Comprehensive organic name reactions and reagents: 2
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| Beschreibung: | XLIX S., S. 1305 - 2292 Ill., graph. Darst. |
| ISBN: | 9780470286630 |
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| 003 | DE-604 | ||
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| 007 | t | ||
| 008 | 081117s2009 ad|| |||| 00||| eng d | ||
| 020 | |a 9780470286630 |9 978-0-470-28663-0 | ||
| 035 | |a (OCoLC)633810894 | ||
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| 040 | |a DE-604 |b ger |e rakwb | ||
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| 100 | 1 | |a Wang, Zerong |e Verfasser |4 aut | |
| 245 | 1 | 0 | |a Comprehensive organic name reactions and reagents |n 2 |c Zerong Wang |
| 264 | 1 | |a Hoboken, NJ |b Wiley |c (2009) | |
| 300 | |a XLIX S., S. 1305 - 2292 |b Ill., graph. Darst. | ||
| 336 | |b txt |2 rdacontent | ||
| 337 | |b n |2 rdamedia | ||
| 338 | |b nc |2 rdacarrier | ||
| 773 | 0 | 8 | |w (DE-604)BV035164063 |g 2 |
| 856 | 4 | 2 | |m Digitalisierung UB Bayreuth |q application/pdf |u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016971140&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |3 Inhaltsverzeichnis |
| 999 | |a oai:aleph.bib-bvb.de:BVB01-016971140 | ||
Datensatz im Suchindex
| _version_ | 1804138328888442880 |
|---|---|
| adam_text | PART TWO
290.
Hajos-Parrish-Eder-Sauer-Wiechert Reaction
....................... 1305
291.
Haller-Bauer Cleavage
.............................................. 1310
292.
Hammick Reaction
................................................. 1314
293.
Hansley-Prelog Acyloin Condensation
............................... 1317
294.
Hantzsch Dihydropyridine Synthesis
................................ 1321
295.
Hantzsch Pyrrole Synthesis
......................................... 1326
296.
Hantzsch Thiazole Synthesis
........................................ 1330
297.
Hass-Bender Oxidation
............................................. 1335
298.
Haworth Methylation
............................................... 1338
CONTENTS
XV
299. Haworth
Synthesis .................................................
1342
300.
Hayashi Rearrangement
............................................ 1347
301.
Heck Reaction
..................................................... 1350
302.
Hegedus
índole
Synthesis
........................................... 1358
303. Helferich
Condensation
............................................. 1363
304. Helferich Glycosylation............................................. 1367
305. Hell-Volhard-Zelinsky
Reaction
..................................... 1371
306. Hemetsberger
Indole
Synthesis......................................
1375
307. Henkel
Reaction....................................................
1379
308. Henry
Reaction ....................................................
1383
309. Herbst-Engel Transamination....................................... 1388
310.
Heron Rearrangement..............................................
1392
311. Herz
Reaction......................................................
1395
312. Heumann Indigo
Process
........................................... 1399
313. Heyns
Rearrangement
.............................................. 1403
314. Hubert-Johnson
Reaction
........................................... 1408
315. Hinsberg Oxindole
Synthesis
........................................ 1415
316. Hinsberg
Reaction
.................................................. 1418
317. Hinsberg Sulfone
Synthesis
......................................... 1422
318. Hinsberg Thiophene
Synthesis
...................................... 1426
319. Hiyama
Coupling
.................................................. 1430
320. Hoch-Campbell
Reaction
........................................... 1434
321. Hock
Rearrangement
............................................... 1438
322. Hofer-Moest
Reaction
.............................................. 1443
323. Hofmann Degradation.............................................. 1447
324. Hofmann Elimination .............................................. 1451
325. Hofmann Isonitrile
Synthesis
....................................... 1457
326. Hofmann
Rule
..................................................... 1460
327. Hofmann-Löffler-Freytag
Reaction
.................................. 1464
328. Hofmann-Martius
Rearrangement
.................................. 1469
329. Hofmann-Sand
Reaction
............................................ 1473
330.
Hooker Oxidation
.................................................. 1477
XVI CONTENTS
331. Horenstein-Pählicke
Reaction
....................................... 1481
332. Horner-Wadsworth-Emmons Olefination............................ 1484
333. Hosomi-Sakurai Allylation.......................................... 1491
334. Houben-Hoesch
Reaction
........................................... 1496
335. Houdry Cracking
Process
........................................... 1501
336. Huisgen
Pyrrole Synthesis..........................................
1504
337. Hunsdiecker
Condensation .........................................
1508
338. Hunsdiecker
Reaction..............................................
1511
339.
Hydroformylation
.................................................. 1516
340. Iodolactonization................................................... 1521
341. Irvine-Purdie Methylation.......................................... 1526
342. Jacobsen
Rearrangement
........................................... 1530
343. Jacobsen-Katsuki Epoxidation...................................... 1534
344.
Janovsky
Reaction..................................................
1542
345. Japp-Klingemann Fischer
Indole
Synthesis..........................
1547
346. Japp-Klingemann
Reaction.........................................
1552
347. Japp-Maitland
Condensation.......................................
1558
348. Johnson
Orthoester Claisen
Rearrangement.........................
1561
349. Jones
Oxidation....................................................
1564
350. Jourdan-Ullmann
Reaction.........................................
1569
351. Julia Olefination ................................................... 1576
352.
Juliá-Colonna
Asymmetric
Epoxidation............................. 1583
353. Kabachnik-Fields
Reaction
......................................... 1588
354. Kahne Glycosylation ............................................... 1593
355. Keck Allylation .................................................... 1597
356. Keck Macrolactonization........................................... 1601
357.
Kemp
Elimination.................................................. 1605
358. Kennedy Oxidative Cyclization ..................................... 1609
359. Kiliani-Fischer
Cyanohydrin Synthesis
.............................. 1613
360.
Kishner Decomposition
............................................. 1617
361. Knoevenagel
Condensation
......................................... 1621
362. Knoevenagel Diazotization
Method
.................................. 1627
CONTENTS
XVii
363.
Knorr
Pyrazole
Synthesis
........................................... 1631
364.
Knorr
Pyrrole Synthesis
............................................ 1634
365.
Knorr Quinoline
Synthesis
.......................................... 1638
366.
Koch-Haaf Carboxylation
.......................................... 1642
367.
Kochi Reaction
..................................................... 1646
368.
Koenigs-Knorr Reaction
............................................ 1650
369.
Kolbe
Electrolysis
.................................................. 1656
370.
Kolbe Nitrile
Synthesis
............................................. 1661
371.
Kolbe-Schmidt Reaction
............................................ 1664
372.
Kondraťeva Pyridine
Synthesis
..................................... 1668
373.
Kornblum Oxidation
............................................... 1672
374.
Kornblum-Delamare Rearrangement
............................... 1675
375.
Kostanecki-Robinson Reaction
...................................... 1679
376.
Kowalski
Ester
Homologation
....................................... 1683
377.
Krapcho Decarboxylation
.......................................... 1687
378.
Kriewitz Condensation
............................................. 1692
379. Kröhnke
Pyridine
Synthesis
........................................ 1695
380. Kuhn-Roth
Oxidation
.............................................. 1699
381. Kuhn-Winterstein
Reduction
....................................... 1703
382.
Kulinkovich Cydopropanation
...................................... 1706
383. Kutscheroff
Acetylene
Hydration ................................... 1710
384.
Lander Rearrangement
............................................. 1713
385.
Larock
Indole
Synthesis
............................................ 1717
386.
Lawesson s Reagent
................................................ 1722
387.
Lebedev Process
.................................................... 1728
388.
Lehmstedt-Tanasescu Reaction
...................................... 1731
389.
Lemieux- Johnson Oxidation
........................................ 1734
390.
Leuckart Reaction
.................................................. 1737
391.
Leuckart Thiophenol Synthesis
..................................... 1743
392.
Levinstein Process
.................................................. 1747
393. Lieben
lodoform
Reaction
.......................................... 1750
394. Liebeskind-Srögl
Cross-Coupling
................................... 1754
XViii
CONTENTS
395. Lindlar
Hydrogénation.............................................
1758
396. Lobry de Bruyn-Alberda van Ekenstein Transformation............. 1763
397.
Lombardo Methylenation
........................................... 1767
398.
Lossen
Rearrangement.............................................
1772
399. Luche
Reaction ....................................................
1777
400. Luche
Reduction...................................................
1782
401. MacDonald-Fischer Degradation.................................... 1787
402. Madelung
Indole
Synthesis .........................................
1791
403.
Maillard
Reaction
.................................................. 1795
404.
Maitland-Japp
Reaction
............................................ 1800
405.
Majetich
Annulation
............................................... 1803
406.
Malaprade Reaction
................................................ 1807
407.
Malonic Ester Synthesis
............................................ 1811
408.
Mandelic Acid Synthesis
............................................ 1816
409.
Mannich Reaction
.................................................. 1820
410.
Marckwald Asymmetric Synthesis
.................................. 1829
411.
Markownikoff Rule and Anti-Markownikoff Rule
................... 1833
412.
Martinet Reaction
.................................................. 1838
413.
Martin s Sulfurane
................................................. 1841
414.
Mattox-Kendall Reaction
........................................... 1845
415.
McCormack
Cycloaddition
......................................... 1849
416.
McFadyen-Stevens Reaction
........................................ 1853
417.
McLafferty Rearrangement
......................................... 1856
418.
McMurry Coupling
................................................ I860
419. Meerwein Arylation................................................ 1866
420.
Meerwein-Ponndorf-Verley Reduction
............................... 1871
421.
Meerwein s Salt
.................................................... 1877
422. Meinwald
Rearrangement
.......................................... 1880
423.
Meisenheimer Complexes
........................................... 1883
424.
Meisenheimer Rearrangement
...................................... 1889
425.
Menke Nitration
...................................................
I893
426.
Menschutkin Reaction
..............................................
I897
CONTENTS
ХІХ
427. Mentzer Pyrone
Synthesis
.......................................... 1901
428. Merrifield
Solid-Phase
Peptide
Synthesis
............................ 1905
429. Meyer-Hartmann
Reaction
......................................... 1910
430. Meyers Aldehyde
Synthesis.........................................
1913
431.
Meyer-Schuster Rearrangement
.................................... 1917
432.
Michael Addition
................................................... 1922
433.
Michaelis-Arbuzov Rearrangement
................................. 1929
434.
Michael-Stetter Reaction
........................................... 1935
435.
Miescher Degradation
.............................................. 1940
436.
Mignonac Reaction
................................................. 1945
437.
Milas Hydroxylation
................................................ 1948
438.
Mislow-Evans Rearrangement
...................................... 1952
439.
Mitsunobu Reaction
................................................ 1955
440.
Moffatt-Swern Oxidation
........................................... 1962
441.
Moore Cyclization
.................................................. 1967
442.
Morgan-Walls Cyclization
.......................................... 1971
443.
Mori-Ban
Indole
Synthesis
.......................................... 1975
444.
Morin Rearrangement
.............................................. 1979
445.
Mosher sAcid
...................................................... 1983
446.
Moureau-Mignonac Ketimine Synthesis
............................. 1988
447.
Mukaiyama Aldol Reaction
......................................... 1991
448.
Mukaiyama-Michael Reaction
...................................... 1996
449.
Miiller-Cunradi-Pieroh Process
..................................... 2000
450.
Myers-Saito Cyclization
............................................ 2003
451.
Nagata Reaction
.................................................... 2007
452.
Nazarov Cyclization
................................................ 2011
453.
Neber
Rearrangement
.............................................. 2017
454. Neber-Bössel
Synthesis
............................................. 2022
455.
Nef
Reaction
....................................................... 2025
456.
Negishi Cross-Coupling
............................................. 2029
457.
Nencki Reaction
.................................................... 2035
458.
Nenitzescu Synthesis
................................................ 2038
XX
CONTENTS
459.
Nenitzescu
índole
Synthesis
......................................... 2042
460.
Newman-Kwart Rearrangement
.................................... 2046
461.
Nicholas Reaction
.................................................. 2049
462.
Niementowski Reaction
............................................. 2054
463. Nierenstein
Reaction
............................................... 2058
464.
Norrish Type I Reaction
............................................ 2062
465.
Norrish Type II Reaction
........................................... 2067
466.
Noyori
Hydrogénation
.............................................. 2072
467.
Nozaki-Hiyama-Kishi Reaction
..................................... 2076
468.
Nysted Reagent
.................................................... 2081
469.
Ohle Quinoxaline Synthesis
......................................... 2084
470.
Oppenauer Oxidation
.............................................. 2088
471.
Orton Rearrangement
.............................................. 2092
472.
Ostromislensky Process
............................................. 2097
473.
Overman Rearrangement
........................................... 2100
474.
Paal-Knorr
Furan
Synthesis
........................................ 2104
475.
Paal-Knorr Pyrrole Synthesis
....................................... 2107
476.
Paneth Technique
.................................................. 2111
477.
Parham Cyclization
................................................ 2114
478.
Parikh-Doering Oxidation
.......................................... 2118
479.
Passerini
Reaction
.................................................. 2121
480. Paterno-Büchi
Reaction
............................................ 2126
481.
Pauson-Khand Reaction
............................................ 2131
482.
Payne Rearrangement
.............................................. 2139
483.
Pearlman s Catalyst
................................................ 2143
484. Pechmann Pyrazole
Synthesis
....................................... 2147
485. Pechmann
Reaction
................................................ 2151
486.
Pellizzari Reaction
................................................. 2157
487.
Perkin Reaction
.................................................... 2160
488.
Perkin Synthesis
................................................... 2164
489.
Perkow Reaction
................................................... 2168
490.
Petasis-Ferrier Rearrangement
..................................... 2173
CONTENTS
ХХІ
491.
Peterson Olefination
................................................ 2176
492. Petrenko-Kritschenko Piperidone
Synthesis
......................... 2182
493. Pfau-Plattner Azulene
Synthesis
.................................... 2185
494. Pfitzinger
Reaction
................................................. 2188
495. Pfitzner-Moffatt
Oxidation
.......................................... 2193
496. Phillips-Ladenburg Benzimidazole
Synthesis
........................ 2197
497. Photo-Fries
Rearrangement
........................................ 2200
498. Pictet-Gams
Synthesis
.............................................. 2206
499. Pictet-Spengler
Reaction
............................................ 2210
500. Piloty-Robinson
Pyrrole Synthesis ..................................
2217
501.
Pinacol
Coupling Reaction
.......................................... 2221
502.
Pinacol
Rearrangement
............................................. 2227
503.
Pinner Condensation
............................................... 2233
504.
Pinner Reaction
.................................................... 2237
505.
Pinner S-Triazine Synthesis
......................................... 2241
506.
Piria Reaction
...................................................... 2244
507.
Plancher
Rearrangement
........................................... 2248
508.
Polonovski Reaction
................................................ 2251
509.
Pomeranz-Fritsch Reaction
......................................... 2256
510.
Ponzio Reaction
.................................................... 2260
511.
Prévost
Reaction
................................................... 2263
512.
Prey Ether Cleavage
................................................ 2267
513.
Prilezhaev Reaction
................................................ 2270
514.
Prins
Reaction
..................................................... 2275
515.
Pudovik Reaction
.................................................. 2280
516.
Pummerer Rearrangement
......................................... 2284
517.
Quelet Reaction
.................................................... 2290
|
| adam_txt |
PART TWO
290.
Hajos-Parrish-Eder-Sauer-Wiechert Reaction
. 1305
291.
Haller-Bauer Cleavage
. 1310
292.
Hammick Reaction
. 1314
293.
Hansley-Prelog Acyloin Condensation
. 1317
294.
Hantzsch Dihydropyridine Synthesis
. 1321
295.
Hantzsch Pyrrole Synthesis
. 1326
296.
Hantzsch Thiazole Synthesis
. 1330
297.
Hass-Bender Oxidation
. 1335
298.
Haworth Methylation
. 1338
CONTENTS
XV
299. Haworth
Synthesis .
1342
300.
Hayashi Rearrangement
. 1347
301.
Heck Reaction
. 1350
302.
Hegedus
índole
Synthesis
. 1358
303. Helferich
Condensation
. 1363
304. Helferich Glycosylation. 1367
305. Hell-Volhard-Zelinsky
Reaction
. 1371
306. Hemetsberger
Indole
Synthesis.
1375
307. Henkel
Reaction.
1379
308. Henry
Reaction .
1383
309. Herbst-Engel Transamination. 1388
310.
Heron Rearrangement.
1392
311. Herz
Reaction.
1395
312. Heumann Indigo
Process
. 1399
313. Heyns
Rearrangement
. 1403
314. Hubert-Johnson
Reaction
. 1408
315. Hinsberg Oxindole
Synthesis
. 1415
316. Hinsberg
Reaction
. 1418
317. Hinsberg Sulfone
Synthesis
. 1422
318. Hinsberg Thiophene
Synthesis
. 1426
319. Hiyama
Coupling
. 1430
320. Hoch-Campbell
Reaction
. 1434
321. Hock
Rearrangement
. 1438
322. Hofer-Moest
Reaction
. 1443
323. Hofmann Degradation. 1447
324. Hofmann Elimination . 1451
325. Hofmann Isonitrile
Synthesis
. 1457
326. Hofmann
Rule
. 1460
327. Hofmann-Löffler-Freytag
Reaction
. 1464
328. Hofmann-Martius
Rearrangement
. 1469
329. Hofmann-Sand
Reaction
. 1473
330.
Hooker Oxidation
. 1477
XVI CONTENTS
331. Horenstein-Pählicke
Reaction
. 1481
332. Horner-Wadsworth-Emmons Olefination. 1484
333. Hosomi-Sakurai Allylation. 1491
334. Houben-Hoesch
Reaction
. 1496
335. Houdry Cracking
Process
. 1501
336. Huisgen
Pyrrole Synthesis.
1504
337. Hunsdiecker
Condensation .
1508
338. Hunsdiecker
Reaction.
1511
339.
Hydroformylation
. 1516
340. Iodolactonization. 1521
341. Irvine-Purdie Methylation. 1526
342. Jacobsen
Rearrangement
. 1530
343. Jacobsen-Katsuki Epoxidation. 1534
344.
Janovsky
Reaction.
1542
345. Japp-Klingemann Fischer
Indole
Synthesis.
1547
346. Japp-Klingemann
Reaction.
1552
347. Japp-Maitland
Condensation.
1558
348. Johnson
Orthoester Claisen
Rearrangement.
1561
349. Jones
Oxidation.
1564
350. Jourdan-Ullmann
Reaction.
1569
351. Julia Olefination . 1576
352.
Juliá-Colonna
Asymmetric
Epoxidation. 1583
353. Kabachnik-Fields
Reaction
. 1588
354. Kahne Glycosylation . 1593
355. Keck Allylation . 1597
356. Keck Macrolactonization. 1601
357.
Kemp
Elimination. 1605
358. Kennedy Oxidative Cyclization . 1609
359. Kiliani-Fischer
Cyanohydrin Synthesis
. 1613
360.
Kishner Decomposition
. 1617
361. Knoevenagel
Condensation
. 1621
362. Knoevenagel Diazotization
Method
. 1627
CONTENTS
XVii
363.
Knorr
Pyrazole
Synthesis
. 1631
364.
Knorr
Pyrrole Synthesis
. 1634
365.
Knorr Quinoline
Synthesis
. 1638
366.
Koch-Haaf Carboxylation
. 1642
367.
Kochi Reaction
. 1646
368.
Koenigs-Knorr Reaction
. 1650
369.
Kolbe
Electrolysis
. 1656
370.
Kolbe Nitrile
Synthesis
. 1661
371.
Kolbe-Schmidt Reaction
. 1664
372.
Kondraťeva Pyridine
Synthesis
. 1668
373.
Kornblum Oxidation
. 1672
374.
Kornblum-Delamare Rearrangement
. 1675
375.
Kostanecki-Robinson Reaction
. 1679
376.
Kowalski
Ester
Homologation
. 1683
377.
Krapcho Decarboxylation
. 1687
378.
Kriewitz Condensation
. 1692
379. Kröhnke
Pyridine
Synthesis
. 1695
380. Kuhn-Roth
Oxidation
. 1699
381. Kuhn-Winterstein
Reduction
. 1703
382.
Kulinkovich Cydopropanation
. 1706
383. Kutscheroff
Acetylene
Hydration . 1710
384.
Lander Rearrangement
. 1713
385.
Larock
Indole
Synthesis
. 1717
386.
Lawesson's Reagent
. 1722
387.
Lebedev Process
. 1728
388.
Lehmstedt-Tanasescu Reaction
. 1731
389.
Lemieux- Johnson Oxidation
. 1734
390.
Leuckart Reaction
. 1737
391.
Leuckart Thiophenol Synthesis
. 1743
392.
Levinstein Process
. 1747
393. Lieben
lodoform
Reaction
. 1750
394. Liebeskind-Srögl
Cross-Coupling
. 1754
XViii
CONTENTS
395. Lindlar
Hydrogénation.
1758
396. Lobry de Bruyn-Alberda van Ekenstein Transformation. 1763
397.
Lombardo Methylenation
. 1767
398.
Lossen
Rearrangement.
1772
399. Luche
Reaction .
1777
400. Luche
Reduction.
1782
401. MacDonald-Fischer Degradation. 1787
402. Madelung
Indole
Synthesis .
1791
403.
Maillard
Reaction
. 1795
404.
Maitland-Japp
Reaction
. 1800
405.
Majetich
Annulation
. 1803
406.
Malaprade Reaction
. 1807
407.
Malonic Ester Synthesis
. 1811
408.
Mandelic Acid Synthesis
. 1816
409.
Mannich Reaction
. 1820
410.
Marckwald Asymmetric Synthesis
. 1829
411.
Markownikoff Rule and Anti-Markownikoff Rule
. 1833
412.
Martinet Reaction
. 1838
413.
Martin's Sulfurane
. 1841
414.
Mattox-Kendall Reaction
. 1845
415.
McCormack
Cycloaddition
. 1849
416.
McFadyen-Stevens Reaction
. 1853
417.
McLafferty Rearrangement
. 1856
418.
McMurry Coupling
. I860
419. Meerwein Arylation. 1866
420.
Meerwein-Ponndorf-Verley Reduction
. 1871
421.
Meerwein's Salt
. 1877
422. Meinwald
Rearrangement
. 1880
423.
Meisenheimer Complexes
. 1883
424.
Meisenheimer Rearrangement
. 1889
425.
Menke Nitration
.
I893
426.
Menschutkin Reaction
.
I897
CONTENTS
ХІХ
427. Mentzer Pyrone
Synthesis
. 1901
428. Merrifield
Solid-Phase
Peptide
Synthesis
. 1905
429. Meyer-Hartmann
Reaction
. 1910
430. Meyers Aldehyde
Synthesis.
1913
431.
Meyer-Schuster Rearrangement
. 1917
432.
Michael Addition
. 1922
433.
Michaelis-Arbuzov Rearrangement
. 1929
434.
Michael-Stetter Reaction
. 1935
435.
Miescher Degradation
. 1940
436.
Mignonac Reaction
. 1945
437.
Milas Hydroxylation
. 1948
438.
Mislow-Evans Rearrangement
. 1952
439.
Mitsunobu Reaction
. 1955
440.
Moffatt-Swern Oxidation
. 1962
441.
Moore Cyclization
. 1967
442.
Morgan-Walls Cyclization
. 1971
443.
Mori-Ban
Indole
Synthesis
. 1975
444.
Morin Rearrangement
. 1979
445.
Mosher'sAcid
. 1983
446.
Moureau-Mignonac Ketimine Synthesis
. 1988
447.
Mukaiyama Aldol Reaction
. 1991
448.
Mukaiyama-Michael Reaction
. 1996
449.
Miiller-Cunradi-Pieroh Process
. 2000
450.
Myers-Saito Cyclization
. 2003
451.
Nagata Reaction
. 2007
452.
Nazarov Cyclization
. 2011
453.
Neber
Rearrangement
. 2017
454. Neber-Bössel
Synthesis
. 2022
455.
Nef
Reaction
. 2025
456.
Negishi Cross-Coupling
. 2029
457.
Nencki Reaction
. 2035
458.
Nenitzescu Synthesis
. 2038
XX
CONTENTS
459.
Nenitzescu
índole
Synthesis
. 2042
460.
Newman-Kwart Rearrangement
. 2046
461.
Nicholas Reaction
. 2049
462.
Niementowski Reaction
. 2054
463. Nierenstein
Reaction
. 2058
464.
Norrish Type I Reaction
. 2062
465.
Norrish Type II Reaction
. 2067
466.
Noyori
Hydrogénation
. 2072
467.
Nozaki-Hiyama-Kishi Reaction
. 2076
468.
Nysted Reagent
. 2081
469.
Ohle Quinoxaline Synthesis
. 2084
470.
Oppenauer Oxidation
. 2088
471.
Orton Rearrangement
. 2092
472.
Ostromislensky Process
. 2097
473.
Overman Rearrangement
. 2100
474.
Paal-Knorr
Furan
Synthesis
. 2104
475.
Paal-Knorr Pyrrole Synthesis
. 2107
476.
Paneth Technique
. 2111
477.
Parham Cyclization
. 2114
478.
Parikh-Doering Oxidation
. 2118
479.
Passerini
Reaction
. 2121
480. Paterno-Büchi
Reaction
. 2126
481.
Pauson-Khand Reaction
. 2131
482.
Payne Rearrangement
. 2139
483.
Pearlman's Catalyst
. 2143
484. Pechmann Pyrazole
Synthesis
. 2147
485. Pechmann
Reaction
. 2151
486.
Pellizzari Reaction
. 2157
487.
Perkin Reaction
. 2160
488.
Perkin Synthesis
. 2164
489.
Perkow Reaction
. 2168
490.
Petasis-Ferrier Rearrangement
. 2173
CONTENTS
ХХІ
491.
Peterson Olefination
. 2176
492. Petrenko-Kritschenko Piperidone
Synthesis
. 2182
493. Pfau-Plattner Azulene
Synthesis
. 2185
494. Pfitzinger
Reaction
. 2188
495. Pfitzner-Moffatt
Oxidation
. 2193
496. Phillips-Ladenburg Benzimidazole
Synthesis
. 2197
497. Photo-Fries
Rearrangement
. 2200
498. Pictet-Gams
Synthesis
. 2206
499. Pictet-Spengler
Reaction
. 2210
500. Piloty-Robinson
Pyrrole Synthesis .
2217
501.
Pinacol
Coupling Reaction
. 2221
502.
Pinacol
Rearrangement
. 2227
503.
Pinner Condensation
. 2233
504.
Pinner Reaction
. 2237
505.
Pinner S-Triazine Synthesis
. 2241
506.
Piria Reaction
. 2244
507.
Plancher
Rearrangement
. 2248
508.
Polonovski Reaction
. 2251
509.
Pomeranz-Fritsch Reaction
. 2256
510.
Ponzio Reaction
. 2260
511.
Prévost
Reaction
. 2263
512.
Prey Ether Cleavage
. 2267
513.
Prilezhaev Reaction
. 2270
514.
Prins
Reaction
. 2275
515.
Pudovik Reaction
. 2280
516.
Pummerer Rearrangement
. 2284
517.
Quelet Reaction
. 2290 |
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| author | Wang, Zerong |
| author_facet | Wang, Zerong |
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| id | DE-604.BV035164069 |
| illustrated | Illustrated |
| index_date | 2024-07-02T22:51:51Z |
| indexdate | 2024-07-09T21:26:27Z |
| institution | BVB |
| isbn | 9780470286630 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-016971140 |
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| physical | XLIX S., S. 1305 - 2292 Ill., graph. Darst. |
| publishDate | 2009 |
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| publisher | Wiley |
| record_format | marc |
| spelling | Wang, Zerong Verfasser aut Comprehensive organic name reactions and reagents 2 Zerong Wang Hoboken, NJ Wiley (2009) XLIX S., S. 1305 - 2292 Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier (DE-604)BV035164063 2 Digitalisierung UB Bayreuth application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016971140&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis |
| spellingShingle | Wang, Zerong Comprehensive organic name reactions and reagents |
| title | Comprehensive organic name reactions and reagents |
| title_auth | Comprehensive organic name reactions and reagents |
| title_exact_search | Comprehensive organic name reactions and reagents |
| title_exact_search_txtP | Comprehensive organic name reactions and reagents |
| title_full | Comprehensive organic name reactions and reagents 2 Zerong Wang |
| title_fullStr | Comprehensive organic name reactions and reagents 2 Zerong Wang |
| title_full_unstemmed | Comprehensive organic name reactions and reagents 2 Zerong Wang |
| title_short | Comprehensive organic name reactions and reagents |
| title_sort | comprehensive organic name reactions and reagents |
| url | http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016971140&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| volume_link | (DE-604)BV035164063 |
| work_keys_str_mv | AT wangzerong comprehensiveorganicnamereactionsandreagents2 |