- 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 and 28:
To Zsuzsanna and Tim
- Page 30 and 31:
Jones et al. 31. On the Use of Immo
- Page 32 and 33:
Jones et al. 5three-phase tests in
- Page 34 and 35:
Jones et al. 7In the HKR of rac-epi
- Page 36 and 37:
Jones et al. 9term performance char
- Page 38 and 39:
Jones et al. 115. A. S. Gruber, D.
- Page 40 and 41:
Moses et al. 132. Supported Re Cata
- Page 42 and 43:
Moses et al. 15perrhenate, followed
- Page 44 and 45:
Moses et al. 17SnCOSnMe 4≡SiOReO
- Page 46 and 47:
Moses et al. 19(AlOSi) of the cube.
- Page 48 and 49:
Moses et al. 212.510 3 k obs / s -1
- Page 50 and 51:
Wang et al. 233. Catalytic Hydrogen
- Page 52 and 53:
Wang et al. 25The rate expressions
- Page 54 and 55:
Wang et al. 27Schiff’s base forma
- Page 56:
Wang et al. 29AcknowledgementsWe gr
- Page 59 and 60:
32Halophosphite LigandsIn 1970, Pru
- Page 61 and 62:
34Halophosphite LigandsThe ligands,
- Page 63 and 64: 36Halophosphite LigandsTable 2 Temp
- Page 65 and 66: 38Halophosphite Ligands3. P. W. N.
- Page 67 and 68: 40Monolithic Bioreactorstrength for
- Page 69 and 70: 42Monolithic BioreactorMenten equat
- Page 72 and 73: Gőbölös et al. 456. Highly Selec
- Page 74 and 75: Gőbölös et al. 47was practically
- Page 76 and 77: Gőbölös et al. 49noteworthy that
- Page 78 and 79: Gőbölös et al. 51Figure 2 NMR sp
- Page 80: Gőbölös et al. 53internal TMS in
- Page 83 and 84: 56Hydrotalcite-like Catalysts[A n-
- Page 85 and 86: 58Hydrotalcite-like Catalystssample
- Page 88 and 89: Mantilla, Tzompantzi, Torres and G
- Page 90 and 91: Mantilla, Tzompantzi, Torres and G
- Page 92: Mantilla, Tzompantzi, Torres and G
- Page 95 and 96: 68Synthesis of MIBKwe examined the
- Page 97 and 98: 70Synthesis of MIBK1412Conversion (
- Page 99 and 100: 72Synthesis of MIBK4,4’-dimethyl
- Page 101 and 102: 74Synthesis of MIBKobtained for MIB
- Page 104 and 105: Ardizzi et al. 7710. The Control of
- Page 106 and 107: Ardizzi et al. 79type acidity at th
- Page 108: Ardizzi et al. 81procedure describe
- Page 111 and 112: 84Phenol Benzoylationconsecutive Fr
- Page 113: 86Phenol BenzoylationThis does not
- Page 118 and 119: Hu et al. 9112. Biphasic Catalytic
- Page 120 and 121: Hu et al. 93Results and DiscussionM
- Page 122 and 123: Hu et al. 95ionic liquid is used in
- Page 124 and 125: Hu et al. 97Figure 4. Schematic flo
- Page 126 and 127: Singh and Chuang 9913. Reaction Pat
- Page 128 and 129: Singh and Chuang 101for O 2 , 40 fo
- Page 130 and 131: Singh and Chuang 103537373650Temp (
- Page 132 and 133: Singh and Chuang 1050.064m/e = 32 (
- Page 134 and 135: Singh and Chuang 107In summary, hyd
- Page 136 and 137: Bacchini et al . 10914. The Transfo
- Page 138 and 139: Bacchini et al . 1111 summarizes th
- Page 140 and 141: Bacchini et al . 113these samples h
- Page 142 and 143: Bacchini et al . 115around 1. The d
- Page 144 and 145: Bacchini et al . 117Experimental Se
- Page 146 and 147: Tanielyan et al. 11915. Transition
- Page 148 and 149: Tanielyan et al. 121We wish to repo
- Page 150 and 151: Tanielyan et al. 123Fig 1a shows th
- Page 152 and 153: Tanielyan et al. 125TEMPO concentra
- Page 154 and 155: Tanielyan et al. 127complete conver
- Page 156 and 157: Tanielyan et al. 129ConclusionsIt h
- Page 158 and 159: Liu, Cant and Smith 13116. The Conv
- Page 160 and 161: Liu, Cant and Smith 133calculated f
- Page 162 and 163: Liu, Cant and Smith 135Table 3. App
- Page 164 and 165:
Liu, Cant and Smith 137noting that
- Page 166 and 167:
Liu, Cant and Smith 139an exact fit
- Page 168 and 169:
Tanielyan et al. 14117. Bromine-Fre
- Page 170 and 171:
Tanielyan et al. 143TEMPO catalyst,
- Page 172 and 173:
mmol),Tanielyan et al. 145catalyst.
- Page 174 and 175:
Miller and Chuang 14718. In situ In
- Page 176 and 177:
Miller and Chuang 1492(a)2359217516
- Page 178 and 179:
Miller and Chuang 151(a)33802973292
- Page 180:
III. Symposium on Catalytic Hydroge
- Page 183 and 184:
156 Raney® Metastable PrecursorsIn
- Page 185 and 186:
158 Raney® Metastable Precursorsfe
- Page 187 and 188:
160 Raney® Metastable Precursorssl
- Page 189 and 190:
162 Raney® Metastable Precursorsfu
- Page 191 and 192:
164 Raney® Metastable Precursorsva
- 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
- Page 243 and 244:
216 Cavitating Ultrasound Hydrogena
- Page 245 and 246:
218 Cavitating Ultrasound Hydrogena
- Page 247 and 248:
220 Cavitating Ultrasound Hydrogena
- Page 249 and 250:
222 Cavitating Ultrasound Hydrogena
- Page 251 and 252:
224 Cavitating Ultrasound Hydrogena
- Page 253 and 254:
226 Cavitating Ultrasound Hydrogena
- Page 255 and 256:
228 Hydrogenation of Pynitrilesuch
- Page 257 and 258:
230 Hydrogenation of Pynitrile%Sele
- Page 259 and 260:
232 Hydrogenation of Pynitrile%Sele
- Page 261 and 262:
234 Hydrogenation of Pynitrile10. A
- Page 263 and 264:
236Deactivation of Catalyst in Suga
- Page 265 and 266:
238Deactivation of Catalyst in Suga
- Page 268 and 269:
Jackson and Spence 24127. Selectivi
- Page 270 and 271:
Jackson and Spence 243been related
- Page 272:
Jackson and Spence 245Acknowledgeme
- 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
- Page 322 and 323:
Pugin et al. 295ferrocene binding m
- Page 324 and 325:
Pugin et al. 297complexes with one
- Page 326 and 327:
Pugin et al. 2993: 50.1 (J pp =50 H
- Page 328 and 329:
Pugin et al. 301temperature, then t
- Page 330 and 331:
Margitfalvi et al. 30335. Catalyst
- Page 332 and 333:
Margitfalvi et al. 305Based on the
- Page 334 and 335:
Margitfalvi et al. 307Table 1. Vari
- Page 336 and 337:
Margitfalvi et al. 309Combination o
- Page 338 and 339:
Margitfalvi et al. 311Figure 1. Map
- Page 340 and 341:
Margitfalvi et al. 313Acknowledgeme
- Page 342 and 343:
Auten, Crump, Singh and Chandler 31
- Page 344 and 345:
Auten, Crump, Singh and Chandler 31
- Page 346 and 347:
Auten, Crump, Singh and Chandler 31
- Page 348 and 349:
Auten, Crump, Singh and Chandler 32
- Page 350:
Auten, Crump, Singh and Chandler 32
- Page 354 and 355:
Falling et al. 32737. Development o
- Page 356 and 357:
Falling et al. 329With these proces
- Page 358 and 359:
Falling et al. 331salt, TOP18 has v
- Page 360 and 361:
Falling et al. 333The catalyst syst
- Page 362 and 363:
Falling et al. 335Normal operation
- Page 364 and 365:
Bianchi, Borzatta, Poluzzi and Vacc
- Page 366 and 367:
Bianchi, Borzatta, Poluzzi and Vacc
- Page 368 and 369:
Bianchi, Borzatta, Poluzzi and Vacc
- Page 370 and 371:
Bianchi, Borzatta, Poluzzi and Vacc
- Page 372 and 373:
Bianchi, Borzatta, Poluzzi and Vacc
- Page 374 and 375:
Griffin, Johnston, Prétôt and van
- Page 376 and 377:
Griffin, Johnston, Prétôt and van
- Page 378 and 379:
Griffin, Johnston, Prétôt and van
- Page 380:
Griffin, Johnston, Prétôt and van
- Page 383 and 384:
356Synthesis of PseudoiononesOOO- H
- Page 385 and 386:
358Synthesis of PseudoiononesMgO Pe
- Page 387 and 388:
360Synthesis of Pseudoionones0.5 wt
- Page 389 and 390:
362Synthesis of PseudoiononesTable
- Page 391 and 392:
364Synthesis of Pseudoiononesstrong
- Page 393 and 394:
366 MIBK Synthesis via CDproduce me
- Page 395 and 396:
368 MIBK Synthesis via CDExperiment
- Page 397 and 398:
370 MIBK Synthesis via CDreboiler p
- Page 399 and 400:
372 MIBK Synthesis via CDIn MIBK, t
- Page 401 and 402:
374 MIBK Synthesis via CDConclusion
- Page 404 and 405:
Sanders et al. 37742. Producing Pol
- Page 406 and 407:
Sanders et al. 379For the purposes
- Page 408 and 409:
Sanders et al. 381corresponding alc
- Page 410 and 411:
Sanders et al. 383polyurethane foam
- Page 412 and 413:
Zoeller and Barnette 38543. Carbony
- Page 414 and 415:
Zoeller and Barnette 387The first s
- Page 416 and 417:
Zoeller and Barnette 389Material ac
- Page 418 and 419:
Zoeller and Barnette 391above 120°
- Page 420 and 421:
Zoeller and Barnette 393tributyl am
- Page 422 and 423:
Hallett, Pollet, Eckert and Liotta
- Page 424 and 425:
Hallett, Pollet, Eckert and Liotta
- Page 426 and 427:
Hallett, Pollet, Eckert and Liotta
- Page 428 and 429:
Hallett, Pollet, Eckert and Liotta
- Page 430 and 431:
Hallett, Pollet, Eckert and Liotta
- Page 432 and 433:
Kiss, Rothenberg and Dimian 40545.
- Page 434 and 435:
Kiss, Rothenberg and Dimian 407C 10
- Page 436 and 437:
Kiss, Rothenberg and Dimian 409Tabl
- Page 438 and 439:
Kiss, Rothenberg and Dimian 411X (m
- Page 440 and 441:
Kiss, Rothenberg and Dimian 413Prep
- Page 442 and 443:
Snåre et al. 41546. Continuous Deo
- Page 444 and 445:
Snåre et al. 417The production of
- Page 446 and 447:
Snåre et al. 419was 15 μm and the
- Page 448 and 449:
Snåre et al. 421to 13% of conversi
- Page 450 and 451:
Snåre et al. 423Ethyl stearate con
- Page 452 and 453:
Snåre et al. 425increase in the fo
- Page 454 and 455:
428Glycerol Hydrogenolysisfundament
- Page 456 and 457:
430Glycerol Hydrogenolysisreaction
- Page 458 and 459:
432Glycerol Hydrogenolysisexpense o
- Page 460 and 461:
434Glycerol Hydrogenolysis[GO], M1.
- Page 462:
436Glycerol HydrogenolysisReference
- Page 465 and 466:
438Sustainable Process Technologyth
- Page 467 and 468:
440Sustainable Process Technologyco
- Page 469 and 470:
442Sustainable Process Technologywi
- Page 471 and 472:
444Sustainable Process TechnologyTh
- Page 474 and 475:
Lee, Shi, Subramaniam and Busch 447
- Page 476 and 477:
Lee, Shi, Subramaniam and Busch 449
- Page 478 and 479:
Lee, Shi, Subramaniam and Busch 451
- Page 480:
VII. Symposium on Other Topics in C
- Page 483 and 484:
...456Chiral BisphospholanesToday,
- Page 485 and 486:
458Chiral BisphospholanesFirst, the
- Page 487 and 488:
460Chiral BisphospholanesInterestin
- Page 490 and 491:
Augustine, Tanielyan, Marin and Alv
- Page 492 and 493:
Augustine, Tanielyan, Marin and Alv
- Page 494 and 495:
Augustine, Tanielyan, Marin and Alv
- Page 496 and 497:
Knifton and Sanderson 46952. Select
- Page 498 and 499:
Knifton and Sanderson 4711414141413
- Page 500:
Knifton and Sanderson 4733. O. C. A
- Page 503 and 504:
476 Palladium LeachingResults and D
- Page 505 and 506:
478 Palladium Leachingtemperatures
- Page 508 and 509:
Arunajatesan, Cruz, Möbus and Chen
- Page 510 and 511:
Arunajatesan, Cruz, Möbus and Chen
- Page 512:
Arunajatesan, Cruz, Möbus and Chen
- Page 515 and 516:
488Profiling of Catalytic Performan
- Page 517 and 518:
490Profiling of Catalytic Performan
- Page 519 and 520:
492Profiling of Catalytic Performan
- Page 521 and 522:
494 Transition Metal Removalmetal r
- Page 523 and 524:
496 Transition Metal RemovalDeloxan
- Page 525 and 526:
498 Transition Metal Removalreduced
- Page 528 and 529:
Durán Pachón and Rothenberg 50157
- Page 530 and 531:
Durán Pachón and Rothenberg 503th
- Page 532:
Durán Pachón and Rothenberg 505Ac
- Page 535 and 536:
508Author IndexDíez Verónica K. 4
- Page 537 and 538:
510Author IndexPhillips Gerald W. 3
- Page 540 and 541:
Catalysis of Organic Reactions 513K
- Page 542 and 543:
Catalysis of Organic Reactions 515c
- Page 544 and 545:
Catalysis of Organic Reactions 517h
- Page 546 and 547:
Catalysis of Organic Reactions 519p