ライフサイエンスコーパス: exchange reaction

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

2 w focusing primarily on GEF distribution and exchange reaction.

3 n much less challenging synthesis by isotope exchange reaction.

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

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

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

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

8 crowave assistance mediate the silyl/acetate exchange reaction.

9 ramework for understanding the complex dimer-exchange reaction.

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

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

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

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

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

15 ocking the formation of intermediates of the exchange reaction.

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

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

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

19 aking these interfaces stable throughout the exchange reaction.

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

21 d with the complex to FUMP for the deuterium exchange reaction.

22 erials is controlled through an intermediate exchange reaction.

23 the 3'-aminooxy oligonucleotides by an oxime exchange reaction.

24 of hybridizing to target RNA through strand-exchange reaction.

25 with the transition state for the deuterium exchange reaction.

26 different exchange pathways for the sulfide exchange reaction.

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

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

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

30 went efficient Ir-catalyzed hydrogen isotope exchange reactions.

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

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

33 rt at quantifying individual thiol/disulfide exchange reactions.

34 tant consequences on the chemistry of ligand exchange reactions.

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

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

37 directional fluxes associated with metabolic exchange reactions.

38 stringent steric requirements for disulfide exchange reactions.

39 uld be induced to dissociate via competitive exchange reactions.

40 common to the decarboxylation and deuterium exchange reactions.

41 immiscible phases by pH changes or by cation-exchange reactions.

42 the NC composition through successive cation exchange reactions.

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

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

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

46 ely linked ligand-binding and conformational exchange reactions.

47 y of subunit composition during assembly and exchange reactions.

48 lease monomeric RRM2 through thiol-disulfide exchange reactions.

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

50 on mechanisms of biphasic nanocrystal ligand-exchange reactions.

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

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

53 an be independently controlled through anion-exchange reactions.

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

55 of all isotopologues involved in the isotope exchange reaction (12)C(16)O(2) + (13)C(16)O(18)O <-> (1

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

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

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

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

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

61 A simple exchange reaction allows extension of nanochemistry to a

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

63 etain their size and shape during the cation-exchange reaction and are either single-layer or a few-l

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

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

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

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

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

76 The exchange reactions are driven by disparate solubilites b

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

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

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

80 Ligand exchange reactions are widely used for imparting new fun

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

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

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

84 exactly hydrolysis influences the DNA strand exchange reaction at the structural level remains to be

85 iciently acidic to initiate dynamic covalent exchange reactions at the orthoester bridgeheads, and as

86 ty, we design a CRISPR-array-mediated primer-exchange-reaction-based biochemical circuit cascade, whi

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

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

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

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

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

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

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

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

95 This exchange reaction between labeled and unlabeled Fdx is c

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

117 Strand exchange reactions catalyzed by phosphorylated versus un

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

119 rs (IERs), which directly monitor changes to exchange reaction conditions.

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

121 This exchange reaction depends mainly on DNA concentration wi

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

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

124 Nucleotide-binding, hydrolysis, and exchange reactions drive significant conformational chan

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

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

127 e, or a nitro group, were tolerated in these exchange reactions, enabling the synthesis of a plethora

128 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

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

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

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

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

133 nthesis in mammalian cells, involving a base-exchange reaction from preexisting phospholipids.

134 ){(WCp)(3)S(4)}] (3) were obtained in ligand exchange reactions from [(PhSn)(4)S(6)] and [M(CO)(3)CpC

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

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

137 immunostaining with signal amplification by exchange reaction (Immuno-SABER), which achieves highly

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

139 ional groups, which can influence a chemical exchange reaction in a subtle but significant way.

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 th of a thin oxide shell, we study the anion exchange reaction in the CsPbX(3) perovskites nanocrysta

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

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

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

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

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

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

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

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

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

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

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

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

162 The strand-exchange reaction is central to homologous recombination

163 The exchange reaction is conducted in deuterated water catal

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

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

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

167 The thiol-disulfide exchange reaction is of specific interest as it has many

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

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

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

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

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

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

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

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

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

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

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

179 doping can be realized via sequential cation-exchange reactions mediated by the Cu(+) ions.

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

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

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

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

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

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

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

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

188 A kinetic study of the hydrogen-deuterium exchange reaction of cyclohexanone in aqueous solution,

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

190 tion state for the OMPDC-catalyzed deuterium exchange reaction of FUMP is ca. 19 kcal/mol smaller tha

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

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

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

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

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

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

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

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

199 Cation exchange reactions of colloidal copper sulfide nanoparti

200 Ion exchange reactions of colloidal nanocrystals provide acc

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

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

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

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

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

206 heterometallic titanium frameworks by metal-exchange reactions of MOF crystals at temperatures below

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

208 rface through the precisely controlled anion exchange reaction, offering a design protocol for tailor

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

210 tero)arylborates (TABs) prepared from ligand-exchange reactions on potassium trifluoroarylborates.

211 ighlight the negative consequences of linker exchange reactions on the compositional integrity of DBB

212 e in situ and real-time monitoring of ligand exchange reactions on the gold surface.

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

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

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

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

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

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

219 thogonal DNA concatemers generated by primer exchange reaction (PER).

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

225 ted, quantum dot and signal amplification by exchange reaction (QD-SABER), for sensitive and multiple

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

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

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

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

232 Here we introduce signal amplification by exchange reaction (SABER), which endows oligonucleotide-

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

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

235 The synthesis proceeds via a cation-exchange reaction starting from single- and multi-layer

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

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

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

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

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

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

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

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

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

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

246 r rheological behavior, related to the swift exchange reactions that have a high activation energy (1

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

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

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

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

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

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

253 ws the equilibrium constant K of the isotope exchange reaction to be determined with an external repr

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

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

256 es by applying up to seven sequential cation-exchange reactions to copper sulfide nanorod precursors.

257 Here we develop cation-exchange reactions to introduce p-type dopants (Cu(+), A

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

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

260 ithin 10 min to 5 h through an I/Zn or Br/Zn exchange reaction using bimetallic reagents of the gener

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

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

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

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

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

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

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

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

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

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

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

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

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

274 Cation exchange reactions were performed in the presence of alk

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

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

277 a refined framework of comparing two toehold exchange reactions, which are competitive strand displac

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

279 level of theory showed high barriers for the exchange reaction, while the addition pathway was more p

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 CD38 then performs a base-exchange reaction with the donor NA group deriving from

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

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

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

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

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

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

290 cally enhanced catalytic performances in H/D exchange reactions with respect to (i) monometallic anal

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

292 Analogous exchange reactions with the single-bonded (CO)(3)CpMo-Mo

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.