ライフサイエンスコーパス: reaction with

1 , resulting in an overall disproportionation reaction with 1 equiv of ethyl arene formed for each equ

2 scence intensity enhancement at 435 nm after reaction with 1 equiv of H2S due to the inhibition of PE

3 of acetic acid from CH4 and CO2 is an ideal reaction with 100 % atom economy, but it is almost impos

4 az, which showed extensive biotransformation reactions with 18 BTPs detected that were mainly formed

5 and the inverse electron-demand Diels-Alder reactions with 3,6-bis(trifluoromethyl)tetrazine were an

6 enation/hydrogenolysis, and cyclization upon reaction with 4-bromobutanal to give the tricyclic skele

7 CuAAC reaction with 5(6)-FAM-azide demonstrated that only cell

8 luding a one-pot version combing the Mannich reaction with a base-mediated halogenation.

9 tion-state calculations for a concerted SNAr reaction with a bromine nucleofug, gives correlations su

10 ransamination, and finally a Pictet-Spengler reaction with a carbonyl cosubstrate.

11 internal alkenes via a catalytic hetero-ene reaction with a chalcogen-based oxidant.

12 , we have performed DFT calculations of this reaction with a cyclic meso anhydride.

13 ifying the surface with EDAC/NHS followed by reaction with a diamine compound.

14 on of methyl 5-hydroxynicotinate followed by reaction with a diene in the presence of triethylamine a

15 in fact effective in catalyzing the reverse reaction with a kcat of 11 +/- 0.4 s(-1) We also quantif

16 allel kinetic resolution (PKR) strategy upon reaction with a pseudoenantiomeric mixture of lithium (R

17 herol and BHT) antioxidants were measured by reaction with a series of 4-alkanoyloxyTEMPO radical pro

18 lo-enolcarbenes was successfully extended to reaction with a stable benzylidene dichlororuthenium com

19 features a late-stage lithiation-borylation reaction with a tertiary amine containing carbenoid.

20 OPA was also found to produce BrC in aqueous reactions with a broad spectrum of amino acids and amine

21 r organ and also an important site of immune reactions with a high density of dendritic cells (DCs),

22 rry out adenosine (A) to inosine (I) editing reactions with a known requirement for duplex RNA.

23 id activates the substrate toward sequential reactions with a nucleophile (epoxide ring-opening by ch

24 nistic studies indicate a complex network of reactions with a number of possible intermediates and me

25 as electrocatalysts or catalysts for various reactions, with a focus on the enhanced performance rela

26 report a single ribozyme that performs both reactions, with a nucleobase serving as initial acceptor

27 Stopping the reaction with acetic acid and a centrifugation/filtratio

28 nexpensive reagents, and reacts in the title reaction with acetonitrile, sodium chloride, and sodium

29 chemiluminescence (MF-CL) methods (based on reactions with acidic permanganate enhanced by formaldeh

30 atalyzed carbomagnesiation of cyclopropenes, reaction with acylsilanes, and addition of THF as cosolv

31 generated kinetin and its isomer, while its reaction with adenosine generated kinetin riboside, as c

32 med with moderate to good yields, while upon reaction with aldehydes, the initial addition product (6

33 , except for a higher rate of injection-site reactions with alirocumab.

34 ethionine, the reactive methyl donor, and by reaction with alkylating agents.

35 cals from arylazo sulfones and their ensuing reaction with allyl sulfones.

36 It was found that the reaction with alpha-substituted five- to seven-membered

37 eagents examined gave exclusive 1,4-addition reactions with alpha,beta-gamma,delta-unsaturated thiol

38 Phosphorus depletion in E. coli after reaction with AMZ, together with evidence of membrane pe

39 More importantly, the post-irradiation reaction with an additional substrate, isotope-labeled C

40 s to trigger the onset of the auto-oxidation reaction with an apparent turnover frequency of 440 s(-1

41 roethanesulfonyl fluoride is made via a neat reaction with an aqueous, nearly saturated potassium bif

42 using digital quantitative polymerase chain reaction with an independent cohort of 63 RRMS patients

43 oop-mediated isothermal amplification (LAMP) reaction with an initial number of DNA strands as low as

44 e activation of coordinated H2O2 followed by reaction with an olefin or H2O2.

45 of a lactam to a thioiminium ion followed by reaction with an organocopper (RCu) reagent and final re

46 as employed in a 2-fold neopentylic coupling reaction with an organolithium reagent derived from the

47 SEC analyses of d-glucose model reactions with and without l-pyroglutamic acid revealed

48 PO) derivatives of variable lipophilicity in reactions with antioxidant Trolox, and as pyrene-fluores

49 ility to additional sulfur incorporation via reaction with aqueous sulfide increased with increasing

50 cleavage was reduced in an organic solvent (reaction with arene radical anions in glyme).

51 anes undergo a stereospecific cross-coupling reaction with aromatic halides in the presence of a pall

52 gaged in a nickel-catalyzed C-C bond-forming reaction with aryl halides.

53 Upon reaction with aryl-N-sulfonylimines, the addition produc

54 then undergoes nickel-catalyzed substitution reactions with aryl halides and triflates and vinyl brom

55 Sulfide and cysteine ligand-exchange reactions with as-synthesized CdSe quantum dots (QDs) ar

56 eby stabilized against the highly exothermic reaction with atmospheric oxygen.

57 The complexation reaction with Au(I) ions spontaneously assembles lumines

58 tion of free diethylnitrosamine, whereas the reaction with azide results in N2O formation; these prod

59 ared using NaCN as the cyanide source, while reaction with B(C6F5)3 provides the cyanoborane derivati

60 (COOLi) and in determining the course of the reaction with bases and alkyl halides 3 are discussed.

61 reactivity as demonstrated in cross-coupling reactions with benzoyl chloride that produce ketones.

62 ed for removal of TFA from the atmosphere by reaction with biogenic Criegee intermediates.

63 pable of finding indirectly dead-end-related reactions with biological importance for the target orga

64 generated from the neutral precatalyst upon reaction with Boc2O, is proposed as the catalytically ac

65 tho-substituted 8-aryl BODIPY derivatives by reaction with borontrifluoride etherate, an overall proc

66 The reaction with both salicylaldehyde and p-tolualdehyde le

67 n two bottom quarks (b) causes the analogous reaction with bottom quarks () to have a much larger ene

68 oited for multifold C-C coupling cyclization reactions with C-C cleavage using symmetrical bisindolyl

69 s is shown to affect C-N bond scission while reactions with C6Cl4O2 or (tht)AuCl afford formal oxidat

70 was isolated and fully characterized in the reaction with carbon dioxide under mild conditions.

71 ng interphase, which minimizes the corrosion reaction with carbonate electrolytes and suppresses dend

72 elf-assembly of an anticipated hexagram upon reaction with Cd(2+) or Fe(2+); however, unexpected pent

73 to metal carboxylate and methane coproducts, reactions with CdMe2 produce surface bound methyl groups

74 he authors show a reactivation strategy by a reaction with cheap sulfur powder under stirring and hea

75 med by similar pathways in both cases (i.e., reactions with chloramines and free chlorine).

76 Family studies, long-range polymerase chain reaction with cloning, and complementary DNA sequencing

77 Further reaction with CO leads to formation of a CO analogue, wh

78 forming of methane (DRM), two key industrial reactions with common elementary steps and intermediates

79 onalized NPs were radiolabeled via a "click" reaction with copper-64 ((64)Cu)-1,4,7-triazacyclononane

80 ough this Communication focuses primarily on reactions with cyanide as nucleophile, preliminary exper

81 The diastereoselectivity of azido-Ugi reaction with cyclic amines was investigated.

82 The normal electron-demand Diels-Alder reactions with cyclopentadiene and the inverse electron-

83 helenalin acetate is not due to irreversible reaction with cysteine residues of C/EBPbeta.

84 r offers a probe having selective, sensitive reaction with cysteine to rapidly produce a reporter who

85 We used 16S rRNA gene polymerase chain reaction with degenerate primers, followed by high-throu

86 Upon reaction with DFOB or DFOB + oxalate, the remaining soli

87 hat matches the experimental values, for the reactions with DHA and Xan (Angew.

88 Analogous reactions with di-tert-butyl peroxide yielded [Cp*2Fe][(

89 ining polymers underwent click-type coupling reactions with dialkynes, while the (iso)cyanate-contain

90 ted quinolines with metal amides followed by reaction with different electrophiles.

91 catalyst was used in batch aerobic oxidation reactions with different primary alcohols and shown to b

92 Its reaction with dioxygen takes place rapidly at ambient co

93 While 1 is stable toward dioxygen, its reaction with dioxygen under NO atmosphere forms the {Fe

94 For gross adulteration levels (>25.0%, w/w) reaction with diphenylamine-sulfuric acid was found adeq

95 works (BRNs) in a cell frequently consist of reactions with disparate timescales.

96 A method whereby reactions with diverse functional groups within a single

97 Upon reaction with either molecular oxygen or di-tert-butylpe

98 embrane protects the metal against parasitic reactions with electrolyte and, for fundamental reasons,

99 se in the formation of Li dendrites and side reactions with electrolyte components, thus potentially

100 pi-system of benzene is highly resistant to reactions with electron-rich and negatively charged orga

101 ess, copper-catalyzed/mediated C-H amination reactions with electron-rich anilines remain an unsolved

102 of forming stable nonvolatile compounds upon reaction with elemental halogens may partially mitigate

103 Drug reaction with eosinophilia and systemic symptoms (DRESS)

104 Drug reaction with eosinophilia and systemic symptoms (DRESS)

105 hey were silylated and subjected to a Perkow reaction with ethyl 3-chloropyruvate.

106 1-aza- and 2-aza-derivatives in Diels-Alder reactions with ethylene and fumaronitrile were investiga

107 ) annulation reaction and multiple catalytic reactions with excellent overall yield.

108 in nitric oxide synthases (NOSs) upon their reaction with excess PN.

109 ns in hydrogen-atom and oxygen-atom transfer reactions, with faster rates corresponding to weaker equ

110 dinuclear zirconium species can catalyze the reaction with feasible energy barriers.

111 acyclic, metal-free, neutral radical L(.) on reaction with FeBr2 .

112 logue to a common fungal metabolite, and its reaction with ferrihydrite and goethite under variable p

113 to replace existing precious-metal-catalyzed reactions with first-row analogs.

114 Its further reaction with fluorobenzene afforded the CAr -H bond act

115 for secondary covalent cross-linking and for reaction with fluorophores for in vitro and in vivo imag

116 A novel catalytic cycle for the reaction with formic acid is proposed and subjected to a

117 Galp-(1-->6)-d-Glcp are formed from acceptor reactions with free Glc and not by rearrangement of Glc

118 Experimental investigation of chemical reactions with full quantum state resolution for all rea

119 le amide base and trapped in a cycloaddition reaction with furan in moderate to good yields.

120 y employing donor-acceptor oxiranes in a new reaction with gamma-hydroxyenones.

121 e and phenol products are released following reaction with H2.

122 Neither reaction with O2 nor reaction with H2O occurs under comparable conditions for

123 based radical species that accumulate during reaction with H2O2 Our results suggest that catalase-ina

124 en substituents geometrically positioned for reaction with halides in solution, halogen bonding was d

125 n ozone and gaseous elemental mercury due to reactions with halogen atoms, influencing atmospheric co

126 ersible during the catalytic process because reaction with HBpin is faster than beta-hydrogen elimina

127 N-Boc-alpha-amino aldehydes in cross-benzoin reactions with heteroaromatic aldehydes is demonstrated.

128 salts and a tertiary amine base promote the reaction with high site-selectivity for either the 3'-po

129 esulting enzyme catalyses a reversible aldol reaction with high stereoselectivity and tolerates a bro

130 oth Mukaiyama-Mannich and oxocarbenium aldol reactions with high efficiency and enantioselectivity.

131 kinetic characterization of electrochemical reactions with high electroanalytical sensitivity.

132 olysis (SJS/TEN) are rare but severe adverse reactions with high mortality.

133 ver, realization of these goals will require reactions with high specificity and precise control.

134 obtained efficiencies of up to 90% for these reactions with high throughput processing up to 120muL o

135 ly involved in the subsequent C-H activation reactions with hydrocarbon solvents reported for some of

136 Subsequent reaction with hydrogen-bond activated dialkyl azodicarbo

137 Subsequent reaction with hydrogen-bond-activated aldimines delivers

138 heterocycles were converted to C-Si bonds by reaction with hydrosilanes under the catalytic action of

139 resols, and methoxyphenols by fast gas-phase reaction with hydroxyl radicals (HO(*)).

140 l sensitizers and DOM isolates revealed that reactions with hydroxyl radicals dominated the transform

141 l glyoxal loss processes such as photolysis, reactions with hydroxyl radicals, and aerosol uptake wer

142 an oxygen-dependent prolyl hydroxylase (PHD) reaction, with hypoxia-inducible factor alpha (HIFalpha)

143 mplex 3 also forms more crowded complexes in reactions with I2, PhCl, and Al2Me6, which generate (C5M

144 rhodium-catalysed asymmetric Suzuki-Miyaura reaction with important partners including aryls, vinyls

145 f advanced catalysts toward oxygen reduction reaction with improving activity and stability is signif

146 rapped, these molecules can undergo chemical reactions with increased rates and with stereoselectivit

147 atures are that mechanochemistry facilitates reactions with insoluble reactants, enables high-yieldin

148 opper(I) sulfide (Cu2 S) NCs through a redox reaction with iodine molecules (I2 ), which formed vacan

149 ct as an unambiguous nucleophile through its reactions with iodomethane, benzophenone and N,N'-di-iso

150 rrocenes undergo one-step carboxamidation by reaction with isocyanates in CF3SO3H solution.

151 ever, the integration of a DNA amplification reaction with its associated detection in a low-cost, po

152 ch will be involved in the second pericyclic reaction with juglone to construct the tetracyclic core

153 wn sequence is predicted based on similarity reactions with known rate constants.

154 en which can generate a reactive peroxide by reaction with [KOt-Bu]4 as indicated by density function

155 Heating aqueous d-glucose model reactions with l-glutamine and l-alanine yielded similar

156 isubstituted selenourea precursors and their reaction with lead oleate at 60-150 degrees C to form ca

157 e actors, audiences may experience autonomic reactions, with less distance, or may have to distance p

158 mutagenic lesions produced endogenously via reactions with lipid peroxidation (LPO) products.

159 f 3.12 and 1.16 the activation energy of the reaction with Lipozyme(R) RM IM and Novozym(R) 435, resp

160 at -70 degrees C is easy to achieve, whereas reaction with lithium-magnesium and lithium-zinc amides

161 um coatings also undergo reversible alloying reactions with lithium ions, facilitating design of high

162 cycloaddition is considered to be a "click" reaction with many applications in chemical biology and

163 hnique to monitor spatially confined surface reactions with mass spectrometry under ambient condition

164 For such a complex reaction with membranes, it has been difficult to uncove

165 robes are capable of performing amalgamation reactions with metal cations, which avoid unwanted side

166 ications are based on whether the elementary reactions with methane proceed by chain or nonchain reac

167 lar, CHA reactions are defined as elementary reactions with methane that result in a discrete methyl

168 ast, CHO reactions are defined as elementary reactions with methane where the carbon atom of the prod

169 nder the main element involved in the direct reactions with methane.

170 rations and the mechanisms of the elementary reactions with methane.

171 Reaction with methyl iodide in the presence of potassium

172 ep to modulate its volume expansion and fast reaction with methylammonium iodide (MAI)/formamidinium

173 rsity of reactions, namely Wittig reactions, reactions with methylene active compounds, formation of

174 MTGase crosslinking reactions with milk proteins stabilize the three-dimensi

175 ur results illustrate Cr(VI) generation from reaction with Mn oxides within structured media simulati

176 e use of (2-arylcyclopropyl)ethanones in the reactions with model 4-bromophenylhydrazine hydrochlorid

177 DRESS) is a rare severe adverse drug-induced reaction with multiorgan involvement.

178 ded sepsis, malignancy, and severe cutaneous reactions with multiorgan failure.

179 e effects (KIEs) tell us about H-abstraction reactions with multispin-state reactivity options?

180 F performs a sequential ordered bi-substrate reaction with MVAPP as the first substrate, consistent w

181 ound to exhibit aromatic C-H activation upon reaction with N,N-diethylaniline, naphthalene, and even

182 N-monochlorovaline, with a slower subsequent reaction with N-monochlorovaline to form N,N-dichloroval

183 ical species acts as an intermediate in this reaction, with NADH and NADPH (the reduced forms of nico

184 or activity; flavin reduction is achieved by reaction with NADPH.

185 Azo-compounds 7 upon further reaction with NaTeC6H5 were reductively cleaved to provi

186 results point to HAT as implausible for the reaction with nitric oxide radical in all the solvents i

187 yrrolidines were synthesized by 1,4-addition reactions with nitroalkanes, followed by reduction and c

188 itu, is exemplified by dipolar cycloaddition reactions with nitrones to give highly substituted 4-nit

189 x with the major sigma factor (sigma(A)) and reaction with NO disassembles this complex.

190 hetero)aromatic amines-essentially a one-pot reaction with no isolation of intermediates; (ii) the al

191 Conversely, reactions with NOB yielded an additional oxidized adduct

192 There were no cross-reactions with non-H5N1 influenza viruses or other avian

193 arbonyl and iminyl chemistry by facilitating reactions with non-nucleophilic reagents.

194 e resulting eta(2)-arenium species undergoes reactions with nucleophiles at the adjacent meta carbon.

195 derivatives, and are also consumed slowly by reactions with nucleophiles.

196 meaningful exposures focuses on adducts from reactions with nucleophilic loci of blood proteins, part

197 e 3 featuring a Si=O-->B interaction through reaction with O2 , N2 O, or CO2 , and formation of silan

198 Neither reaction with O2 nor reaction with H2O occurs under comp

199 ropose that the partial reversibility of the reaction with O2 results from the four-electron reductio

200 functions as the sensory module, undergoing reaction with O2 that leads to conversion to a [2Fe-2S]

201 In addition to reaction with O2, cis-[Pd(IPr)2(eta(2)-O2)] reacts at lo

202 The related reaction with [(OEP)Ru(NO)(5-MeIm)](+) generates the (OE

203 widely used herbicide, and its heterogeneous reaction with OH radicals is important for assessing its

204 ric sink for (CF3)2CFCN was determined to be reaction with OH radicals.

205 The two carbamates were subjected to reaction with (*)OH, persistent DPPH(*) and galvinoxyl r

206 es photodegradation by direct photolysis, by reactions with (*)OH and CO3(*-), and possibly also with

207 hoton-generated cyclooctynes undergo a SPAAC reaction with organic azides, yielding the expected tria

208 15%) Faradaic yield, likely due to competing reactions with organics.

209 etection limit of 60ng/ml and shows no cross-reaction with other analogous organophosphates or metal

210 nce for acid production from indoor chemical reactions with ozone was found.

211 in a GSH and GSSG mixture via a 1,4-addition reaction with p-benzoquinone (BQ), followed by enzymatic

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

213 es were not protected from DMS and showed no reaction with permanganate.

214 ypes of reactive species involved in primary reactions with PFOA showed that hydroxyl and superoxide

215 mples demonstrating such selectivity include reactions with: phenolics, through dearomatizing ortho-s

216 re pyrrolidine-based carbonate was used, the reaction with phenols proceeds via a bicyclic aziridiniu

217 isphosphine ligands and activated in situ by reaction with pinacolborane (HBpin).

218 olkit and the frequent failure of even these reactions with polar and functionalized substrates.

219 sign principles for programmable biochemical reactions with potential applications to autonomous sens

220 negative charge at the oxygen end that upon reaction with PPh3 and benzoic acid afford Ph3P horizont

221 used as electrophiles in asymmetric Mannich reactions with pyrazolones.

222 e corresponding pyridyl cryptands 3 and 4 by reaction with pyridine-2,6-dicarbonyl chloride.

223 and [IMesH][C14H8O2B(C6F5)2] (12), while the reactions with quinuclidine and DMAP afforded the specie

224 Unfortunately, carrying out reactions with radicals in an enantiocontrolled fashion

225 Anaphylaxis is a serious systemic allergic reaction with rapid onset and potentially life-threateni

226 f iron oxide particles as a result of either reaction with reducing moieties, light-mediated ligand t

227 These reactions with rLb6H were highly specific (98.5%) when c

228 N3-Methyladenine (3-MeA) is formed in DNA by reaction with S-adenosylmethionine, the reactive methyl

229 and formation of silanethione borane 4 from reaction with S8 .

230 In assembly reactions with saturating profilin, approximately 85% of

231 The compatibility of this reaction with secondary free amines and anilines also ov

232 Upon tandem Diels-Alder reactions with several symmetrical as well as unsymmetri

233 iated ligand to metal charge transfer and/or reaction with siderophores.

234 talytic Cu/aminoxyl-driven alcohol oxidation reactions, with similar findings.

235 ultiple interdiffusion pathways for complete reaction with SnI2 .

236 ute configuration was determined by chemical reactions with sodium borohydride, hydrogen peroxide, al

237 led that radical mechanisms are preferred in reactions with sterically hindered coupling partners wit

238 outliers to the Bronsted correlation are the reactions with sterically hindered pyridines, which appa

239 tion between neutral and anionic phases upon reaction with stoichiometric amounts of halide or pseudo

240 Reaction with styryl bromide via O-styrylation, Claisen

241 ve deaggregation, and at other times include reaction with substrate.

242 acyl chlorides or carboxylic acids and their reaction with sugar azides.

243 ttributed to direct electron transfer and to reactions with surface-bound reactive chlorine species.

244 the free energy DeltaG degrees PCET for the reaction with TEMPO (-48.4 kJ mol(-1)) are very similar

245 d on ZrO2, which results in a more efficient reaction with TEOA.

246 eduction to the corresponding aldehydes, and reaction with tert-butyl (triphenylphosphoranylidene)ace

247 trofurans undergo intramolecular Diels-Alder reactions with tethered electron-poor dienophiles more r

248 2 + 2] cycloaddition-retroelectrocyclization reaction with tetracyanoethylene (TCNE) and 7,7,8,8-tetr

249 pollen allergen Bet v 1 and subsequent cross-reaction with the apple protein Mal d 1.

250 However, the reaction with the bis-silylated cluster [Ge9{Si(TMS)3}2]

251 ted more slowly, which ensures more complete reaction with the contaminant.

252 In contrast, the analogous reaction with the Cp(Bn) derivative [Cp(Bn)Fe(mu-Br)]2 (

253 zed via a domino addition-Wittig olefination reaction with the cumulated ylide Ph3PCCO.

254 erent rates: kobs1, which corresponds to its reaction with the deprotonated form of the substrate, an

255 iron(II)-SciOPP complexes are consumed upon reaction with the electrophile with concomitant generati

256 an forge interstrand DNA-DNA cross-links via reaction with the exocyclic amino group on a nearby 2-de

257 etention of oscillatory behavior for the B-Z reaction with the formation of giant vesicles bring a ne

258 The corresponding product from reaction with the new Bi(II) radical Bi(NON(Ardouble dag

259 A domino reaction with the organocatalytic enantioselective Micha

260 g CPP precursor was used for the Diels-Alder reaction with the parent benzyne or 3,6-dimethoxybenzyne

261 bstrate, and kobs2, which corresponds to its reaction with the protonated form of the substrate.

262 oxidative removal of Mn(II) from solution by reaction with the reactive oxidant species produced thro

263 ion and added functionality through chemical reaction with the retained phase.

264 ng a regio- and stereoselective oxyamination reaction with the same nitrene reagent generated in stoi

265 omplex of a ligand-centered radical, whereas reaction with the stronger oxidant AgBF4 formed the meta

266 the release of phenylalanine amino acid in a reaction with the yeast enzyme of phenylalanine ammonia

267 AA caused by chlorine follows a second-order reaction, with the rate constant k1 is 5.0 x 10(4) M(-1)

268 mature cell failure as a result of parasitic reactions with the anode.

269 substituted alkenes through cross-metathesis reactions with the commercially available, inexpensive a

270 Subsequent bioorthogonal reactions with the fluorophore-conjugated DpTz reagents

271 Reactions with the highest agreement between simulations

272 Reactions with the N-based nucleophile diethylamide resu

273 s for the design of new amide cross-coupling reactions with the N-C(O) amide bond cleavage as a key s

274 has inspired original methodologies to probe reactions, with the aim to rationalize unknown mechanism

275 is and low-temperature water-gas shift (LTS) reactions, with the choice of precursor phase strongly i

276 followed by a description of stoichiometric reactions, with the competition between the C-H and C-F

277 been available on early Earth from prebiotic reactions, with the goal of making the model less discon

278 ides and aliphatic carboxylic acids based on reactions with TMMS and one or two CAD experiments.

279 ducts that had lost a methanol molecule upon reactions with TMMS.

280 ron hydroxylase intermediate formed during a reaction with toluene.

281 a key role in atmospheric chemistry through reactions with trace species that can lead to aerosol pa

282 Studies of the reaction with tris(pentafluorophenyl)borane (B(C6F5)3),

283 e quenching by the probes, but not for their reaction with Trolox.

284 r substrate radicals was observed during the reaction with Trp or any molecule within a tested panel

285 ilms that are powered by DNA strand exchange reactions with two different domains that can respond to

286 can participate in 1,3-dipolar cycloaddition reactions with two maleimides that differ in the relativ

287 acetylation at the 2-position and subsequent reaction with typing antiserum 35a.

288 ct, requirement of toxic catalysts, and side reactions with unintended biomolecules.

289 o decades, the demand for new chemoselective reactions with unique abilities, and those compatible wi

290 In notable contrast to reactions with unsubstituted allylboronic acid pinacol e

291 about the formation of CO2 adducts from its reaction with various amine-functionalized SBA-15 contai

292 without cleavage of the 1,2,3-dithiazole by reaction with various nucleophiles, giving access to 4-[

293 Gibbs free energies of reactions with various free radicals indicate that syn-D

294 Compound 6 can be used directly in SN2@P reactions with various nucleophiles to yield valuable P-

295 indicate that carbamates can undergo direct reactions with various radical species, oxidizing themse

296 amine-squaramide catalyzed C-C bond forming reactions with vinyl ketones or Morita-Baylis-Hillmann-t

297 lar ratios of >/=0.3, effectively eliminates reaction with water, but retains significant reactivity

298 syn- and anti-CH3 CHOO remain inert towards reaction with water.

299 hiral ligands for transition-metal-catalyzed reactions with well-defined reaction mechanisms but mult

300 -allenoate 10aa in 68% yield and 96% ee upon reaction with ZnI2.