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Smith M.B., March J. — March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure |
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Предметный указатель |
Alcohols by reduction aldehydes or ketones 1197—1203
Alcohols by the Baeyer-Villiger reaction 1644
Alcohols by the Barbier reaction 1205
Alcohols by the Bouveault-Blanc procedure 1551
Alcohols by the Cannizzaro reaction 1200 1564 1644
Alcohols by the Demyanov rearrangement 1644
Alcohols by the Tamao-Fleming oxidation 482
Alcohols by the Wittig rearrangement 1421 1644
Alcohols by Wagner-Meerwein rearrangement 1644
Alcohols conversion to ethers 479
Alcohols coupling by 544
Alcohols cyclic, oxidative cleavage 1521
Alcohols cyclic, transannular etherincation 920
Alcohols dehydration of 479 1326
Alcohols dehydration, and Zaitsev’s rule 1327
Alcohols dehydrogenation 1515
Alcohols enzymatic oxidation 1517
Alcohols epoxy, ring opening 462
Alcohols from acetals 1643
Alcohols from acid derivatives 567 1214 1551 1644
Alcohols from alcohols 1393 1643
Alcohols from aldehydes 719 1564 1643—1644
Alcohols from aldehydes and organometallics 1209—1211
Alcohols from alkaline cleavage of ethers 1644
Alcohols from alkanes 1533
Alcohols from alkenes 914 974 993 1643 1643 1644
Alcohols from alkenes, reagents for 914
Alcohols from allylic alcohols 1643
Alcohols from allylic silanes 1643
Alcohols from allylic silanes to aldehydes 1644
Alcohols from amides 1644
Alcohols from amines 494 1398 1643
Alcohols from anhydrides 1644
Alcohols from aromatic compounds 719 1643
Alcohols from boradioxolanes 1422
Alcohols from boranes 796 1422 1423 1644
Alcohols from carboxylic acids 1549 1644
Alcohols from contraction of rings 1644
Alcohols from cyclopropanes 1643
Alcohols from epoxides 529 546 1643
Alcohols from esters 1214 1551 1643 1644
Alcohols from ethers 1421 1643
Alcohols from expansion of rings 1644
Alcohols from Grignard reagents and aldehydes or ketones 795 1205—1209 1644
Alcohols from hydrolysis of alkyl halides 1643
Alcohols from hydrolysis of carboxylic esters 1643
Alcohols from hydrolysis of enol acetals 1643
Alcohols from hydrolysis of enol ethers 1643
Alcohols from hydrolysis of inorganic esters 1643
Alcohols from hydrolysis of ortho esters 1643
Alcohols from hydrolysis of sulfonic esters 1643
Alcohols from hydroperoxides 1558 1644
Alcohols from hydroxyalkylation of aromatic rings 1643
Alcohols from hydroxylation at an aliphatic carbon 1643
Alcohols from hydroxylation of silanes 482
Alcohols from hydroxymethylation of aromatic rings 1643
Alcohols from ketones 719 1209—1211 1643—1644
Alcohols from nitrites 1644
Alcohols from organolithium reagents and aldehydes or ketones 1205—1209 1644
Alcohols from organometallic compounds and alcohols 1643
Alcohols from organometallic compounds and aldehydes 1644
Alcohols from organometallic compounds and epoxides 1643
Alcohols from organometallic compounds and ketones 1644
Alcohols from organometallic reagents and oxygen 1643
Alcohols from ortho esters 1643
Alcohols from ozonides 1644
Alcohols from peroxides 1558
Alcohols from radicals and aldehydes or ketones 1644
Alcohols from rearrangement of alcohols 1644
Alcohols from rearrangement of alkenes 1644
Alcohols from rearrangement of ethers 1644
Alcohols from rearrangements of allylic ethers 1644
Alcohols from rearrangements of allylic sulfoxides 1644
Alcohols from reduction of esters 1644
Alcohols from transesterification 1643
Alcohols hydrogenation of 527
Alcohols hydrogenolysis of 527
Alcohols methyl and the haloform reaction 813
Alcohols methyl optically active, by hydroboration 1014
Alcohols methyl order of acid strength 350
Alcohols methyl oxidation to aldehydes or ketones 1514—1517
Alcohols methyl oxidation to cyclic ethers 919
Alcohols methyl oxidation with Bacillus steamthermophilus 1517
Alcohols methyl oxidation with chromate, mechanism 1517
Alcohols methyl oxidation with chromic acid 1515
Alcohols methyl oxidation with chromium derivatives 1537
Alcohols methyl oxidation with Collins’ reagent 1514
Alcohols methyl oxidation with Corey’s reagent 1515
Alcohols methyl oxidation with DMSO-based reagents 1515—1516
Alcohols methyl oxidation with Fremy's salt 1515
Alcohols methyl oxidation with hypervalent iodine reagents 1516
Alcohols methyl oxidation with Jones reagent 1514
Alcohols methyl oxidation with nitroxyl radical 1515
Alcohols methyl oxidation with oxoammonium salts 1515
Alcohols methyl oxidation with permanganate, and ultrasound 1515
Alcohols methyl oxidation with pyridinium chlorochromate 1514
Alcohols methyl oxidation with pyridinium dichromate 1514
Alcohols methyl oxidation with ruthenium tetroxide 1515
Alcohols methyl oxidation with TEMPO-NCS 1515
Alcohols methyl oxidation with zirconocene complexes 1515
Alcohols methyl oxidation withTPAP 1515
Alcohols methyl oxidation, and microwaves 1515
Alcohols methyl photochemical addition to alkenes 997
Alcohols oxidation of silanes 1643
Alcohols oxidative dehydrogenation with copper chromite 1515
Alcohols reaction with 493
Alcohols reaction with and 519
Alcohols reaction with acyl halides 482
Alcohols reaction with aldehydes or ketones 1180
Alcohols reaction with alkenes 996
Alcohols reaction with alkyl halides 564
Alcohols reaction with amides 488
Alcohols reaction with anhydrides 483
Alcohols reaction with aryl halides 870
Alcohols reaction with carbon disulfide 1184
Alcohols reaction with carboxylic acids 484—486
Alcohols reaction with chlorotrimethylsilane 527
Alcohols reaction with cyanogen chloride 1183
Alcohols reaction with DAST 519
Alcohols reaction with diazo compounds 479
Alcohols reaction with diazomethane 479
Alcohols reaction with dihydropyran 996
Alcohols reaction with diisopropyl azodicarboxylate 502
Alcohols reaction with enol esters 487
Alcohols reaction with enol ethers 487
Alcohols reaction with esters 486
Alcohols reaction with ethers 480
Alcohols reaction with Grignard reagents 526
Alcohols reaction with HI 518
Alcohols reaction with hydrazoic acid 502
Alcohols reaction with isocyanates 1182—1183
Alcohols reaction with isothiocyanates 1183
Alcohols reaction with lactones 487
Alcohols reaction with Lawesson’s reagent 496
Alcohols reaction with lead tetraacetate 919
Alcohols reaction with nitrites 1183 1244
Alcohols reaction with nitrous acid 493
Alcohols reaction with onium salts 482
Alcohols reaction with phosgene 483
Alcohols reaction with phosphorus halides 518
Alcohols reaction with sulfonamides 576
Alcohols reaction with sulfonyl chlorides 576
Alcohols reaction with sulfur trioxide 493
Alcohols reaction with thionyl chloride 493 518
Alcohols reaction with triflic anhydride 493
Alcohols reaction with trimethylaluminum 544
Alcohols reactivity with alkenes 996
Alcohols reagents for hydrogenolysis 527
Alcohols vinyl cyclic, and sigmatropic rearrangements 1440
Alcohols, alkenyl, fragmentation 1351
| Alcohols, alkynyl, dehydration of 1327
Alcohols, allylic by Mislow-Evans rearrangement 1455
Alcohols, allylic coupling with Grignard reagents 545
Alcohols, allylic from aldehydes and allylsilanes 1211
Alcohols, allylic from alkene snlfoxides 1455
Alcohols, allylic from epoxides 1329
Alcohols, allylic reduction, reagents for 1009
Alcoholysis of acyl halides 482
Alcoholysis of amides 488
Alcoholysis of anhydrides 483
Alcoholysis of epoxides 481
Alcoholysis of esters 486
Alcoholysis of lactones 487
Aldehydes acylation of 1245
Aldehydes addition of boranes 1210
Aldehydes addition to alkenes 1033
Aldehydes and Benedict’s solution 917
Aldehydes and Fehling’s solution 917
Aldehydes and Gomberg-Bachmann pinacol synthesis 1560
Aldehydes and hydroxyalkylation of aromatic rings 719
Aldehydes and radical cyclization 1244
Aldehydes and the Barbier reaction 1205
Aldehydes and the Bouveault-Blanc reaction 1199
Aldehydes and the Cannizzaro reaction 1200 1564
Aldehydes and the Claisen reaction 1224
Aldehydes and the Darzen’s glycidic ester condensation 1230
Aldehydes and the Eschweiler-Clarke reaction 1188
Aldehydes and the Fischer indole synthesis 1453
Aldehydes and the Knoevenagel reaction 1225—1228
Aldehydes and the Leuckart reaction 1188
Aldehydes and the Meerwein-Ponndorf-Verley reduction 1199
Aldehydes and the Passerini reaction 1252
Aldehydes and the Paterno-Bchi reaction 1249
Aldehydes and the Perkin reaction 1229
Aldehydes and the Sonn-Mueller method 534
Aldehydes and the Wallach reaction 1188
Aldehydes by Hofmann rearrangement 1645
Aldehydes by hydrolysis of imines 552
Aldehydes by McFadyen — Stevens reduction 534
Aldehydes by Oppenauer oxidation 1516
Aldehydes by pinacol rearrangement 1645
Aldehydes by reduction of amides 1550
Aldehydes by Stephen reduction 1204
Aldehydes by Swern oxidation 1516
Aldehydes by the Barton reaction 1463 645
Aldehydes by the Dess-martin periodinane 1516
Aldehydes by the Etard reaction 1646
Aldehydes by the Gatterman reaction 1645
Aldehydes by the Krohnke reaction 1536
Aldehydes by the Meyers synthesis 558
Aldehydes by the Nef reaction 1178 1645
Aldehydes by the Oppenauer oxidation 1199
Aldehydes by the oxo process 1645
Aldehydes by the Pummerer rearrangement 1566
Aldehydes by the Reimer — Tiemann reaction 1645
Aldehydes by the Rosenmund reduction 532
Aldehydes by the Sommelet reaction 1536
Aldehydes by the Sonn — Mueller method 1204
Aldehydes by the Vilsmeier reaction 1645
Aldehydes by the Wacker process 1538
Aldehydes conversion to amides 925
Aldehydes decarbonylation 944
Aldehydes decarbonylation and radical rearrangement 1389
Aldehydes dissolving metal reductions 1199—1200
Aldehydes enolate anion of also see “Enolate anions”
Aldehydes from -halo amides and NaOBr 1645
Aldehydes from -hydroxy amides and NaOBr 1645
Aldehydes from -hydroxy alkenes 1645
Aldehydes from -amino halides 1645
Aldehydes from -hydroxy halides 1645
Aldehydes from acid derivatives 1644
Aldehydes from activated methyl groups 1646
Aldehydes from acyl halides 532 533
Aldehydes from acyl sulfonylhydrazides 534
Aldehydes from alcohols 1514—1517 1645
Aldehydes from aldehydes 1401 1644 1645
Aldehydes from alkanes 1645
Aldehydes from alkyl halides 562 1535 1644 1646
Aldehydes from allylic alcohols, arylation of 1645
Aldehydes from amides 533
Aldehydes from amines 1646
Aldehydes from anhydrides 533
Aldehydes from aromatic compounds 1645
Aldehydes from aryl acetic acids 1645
Aldehydes from aryl iodides 1645
Aldehydes from aryl nitro compounds 1645
Aldehydes from arylmethanes 1646
Aldehydes from boranes 1423 1644 1645
Aldehydes from carboxylic acid salts 1644
Aldehydes from carboxylic acids, reagents for 532 533
Aldehydes from dialkylformamides 568
Aldehydes from diazo aldehydes 1644
Aldehydes from diazonium salts 1645
Aldehydes from dithianes 1644
Aldehydes from enol ethers 1329
Aldehydes from epoxides 1398
Aldehydes from esters 1646
Aldehydes from formamides 1644—1645
Aldehydes from formates 1644
Aldehydes from formic acid 1644
Aldehydes from glycidic acids 809 1645
Aldehydes from Grignard reagents 801
Aldehydes from homologation of aldehydes 1645
Aldehydes from hydration of acetylene 1645
Aldehydes from hydroformylation of alkenes 1645
Aldehydes from hydrolysis of -acetoxy sulfides 1646
Aldehydes from hydrolysis of acetals 1644
Aldehydes from hydrolysis of C=N compounds 1645
Aldehydes from hydrolysis of enol esters 1644
Aldehydes from hydrolysis of enol ethers 1644
Aldehydes from hydrolysis of gem-dihalides 1644
Aldehydes from hydrolysis of hydrazones 1645
Aldehydes from hydrolysis of imines 1645
Aldehydes from hydrolysis of metalated aldimines 1645
Aldehydes from hydrolysis of oximes 1645
Aldehydes from hydrolysis of primary nitro compounds 1645
Aldehydes from hydrolysis of thioacetals 1644
Aldehydes from hydrolysis of unsaturated boranes 1645
Aldehydes from hydroperoxides 1645
Aldehydes from imines 532 1177 1644
Aldehydes from methyl groups 1463
Aldehydes from nitrites 1204 1645
Aldehydes from nitro compounds 1178 1537 1646
Aldehydes from organolithium reagents 801
Aldehydes from organometallic compounds 1645
Aldehydes from oxazines 1644
Aldehydes from oximes 1463 1645
Aldehydes from rearrangement of ally lie ethers 1645
Aldehydes from rearrangement of allylic vinylic ethers 1645
Aldehydes from rearrangement of diols 1645
Aldehydes from Reissert compounds 533
Aldehydes from sulfoxides 1566
Aldehydes from thiazoles 559
Aldehydes from thioaldehydes 1185
Aldehydes from thioesters 533
Aldehydes from unsaturated aldehydes 1645
Aldehydes from vinyl ethers 1645
Aldehydes from-1,2-diols 1645
Aldehydes from-1,3-diols 1645
Aldehydes fromalkenes 1037 1522 1525—1526 1537—1538 1645 1646
Aldehydes fromdiols 1519—1521 1645
Aldehydes fromketones 1645
Aldehydes halo, from aldehydes 775
Aldehydes halogenation, mechanism of 776
Aldehydes homologation of 1407
Aldehydes hydrogenation of 1198
Aldehydes hydroxy see “Hydroxy Aldehydes”
Aldehydes in the Mannich reaction 1189
Aldehydes in the Mukaiyama aldol reaction 1223
Aldehydes keto-enol tautomerism 774
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