Catalysis of Organic..

More documents

Recommendations

Info

xxiiiChronology of Organic ReactionsCatalysis Society ConferencesConf Year Chair Location ProceedingsPublisher1 1967 Joseph O'Connor New York City NYAS2 1969 Joseph O'Connor New York CityNYAS3 1970 Mel Rebenstrot New York City NYAS4 1973 Paul Rylander New York City NYAS5 1974Paul Rylander& Harold Greenfield Boston Academic Press6 1976 Gerry Smith Boston Academic Press7 1978 Bill Jones Chicago Academic Press8 1980 Bill Moses New Orleans Academic Press9 1982 John KosakSouthCharleston Dekker10 1984 Bob Augustine Williamsburg Dekker11 1986Paul Rylander& Harold Greenfield Savannah Dekker12 1988 Dale Blackburn San Antonio Dekker13 1990 Bill Pascoe Boca Raton Dekker14 1992Tom Johnson& John Kosak Albuquerque Dekker15 1994Mike Scaros& Mike Prunier Phoenix Dekker16 1996 Russ Malz Atlanta Dekker17 1998 Frank Herkes New Orleans Dekker18 2000 Mike Ford Charleston Dekker19 2002 Dennis Morrell San Antonio Dekker20 2004 John Sowa Hilton Head CRC Press21 2006 Steve Schmidt Orlando CRC Press
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 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
Page 66 and 67: Lathouder, Kapteijn and Moulijn 395
Page 68 and 69: Lathouder, Kapteijn and Moulijn 41p
Page 70: Lathouder, Kapteijn and Moulijn 43m
Page 73 and 74:
46Preparation of 4-Aminocarboxylic
Page 75 and 76:
Page 77 and 78:
Page 79 and 80:
Page 82 and 83:
Tzompantzi, Valente, Cantú and Gó
Page 84 and 85:
Page 86:
Page 89 and 90:
62Isobutene TrimerizationResults an
Page 91 and 92:
64Isobutene TrimerizationFigure 4 R
Page 94 and 95:
Canning, Gamman, Jackson and Urquar
Page 96 and 97:
Page 98 and 99:
Page 100 and 101:
Page 102:
Page 105 and 106:
78Methylation of Catecholthe use of
Page 107 and 108:
80Methylation of CatecholThe main r
Page 110 and 111:
Ardizzi et al. 8311. The Environmen
Page 112 and 113:
Ardizzi et al. 85the selectivity to
Page 114:
Ardizzi et al. 87Experimental Secti
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:
Page 245 and 246:
Page 247 and 248:
Page 249 and 250:
Page 251 and 252:
Page 253 and 254:
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:
Page 346 and 347:
Page 348 and 349:
Page 350:
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:
Page 368 and 369:
Page 370 and 371:
Page 372 and 373:
Page 374 and 375:
Griffin, Johnston, Prétôt and van
Page 376 and 377:
Page 378 and 379:
Page 380:
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:
Page 426 and 427:
Page 428 and 429:
Page 430 and 431:
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:
Page 478 and 479:
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:
Page 494 and 495:
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:
Page 512:
Page 515 and 516:
488Profiling of Catalytic Performan
Page 517 and 518:
Page 519 and 520:
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
show all

Catalysis of Organic..

You also want an ePaper? Increase the reach of your titles

Delete template?

Save as template?