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I. Symposium on <strong>Catalysis</strong> in <strong>Organic</strong> Synthesis1
Page 2: Catalysis ofOrganic Reactions
Page 5 and 6: 14. Catalyst Manufacture: Laborator
Page 7 and 8: 62. Catalysis of Organic Reactions,
Page 9 and 10: 108. Metal Oxides: Chemistry and Ap
Page 11: CRC PressTaylor & Francis Group6000
Page 14: xiii14. The Transformation of Light
Page 18 and 19: xviien Catalisis y Petroquimica (UN
Page 20: xix56. Transition Metal Removal fro
Page 24: xxiiiChronology of Organic Reaction
Page 27: To Zsuzsanna and Tim
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
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Page 66 and 67: Lathouder, Kapteijn and Moulijn 395
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Page 73 and 74: 46Preparation of 4-Aminocarboxylic
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52Preparation 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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