ライフサイエンスコーパス: hydrogenation

1 pper(I) catalysis followed by Pd/C catalytic hydrogenation.

2 solated, fully characterized, and applied in hydrogenation.

3 ion and Fischer-Tropsch based carbon dioxide hydrogenation.

4 ative followed by a stereoselective Crabtree hydrogenation.

5 etalization/elimination followed by an ionic hydrogenation.

6 double bond has to be encapsulated to effect hydrogenation.

7 selective precatalysts for asymmetric alkene hydrogenation.

8 nogashira cross-coupling, and regioselective hydrogenation.

9 beta-sheet structures by self-assembly upon hydrogenation.

10 and atom-economical, enabled by a Shenvi-HAT hydrogenation.

11 the reduction of a nitrostyrene by transfer hydrogenation.

12 ior chemoselectivity and regioselectivity in hydrogenation.

13 s rule and affords E-alkenes by direct trans-hydrogenation.

14 in photocatalytic and electrocatalytic CO(2) hydrogenation.

15 tion was successfully achieved by Pearlman's hydrogenation.

16 ies and introduces a new approach to radical hydrogenation.

17 3) catalyst for methanol synthesis via CO(2) hydrogenation (300 degrees C, 20 bar) by combining X-ray

18 highly stereoselective substrate-controlled hydrogenation, a Lewis acid catalyzed anomeric reduction

19 -Buchi [2 + 2] photocycloaddition, catalytic hydrogenation, acid-catalyzed cyclization to form the ra

20 atalytic regimes are identified during CO(2) hydrogenation: activation, stable performance, and deact

21 C (BTC(3-) =benzenetricarboxylate) exhibited hydrogenation activity, while other isostructural monome

22 eassessing the nature of the active transfer hydrogenation agent: experimentally, a gel is observed i

23 selective transformations of the products by hydrogenation, allylation, and isomerization.

24 During this synthesis, it was found that gem-hydrogenation also provides opportunities for C-H functi

25 d on the two tandem catalytic reactions: DPA hydrogenation and (Z)-stilbene isomerization.

26 pincer ligands in first-row transition metal hydrogenation and dehydrogenation catalysis and related

27 tions of this work are broadly applicable to hydrogenation and dehydrogenation catalysis and, in part

28 important in many transition metal catalyzed hydrogenation and dehydrogenation reactions.

29 leophiles with allylic fluorides followed by hydrogenation and diastereoselective Friedel-Crafts cycl

30 n different ways, leading to products of B=B hydrogenation and dihalogenation as well as halide excha

31 catalytic reaction as well as regioselective hydrogenation and double condensation to form cyclopenta

32 ls and their catalytic applications in CO(x) hydrogenation and electrochemical hydrogen evolution rea

33 This was quantified using alkyne hydrogenation and H-atom transfer reactions with phenoxy

34 talytic activities of iron carbides in CO(x) hydrogenation and HER and the correlation between struct

35 eters on the valorisation of biomass through hydrogenation and hydrodeoxygenation, oxidation, reformi

36 for use as a reagent in remote, Pd-catalyzed hydrogenation and hydrogenolysis reactions.

37 Intermolecular transfer hydrogenation and hydrothiolation under analogous condit

38 mation 1,3-trans-dihydrotriboranes by formal hydrogenation and insertion of a borylene unit into the

39 Two hydrogenation and one C-C bond coupling products are ide

40 This approach offers a new strategy for (de)hydrogenation and other catalytic transformations mediat

41 ot, two-step reaction involving Pd-catalyzed hydrogenation and polycondensation with an aromatic dial

42 tunities for optimizing selectivity in CO(2) hydrogenation and producing high-grade methanol.

43 entities of catalytic intermediates in ester hydrogenation and related transformations.

44 which is proposed to be responsible for the hydrogenation and the formation of hydrogen.

45 upported catalyst was selective for ethylene hydrogenation and the zeolite-supported catalyst selecti

46 Relevant to a range of hydrogenations and reductions is the modulation of the h

47 The activation, hydrogenation, and covalent coupling of polycyclic aroma

48 product selectivity in thermocatalytic CO(2) hydrogenation, and low efficiency and selectivity in pho

49 yfluorinated ether acids containing a single hydrogenation, and previously unreported perfluorinated

50 e of the vinyl phosphonates was subjected to hydrogenation, and the resulting saturated phosphonates

51 ased under the conditions of catalytic ester hydrogenation, and time-course studies show that this re

52 , the technique was applied to an asymmetric hydrogenation, and various interferents expected to be p

53 ns, C-H functionalizations, polymerizations, hydrogenations, and reductive couplings, among others.

54 rs, void-confinement effects in liquid-phase hydrogenation are investigated in a two-chamber reactor.

55 cenes (DBAs) are introduced as catalysts for hydrogenation as well as hydride-transfer reactions.

56 meability, promotes CO(2) transportation and hydrogenation, as well as suppresses the hydrogen evolut

57 group and the electrode surface inhibits the hydrogenation at all platinum surfaces.

58 and with much higher voltage efficiency than hydrogenation at an electrode.

59 hibiting exceptional high activity for CO(2) hydrogenation at low temperatures (160-200 degrees C) wi

60 omplex is a highly active catalyst for ester hydrogenation at room temperature, giving up to 15 500 t

61 g capacity to direct the asymmetric transfer hydrogenation (ATH) of ketones in the presence of [(aren

62 tones were reduced using asymmetric transfer hydrogenation (ATH) through a dynamic kinetic resolution

63 ractical method based on asymmetric transfer hydrogenation (ATH) to control the planar chirality of a

64 efficient metal-free catalysts for catalytic hydrogenation, but their performance in chemoselective h

65 as chemisorption (CO(2) removal), catalytic hydrogenation (C(2)H(2) conversion), and cryogenic disti

66 ynes, hydrogenation of nitroaromatics, CO(2) hydrogenation, C-C coupling, and methane oxidation.

67 As a result, hydrogenation can be performed electrochemically with pr

68 gen atoms to the host metal, where selective hydrogenation can then occur.

69 The use of 3d metals in de/hydrogenation catalysis has emerged as a competitive fie

70 Heterogeneous hydrogenation catalysis is a promising approach for trea

71 The data are most consistent with hydrogenation catalysis prompted by an unobserved multim

72 ous media and provides a basis for enhancing hydrogenation catalysis under mild conditions via electr

73 mprise the free energy landscape of transfer hydrogenation catalysis.

74 We identified the actual hydrogenation catalyst as a K-Mn-bimetallic species and

75 amolecular strategy where encapsulation of a hydrogenation catalyst enables selective olefin hydrogen

76 thorough thermochemical analysis of the (de)hydrogenation catalyst, (PNP)Ru-Cl (PNP = 2,6-bis(di-ter

77 rthogonal Pd NP sites in 1-OTf-Pd(NP) as the hydrogenation catalyst.

78 sted in developing innovative carbon dioxide hydrogenation catalysts, and the pace of progress in thi

79 tibility of the generated thiol with typical hydrogenation catalysts.

80 n recent developments in main group mediated hydrogenation chemistry and catalysis using "frustrated

81 using a palladium membrane reactor to drive hydrogenation chemistry with electricity while bypassing

82 physically separate the electrochemical and hydrogenation chemistry.

83 The physical separation of the hydrogenation compartment from the electrolysis compartm

84 When generated in situ under catalytic hydrogenation conditions, electrophilic addition to the

85 lternative two-step procedure and controlled hydrogenation conditions.

86 This formate intermediate exhibits fast hydrogenation conversion to methoxy.

87 Here we report a new approach to radical hydrogenation: cooperative hydrogen atom transfer (cHAT)

88 a detailed analysis of catalytic reactions: hydrogenation, dehydrogenation, hydrogenolysis, oxidativ

89 deoxydehydration, haloperoxidase, cyanation, hydrogenation, dehydrogenation, ring-opening metathesis

90 merization of n-hexane, a reaction requiring hydrogenation/dehydrogenation and moderate to strong Bro

91 terparts recently allowed for the control of hydrogenation/dehydrogenation processes, yielding drasti

92 diastereomer to that expected for productive hydrogenation demonstrating a Curtin-Hammett kinetic reg

93 lectrocyclization reaction, a stereospecific hydrogenation driven by thermodynamic conformational sta

94 iled mechanistic studies of electrocatalytic hydrogenation (ECH) in aqueous solution over skeletal ni

95 temperatures are needed for electrocatalytic hydrogenation (ECH) to upgrade the feedstocks.

96 ally thin MoSe(2) deposits to study possible hydrogenation effects on select architectures using in-s

97 The fast hydrogenation enabled by the presence of phenol and appl

98 correlation between singlet-triplet gaps and hydrogenation enthalpies was observed.

99 iloxy carbenes were explored on the basis of hydrogenation enthalpies.

100 ucts can be further functionalized, e.g., by hydrogenation, epoxidation, or dihydroxylation to furnis

101 rogenation catalyst enables selective olefin hydrogenation, even in the presence of multiple sites of

102 de moiety at room temperature and exhaustive hydrogenation followed by reductive detosylation and spo

103 The catalytic activity in DPA hydrogenation follows the order Ni-Ga > Ni-La > Ni-Y > N

104 O(2)) conversion and methanol yield in CO(2) hydrogenation for methanol production.

105 a single-crystal to single-crystal solid/gas hydrogenation from a norbornadiene precursor, and its st

106 Reduction of the ynimides with Pd-catalyzed hydrogenation generates ethyleneimides with easily remov

107 Asymmetric hydrogenation has evolved as one of the most powerful to

108 rated precursors to perform PHIP by side arm hydrogenation has recently opened new possibilities for

109 etero)biaryl cross-coupling, borylation, and hydrogenation in a redox catalytic regime involving S(4)

110 H(12))][BAr(F)(4)] can be prepared by simple hydrogenation in a solid/gas single-crystal to single-cr

111 outline a series of experiments showing how hydrogenation in the palladium membrane reactor proceeds

112 n and in-situ Raman spectroscopy analysis of hydrogenation in ultrathin crystalline MoSe(2) deposits.

113 ng a green and sustainable approach based on hydrogenation, in the presence of a ruthenium pincer cat

114 in a-Si:H NPs in the visible range caused by hydrogenation-induced bandgap renormalization, producing

115 Moreover, it is shown that catalytic trans-hydrogenation is by no means a singularity: rather, the

116 cing equivalents for both hydrogenolysis and hydrogenation is exclusively H(2)/D(2(g)) rather than th

117 nondemanding alkene substituent, the rate of hydrogenation is not sensitive to the distance between t

118 s methanol synthesis catalysts through CO(2) hydrogenation is one of the major topics in CO(2) conver

119 In many instances the hydrogenation is stereospecific in the regard that the E

120 ey concept in using bimetallic catalysts for hydrogenation is that the active metal supplies hydrogen

121 ional design strategy in selective acetylene hydrogenation is to maximize the number of (111) sites i

122 are shown to be caused by differences in the hydrogenation mechanism between the electrochemical and

123 Our observations support a hydrogenation mechanism involving the Mn-H complex.

124 lyst follows the prototypical "outer sphere" hydrogenation mechanism, comprehensive studies of temper

125 transformation to methane via a direct CO(2) hydrogenation mechanism.

126 quid fuels, and alcohols through two leading hydrogenation mechanisms: methanol reaction and Fischer-

127 enzymatic sequence, in which stereoselective hydrogenation, Mitsunobu reaction, and regio- and stereo

128 Subsequent phenol hydrogenation occurs much more slowly (k(2) = 0.0052 s(-

129 O(2) and Ph(2) CO reduction by Et(3) SiH and hydrogenation of 1,1-diphenylethylene using 1,4-cyclohex

130 300 degrees C for 24 h and during catalytic hydrogenation of 1-hexene at 25 degrees C in the liquid

131 in tritium-labeled form ([(3)H]PSB-1584) by hydrogenation of a hexenyl-substituted precursor with tr

132 The catalytic hydrogenation of a metal nitride to produce free ammonia

133 eatures an enantioselective partial transfer hydrogenation of a naphthyridine using a chiral phosphor

134 atalytic conditions, we also demonstrate the hydrogenation of a polyurethane to produce diol, diamine

135 this work, the stereoselective heterogeneous hydrogenation of a tetrasubstituted indolizine was studi

136 chemistry is demonstrated by the successful hydrogenation of a wide variety of electronically and st

137 Comparison with results obtained for the hydrogenation of acetone featuring an isolated carbonyl

138 elf-adjusting surface that is active for the hydrogenation of acetone over a wide range of reaction c

139 roup renders these surfaces inactive for the hydrogenation of acetone.

140 Herein, we investigate hydrogenation of acetylene to ethylene using kinetic Mon

141 bits excellent catalytic performance in semi-hydrogenation of acetylene with 100% conversion and 85.1

142 p to 10 000) were achieved in the asymmetric hydrogenation of aliphatic carbocyclic and heterocyclic

143 impact the enantioselectivity of asymmetric hydrogenation of alkenes and imines.

144 Herein, we report an electrochemical hydrogenation of alkenes, alkynes, and ketones using amm

145 ant transition metal catalysts for selective hydrogenation of alkynes remains a challenge in both ind

146 onohydric and polyhydric alcohols, selective hydrogenation of alkynes, hydrogenation of nitroaromatic

147 In the semi-hydrogenation of alkynes, the nuclearity primarily impac

148 The activation of CO(2) and hydrogenation of all the surface oxygenate intermediates

149 Selective hydrogenation of alpha,beta-unsaturated aldehydes to uns

150 The asymmetric hydrogenation of alpha,beta-unsaturated carboxylic acids

151 nteresting performance in the chemoselective hydrogenation of alpha,beta-unsaturated organic compound

152 mical changes that manifest as toposelective hydrogenation of alternating rings on the surface of the

153 ative Heck arylation that relies on transfer hydrogenation of an acceptor olefin is developed with ex

154 sly shown to be effective for the asymmetric hydrogenation of aryl ketones is also a very effective c

155 states I and III, and proved useful for the hydrogenation of azoarenes and the partial reduction of

156 were applied in the Rh-catalyzed asymmetric hydrogenation of benchmark substrates furnishing enantio

157 The hydrogenation of benzaldehyde to benzyl alcohol on carbo

158 de complex catalyzes the asymmetric transfer hydrogenation of benzils from 2-propanol.

159 with phosphine ligand enabled the efficient hydrogenation of benzoic acid (BA) over Ru nanoparticles

160 The asymmetric hydrogenation of biomass-derived molecules for the prepa

161 Specifically, Ir-catalyzed hydrogenation of BN-[10]CPP selectively reduces the BN h

162 We report the hydrogenation of carbamates and urea derivatives, two of

163 The catalytic hydrogenation of carbon dioxide holds immense promise fo

164 This composition indicates hydrogenation of carbon monoxide-rich ice and/or energet

165 catalyst has been developed for the transfer hydrogenation of carbon-carbon multiple bonds.

166 tificial catalysts developed to date for the hydrogenation of carbonyl functionalities (loadings up t

167 or CH(4) production via a photodriven formal hydrogenation of CO to CH(4) was also found.

168 sisted route for low temperature homogeneous hydrogenation of CO to methanol is described.

169 The hydrogenation of CO(2) in the presence of amines to form

170 tituted nitroaromatics (>99 %) and gas-phase hydrogenation of CO(2) to CO (>98 %).

171 2)O(3), and has 100% selectivity towards the hydrogenation of CO(2) to CO with a turnover frequency o

172 Amine-assisted homogeneous hydrogenation of CO(2) to methanol is one of the most ef

173 o be efficacious catalysts for the gas-phase hydrogenation of CO(2).

174 nzene and tetrahydroquinoline as well as for hydrogenation of common unsaturated functionalities, inc

175 Using a sequential epoxidation and hydrogenation of crotonic acid leads to 29 % yield of be

176 We show the two-step hydrogenation of dimethyl acetylenedicarboxylate with pa

177 or Ga), were investigated for the selective hydrogenation of diphenylacetylene (DPA) to (E)-stilbene

178 cking reaction pathways of further catalytic hydrogenation of DMF to N(CH(3))(3).

179 discovery that complex 1 also catalyzes the hydrogenation of ethene under ambient conditions.

180 This catalyst was used for the hydrogenation of ethylene in a flow reactor.

181 this zinc pincer system, base-free catalytic hydrogenation of imines and ketones is demonstrated.

182 nd chemoselective manganese catalyst for the hydrogenation of imines.

183 l complex was therefore able to catalyze the hydrogenation of in situ formed formamides to methanol.

184 The only recently discovered gem-hydrogenation of internal alkynes is a fundamentally new

185 as versatile precatalysts for the asymmetric hydrogenation of isocoumarines, benzothiophene 1,1-dioxi

186 ly active species in the asymmetric transfer hydrogenation of ketones formed upon reaction of [Fe(CNC

187 ring resistance of these clusters during the hydrogenation of light olefins.

188 A rhodium-catalyzed method for the hydrogenation of N-heteroarenes is described.

189 The hydrogenation of N-substituted vinylphosphonates using r

190 ant material was tested in the heterogeneous hydrogenation of nitriles to the corresponding primary a

191 lcohols, selective hydrogenation of alkynes, hydrogenation of nitroaromatics, CO(2) hydrogenation, C-

192 The asymmetric catalytic hydrogenation of olefins is one of the most widely studi

193 Catalytic hydrogenation of olefins was also facilitated by the sul

194 has been successfully used in the asymmetric hydrogenation of olefins with poorly coordinative or non

195 the different stereochemical outcomes in the hydrogenation of olefins.

196 hite ligands for the Rh-catalyzed asymmetric hydrogenation of olefins.

197 theory calculations indicate that P promotes hydrogenation of OOH* to H(2)O(2) by weakening the Pt-OO

198 , substantially extending the application of hydrogenation of organosulfur compounds.

199 dride BaGa(2)H(2), effectively catalyzes the hydrogenation of phenylacetylene into styrene and ethylb

200 In addition, the hydrogenation of polyaromatic N-heteroarenes exhibited u

201 is (trifluoromethyl)- cyclohexanes by direct hydrogenation of precursor tetrakis- or hexakis- (triflu

202 a very effective catalyst for the asymmetric hydrogenation of prochiral aryl imines activated with N-

203 n is highlighted for the asymmetric transfer hydrogenation of prochiral imines using [Cp*Ir(biot-p-L)

204 o higher pairwise selectivity (6.1 %) in the hydrogenation of propene than any previously reported mo

205 ulations define a mechanism for the transfer hydrogenation of propene with (n)BuNH(2) and HBpin that

206 se Rh(2+) sites are active for the catalytic hydrogenation of propylene to propane at room temperatur

207 nthesis of enantiomerically pure benzoins by hydrogenation of readily available benzils has been long

208 Such gem-hydrogenation of stable carbogenic compunds is a fundame

209 lly characterized, and it promotes exclusive hydrogenation of styrene in the presence of 50 bar of H(

210 y and excellent selectivity for liquid-phase hydrogenation of substituted nitroaromatics (>99 %) and

211 able, highly enantio- and diastereoselective hydrogenation of such olefins and the mechanistic insigh

212 suggests that this interaction promotes the hydrogenation of surface-bound CO to ethylene.

213 stoichiometry allows for semi- and complete hydrogenation of terminal alkynes.

214 tivates the Pt(111) and Pt(100) surfaces for hydrogenation of the acetyl substituent.

215 This paper studies the electrochemical hydrogenation of the carbonyl functional group of acetop

216 Hydrogenation of the chiral p-methoxybenzyl azetine-2-ca

217 Reduction of the ester moiety and hydrogenation of the exo-methylene double bond of the bi

218 Hydrogenation of the four carbon-carbon triple bonds pro

219 ol, alpha-C-H activation of the nitrile, and hydrogenation of the in-situ-formed unsaturated intermed

220 The hydrogenation of the indolizine ring was shown to be dia

221 is otherwise active for the electrochemical hydrogenation of the isolated carbonyl functional group

222 Direct hydrogenation of thioesters with H(2) provides a facile

223 Here, we report an efficient and selective hydrogenation of thioesters.

224 (Beg = ethylene glycolatoboryl) promote the hydrogenation of trisubstituted alkenes by enabling irre

225 However, the asymmetric hydrogenation of unfunctionalized tetrasubstituted acycl

226 For the hydrogenation of unsaturated compounds, we identified Li

227 Catalytic hydrogenation of unsaturated hydrocarbons at room temper

228 on pathways to achieve otherwise challenging hydrogenations of trisubstituted alkenes.

229 Hydrogenation, on the other hand, is accomplished at tem

230 Bu) for both amine formylation and formamide hydrogenation, only catalyst Ru-Macho (R = Ph) provided

231 dolinones are obtained by hydration, partial hydrogenation, or hydroxyacyloxylation of the ynamide mo

232 It is found that hydrogenations over PdCu@HCS are shape-selective catalys

233 ion, but their performance in chemoselective hydrogenation, particularly in heterogeneous systems, ha

234 Asymmetric imine hydrogenation, particularly with iridium catalysts, is w

235 en the electrochemical and the H(2) -induced hydrogenation pathways.

236 C NPs, we evaluated the thermochemical CO(2) hydrogenation performance of alpha-MoC(1-x) NPs disperse

237 Moreover, the hydrogenation proceeds under mild pressure (20 bar).

238 e monomers (and oligomers) obtained from the hydrogenation process can be dehydrogenated back to a po

239 ted alkanes via a tandem dehydroalkoxylation-hydrogenation process under relatively mild conditions.

240 e-pot Suzuki-Miyaura cross-coupling/transfer-hydrogenation process.

241 isolated Ni sites to optimize acetylene semi-hydrogenation processes.

242 he olefin governs the stereochemistry of the hydrogenation, producing an enantiodivergent outcome.

243 Partial hydrogenation products were obtained in three steps from

244 hosphine catalysts, well-known in asymmetric hydrogenation, racemic secondary alcohols are shown to c

245 In contrast, the hydrogenation rate is not affected when H(2) is used as

246 s, such as substituted phenols, enhances the hydrogenation rate of the aldehyde by two effects, that

247 adsorbed species on the Rh surface enhances hydrogenation rates of reaction intermediates.

248 node and the influence of H(2)O on the CO(2) hydrogenation reaction at 170 degrees C, through steady

249 Integrating the hydrogenation reaction into the chip minimizes polarizat

250 ing framework Sn atoms catalyze the transfer hydrogenation reaction of cyclohexanone in a 2-butanol s

251 The hydrogenation reaction of these CO(2)-derived compounds,

252 in liquids; it allows in-line monitoring of hydrogenation reactions and can be used to determine the

253 de-based materials for ammonia synthesis and hydrogenation reactions in general.

254 nstrate the optimization of the Pd-catalyzed hydrogenation reactions of styrene, phenylacetylene, cyc

255 les were used as substrates in heterogeneous hydrogenation reactions to afford new fused indolines in

256 es for green chemistry such as aqueous phase hydrogenation reactions which benefit from enhanced hydr

257 based on spin density analysis, isogyric and hydrogenation reactions, HOMA, NICS, and ACID calculatio

258 Pd-catalyzed processes, i.e., couplings and hydrogenation reactions, including multistep processes.

259 e is the canonical course of metal catalyzed hydrogenation reactions.

260 re, and its unique catalytic performance for hydrogenation reactions.

261 modifying film, strong CO(2) adsorption and hydrogenation reactivity could be restored.

262 le-atom catalysts (SACs) to high-temperature hydrogenation requires materials that thermodynamically

263 red by kinetic resolution through asymmetric hydrogenation, resulting in an ee of up to 98%.

264 These two effects enable a hydrogenation route, in which phenol acts as a conduit f

265 s a variety of functional groups, among them hydrogenation sensitive examples such as an olefin, a ke

266 to a palladium-catalyzed carboetherification/hydrogenation sequence on propargylic amines, providing

267 featuring dehydration, oligomerization, and hydrogenation, the consolidated alcohol dehydration and

268 In catalysts for CO(2) hydrogenation, the interface between metal nanoparticles

269 ytic performance of catalysts for oxidation, hydrogenation, the water-gas shift reaction, and others,

270 yclizations, and a highly diastereoselective hydrogenation to assemble multigram quantities of the tr

271 Finally, CO(2) capture from ambient air and hydrogenation to CH(3)OH was demonstrated.

272 (rWGS) but are unable to conduct its further hydrogenation to CH(4) (or MeOH), for which Ni clusters

273 en subjected to a Noyori asymmetric transfer hydrogenation to establish the stereogenic center at C-1

274 e kinetics of nonfaradaic Pd-catalyzed CO(2) hydrogenation to formate and find that the reaction can

275 swing promotes the rate of nonfaradaic CO(2) hydrogenation to formate by nearly 3 orders of magnitude

276 utylphosphinito)phenyl) that catalyzes CO(2) hydrogenation to formate with faster rates at lower temp

277 guided the selection of conditions for CO(2) hydrogenation to formate with high activity (up to 364 h

278 st shows a carbon dioxide conversion through hydrogenation to hydrocarbons in the aviation jet fuel r

279 manganese nitride ((tBu)Salen)Mn=N underwent hydrogenation to liberate free ammonia with up to 6 tota

280 test pressure (3 MPa) reveal that the CO(2) hydrogenation to methanol on the CZZ catalysts follows t

281 3)O intermediates, that more readily undergo hydrogenation to methanol than the C-O dissociation asso

282 the feedstock gas is not favorable for CO(2) hydrogenation to methanol, causing low activity and poor

283 (120-150 degrees C, 50 bar) carbon monoxide hydrogenation to methanol.

284 ce of Cu-ZnO-ZrO(2) (CZZ) catalyst for CO(2) hydrogenation to methanol.

285 hod, showing excellent performance for CO(2) hydrogenation to methanol.

286 kene migratory insertion (and hence transfer hydrogenation) to dominate.

287 hydrophobic Sn-Beta stabilizes the transfer hydrogenation transition state to a greater extent than

288 The hydrogenation typically proceeds in two steps.

289 nalities are accessible for electrocatalytic hydrogenation under a set of reaction conditions?

290 Thiocarbamates and thioamides also undergo hydrogenation under similar conditions, substantially ex

291 reported to be active precatalysts for ester hydrogenation, undergo dehydroalkylation on heating in t

292 A catalytic transfer-hydrogenation utilizing a well-defined Bi(I) complex as

293 Radical hydrogenation via hydrogen atom transfer (HAT) to alkene

294 Kinetic studies on pyridine hydrogenation were conducted with each of the isolated r

295 ne, traditionally challenging substrates for hydrogenation, were successfully hydrogenated using the

296 ive catalyst for methanol synthesis in CO(2) hydrogenation which exhibits good activity and stability

297 uch design is particularly desired for CO(2) hydrogenation, which is characterized by complex pathway

298 ation step, which is conducted as a transfer hydrogenation with aqueous, buffered sodium formate as t

299 f dinitrogen (N(2) ) to nitride (N(3-) ) and hydrogenation with dihydrogen (H(2) ) to yield ammonia (

300 unactivated alkenes such as 1-hexene undergo hydrogenation within 1 h at room temperature.