the equation m proportional, vari

131 suitable substrates to the selenium-lithium exchange reactions followed by trapping with aldehydes a

132 hiol-containing proteins through a disulfide exchange reaction, followed by on-resin protein digestio

133 d useful guides to the application of cation-exchange reactions for the synthesis of a broader range

134 r via a monomer (i.e., donor)-induced ligand-exchange reaction forming Cp3Ln in equilibrium (e.g., fo

135 hydrocarbon group) undergo a stoichiometric exchange reaction, forming hybridized CH3S-Au-SPh comple

136 2N]-) in optically pure form by a simple ion exchange reaction from corresponding chloride salts that

137 -catalyzed homologous DNA pairing and strand exchange reaction have also been identified.

138 onducting gas phase hydrogen/deuterium (H/D) exchange reactions (HDX) in real time without the need f

139 entangled spin-order of parahydrogen and an exchange reaction in a low magnetic field of 10(-)(3) Te

140 lts constitute the first example of a ligand exchange reaction in a thiolate-protected gold cluster w

141 ugate that is radiolabeled in a 1-step (18)F exchange reaction in high yield and with high specific a

142 f the rate constant for pyridine ligand edge exchange reaction in one of the cages and for the unusua

143 cyclization in formation of cADPR to a base-exchange reaction in the generation of NAADP.

144 er occurs upon each binding event, to a fast exchange reaction in the Tyr L162 mutant, where dissocia

145 olesterol (25OH) competitively inhibits this exchange reaction in vitro and causes the constitutive l

146 crA can inhibit the RecA-mediated DNA strand exchange reaction in vitro.

147 ntum dots (QDs) using a postsynthetic cation exchange reaction in which Pb is exchanged for Ag.

148 We studied cation exchange reactions in colloidal Cu(2-x)Se nanocrystals (

149 We have investigated cation exchange reactions in copper selenide nanocrystals using

150 ll as mechanochromic behavior based on metal-exchange reactions in metallopolymers imbibed with an au

151 tudied SC-SC transformations involve solvent exchange reactions in porous coordination polymers or me

152 agnostic applications, similar to how strand exchange reactions in solution have been used for transd

153 ication for broadening due to conformational exchange reactions in the intact photoreceptor domain, w

154 nt mechanism underlying highly dynamic lipid exchange reactions in the lysosomal compartment that sha

155 alkoxy-terminated surfaces and their ligand exchange reactions in the presence of various alkenes an

156 Its presence in DNA strand-exchange reactions in vitro results in a significant sti

157 of the resulting products that undergo thiol-exchange reactions in vivo.

158 Kinetic studies suggested that linker exchange reactions in ZIF-8 proceed via a competition be

159 ability to monitor this challenging cluster exchange reaction indicates that real-time Fe-S cluster

160 tegy, including sequential anion- and cation-exchange reactions, integrates two distinct sulfide semi

161 yclohexadienyl radical, we conclude that the exchange reaction involves a radical intermediate and re

162 With the more sterically hindered exchange reaction involving t-butyl mercaptide and di-t-

163 lthough growing evidence suggests that redox exchange reactions involving CD4 disulfides, potentially

164 It is concluded that the observed exchange reaction is between 13CO and CODH-bound 13CO2 b

165 The vanadium self-exchange reaction is ca. 10(6) slower than that for the

166 The exchange reaction is conducted in deuterated water catal

167 The mechanism of the exchange reaction is confirmed by a DFT study to involve

168 g strategy based on a photodynamic disulfide exchange reaction is demonstrated.

169 We have found that this exchange reaction is first order in dinitrogen and relat

170 Substrate inhibition of the thiol-disulfide exchange reaction is less severe in the I12S and I12A mu

171 ntegration and dissociation of H2AX and this exchange reaction is mainly catalyzed by FACT among the

172 The k phi of the H-D exchange reaction is obtained from the mass spectrum ref

173 ggest that either a two- or three-coordinate exchange reaction is preferred and that it is unlikely t

174 nd cold conditions, where the amide hydrogen exchange reaction is quenched (pH 2.5, 0 degrees C).

175 After a given period of deuteration, the exchange reaction is quenched by acidification (pH 2.5)

176 The thiol-disulfide exchange reaction is the rate-limiting step in the reduc

177 rification of nanocrystals as well as ligand exchange reactions is discussed.

178 Reactivity in ligand exchange reactions is found to contrast significantly to

179 heterostructures, formed upon partial cation exchange reactions, is intimately connected not only to

180 ynamic covalent chemistry (DCC) of disulfide exchange reactions, is presented.

181 cond-order rate constant for these deuterium exchange reactions [(k(E))(P)] equals 0.25 M(-1) s(-1).

182 inum hydroxide allows progress of the cation exchange reaction leading to hardness removal.

183 ed base pairs that impede uncatalyzed strand exchange reactions led to a significant decrease of the

184 This impairment of apoA-I exchange reaction may be a trait of dysfunctional HDL co

185 eory calculations were used to elucidate the exchange reaction mechanism in 1,2-dialkoxybenzenes.

186 Faster ion exchange reactions (Na(+)-K(+), Mg(2+)-K(+), and Ca(2+)-

187 ICAACs as compared to CAACs allow for ligand exchange reactions not only at a metal center, but also

188 In most instances, oxygen-sulfur exchange reactions (O/S ERs), which would generate rando

189 pid intra- and intermolecular hydride/proton exchange reactions observed for 4.

190 alculations, it is shown that these "ligand" exchange reactions occur via an associative mechanism as

191 tion, we find that a concentration-dependent exchange reaction occurs which turns over the bound prot

192 A Cl/H exchange reaction of 2 using potassium trisec.-butylborh

193 The exchange reaction of 2 with Ph3SnH gave Pt(SnPh3)3(CNBu(

194 nthetic approach is based on a metal-halogen exchange reaction of 2-iodobiphenyl derivative and his s

195 The deuterium exchange reaction of FEU is accelerated 1.8 x 10(4)-fold

196 tetramer stability, we measured the subunit exchange reaction of p53 family homotetramers by nanoflo

197 emical denaturant dependence of the slow H/D exchange reaction of the imidazole C(2) proton in histid

198 idazolate, is an active catalyst for the H/D exchange reaction of various substrates using CDCl3 as D

199 een probed with DFT calculations on the self-exchange reactions of 1c + 2c and on monocationic ruthen

200 Strikingly, the Br/H ligand exchange reactions of 3 using potassium hydride as a hyd

201 ype- and K12G mutant TIM-catalyzed deuterium exchange reactions of [1-(13)C]GA, respectively, to form

202 d pD 7.0 was found to catalyze the deuterium exchange reactions of [1-(13)C]glycolaldehyde ([1-(13)C]

203 ry of base-catalyzed 1,2-elimination and H/D exchange reactions of carbonyl compounds, we have found

204 Ion exchange reactions of colloidal nanocrystals provide acc

205 Hydrogen-deuterium exchange reactions of deprotonated amino acids and small

206 ing appears to be more important in the self-exchange reactions of dialkylhydroxylamines than of aryl

207 minescence of ruthenium compounds and ligand exchange reactions of iron complexes using UV-vis spectr

208 Fluoride-azide exchange reactions of Me3SiN3 with MnF2 and MnF3 in acet

209 rium and the morphology change in the cation-exchange reactions of metal chalcogenide nanocrystals, C

210 chemical investigations of the SN2 identity exchange reactions of methyl, ethyl, propyl, allyl, benz

211 on undergoes pH-dependent hydrogen-deuterium exchange reaction, of which the rate constant ( k phi) r

212 ted for measurements were obtained by ligand-exchange reactions on AuNCs grown at the water/toluene i

213 ability to promote DNA annealing and strand exchange reactions on free as well as RPA-coated substra

214 of Cl can be facilitated by either a ligand exchange reaction or the dissociation of Cl upon increas

215 e that it can be combined with metal-halogen exchange reactions or a variety of directed ortho metala

216 While theoretical models invoke ion-neutral exchange reactions outside the protoplanetary disk and p

217 Chemical transformations like cation exchange reactions overcome a limitation in traditional

218 /desorption at the molecular-scale elucidate exchange reaction pathways.

219 Here, we introduce the concept of primer exchange reaction (PER) cascades, which grow nascent sin

220 Mass action law equations for ion-exchange reactions predicted similar trends in a qualita

221 of both the kinetically labile metal-ligand exchange reactions prior to oxidation and the kineticall

222 These alkyne exchange reactions proceed regioselectively and can tole

223 hypobromous acid generated through a halogen exchange reaction produced an additional 4'-brominated g

224 miting ssDNA; and (3) no formation of strand exchange reaction products.

225 the dihydrogen complexes, as well as isotope exchange reactions, provide evidence for proposed ionic

226 y dissolution as Ag(+) and subsequent cation exchange reactions regardless of the applied silver form

227 Other mechanisms such as ion exchange reactions remain speculative.

228 s limited by the rate of the thiol-disulfide exchange reaction required to regenerate the free enzyme

229 competitive inhibitor of the thiol-disulfide exchange reaction required to regenerate the free form o

230 Unlike strand-annealing, the strand-exchange reaction requires nucleotide hydrolysis and gre

231 peptides, are involved in disulfide-dithiol exchange reaction, resulting in formation of adventitiou

232 er levels of initiators for thiol-disulphide exchange reactions, resulting in an increase in the rate

233 , (t)Bu(2)NO((*)/H), and Ph(2)NO((*)/H) self-exchange reactions reveal why the phenyl groups make the

234 structural snapshots of the full nucleotide exchange reaction sequence together with the G-protein s

235 compounds is easily adjusted by simple anion exchange reactions so that the compounds can be made sol

236 der kinetics, observed for all the is otopic exchange reactions studied over the entire time scale th

237 fluorescence with a toehold-mediated strand exchange reaction termed one-step strand displacement (O

238 clophane is much less prone to halogen-metal exchange reactions than its constitutional pseudo-ortho

239 sing a low-temperature solution-based cation exchange reaction that creates a heteroepitaxial junctio

240 nated by a glycolytically mediated Pi<-->ATP exchange reaction that is unrelated to mitochondrial fun

241 utcome for the H + H2 --> H2 + H bimolecular exchange reaction that it might seem further experiments

242 inal step of the reaction, a thiol-disulfide exchange reaction that regenerates the free enzyme and f

243 r regulatory sites via an ATP-driven histone exchange reaction that replaces nucleosomal H2A with H2A

244 Here we propose a novel cation exchange reaction that takes advantage of the reducing p

245 as an effective new reagent for direct Zn-I exchange reactions that allow the preparation and struct

246 D51 protein catalyzes DNA pairing and strand exchange reactions that are central to homologous recomb

247 ut, due to its transient nature and chemical exchange reactions that complicate NMR detection, its ac

248 present a systematic investigation of cation-exchange reactions that involve the displacement of Mn(2

249 hesis to the possibility of metal and linker exchange reactions that may lead to defects and disorder

250 While nanocrystal ion-exchange reactions that retain anion sublattice features

251 In this exchange reaction the final stoichiometry of the NCs can

252 alogenation, rather than the thiol-disulfide exchange reaction, the relatively modest inhibition of t

253 for Li-ion battery positive electrodes, ion exchange reactions, the formation of nanoporous material

254 insights into the mechanism of the pi-ligand exchange reactions; the cycloalkene forms a complex with

255 compensating for its accelerated nucleotide exchange reaction through the expression of the GTPase-a

256 ons that form during the hydroxide-catalyzed exchange reaction to examine how well the predicted ther

257 with a Sir2 reaction intermediate via a base-exchange reaction to reform NAD(+) at the expense of dea

258 The NCCs were porous and allowed fast cation exchange reaction to release an ultralarge number of Zn(

259 s generally couples chemical thiol-disulfide-exchange reactions to a physical conformational folding

260 performed through postsynthesis ligand place-exchange reactions to validate the existence of the tetr

261 retical studies of the intermolecular proton exchange reactions underlying the isomerization of [Ni(P

262 amic processes involved in the triggered ion-exchange reaction upon activation of the photoactive com

263 c CsPbI3 has been developed through a halide exchange reaction using films of sintered CsPbBr3 nanocr

264 r the first time to follow a Li(+)/Na(+) ion exchange reaction using in situ powder neutron diffracti

265 We demonstrate that, via controlled anion exchange reactions using a range of different halide pre

266 source avoids, or minimizes, undesired back-exchange reactions usually encountered during deuterium

267 hai1-D229N/Galphai1-D231N) on the nucleotide exchange reaction was furthermore elucidated.

268 ionality of the Ric-8BFL-catalyzed Galpha(s) exchange reaction was GTP-dependent.

269 lfate, the enthalpy associated with two S-Se exchange reactions was calculated.

270 ns, the scope of existing nanocrystal cation-exchange reactions was expanded to include 3d transition

271 as well as in the EF-Ts-mediated nucleotide exchange reaction, we performed a comparative rapid kine

272 nd its ability to catalyze bidirectional ion-exchange reactions, we propose a structure model for the

273 vironment, where the cations involved in the exchange reaction were preferentially solvated in differ

274 Degenerate hydrogen exchange reactions were calculated for 3H(2) --> 3H(2) i

275 On the basis of model reactions, exchange reactions were evidenced, which convert the cyc

276 ete 3-fold activation of a zincate in a Zn-I exchange reaction which, in turn, can efficiently be use

277 18O + 32O2 --> O3(*) --> 16O + 34O2 isotope exchange reaction (which proceeds on the same potential

278 mined primarily by the O((1)D)+CO(2) isotope exchange reaction, which promotes a stochastic isotopolo

279 e crystal remains intact during these ligand-exchange reactions, which occur within the crystal and d

280 The method is based on the acid-nitrile exchange reaction with acetonitrile, used as the solvent

281 apsulate F(-) in solution, where a deuterium-exchange reaction with DMSO-d(6) can be monitored by (19

282 properties can be readily tuned by an anion-exchange reaction with good morphology preservation.

283 CO(2) can be satisfactorily explained by the exchange reaction with O((1)D).

284 that [Au(CN)2]- can participate in a ligand exchange reaction with the cysteine thiolate at 338 such

285 f this unique architecture to perform cation exchange reactions with Ag(+) and Pd(2+), thus demonstra

286 Sulfide and cysteine ligand-exchange reactions with as-synthesized CdSe quantum dots

287 on pathway for degenerate thiolate-disulfide exchange reactions with dimethyl disulfide has been show

288 onding metal fluorides MF4 by fluoride-azide exchange reactions with Me3 SiN3 in the presence of two

289 These defects promote molecular exchange reactions with n-dodecanethiol molecules, leadi

290 ures and used as the host material in cation exchange reactions with Pb(2+) ions.

291 ing was observed using (13)C labeled CO, and exchange reactions with phosphines afford the correspond

292 Additionally, it is able to undergo anion-exchange reactions with small ions such as carbonate, ox

293 iochemical reconstitutions of the DNA strand exchange reactions with total internal reflection fluore

294 hanging films that are powered by DNA strand exchange reactions with two different domains that can r

295 Systematic effects like spurious exchange reactions with wall materials and others are co

296 induced ortho-metalation/LaCl(3).2LiCl metal exchange, reaction with N-Boc pyrrolidin-3-one (5), and

297 in both the kinetics and the pattern of the exchange reaction, with the p53 and p63 tetramers exhibi

298 The possibility to perform an anion-exchange reaction within the layer was demonstrated.

299 s cannot be reduced before or during the H/D exchange reaction without affecting the protein higher-o

300 igher MABr concentration enhances I-Br anion exchange reaction, yielding poorer device performance.