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Jackson and Spence 245AcknowledgementsThe authors would like to acknowledge the ATHENA project, which is funded bythe Engineering & Physical Sciences Research Council (EPSRC) <strong>of</strong> the U.K. andJohnson Matthey plc.References1. Li Zon Gva and Kim En Kho, Kinet. Katal., 29, 381 (1988).2. A. N. R. Bos and K. R. Westerterp, Chem. Eng. Process., 32, 1 (1993).3. F. King, S. D. Jackson and F. E. Hancock, Chemical Industries (Dekker), 68,(Catal. Org. React.), 53-64 (1996).4. C. A. Hamilton, S. D. Jackson, G. J. Kelly, R. R. Spence and D. de Bruin, Appl.<strong>Catalysis</strong> A, 237, 201 (2002)5. S. D. Jackson and G. J. Kelly, Curr. Top. Catal. 1, 47 (1997).
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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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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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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
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114Oxidation of n-Pentanethe presen
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116Oxidation of n-PentaneIn the mec
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118Oxidation of n-PentaneReferences
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120TEMPO Oxidation of Alcoholsthe u
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122TEMPO Oxidation of AlcoholsThe r
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124TEMPO Oxidation of Alcoholsany d
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126TEMPO Oxidation of Alcoholsconce
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128TEMPO Oxidation of AlcoholsMNT :
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130TEMPO Oxidation of Alcoholsuptak
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132Aminoalcohols to Aminocarboxylic
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142Bromine-Free TEMPO-Based Catalys
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148CO OxidationP25 TiO 2 , respecti
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150CO Oxidation0.02(a)21802110(b)21
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152CO Oxidationcarboxylate species
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Yamauchi 15519. 2006 Murray Raney A
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Yamauchi 157transformation is schem
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Yamauchi 159The X-ray diffraction p
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Yamauchi 161was -0.0009, -0.0032 an
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Yamauchi 163shown in Fig. 12. It wa
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Yamauchi 165These fine particles we
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168Nitrobenzene Hydrogenationfurthe
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170Nitrobenzene Hydrogenationhydrog
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172Nitrobenzene HydrogenationThe co
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174Nitrobenzene HydrogenationHence
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176Nitrobenzene Hydrogenation10. G.
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178 Hydrogenation of Dehydrolinaloo
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188Modeling Mass Transfer Hydrogena
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Page 221 and 222: 194Modeling Mass Transfer Hydrogena
Page 223 and 224: 196Modeling Mass Transfer Hydrogena
Page 225 and 226: 198 Fructose HydrogenationHOHCCH 2O
Page 227 and 228: 200 Fructose HydrogenationTable 1.
Page 229 and 230: 202 Fructose Hydrogenationmmol form
Page 231 and 232: 204 Fructose Hydrogenationthe subst
Page 233 and 234: 206 Fructose Hydrogenationcleave th
Page 235 and 236: 208 Fructose Hydrogenationfulfills
Page 237 and 238: 210 Fructose Hydrogenationis not th
Page 240 and 241: Disselkamp et al. 21324. Cavitating
Page 242 and 243: Disselkamp et al. 215column. In a p
Page 244 and 245: Disselkamp et al. 217selectivity es
Page 246 and 247: Disselkamp et al. 219hydrogenated (
Page 248 and 249: Disselkamp et al. 221A somewhat mor
Page 250 and 251: Disselkamp et al. 223Scheme 4.cis-2
Page 252 and 253: Disselkamp et al. 225conventional c
Page 254 and 255: Ostgard et al. 22725. The Treatment
Page 256 and 257: Ostgard et al. 229Table 1. The reac
Page 258 and 259: Ostgard et al. 231metal atoms. Thes
Page 260 and 261: Ostgard et al. 233In conclusion, th
Page 262 and 263: Kuusisto, Mikkola and Salmi 23526.
Page 264 and 265: Kuusisto, Mikkola and Salmi 237100A
Page 266: Kuusisto, Mikkola and Salmi 2399. B
Page 269 and 270: 242 1-Phenyl-1-Propyneof cis-β-met
Page 271: 244 1-Phenyl-1-Propynealkene. When
Page 275 and 276: 248Homogeneous Hydrogenationthe pre
Page 277 and 278: 250Homogeneous Hydrogenationmetal s
Page 279 and 280: 252Homogeneous Hydrogenation2. R. R
Page 281 and 282: 254 Amination of Isobutanolnotewort
Page 283 and 284: 256 Amination of Isobutanoland (iBu
Page 286: 259IV. Symposium on Novel Methods i
Page 289 and 290: 262Find the Best Catalystquantitati
Page 291 and 292: 264Find the Best CatalystSTARTcreat
Page 293 and 294: 266Find the Best CatalystNHNPNO NNC
Page 295 and 296: 268Find the Best CatalystFigure 4.
Page 297 and 298: 270Find the Best Catalyst14. For a
Page 299 and 300: 272 Acidic Ionic LiquidsThe effect
Page 301 and 302: 274 Acidic Ionic Liquidssites for H
Page 303 and 304: 276 Acidic Ionic Liquids102.2 ppm 9
Page 305 and 306: 278 Acidic Ionic LiquidsClClClClClC
Page 307 and 308: 280 Acidic Ionic Liquids9. E. J. An
Page 309 and 310: 282 Chemoselective Hydrogenationthe
Page 311 and 312: 284 Chemoselective HydrogenationThe
Page 313 and 314: 286 Chemoselective HydrogenationCNN
Page 315 and 316: 288 Chemoselective Hydrogenation11.
Page 317 and 318: 290 Hydrogenolysis over Structured
Page 320 and 321: 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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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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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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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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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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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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488Profiling 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
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