Catalysis of Organic..

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Catalysis of Organic Reactions 517hydroxybenzophenone 11 83hydroxyl capping 2 13immobilization 12 91information mining 35 303infrared spectroscopy 13, 18, 36 99, 147, 315ionic liquid 12, 37 91, 327chloroaluminate 31 271isobutanol 29 253isobutene 8 61isobutylene 52 469isomerization 22, 37 187, 327cis-trans 6 45(Z) – (E) 28 247double bond 28 247ketoesters 43 385kinetic resolution 1 3kinetics 2 13lactose 22 187D- 26 235Lewis acid 37 327ligand design 30 261linalool 21 177maleic anhydride 14 109mannitol 23 197mass-transfer limitation 22 187mechanical alloying 19 155mechanism 20 167mesityl oxide 7 55metal scavengers 56 493metastable phase 19 155methyl isobutyl ketone 9, 41, 54 67, 365, 481synthesis 41 365methyl pivaloylacetate 43 385methylation of diphenols 10 77methyltrioxorhenium 2 13MgO-based catalysts 40 355microchannel reactor 12 91modeling 22 187modification 27 241monolithicreactor 33 289stirrer 5 39montmorillonite 38 337nanoclusters 57 501nanoparticles 57 501natural oil polyol 42 377NBS promoted 15 119
518 Keyword IndexNi, activated 25 227Ni/Re/TiO2 catalyst 33 289nickel 9 67nitrate promoted 15 119nitrile 25 227nitro groups 32 281nitrobenzene 20 167nitrosobenzene 20 167NMR 6 45Noyori hydrogenation 51 463olefin 8 61metathesis 2 13oligomerization 8 61organotin 37 327oxidant NaOCl 17 141oxidation 49 447alcohol 15, 17 119, 141catalytic 18 147CO 36 315hydrocarbon 12 91liquid phase 17 141partial 13 99selective 14, 17 109, 141selective aerobic 15 119selective to aldehyde 17 141TEMPO catalyzed 17 141oxidation state of palladium/carbon 53 475oxidative dehydrogenation 16 131oxides, mixed metal 45 405oxo reaction 4 31palladium 9, 21, 27, 67, 177, 241,55, 56, 57 487, 493, 501palladium leaching 53 475palladium/carbon 3, 20, 53 23, 167, 475heat treatment of 53 475paraffin 46 415pentane, n- 14 109peroxycarbonic acid 49 447phase transfer catalysis 44 395phenol benzoylation 11 83phenylbenzoate 11 83phosphonium 37 327phosphorus ligand 4 31phthalic anhydride 14 109pilot plant 41 365platinum catalyst 54 481polyethyleneimine 5 39
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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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198 Fructose HydrogenationHOHCCH 2O
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200 Fructose HydrogenationTable 1.
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202 Fructose Hydrogenationmmol form
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204 Fructose Hydrogenationthe subst
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206 Fructose Hydrogenationcleave th
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208 Fructose Hydrogenationfulfills
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210 Fructose Hydrogenationis not th
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Disselkamp et al. 21324. Cavitating
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Disselkamp et al. 215column. In a p
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Disselkamp et al. 217selectivity es
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Disselkamp et al. 219hydrogenated (
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Disselkamp et al. 221A somewhat mor
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Disselkamp et al. 223Scheme 4.cis-2
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Disselkamp et al. 225conventional c
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Ostgard et al. 22725. The Treatment
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Ostgard et al. 229Table 1. The reac
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Ostgard et al. 231metal atoms. Thes
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Ostgard et al. 233In conclusion, th
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Kuusisto, Mikkola and Salmi 23526.
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Kuusisto, Mikkola and Salmi 237100A
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Kuusisto, Mikkola and Salmi 2399. B
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242 1-Phenyl-1-Propyneof cis-β-met
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244 1-Phenyl-1-Propynealkene. When
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Musolino, Apa, Donato and Pietropao
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Gőbölös and Margitfalvi 25329. R
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Gőbölös and Margitfalvi 255maxim
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Gőbölös and Margitfalvi 257Y=421
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Rothenberg et al. 26130. How to Fin
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Rothenberg et al. 263By dividing th
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Rothenberg et al. 265pre-define the
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Rothenberg et al. 267Table 1. Parti
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Rothenberg et al. 269Experimental S
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Angueira and White 27131. Novel Chl
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Angueira and White 273optimizedgeom
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Angueira and White 275F igure 4 - c
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Angueira and White 277Table 1. 27 A
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Angueira and White 279obtained from
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Robitaille, Clément, Chapuzet and
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Cao, White, Wang and Frye 28933. Se
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Cao, White, Wang and Frye 291Experi
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294Chiral Ferrocene Ligandsnew Twin
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296Chiral Ferrocene LigandsTable 1.
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298Chiral Ferrocene Ligandsprevents
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300Chiral Ferrocene LigandsConclusi
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302Chiral Ferrocene Ligandsextracte
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304 Catalyst Library DesignIn gas p
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306 Catalyst Library Designd−(b 0
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308 Catalyst Library DesignBasic Pr
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310 Catalyst Library DesignD in com
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312 Catalyst Library DesignCatalyst
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314 Catalyst Library Design27. S. H
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316 Dendrimer TemplatesWe are devel
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318 Dendrimer TemplatesThe differen
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320 Dendrimer TemplatesWe encounter
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322 Dendrimer TemplatesThe 100 cm -
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V. Symposium on Acid and Base Catal
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328Rearrangement of 3,4-Epoxy-1-But
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3382,5-Dimethyl-2,4-Hexadieneharves
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3402,5-Dimethyl-2,4-Hexadienestabil
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3422,5-Dimethyl-2,4-Hexadiene10086Y
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3442,5-Dimethyl-2,4-Hexadienereacti
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3462,5-Dimethyl-2,4-Hexadiene8. www
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348Heteropoly AcidsSOOO O+ +OS1 2 3
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350Heteropoly AcidsTable 3. Acylati
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352Heteropoly AcidsSiO 2 is the bes
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Diez, Di Cosimo and Apesteguia 3554
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Diez, Di Cosimo and Apesteguia 357T
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Diez, Di Cosimo and Apesteguia 359A
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Diez, Di Cosimo and Apesteguia 361I
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Diez, Di Cosimo and Apesteguia 3630
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O’Keefe, Jiang, Ng and Rempel 365
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VI. Symposium on “Green” Cataly
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378 Polyurethane from Natural OilMe
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380 Polyurethane from Natural Oilco
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382 Polyurethane from Natural Oilfr
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384 Polyurethane from Natural OilTh
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386 Carbonylation of Chloropinacolo
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396 Recycling Homogeneous Catalysts
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406“Green” Catalysts for Biodie
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416 Production of BiodieselTable 1.
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418 Production of Biodieselto a mas
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420 Production of BiodieselEthyl st
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422 Production of Biodiesel10080Sel
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424 Production of Biodieselproduct
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Marincean et al. 42747. Glycerol Hy
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Marincean et al. 429Experimental Se
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Marincean et al. 431neutralize all
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Marincean et al. 433suggesting that
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Marincean et al. 435increasing from
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Kocal 43748. Developing Sustainable
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Kocal 439description of the four st
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Kocal 441metallurgy in parts of the
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Kocal 443that capital investment co
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Kocal 4455. J.J. Siirola, An Indust
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448Propylene Oxidation to POSupercr
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450Propylene Oxidation to POTable 1
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452Propylene Oxidation to PO
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Riermeier et al. 45550. catASium ®
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Riermeier et al. 457It is interesti
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Riermeier et al. 459Reaction of the
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Riermeier et al. 461References1. I.
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464 Chiral 2-Amino-1-Phenylethanolp
Page 493 and 494: 466 Chiral 2-Amino-1-PhenylethanolI
Page 495 and 496: 468 Chiral 2-Amino-1-Phenylethanola
Page 497 and 498: 470 t-Butanol DehydrationResults an
Page 499 and 500: 472 t-Butanol Dehydrationcomprises
Page 502 and 503: Pohlmann et al 47553. Leaching Resi
Page 504 and 505: Pohlmann et al 477this study. In th
Page 506: Pohlmann et al 479Experimental Sect
Page 509 and 510: 482 Reductive AlkylationSince the p
Page 511 and 512: 484 Reductive AlkylationTable 2. Re
Page 514 and 515: Wolf, Seebald and Tacke 48755. Acce
Page 516 and 517: Wolf, Seebald and Tacke 489100Norma
Page 518 and 519: Wolf, Seebald and Tacke 4911,88Figu
Page 520 and 521: Woods et al. 49356. Transition Meta
Page 522 and 523: Woods et al. 495Effect of oxidation
Page 524 and 525: Woods et al. 497
Page 526: Woods et al. 499removed the samples
Page 529 and 530: 502 Electroreductive Catalytic Ullm
Page 531 and 532: 504 Electroreductive Catalytic Ullm
Page 534 and 535: Catalysis of Organic Reactions 507A
Page 536 and 537: Catalysis of Organic Reactions 509K
Page 538: Catalysis of Organic Reactions 511T
Page 541 and 542: 514 Keyword Indexcarboncarbon dioxi
Page 543: 516 Keyword Indexethanolamine 16 13
Page 547: 520 Keyword Indexsuccinimido ketone
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