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xvi34. Twinphos: A New Family of Chiral Ferrocene Tetra-Phosphine Ligands forAsymmetric Catalytic Transformations 293Benoit Pugin, Heidi Landert, Martin Kesselgruber, Hans Meier, Richard Sachleben, FelixSpindler and Marc ThommenSolvias AG, Klybeckstrasse 19, Postfach CH 4002, Basel, Switzerland35. Catalyst Library Design for Fine Chemistry Applications 303József L. Margitfalvi, András Tompos, Sándor Gőbölös, Emila Tálas and MihályHegedűsChemical Research Center, Institute of Surface Chemistry and Catalysis, Department ofOrganic Catalysis, 1025 Budapest, Pusztaszeri ut 59-67Hungary36. Dendrimer Templates for Pt and Au Catalysts 315Bethany J. Auten, Christina J. Crump, Anil R. Singh and Bert D. ChandlerDepartment of Chemistry, Trinity University, 1 Trinity Place,San Antonio, TX 78212-7200V. Symposium on Acid and Base Catalysis 32537. Development of an Industrial Process for the Lewis Acid/Iodide Salt-CatalyzedRearrangement of 3,4-Epoxy-1-Butene to 2,5-Dihydrofuran 327Stephen N. Falling 1 , John R. Monnier, 1,2 Gerald W. Phillips 1 , Jeffrey S. Kanel 1 , andStephen A. Godleski 31 Eastman Chemical Company Research Laboratories, Bldg. 150B, P.O. Box 1972Kingsport, TN 37662-51502 Department of Chemical Engineering, University of South Carolina,Columbia, SC, 292083 Eastman Kodak Company, Rochester, New York, 1465038. A New Economical and Environmentally Friendly Synthesis of2,5-Dimethyl-2,4-Hexadiene 337Alessandra O. Bianchi a , Valerio Borzatta a , Elisa Poluzzi a and Angelo Vaccari ba Endura SpA, Viale Pietramellara 5, 40012 Bologna (Italy)b Dipartimento di Chimica Industriale e dei Materiali, Alma Mater Studiorum Universitàdi Bologna, Viale del Risorgimento 4, 40136 Bologna, Italy39. Supported Heteropoly Acid Catalysts for Friedel-Crafts Acylation 347Kenneth G. Griffin 1 , Peter Johnston 1 , Roger Prétôt 2 , Paul A. van der Schaaf 21 Johnson Matthey plc, Catalyst Development, Royston, SG8 5HE, UK2 Ciba Specialty Chemicals Inc., CH-4002 Basel, Switzerland40. Synthesis of Pseudoionones by Aldol Condensation of Citral with Acetone onLi-Modified MgO Catalysts 355Veronica K. Díez, Juana I. Di Cosimo and Carlos ApesteguíaCatalysis Science and Engineering Research Group (GICIC), Instituto de Investigaciones
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Page 9 and 10: 108. Metal Oxides: Chemistry and Ap
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Page 22: xxiBoard of EditorsStephen R. Schmi
Page 26 and 27: xxvPrefaceThis volume of Catalysis
Page 28: I. Symposium on Catalysis in Organi
Page 31 and 32: 4Immobilized Metal Complex Catalyst
Page 37 and 38: 10Immobilized Metal Complex Catalys
Page 39 and 40: 12Immobilized Metal Complex Catalys
Page 41 and 42: 14Supported Re Catalysts for Olefin
Page 51 and 52: 24Hydrogenation of a Schiff’s Bas
Page 58 and 59: Puckette 314. Halophosphite Ligands
Page 60 and 61: Puckette 33initial results were bot
Page 62 and 63: Puckette 35expense of catalyst acti
Page 64 and 65: Puckette 372 1 Mixed 2- 71% Nonyl A
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Lathouder, Kapteijn and Moulijn 395
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Lathouder, Kapteijn and Moulijn 41p
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Lathouder, Kapteijn and Moulijn 43m
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46Preparation of 4-Aminocarboxylic
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Tzompantzi, Valente, Cantú and Gó
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62Isobutene TrimerizationResults an
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64Isobutene TrimerizationFigure 4 R
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Canning, Gamman, Jackson and Urquar
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78Methylation of Catecholthe use of
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80Methylation of CatecholThe main r
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Ardizzi et al. 8311. The Environmen
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Ardizzi et al. 85the selectivity to
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Ardizzi et al. 87Experimental Secti
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Hu et al. 9112. Biphasic Catalytic
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Hu et al. 93Results and DiscussionM
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Hu et al. 95ionic liquid is used in
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Hu et al. 97Figure 4. Schematic flo
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Singh and Chuang 9913. Reaction Pat
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Singh and Chuang 101for O 2 , 40 fo
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Singh and Chuang 103537373650Temp (
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Singh and Chuang 1050.064m/e = 32 (
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Singh and Chuang 107In summary, hyd
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Bacchini et al . 10914. The Transfo
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Bacchini et al . 1111 summarizes th
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Bacchini et al . 113these samples h
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Bacchini et al . 115around 1. The d
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Bacchini et al . 117Experimental Se
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Tanielyan et al. 11915. Transition
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Tanielyan et al. 121We wish to repo
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Tanielyan et al. 123Fig 1a shows th
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Tanielyan et al. 125TEMPO concentra
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Tanielyan et al. 127complete conver
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Tanielyan et al. 129ConclusionsIt h
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Liu, Cant and Smith 13116. The Conv
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Liu, Cant and Smith 133calculated f
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Liu, Cant and Smith 135Table 3. App
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Liu, Cant and Smith 137noting that
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Liu, Cant and Smith 139an exact fit
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Tanielyan et al. 14117. Bromine-Fre
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Tanielyan et al. 143TEMPO catalyst,
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mmol),Tanielyan et al. 145catalyst.
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Miller and Chuang 14718. In situ In
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Miller and Chuang 1492(a)2359217516
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Miller and Chuang 151(a)33802973292
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III. Symposium on Catalytic Hydroge
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156 Raney® Metastable PrecursorsIn
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158 Raney® Metastable Precursorsfe
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160 Raney® Metastable Precursorssl
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162 Raney® Metastable Precursorsfu
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164 Raney® Metastable Precursorsva
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Gelder, Jackson and Lok 16720. Comp
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Gelder, Jackson and Lok 169hydrogen
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Gelder, Jackson and Lok 171more rap
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Gelder, Jackson and Lok 173and that
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Gelder, Jackson and Lok 175measured
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Nikoshvili et al . 17721. Selective
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Nikoshvili et al . 179Experimental
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Nikoshvili et al . 181gasometrical
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Nikoshvili et al . 183causes the se
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Nikoshvili et al . 185determined th
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Salmi et al. 18722. Modeling and Op
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Salmi et al. 189andn−1( ) ( 1)) 1
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Salmi et al. 191dci= Niap− NGLiaG
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Salmi et al. 193of adsorption and t
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Salmi et al. 195Notationaa pa GLAcd
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Ostgard et al . 19723. The Effects
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Ostgard et al . 199not the ionic sa
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Ostgard et al . 201-2-0,9 -0,7 -0,5
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Ostgard et al . 2032,22Figure 8 NiM
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Ostgard et al . 205Max Act., mol/(m
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Ostgard et al . 207Flat Adsorbtion
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Ostgard et al . 209product mixture.
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Ostgard et al . 2116. M. Makkee, A.
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214 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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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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