ライフサイエンスコーパス: reaction of

1 Reaction of 1 with P(t-Bu)3 affords the zwitterion 3-(t-

2 In contrast, the reaction of 1 with PPh3 proceeds to give two regioisomer

3 ly, 4(*) may also be synthesized directly by reaction of 1 with sulfur (in a 1:4 ratio) in THF.

4 by migration of a MIDA-boryl group (for the reaction of 1) and hydrogen (for the reaction of 24), to

5 In the rearrangement step for the reaction of 1, the MIDA-boryl group migrates easily, pro

6 t light-activated electrocyclic ring-opening reaction of 1,3-cyclohexadiene is a fundamental prototyp

7 [3,3]-sigmatropic rearrangement/Diels-Alder reaction of 1,9-dien-4-yne esters is described.

8 of the protonation step in the ring-opening reactions of 1,3-benzoxazines with thiols in absence of

9 Gas-phase ion/ion reactions of (13)C-TrEnDi-modified phosphatidylethanolam

10 (18)F-SO3F(-) was synthesized by reaction of (18)F(-) with SO3-pyridine complex in MeCN a

11 The 1:1 reaction of 1a or 1b with 5a or 5b yields the unknown mo

12 The reaction of 2,5-dihydro-1H-phosphole 1-oxide 1 with ArB(

13 uoride-promoted vinylogous Mukaiyama-Michael reaction of 2-[(trimethylsilyl)oxy]furan with diverse al

14 On the other hand, the reaction of 2-aminophenols/anilines produced the corresp

15 sodium benzenetellurolate, NaTeC6H5, and by reaction of 2-bromo-3-nitrobenzamides with Na2Se2.

16 Furthermore, the reaction of 2-furanmethanol with adenine in the presence

17 enantioselective Michael-acetalization-Henry reaction of 2-hydroxynitrostyrene and 5-oxohexanal was d

18 atives via a one-pot copper catalyzed tandem reaction of 2-iodobenzamides with 2-iodobenzylcyanides h

19 for the reaction of 1) and hydrogen (for the reaction of 24), to give the same BF3-coordinated alpha-

20 rlying thermodynamic factors controlling the reactions of 25 and its reaction partners, and a detaile

21 Further reaction of 3 with 2 equiv of elemental sulfur in THF af

22 ring) indoles and 1-benzothiophenes from the reaction of 3-alkenylpyrroles/-thiophenes as C4 synthons

23 A cascade reaction of 3-ylidene oxindoles with phenols and beta-na

24 A systematic study of the N-substitution reactions of 3-substituted pyrazoles under basic conditi

25 0.3% contribution to SOA growth from direct reactions of (3)IC* with limonene, isoprene, alpha-pinen

26 rbazole has been prepared by cyclomerization reaction of 4,5-bis(6-carbazole-9-yl-hexylsulfanil)phtha

27 The formation of BrC in the reaction of 4-OPA with AS and ammonium nitrate was great

28 cient, solvent-free, and eco-friendly domino reaction of 5/6-membered cyclic sulfamidate imines with

29 Thus, reactions of 5, triflic acid, and either N-methylpyrrole

30 Finally, the hydrophosphination reaction of [60]fullerene by the sec-phosphine borane co

31 osphination and the retro-hydrophosphination reactions of [60]fullerene/phosphine borane compounds of

32 rease in the overpotential for the oxidation reaction of A and G.

33 Reaction of a C-based nucleophile, namely the phenyl ani

34 the case of para-substituted phenols, after reaction of a dilithio phenolate species with a boronic

35 ound 320-350 K observed in the isomerization reaction of a hydroxycarbene into an aldehyde.

36 its as well as the transannular ring closure reaction of a nonconjugated diyne.

37 ochastically generated from the ring-opening reaction of a spiropyran, we provide mechanistic insight

38 e hinge region by the protein trans-splicing reaction of a split intein to generate BsAbs without hea

39 ted acid catalysts of the hetero-Diels-Alder reaction of a wide variety of aldehydes and dienes to gi

40 ty was observed in solution, but solid-state reactions of a 1:1 complex as a suspension or a thin fil

41 concentrated solar energy mediated by redox reactions of a metal oxide.

42 nt alkyl-alkyl cross-coupling, specifically, reactions of a racemic pyrrolidine-derived nucleophile w

43 Along with the model reaction of acetone addition to propyne and allene, the

44 ncement was quantified and attributed to the reaction of activated O atom within the solvent cage pri

45 The bimolecular rate constant for reaction of alanine with OPA is found to be 84 +/- 10 an

46 atalyzed enantioselective reductive coupling reactions of aldehydes and alkynes have been developed.

47 The enantioselectivity of amine-catalyzed reactions of aldehydes with electrophiles is often expla

48 The corresponding reaction of alkenes with aryl-1,3-butadiynes, ethynylogo

49 ehensive mechanism for the gold(I)-catalyzed reaction of alkynes with alkenes is proposed on the basi

50 Despite the myriad of Au(I)-catalyzed reactions of alkynes, the mono Au(I)-catalyzed pendant t

51 Two CuCN-mediated rearrangement reactions of allenylcyclopropanols to cyclopentenones ha

52 ficient copper-catalyzed carbenoid insertion reaction of alpha-diazo carbonyl compounds into Si-H and

53 irst visible light-induced Pd-catalyzed Heck reaction of alpha-heteroatom substituted alkyl iodides a

54 -carboxylates through the one-pot sequential reaction of alpha-lithiated alkoxyallenes with isothiocy

55 he mechanism, scope, and applications of the reactions of alpha-imino esters and related compounds in

56 ange of illustrative examples, including the reactions of alpha-lithiated haloalkanes, epoxides, and

57 We report non-decarbonylative Mizoroki-Heck reactions of amide derivatives.

58 The reactions of ammonia with HOCl or HOBr that lead to dich

59 atalysis can also be extended to the one-pot reactions of ammonium formate, 2-nitroacetophenone, and

60 hiolate [Cu(II)]-SR intermediate formed upon reaction of an additional equiv thiol with [Cu(II)]-OH.

61 Herein, a new reaction of an alkyl iodide (R-I) with an azide anion (N

62 acetates is a rare example of a Type I DyKAT reaction of an allene, the first example of DyKAT in a c

63 in situ allylic strain controlled retro-ene reaction of an allyl diazene, i.e., an allylic diazene r

64 p is an intramolecular [3 + 2]-cycloaddition reaction of an in situ generated azomethine ylide onto a

65 the first time by a one-pot Knoevenagel-IMDA reaction of an l-phenylalanine-derived tetramic acid and

66 cations have also been synthesized from the reaction of an NHC with phenylethynyl bromide or 1,4-bis

67 5)2 isomer was deduced, which showed typical reactions of an oxygen/boron frustrated Lewis pair.

68 dose (with additional lower steps for index reactions of anaphylaxis).

69 es capitalizing on the highly stereospecific reaction of anomeric nucleophiles.

70 -kinetic isotope effects ((18)O-KIE) for the reactions of aqueous O2, and studied the impact of radic

71 ing from 2005 to 2017 concerning the organic reactions of aromatic ligands eta(2)-coordinated to tung

72 A simple formylation reaction of aryl halides, aryl triflates, and vinyl brom

73 II) -catalyzed ortho C-H alkoxycarbonylation reaction of aryl silanes toward active hexafluoroisoprop

74 Cross-coupling reactions of aryl groups with alpha-fluoro carbonyl comp

75 ple and an efficient one-pot three-component reaction of arylamines, aromatic aldehydes, and cyclic k

76 ivity was employed in the diastereoselective reaction of arylboron reagents with substrates containin

77 quinazolines has been realized by the direct reaction of aryldiazonium salts with two equivalent of n

78 The halogen-mediated cyclization reaction of aryldiynes to produce halogenated indeno[1,2

79 per-free rhodium-catalyzed C-H acetoxylation reaction of azaindoles has been achieved at near ambient

80 The reaction of benzaldimine with a methoxycarbonyl group in

81 giochemical control of the cyclocondensation reaction of beta-enamino diketones with arylhydrazines.

82 ble-sidearmed bisoxazoline complex catalyzed reactions of beta-triisopropylsilyl-substituted enoldiaz

83 Reaction of bis-(2,6-diisopropylphenyl)-imidazol-2-ylide

84 Enantioconvergent arylation reactions of boronic acids and racemic beta-stereogenic

85 ect the carer negatively and cause emotional reactions of burden and stress.

86 the theoretical and experimental studies of reactions of C1 molecules (CO, CO2, CH3OH, etc.), the re

87 Finally, the chemical reaction of [C2mim][OAc] with a cysteine-containing biom

88 The reaction of (C5 Me5 )2 Th(CH3 )2 with the phosphonium sa

89 The Fe(II)8L6 cage also enabled the reaction of C60 and anthracene to yield the bisadducts s

90 The reaction of C6F5H and H2C horizontal lineCHSiMe3 with ca

91 The tetraoxane products generally formed in reactions of carbonyl and dicarbonyl compounds with H2 O

92 9 CBDs: second-order rate constants for the reactions of CBDs with ozone (kO3) (<0.1-7.9 x 10(3) M(-

93 This seems problematic because the reaction of CH4 and water to generate methanol and H2 is

94 The reaction of chiral N-tert-butanesulfinyl aldimines with

95 nclude the highly regio- and stereoselective reactions of chiral N-sulfinyl metallodienamines (NSMDs)

96 free energies of activation and kexp for 31 reactions of Cl(*) with organic compounds.

97 Consideration of reactions of (*)ClO and its daughter products (e.g., ClO

98 sition of water and methanol, as well as the reactions of CO and CO2 over TMC surfaces.

99 Visualization of a phase reaction of composite nanomaterials with high spatial an

100 =hexaazatrinaphthylene) proceeds through the reaction of Cp*2 Ln(BPh4 ) with HAN under strongly reduc

101 activation free energies for the Diels-Alder reactions of cyclic 1-azadienes are 10-14 kcal mol(-1) h

102 ) bond formation in the copper(I)-catalyzed reaction of cyclopropanols with diazo esters.

103 ted by periplasmic oxidation and cyclization reactions of d-tyrosine and l-diaminobutyric acid.

104 Experiments involved reactions of d-xylose, d-arabinose and d-ribose with gly

105 y steps are the use of rhodium(II)-catalyzed reactions of diazocarbonyl compounds to generate the fou

106 s for some hydrolysis and disproportionation reactions of dichloramine, monobromamine, and bromochlor

107 The reaction of dichloro ketones with azide anions provides

108 nanostructures at the MWCNT/Cu interface by reaction of diffused Cr atoms and amorphous carbon of MW

109 ic intra- and intermolecular C-H activation; reactions of dioxygen with Pt(II) complexes that may be

110 (BMCs) that encapsulate sequential enzymatic reactions of diverse metabolic pathways.

111 cades, the precise events taking place after reaction of DNA nucleobases with OH radical have been wi

112 The chemoselective reaction of donor/acceptor (D/A) and acceptor/acceptor (

113 droboration and palladium-catalyzed coupling reactions of E-1,2-dichloroethene.

114 An efficient dual-metal catalyzed reaction of electron-deficient o-chlorovinylpyridines wi

115 d-catalyzed Heck-type coupling (Matsuda-Heck reaction) of electron rich arene diazonium salts with el

116 The traceless Petasis borono-Mannich reaction of enals, sulfonylhydrazines, and allylboronate

117 Diastereoselective multicomponent reactions of enantioenriched 4-nitroprolinates, obtained

118 Highly selective divergent cycloaddition reactions of enoldiazo compounds and alpha-diazocarboxim

119 This comprehensive review on cycloaddition reactions of enoldiazo compounds, with emphasis on metho

120 nd phloroglucinolysis allowed us to describe reaction of epicatechin and acetaldehyde.

121 ert atmosphere was governed by decomposition reactions of esterified compounds.

122 The catalytic reaction of ethyl 3-(trimethylsilyl)propiolate and methy

123 (ONOO(-)) arising from the diffusion-limited reaction of exogenous NO and endogenous superoxide (O2(*

124 ative reverse transcription polymerase chain reaction of extracellular purine degrading enzymes and P

125 Reaction of Fe(OH)2(s) in the presence of Cr(III) result

126 Reaction studies demonstrate that reaction of FeBr2(SciOPP) with 1 equiv (triisopropylsily

127 In this work, the reverse reaction of FHL is unlocked.

128 A mild, asymmetric Heck-Matsuda reaction of five-, six- and seven-membered ring alkenes

129 conformational change in the oxidative half-reaction of FMOs.

130 = 1718 h(-1) and Ea = 31 kJ/mol) and one-pot reactions of formic acid, 2-nitrophenol, and aldehydes i

131 Two named reactions of fundamental importance and paramount utilit

132 rate of force-accelerated retro-Diels-Alder reactions of furan/maleimide adducts.

133 -inspired enantioselective rhodium-catalyzed reaction of gamma-substituted enoldiazoacetamide with ni

134 phenols by this method is a well-recognized reaction of general utility, the associated para-selecti

135 by using Cre-reporter mice, polymerase chain reaction of genomic DNA, and quantitation of Bmp6 messen

136 NO determination was based on the reaction of Griess.

137 ery first time via the bimolecular gas-phase reaction of ground-state carbon atoms with 1,3,5-cyclohe

138 he very detailed dynamics of the abstraction reactions of ground-state methane (and isotopologues) wi

139 The efficient Suzuki-Miyaura cross-coupling reaction of halogenated aminopyrazoles and their amides

140 It involves the reaction of halogens or halides with hydrocarbons, leadi

141 The direct amination reaction of heterocyclic thiols has been developed in th

142 efficient organocatalyst for the asymmetric reaction of homophthalic anhydride with imines.

143 nalysis was demonstrated using proteome-wide reactions of HT-29 cell lysates with a model probe of th

144 Reaction of [(i) Pr2 NN]Cu(NCMe) with bulkier azides N3

145 atic interactions for describing the binding reactions of IDPs.

146 lated to be 16 h, indicating the significant reaction of IMD over the course of a day.

147 The reaction of indoles leads to the formation of chiral C-N

148 meet the specific needs of a metal-catalyzed reaction of interest.

149 t into the source of the regioselectivity in reactions of internal alkynes.

150 combination of ion intercalation with redox reactions of iodine allows for developing rechargeable i

151 the porous carbon skeleton facilitates redox reactions of iodine and ion intercalation.

152 has been reported in 2012, which employs the reaction of iodoalkyl radical with molecular oxygen: for

153 Kinetic studies on the reactions of iron complexes supported by the TPA (tris(p

154 by utilizing the catalytic enolate arylation reaction of ketones in conjunction with several 3-bromoi

155 In contrast, the reaction of L(-) with CuI formed the unique, neutral Cu2

156 ed that can be formed at room temperature by reaction of [(L)2Ni(II)2(mu-X)3]X (X = Cl or Br) with Na

157 The reaction of LGa (L = Dipp(4-(Dipp-imino)pent-2-en-2-yl)a

158 a-ketocarboxylates 1(COOLi), prepared by the reaction of lithium enolates 2(Li(+)) with carbon dioxid

159 Around 50% of CO2 was formed from thermal reactions of lower molecular weight compounds that repre

160 d anion-pi catalysts to explore the addition reaction of malonic acid half thioesters to enolate acce

161 The reaction of MBH bromides with 2-aminopyridines takes pla

162 This review covers the functionalization reactions of meso-arylcorroles, both at the inner core,

163 he dry reforming of methane (DRM), i.e., the reaction of methane and CO2 to form a synthesis gas, con

164 The ring contraction reaction of methoxy- or phenylthio-diazepinones under ac

165 rent activities in the Morita-Baylis-Hillman reaction of methyl acrylate with benzaldehyde derivative

166 Palladium(II)-catalyzed C-H carbonylation reactions of methylene C-H bonds in secondary aliphatic

167 ed can be used to calculate the rates of the reactions of Michael acceptors 1 and 2 with any nucleoph

168 l acceptors, we measured the kinetics of the reactions of monoacceptor-substituted ethylenes (H2C hor

169 effect of oxalic acid (OxA) on NPF from the reaction of MSA and methylamine (MA) at 1 atm and 294 K

170 strates that the activation of self-cleavage reaction of MyRF is independent of the presence of its N

171 The mechanism of reaction of N-(3-pyridyl)aldimines with olefins can be e

172 Fs) as additives is herein described for the reaction of n-alkyl aldehydes in the presence of methylv

173 A cascade reaction of N-aryl-alpha,beta-unsaturated nitrones and e

174 ved in the intermolecular [3 + 2] annulation reaction of N-cyclopropylaniline (CPA, 1) and styrene 2

175 trans steroid-fulleropyrrolidines hybrids by reaction of N-metalated azomethine ylides [Cu(II) or Ag(

176 We describe here the reaction of N-nucleophiles with the amino acid dehydroal

177 Strategies relying on intramolecular reactions of N-acyliminium intermediates, also referred

178 In the reactions of N-alkylamides and N-alkylphthalimides with

179 egioselectivity in Zn-catalyzed allenylation reactions of N-protected l-alpha-amino aldehydes is repo

180 NO3 )4 ](+) (3), a complex obtained from the reaction of [(N4Py)Fe(II) (NCMe)](2+) with 2 equiv CAN o

181 Reaction of [NBu4][LCu(II)OH] with excess ROOH (R = cumy

182 The reactions of nitramine, N-methyl nitramine, and N,N-dime

183 The reaction of nitrite with different amino acids containin

184 agents for Corey-Chaykovsky cyclopropanation reactions of nitro styrenes.

185 This one-pot reaction of Nitron provides access to a range of previou

186 The reaction of o-phthalaldehyde (OPA) with alanine in the p

187 O2, the weakness of the O-O sigma bond makes reactions of O2, which eventually lead to cleavage of th

188 fter the proposal of the main routes for the reaction of (*)OH with adenine, the present work demonst

189 The unexpected reaction of one of these 1,4-oxazepanes in the presence

190 e intermediate structures delivered from the reaction of ortho-quinones with alpha-amino acids were d

191 dence of the role of the defects in chemical reaction of oxide surfaces with both water and Pb-contai

192 g (i.e., metal-mediated and metal-catalyzed) reactions of oximes.

193 ible ring-opening addition and fragmentation reaction of p-cresol-based N-phenylbenzoxazine with alip

194 e of this review is to describe the field of reactions of partially fluorinated substrates with trans

195 ompletely characterized, we investigated the reaction of PDI with the biological oxidant peroxynitrit

196 ess these issues by tuning the isomerization reactions of photo/thermoswitches.

197 Initially, the corresponding reactions of (PhS)2 and (PhTe)2 were shown to give the s

198 The electron-induced reaction of physisorbed vinyl bromide (ViBr) and allyl b

199 t of 2.60 x 10(-4) mA cm(-2) , a rapid redox reaction of polysulfide, and therefore improved sulfur u

200 tallic arrays can be formed spontaneously by reaction of precursor molecular rotor molecules with a m

201 Selective reaction of primary alcohols in the presence of secondar

202 st-dependent divergent reaction pathways for reactions of propargyl aryldiazoacetates are disclosed.

203 ve developed a copper-catalyzed substitution reaction of propargylic ammonium salts with aryl Grignar

204 The second-order rate constant for the reaction of [(PyPz)Fe(III)(OH) (OH2)](4+) with xanthene

205 The cycloadduct derived from reaction of pyrazinone and maleic anhydride underwent se

206 The reaction of pyrazoles and benzpyrazoles onto alkynes tak

207 nd (iso)quinoline can be synthesized through reaction of pyridyl radicals with 1,3-butadiene or seque

208 A two-step, one-flask reaction of pyrrole and pentafluorobenzaldehyde was inve

209 The reverse hydrogenation reaction of quinoline derivatives (H2 storage) was also

210 This is particularly the case for reactions of radicals generated using the classical reag

211 complete energy diagram for the regeneration reaction of rhodopsin.

212 Reaction of RS(-) with CO2 produces a terminal, sulfur-b

213 NO formation from thiols occurs from the reaction of RSNO and a copper(II) thiolate [Cu(II)]-SR i

214 nalysis of the heterolytic hydrogen cleavage reaction of ruthenium PNN complexes of Milstein and the

215 Here, mechanistic investigations on reactions of saturated NHC SIMes (SIMes=[:C{N(2,4,6-Me3

216 The reaction of secondary alcohols proceeds stereospecifical

217 Reactions of silylated clusters [Ge9{Si(TMS)3}3](-) or [

218 atalytic reductive methylenecyclopropanation reaction of simple olefins, utilizing 1,1-dichloroalkene

219 ted which may enable coupled electrochemical reactions of single redox molecules.

220 ate-of-the-art in terms of direct alkylation reactions of some carbonyl groups.

221 t studies show that PCM can promote chemical reactions of sorbed contaminants at ordinary temperature

222 es of advanced solid tumors leads to a chain reaction of stimuli that enhances the expression of prot

223 zation based on Michael addition-elimination reaction of structurally diverse beta-ketoenols with ami

224 oselective intramolecular C-H bond amination reactions of sulfonyl azides.

225 Applying these methods to the reaction of syngas on rhodium(111), we identify the most

226 In addition, the reaction of TEMPO with Lewis acid and Cp*2Fe afforded [C

227 nt reactions are compared with a related HAT reaction of TEMPOH, with the 2,4,6-tri-tert-butylphenoxy

228 d from all sp(2) carbons by C=C condensation reactions of tetrakis(4-formylphenyl)pyrene and 1,4-phen

229 ) and an asymmetric [2]catenane (AC.7PF6) on reaction of the 1:1 complex with diazapyrene and bipyrid

230 red products in a single operation while the reaction of the aldehyde precursors required a one-pot t

231 osition, which catalyzes the first enzymatic reaction of the amplification loop of the alternative pa

232 eported, enantioselective conjugate addition reaction of the barbituric acid pharmacaphore to nitroal

233 ne (BCN) polycations were synthesized by the reaction of the bivalent electrophile thiabicyclo[3.3.1]

234 oselective intramolecular Diels-Alder (IMDA) reaction of the camphanate-containing triene intermediat

235 f the possible transition states of the IMDA reaction of the camphanate-containing triene were obtain

236 Reaction of the cyclic guanidine TolN horizontal lineSIM

237 key step in the synthesis of 1 and 2 is the reaction of the dianion of pyrrole-1,2,5-tricarboxylic a

238 Here, the reaction of the diketiminate-supported cobalt(I) complex

239 thalides with Meerwein's reagent followed by reaction of the ensuing salts with pyrrole, results in t

240 etic resolutions can be expected because the reaction of the even more sterically demanding rac-2-flu

241 tion mechanism was responsible for the rapid reaction of the faster substrate was excluded through (1

242 w that self-assembly reduces the rate of the reaction of the fatty acid with ozone, and that lyotropi

243 s added first followed by TMSOTf, no further reaction of the formed ester was detected.

244 fides (RSSH) are formed endogenously via the reaction of the gaseous biotransmitter hydrogen sulfide

245 The reaction of the ketone precursors could directly lead to

246 In addition, the reaction of the NHC-iodosilicon(I) dimer [IAr (I)Si:]2 (

247 Reaction of the purified protein, in detergent, with the

248 methanesulfonamides with n-BuLi, followed by reaction of the resulting carbanion with methyl esters o

249 of isoamyl nitrite followed by condensation reaction of the resulting HOOC-Phe-SWCNT with 1-(3-amino

250 In the absence of H2, reaction of the rhodium-hydrido dicarbonyl with allylben

251 compared to the dark controls mainly due to reaction of the tartaric acid photodegradation product g

252 The photochemical electrocyclization reaction of the title compound in the presence of beta-c

253 e way to generate the singlet carbene is the reaction of the triplet with water molecules by annealin

254 The rates of the reactions of the arylsulfonyl-substituted carbanions car

255 Reactions of the BH4(-) anion with equimolar amounts of

256 ses may also occur in a detached way via the reactions of the catalytic intermediates with the starti

257 cleic acids or polyP modulate the individual reactions of the contact pathway have been lacking.

258 nate-to-isocyanate sigmatropic rearrangement reactions of the corresponding allyl carbamates.

259 ereoselective Pt(IV)-catalyzed cycloaddition reactions of the corresponding quinone methides with cha

260 Intramolecular ring-closure reactions of the morpholine moiety with the flanking mes

261 erall performance and elucidate the limiting reactions of the photobioelectrochemical cell.

262 s to aqueous partitioning and particle-phase reactions of the photooxidation product glyoxal.

263 Reactions of the Sn(II) hydrides [ArSn(mu-H)]2 (1) (Ar =

264 m transfer is the preferred mechanism in the reactions of the two carbamates with the radicals.

265 y theoretical calculations conducted for the reactions of the two N-oxyl radicals with toluene, which

266 g mechanism could facilitate the consecutive reactions of the two-step indirect pathway of Cys-tRNA(C

267 Because the kinetics and products of the reaction of these oxidants with PDI remain incompletely

268 The different rates of reaction of these products with a dienophile through the

269 The photoisomerization reaction of these proteins has been studied outside cell

270 The subsequent reactions of these first formed excited species lead to

271 Several reactions of these nucleophiles with benzylidenemalononi

272 Despite this, reactions of these types of borylimides with C-H or C id

273 thiazoles 1 by an yttrium-triflate-catalyzed reaction of thiocarboxylic acids 2 with isocyanides 3.

274 Reaction of thiolate 1 with carbene-stabilized diiodo-bi

275 In contrast to NO generation upon reaction of thiols at iron nitrite species, at copper th

276 4 (TMO)-like spinel phase resulting from the reaction of TiO2 with the surface LNMO.

277 The ring-opening reaction of trans-2-aroyl-3-styrylcyclopropane-1,1-dicar

278 rization of intermediates formed through the reaction of transition-metal complexes with dioxygen (O2

279 These inverse electron-demand Diels-Alder reactions of triazines have wide applications in bioorth

280 A detailed study of the reaction of trifluoroacetylated acetylenes and aryl (alk

281 The reaction of trifluoromethylated ynones with aryl (alkyl)

282 The reaction of triplet tetrachlorocyclopentadienylidene wit

283 On the other hand, reaction of two equivalents of CuBr2 with compounds 1 ga

284 nvestigating the coupled folding and binding reaction of two intrinsically disordered proteins and th

285 etric signature was monitored via the anodic reaction of tyrosine and tryptophan residues.

286 Alternatively, reaction of [U(Tren(TIPS) )(PH)][Na(12C4)2 ] (5, 12C4=12

287 Reaction of [U(Tren(TIPS) )(PH2 )] (1, Tren(TIPS) =N(CH2

288 g for the multichannel, addition-elimination reactions of unsaturated hydrocarbons with O atoms, and

289 reactive carbonyl oxides that are formed in reactions of unsaturated hydrocarbons with ozone (ozonol

290 for the enantioselective [4 + 1] annulation reaction of vinyl benzoxazinones and sulfur ylides in go

291 ic procedure involved two key steps: (1) the reaction of vinyl magnesium bromide with 2,2-dimethyl-6-

292 on and the regioselectivity of the catalytic reactions of vinylarenes.

293 This is because the other half reaction of water splitting, i.e., oxygen evolution reac

294 view, we summarize the general trends in the reactions of water and C1 molecules over transition meta

295 of C1 molecules (CO, CO2, CH3OH, etc.), the reactions of water will also be reviewed because water p

296 e 204 reports of radiopharmaceutical adverse reactions, of which 13 were considered invalid, primaril

297 gine) temperatures that promote the chemical reaction of WS2 with the aluminium matrix.

298 vision of the mechanism of the deoxygenation reaction of xanthates using R3B and water (Wood deoxygen

299 tic method of substituted triptycenes by the reaction of ynolates and arynes.

300 elemental combination method via the direct reaction of zirconium powders with red phosphorus, and c