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Catalysis ofOrganic Reactions
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14. Catalyst Manufacture: Laborator
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62. Catalysis of Organic Reactions,
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108. Metal Oxides: Chemistry and Ap
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CRC PressTaylor & Francis Group6000
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xiii14. The Transformation of Light
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xviien Catalisis y Petroquimica (UN
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xix56. Transition Metal Removal fro
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xxiiiChronology of Organic Reaction
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To Zsuzsanna and Tim
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Jones et al. 31. On the Use of Immo
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Jones et al. 5three-phase tests in
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Jones et al. 7In the HKR of rac-epi
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Jones et al. 9term performance char
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Jones et al. 115. A. S. Gruber, D.
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Moses et al. 132. Supported Re Cata
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Moses et al. 15perrhenate, followed
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Moses et al. 17SnCOSnMe 4≡SiOReO
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Moses et al. 19(AlOSi) of the cube.
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Moses et al. 212.510 3 k obs / s -1
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Wang et al. 233. Catalytic Hydrogen
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Wang et al. 25The rate expressions
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Wang et al. 27Schiff’s base forma
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Wang et al. 29AcknowledgementsWe gr
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32Halophosphite LigandsIn 1970, Pru
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34Halophosphite LigandsThe ligands,
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36Halophosphite LigandsTable 2 Temp
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38Halophosphite Ligands3. P. W. N.
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40Monolithic Bioreactorstrength for
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42Monolithic BioreactorMenten equat
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Gőbölös et al. 456. Highly Selec
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Gőbölös et al. 47was practically
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Gőbölös et al. 49noteworthy that
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Gőbölös et al. 51Figure 2 NMR sp
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Gőbölös et al. 53internal TMS in
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56Hydrotalcite-like Catalysts[A n-
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58Hydrotalcite-like Catalystssample
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Mantilla, Tzompantzi, Torres and G
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Mantilla, Tzompantzi, Torres and G
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Mantilla, Tzompantzi, Torres and G
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68Synthesis of MIBKwe examined the
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70Synthesis of MIBK1412Conversion (
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72Synthesis of MIBK4,4’-dimethyl
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74Synthesis of MIBKobtained for MIB
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Ardizzi et al. 7710. The Control of
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Ardizzi et al. 79type acidity at th
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Ardizzi et al. 81procedure describe
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84Phenol Benzoylationconsecutive Fr
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86Phenol BenzoylationThis does not
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II. Symposium on Catalytic Oxidatio
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92Oxidation with Microchannel Immob
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94Oxidation with Microchannel Immob
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96Oxidation with Microchannel Immob
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98Oxidation with Microchannel Immob
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100 Propylene Partial OxidationThe
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102 Propylene Partial OxidationSiO
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104 Propylene Partial Oxidation0.01
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106 Propylene Partial Oxidation0.02
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108 Propylene Partial OxidationRefe
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110Oxidation of n-Pentanemethacryli
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112Oxidation of n-PentaneFReqox1ox2
- Page 141 and 142: 114Oxidation of n-Pentanethe presen
- Page 143 and 144: 116Oxidation of n-PentaneIn the mec
- Page 145 and 146: 118Oxidation of n-PentaneReferences
- Page 147 and 148: 120TEMPO Oxidation of Alcoholsthe u
- Page 149 and 150: 122TEMPO Oxidation of AlcoholsThe r
- Page 151 and 152: 124TEMPO Oxidation of Alcoholsany d
- Page 153 and 154: 126TEMPO Oxidation of Alcoholsconce
- Page 155 and 156: 128TEMPO Oxidation of AlcoholsMNT :
- Page 157 and 158: 130TEMPO Oxidation of Alcoholsuptak
- Page 159 and 160: 132Aminoalcohols to Aminocarboxylic
- Page 161 and 162: 134Aminoalcohols to Aminocarboxylic
- Page 163 and 164: 136Aminoalcohols to Aminocarboxylic
- Page 165 and 166: 138Aminoalcohols to Aminocarboxylic
- Page 167 and 168: 140Aminoalcohols to Aminocarboxylic
- Page 169 and 170: 142Bromine-Free TEMPO-Based Catalys
- Page 171 and 172: 144Bromine-Free TEMPO-Based Catalys
- Page 173 and 174: 146Bromine-Free TEMPO-Based Catalys
- Page 175 and 176: 148CO OxidationP25 TiO 2 , respecti
- Page 177 and 178: 150CO Oxidation0.02(a)21802110(b)21
- Page 179 and 180: 152CO Oxidationcarboxylate species
- Page 182 and 183: Yamauchi 15519. 2006 Murray Raney A
- Page 184 and 185: Yamauchi 157transformation is schem
- Page 186 and 187: Yamauchi 159The X-ray diffraction p
- Page 188 and 189: Yamauchi 161was -0.0009, -0.0032 an
- Page 190 and 191: Yamauchi 163shown in Fig. 12. It wa
- Page 194 and 195: Gelder, Jackson and Lok 16720. Comp
- Page 196 and 197: Gelder, Jackson and Lok 169hydrogen
- Page 198 and 199: Gelder, Jackson and Lok 171more rap
- Page 200 and 201: Gelder, Jackson and Lok 173and that
- Page 202 and 203: Gelder, Jackson and Lok 175measured
- Page 204 and 205: Nikoshvili et al . 17721. Selective
- Page 206 and 207: Nikoshvili et al . 179Experimental
- Page 208 and 209: Nikoshvili et al . 181gasometrical
- Page 210 and 211: Nikoshvili et al . 183causes the se
- Page 212 and 213: Nikoshvili et al . 185determined th
- Page 214 and 215: Salmi et al. 18722. Modeling and Op
- Page 216 and 217: Salmi et al. 189andn−1( ) ( 1)) 1
- Page 218 and 219: Salmi et al. 191dci= Niap− NGLiaG
- Page 220 and 221: Salmi et al. 193of adsorption and t
- Page 222 and 223: Salmi et al. 195Notationaa pa GLAcd
- Page 224 and 225: Ostgard et al . 19723. The Effects
- Page 226 and 227: Ostgard et al . 199not the ionic sa
- Page 228 and 229: Ostgard et al . 201-2-0,9 -0,7 -0,5
- Page 230 and 231: Ostgard et al . 2032,22Figure 8 NiM
- Page 232 and 233: Ostgard et al . 205Max Act., mol/(m
- Page 234 and 235: Ostgard et al . 207Flat Adsorbtion
- Page 236 and 237: Ostgard et al . 209product mixture.
- Page 238: Ostgard et al . 2116. M. Makkee, A.
- Page 241 and 242: 214 Cavitating Ultrasound Hydrogena
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216 Cavitating Ultrasound Hydrogena
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218 Cavitating Ultrasound Hydrogena
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220 Cavitating Ultrasound Hydrogena
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222 Cavitating Ultrasound Hydrogena
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224 Cavitating Ultrasound Hydrogena
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226 Cavitating Ultrasound Hydrogena
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228 Hydrogenation of Pynitrilesuch
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230 Hydrogenation of Pynitrile%Sele
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232 Hydrogenation of Pynitrile%Sele
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234 Hydrogenation of Pynitrile10. A
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236Deactivation of Catalyst in Suga
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238Deactivation of Catalyst in Suga
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Jackson and Spence 24127. Selectivi
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Jackson and Spence 243been related
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Jackson and Spence 245Acknowledgeme
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248Homogeneous Hydrogenationthe pre
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250Homogeneous Hydrogenationmetal s
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252Homogeneous Hydrogenation2. R. R
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254 Amination of Isobutanolnotewort
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256 Amination of Isobutanoland (iBu
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259IV. Symposium on Novel Methods i
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262Find the Best Catalystquantitati
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264Find the Best CatalystSTARTcreat
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266Find the Best CatalystNHNPNO NNC
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268Find the Best CatalystFigure 4.
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270Find the Best Catalyst14. For a
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272 Acidic Ionic LiquidsThe effect
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274 Acidic Ionic Liquidssites for H
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276 Acidic Ionic Liquids102.2 ppm 9
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278 Acidic Ionic LiquidsClClClClClC
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280 Acidic Ionic Liquids9. E. J. An
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282 Chemoselective Hydrogenationthe
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284 Chemoselective HydrogenationThe
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286 Chemoselective HydrogenationCNN
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288 Chemoselective Hydrogenation11.
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290 Hydrogenolysis over Structured
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Pugin et al. 29334. Twinphos: A New
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Pugin et al. 295ferrocene binding m
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Pugin et al. 297complexes with one
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Pugin et al. 2993: 50.1 (J pp =50 H
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Pugin et al. 301temperature, then t
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Margitfalvi et al. 30335. Catalyst
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Margitfalvi et al. 305Based on the
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Margitfalvi et al. 307Table 1. Vari
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Margitfalvi et al. 309Combination o
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Margitfalvi et al. 311Figure 1. Map
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Margitfalvi et al. 313Acknowledgeme
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Auten, Crump, Singh and Chandler 31
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Auten, Crump, Singh and Chandler 31
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Auten, Crump, Singh and Chandler 31
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Auten, Crump, Singh and Chandler 32
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Auten, Crump, Singh and Chandler 32
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Falling et al. 32737. Development o
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Falling et al. 329With these proces
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Falling et al. 331salt, TOP18 has v
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Falling et al. 333The catalyst syst
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Falling et al. 335Normal operation
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Bianchi, Borzatta, Poluzzi and Vacc
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Bianchi, Borzatta, Poluzzi and Vacc
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Bianchi, Borzatta, Poluzzi and Vacc
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Bianchi, Borzatta, Poluzzi and Vacc
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Bianchi, Borzatta, Poluzzi and Vacc
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Griffin, Johnston, Prétôt and van
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Griffin, Johnston, Prétôt and van
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Griffin, Johnston, Prétôt and van
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Griffin, Johnston, Prétôt and van
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356Synthesis of PseudoiononesOOO- H
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358Synthesis of PseudoiononesMgO Pe
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360Synthesis of Pseudoionones0.5 wt
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362Synthesis of PseudoiononesTable
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364Synthesis of Pseudoiononesstrong
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366 MIBK Synthesis via CDproduce me
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368 MIBK Synthesis via CDExperiment
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370 MIBK Synthesis via CDreboiler p
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372 MIBK Synthesis via CDIn MIBK, t
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374 MIBK Synthesis via CDConclusion
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Sanders et al. 37742. Producing Pol
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Sanders et al. 379For the purposes
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Sanders et al. 381corresponding alc
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Sanders et al. 383polyurethane foam
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Zoeller and Barnette 38543. Carbony
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Zoeller and Barnette 387The first s
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Zoeller and Barnette 389Material ac
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Zoeller and Barnette 391above 120°
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Zoeller and Barnette 393tributyl am
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Hallett, Pollet, Eckert and Liotta
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Hallett, Pollet, Eckert and Liotta
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Hallett, Pollet, Eckert and Liotta
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Hallett, Pollet, Eckert and Liotta
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Hallett, Pollet, Eckert and Liotta
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Kiss, Rothenberg and Dimian 40545.
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Kiss, Rothenberg and Dimian 407C 10
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Kiss, Rothenberg and Dimian 409Tabl
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Kiss, Rothenberg and Dimian 411X (m
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Kiss, Rothenberg and Dimian 413Prep
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Snåre et al. 41546. Continuous Deo
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Snåre et al. 417The production of
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Snåre et al. 419was 15 μm and the
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Snåre et al. 421to 13% of conversi
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Snåre et al. 423Ethyl stearate con
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Snåre et al. 425increase in the fo
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428Glycerol Hydrogenolysisfundament
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430Glycerol Hydrogenolysisreaction
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432Glycerol Hydrogenolysisexpense o
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434Glycerol Hydrogenolysis[GO], M1.
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436Glycerol HydrogenolysisReference
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438Sustainable Process Technologyth
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440Sustainable Process Technologyco
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442Sustainable Process Technologywi
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444Sustainable Process TechnologyTh
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Lee, Shi, Subramaniam and Busch 447
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Lee, Shi, Subramaniam and Busch 449
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Lee, Shi, Subramaniam and Busch 451
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VII. Symposium on Other Topics in C
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...456Chiral BisphospholanesToday,
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458Chiral BisphospholanesFirst, the
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460Chiral BisphospholanesInterestin
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Augustine, Tanielyan, Marin and Alv
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Augustine, Tanielyan, Marin and Alv
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Augustine, Tanielyan, Marin and Alv
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Knifton and Sanderson 46952. Select
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Knifton and Sanderson 4711414141413
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Knifton and Sanderson 4733. O. C. A
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476 Palladium LeachingResults and D
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478 Palladium Leachingtemperatures
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Arunajatesan, Cruz, Möbus and Chen
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Arunajatesan, Cruz, Möbus and Chen
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Arunajatesan, Cruz, Möbus and Chen
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488Profiling of Catalytic Performan
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490Profiling of Catalytic Performan
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492Profiling of Catalytic Performan
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494 Transition Metal Removalmetal r
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496 Transition Metal RemovalDeloxan
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498 Transition Metal Removalreduced
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Durán Pachón and Rothenberg 50157
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Durán Pachón and Rothenberg 503th
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Durán Pachón and Rothenberg 505Ac
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508Author IndexDíez Verónica K. 4
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510Author IndexPhillips Gerald W. 3
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Catalysis of Organic Reactions 513K
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Catalysis of Organic Reactions 515c
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Catalysis of Organic Reactions 517h
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Catalysis of Organic Reactions 519p