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Авторизация |
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Smith M.B., March J. — March's Advanced Organic Chemistry: Reactions, Mechanisms, and Structure |
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Предметный указатель |
Amides from rearrangement of oximes 1653
Amides from transamidation 1652
Amides fromketenes 1001 1653
Amides hydrolysis and diazonium ions 475
Amides hydrolysis and radiolabeling 476
Amides hydrolysis of 474—476
Amides hydrolysis, rate of reaction 475
Amides imidazolide, reaction with alcohols 488
Amides indirectly from aldehydes 1653
Amides methyl, from isocyanates 1555
Amides potassium, reaction with K and aryl diethyl phosphates 866
Amides protecting groups for amines 697
Amides reaction with 1464
Amides reaction with acid derivatives 514
Amides reaction with alcohols 488
Amides reaction with aldehydes 1187
Amides reaction with alkenes 1001
Amides reaction with amines 503
Amides reaction with ammonium salts 512
Amides reaction with Grignard reagents 1214
Amides reaction with Lawesson’s reagent 1184
Amides reaction with NaOBr 1411
Amides reaction with organocerinm reagents 1215
Amides reaction with organolithium reagents 568
Amides reaction with oxalyl chloride 515
Amides reduction to aldehydes, reagents for 533
Amides reduction with 1549
Amides sulfenylation of 783
Amides twisted 185
Amides, conjugated from vinyltin reagents 1218
Amides, conjugated halogenation of 501
Amides, conjugated reaction with aldehydes 1212
Amidines Amidomethylation, of phenols 722
Amidines from addition of amines to ketenimines 1653
Amidines from addition of ammonia or amines to nitriles 1653
Amidines from amines 1001
Amidines from ammonia 1191
Amidines from animation of imidates 1653
Amidines from imidates 510
Amidines from ketenimines 1001
Amidines from nitriles 1191
Aminals 1186
Aminals, from addition of amines to aldehydes or ketones 1654
Amination, reductive 1188
Amine alcohols, oxidative cleavage 1520
Amine alkenes from alkenes 782
Amine alkenes frombicyclic amines 1511—1512
Amine anions see “Amide bases”
Amine ditosylates, as leaving groups 447
Amine halides, fragmentation reactions 1345
Amine ketones and Mannich bases 1189
Amine ketones by the Mannich reaction 1189
Amine ketones by the Neber rearrangement 1410
Amine ketones, from oxime tosylates 1410
Amine N-oxides and Cope elimination 1333
Amine N-oxides and elimination of aziridines 1343
Amine N-oxides from amines 1541
Amine N-oxides from oxidation of tertiary amines 1654
Amine N-oxides pyrolysis of 1333
Amine N-oxides reduction with 1557
Amine N-oxides spin traps 239
Amine N-oxides thermolysis of 1420
Amine-Claisen rearrangement 1452
Amines also see “Diamines”
Amines acylation 511
Amines aliphatic, reaction with nitrous acid 816
Amines alkylation of 501 552
Amines alkylation, catalysts for 501
Amines allylic, reaction with Grignard reagents 1025
Amines allylic, reductive cleavage 1559
Amines and acidity 344
Amines and base strength 346
Amines and Birch reduction 1012
Amines and elimination of snlfonyl halides 1338
Amines and exhanstive alkylation 500
Amines and Li, reduction of carboxylic acids 532
Amines and Li, reduction of esters 529
Amines and Michael addition to alkenes 1000
Amines and Michael reactions 1023
Amines and optical activity 129—130
Amines and phase transfer 501
Amines and pyramidal inversion 129
Amines and radical cyclization 1244
Amines and the Ing-Manske procedure 513
Amines and the Mannich reaction 1655
Amines and the Menshutkin reaction 499
Amines aromaticity, resonance effects 344
Amines as catalysts, for the Knoevenagel reaction 1226
Amines base strength, table 346
Amines bicyclic, from N-chloroamines 1416
Amines bicyclic, reaction with mercuric acetates 1512
Amines by Hofmann elimination 1655
Amines by the Bncherer reaction 1654
Amines by the Bonveanlt reaction 1214
Amines by the Chichibabin reaction 1654
Amines by the Curtins rearrangement 1655
Amines by the Delepine reaction 501
Amines by the Emde rednction 530
Amines by the Eschweiler — Clarke reaction 1188
Amines by the Fischer — Hepp rearrangement 1654
Amines by the Gabriel synthesis 500 513 1654
Amines by the hctcroatom Diels Alder reaction 1655
Amines by the Hofmann rearrangement 1411
Amines by the Hofmann — Loffler reaction 1655
Amines by the Leuckart reaction 1188
Amines by the Lossen rearrangement 1413 1655
Amines by the Mitsunobn reaction 502
Amines by the Schmidt reaction 1413 1655
Amines by the Sommelet — Hauser rearrangement 877 1420 1654
Amines by the Staudinger reaction 1555
Amines by the Stevens rearrangement 1419 1655
Amines by the Wallach reaction 1188
Amines chiral, from organolithium addition to imines 1216
Amines chloro, from alkenes 1045
Amines cleavage with phenyl chloroformate 522
Amines conversion to alkyl iodides 522
Amines conversion to azetidines 501
Amines conversion to carbocations 787
Amines cyclic, by the Hofmann — Loffler reaction 1462
Amines cyclic, cleavage with cyanogen bromide 523
Amines cyclic, from lactams 1535
Amines cyclic, from N-chloroamines 1462
Amines cyclic, oxidation of 1535
Amines dealkylation 1559
Amines deamination 1548
Amines dehydrogenation, reagents for 1518
Amines diamines see “Diamines”
Amines diazotization of 816 1382
Amines diazotization with metal halides 522
Amines dichloro, pyrolysis of 1348
Amines formyl 1188
Amines formylation of 820
Amines from active hydrogen compounds 1655
Amines from alcohols 502 1654
Amines from aldehydes 552 1187—1189 1655
Amines from alkanes 1654
Amines from alkenes 999 1654 1655
Amines from alkyl halides 499—501
Amines from alkylnitrilium ions 1204
Amines from amides 1549 1559
Amines from amine ethers 1654
Amines from amine oxides 1655
Amines from amines 503 999 1558 1654 1655
Amines from amino acids 1654
Amines from amino ethers 546
Amines from ammonia 1654 1655
Amines from ammonium hydroxides 1655
Amines from ammonium salts 530 877 1419—1421 1654 1655
Amines from aromatic amines 1654
Amines from aromatic ammonium salts 1654
| Amines from aromatic compounds 1654
Amines from aryl halides 1654
Amines from azides 781 1555 1655
Amines from aziridines 531 548 1654
Amines from azo compounds 1655
Amines from azoxy compounds 1655
Amines from boranes 799
Amines from C=N compounds 1216
Amines from carboxylic acids 1655
Amines from cyanoamines 1654
Amines from cyanohydrins 502
Amines from diazo compounds 504
Amines from ethers 1654
Amines from formamides 1655
Amines from heterocyclic compounds 1654
Amines from hydrazo compounds 1655
Amines from hydrazones 1655
Amines from hydrocarbons 505
Amines from hydrolysis of amides 1654
Amines from hydrolysis of cyanamides 1655
Amines from hydrolysis of enamines 1655
Amines from hydrolysis of imines 1655
Amines from hydrolysis of iminium ions 1655
Amines from hydrolysis of phthalimides 1654
Amines from hydrolysis of sulfonamides 1654
Amines from hydroxylamines 1554 1655
Amines from imines 1203 1655
Amines from iminium salts 1216
Amines from isocyanates 1411 1413 1655
Amines from isothiocyanates 1655
Amines from N-nitroso amines 1556
Amines from N-nitroso compounds 1655
Amines from naphthols 1654
Amines from nitriles 1204 1655
Amines from nitrilium ions 1655
Amines from nitro compounds 1552—1554 1655
Amines from nitroso compounds 1655
Amines from O-acyl hydroxamic acids 1413
Amines from organometallic compounds 799 1654 1655
Amines from oxetanes 506
Amines from ozonides 1655
Amines from rearrangement of acyl azides 1655
Amines from rearrangement of ammonium salts 1655
Amines from rearrangement of aryl alkyl ammonium salts 1654
Amines from rearrangement of aryl hydroxylamines 1654
Amines from rearrangement of arylamines 1654
Amines from rearrangement of benzidines 1655
Amines from rearrangement of benzylic ammonium salts 1654
Amines from rearrangement of hydroxamic acids 1655
Amines from rearrangement of N-haloamines 1655
Amines from rearrangement of N-nitroamines 1654
Amines from rearrangement of N-nitrosoamines 1654
Amines from rearrangement of triazencs 1654
Amines from rearrangement of triazencs ammonium salts 1655
Amines from thioamides 1654
Amines from transamination 1654
Amines fromketones 1187—1189
Amines fromoximes 1554—1555 1655
Amines halo, reagents for their preparation 819
Amines methyl, from isothiocyanates 1555
Amines methylation with diazomethane 504
Amines N,N-dichloro, rearrangement of 1410
Amines N-arylation of 501
Amines N-chloro, reaction with in methanol 1416
Amines N-chloro, reaction with alkenes 1045
Amines N-halo, and the Stieglitz rearrangement 1417
Amines N-iodo, photolysis of 1463
Amines N-methyl, from reduction of isonitriles 1204
Amines order of base strength 349
Amines oxidation of 1535—1536 1539
Amines oxidation with hydrogen peroxide 1141
Amines oxidation with peroxides 1541
Amines oxidation with peroxyacids 1541
Amines protection of 577 697
Amines reaction with 820 1192
Amines reaction with 1192
Amines reaction with 1539
Amines reaction with 494
Amines reaction with acids derivatives 512
Amines reaction with aldehydes or ketones 1185—1187
Amines reaction with alkenes 999 1056
Amines reaction with alkoxyphosphonium perchlorates 502
Amines reaction with alkynes 1000
Amines reaction with amide bases 503
Amines reaction with amides 503
Amines reaction with aryl halides 864
Amines reaction with azides 781
Amines reaction with aziridines 505
Amines reaction with chloroform 506
Amines reaction with chloroformates 507
Amines reaction with CO 820
Amines reaction with cyanogen bromide 522
Amines reaction with diazo compounds 504
Amines reaction with diazoalkanes 1217
Amines reaction with diynes 1000
Amines reaction with esters 510
Amines reaction with hydroxylamine-O-sulfonic acid 530
Amines reaction with hypobromites 819
Amines reaction with hypochlorites 819
Amines reaction with hypohalites 819
Amines reaction with isocyanates 1191
Amines reaction with isocyanic acid 1191
Amines reaction with isopropenyl formate 511
Amines reaction with isothiocyanates 1191
Amines reaction with ketenimines 1001
Amines reaction with ketones 552
Amines reaction with N-chloromethyl lactams 500
Amines reaction with NaOCl 1518
Amines reaction with NCS 500
Amines reaction with nitric acid-acetic anhydride 818
Amines reaction with nitrous acid 816—817 1398
Amines reaction with NOCl 818
Amines reaction with organocuprates 800
Amines reaction with organolithium reagents 500
Amines reaction with oxetanes 505
Amines reaction with Oxone 1540
Amines reaction with phenol and formaldehyde 722
Amines reaction with phosgene 507
Amines reaction with pyrylium ions 1186
Amines reaction with sulfonyl chlorides 576—577
Amines reduction by Katritzky pyrylium-pyridinium method 530
Amines reductive alkylation 1188
Amines test for primary amines 506
Amines, aromatic also see “Aniline derivatives”
Amines, aromatic and Friedel — Crafts alkylation 709
Amines, aromatic by the Goldberg reaction 864
Amines, aromatic coupling with diazonium salts 700
Amines, aromatic formylation by the Duff reaction 717
Amines, aromatic from aromatic compounds 701
Amines, aromatic from aryl halides 864
Amines, aromatic from aryl nitrogen compounds 1559
Amines, aromatic from hydroxyl amines 878
Amines, aromatic fromazides 701
Amines, aromatic oxidation of 1539
Amines, aromatic oxidation with nitric acid 697
Amines, aromatic reaction with nitrons acid 699
Amines, aromatic reaction with nitroso compounds 818
Amines, aromatic removal by dediazoniation 935
Amines, aromatic with 701
Aminium radical cations 909
Aminium radical ion 701
Amino acids acylation of 812
Amino acids and the Dakin — West reaction 812
Amino acids aryl, preparation of 720
Amino acids by the Hermann reaction 1656
Amino acids by the Sorensen reaction 549 1656
Amino acids by the Strecker synthesis 1656
Amino acids conversion to lactams 508
Amino acids diazotization 522
Amino acids from -lactones 1656
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