The chemistry of heterocycles: structure, reactions, syntheses, and applications
Gespeichert in:
| Hauptverfasser: | , |
|---|---|
| Format: | Buch |
| Sprache: | German |
| Veröffentlicht: |
Weinheim
Wiley-VCH
2003
|
| Ausgabe: | 2., completely rev., and enl. ed. |
| Schlagworte: | |
| Online-Zugang: | Inhaltsverzeichnis |
| Beschreibung: | XVI, 556 S. |
| ISBN: | 3527307206 |
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| 245 | 1 | 0 | |a The chemistry of heterocycles |b structure, reactions, syntheses, and applications |c Theophil Eicher ; Siegfried Hauptmann |
| 250 | |a 2., completely rev., and enl. ed. | ||
| 264 | 1 | |a Weinheim |b Wiley-VCH |c 2003 | |
| 300 | |a XVI, 556 S. | ||
| 336 | |b txt |2 rdacontent | ||
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| 338 | |b nc |2 rdacarrier | ||
| 650 | 4 | |a Chimie des composés hétérocycliques | |
| 650 | 7 | |a Compostos heterocíclicos |2 larpcal | |
| 650 | 7 | |a Química |2 larpcal | |
| 650 | 4 | |a Heterocyclic chemistry | |
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Datensatz im Suchindex
| _version_ | 1804130023280476160 |
|---|---|
| adam_text | Titel: The chemistry of heterocycles
Autor: Eicher, Theophil
Jahr: 2003
XI
Contents
Abbreviations and Symbols.........................................................................................................XV
1 The Structure of Heterocyclic Compounds..............................................................1
2 Systematic Nomenclature of Heterocyclic Compounds.........................................5
2.1 Hantzsch-Widman Nomenclature..............................................................................................6
2.2 Replacement Nomenclature......................................................................................................11
2.3 Examples of Systematic Nomenclature....................................................................................12
2.4 Important Heterocyclic Systems...............................................................................................16
3 Three-Membered Heterocycles....................................................................................17
3.1 Oxirane.....................................................................................................................................17
3.2 Thiirane....................................................................................................................................24
3.3 2//-Azirine................................................................................................................................26
3.4 Aziridine...................................................................................................................................28
3.5 Dioxirane..................................................................................................................................32
3.6 Oxaziridine...............................................................................................................................32
3.7 3//-Diazirine.............................................................................................................................34
3.8 Diaziridine................................................................................................................................35
References................................................................................................................................37
4 Four-Membered Heterocycles......................................................................................38
4.1 Oxetane.....................................................................................................................................38
4.2 Thietane....................................................................................................................................41
4.3 Azete.........................................................................................................................................42
4.4 Azetidine..................................................................................................................................43
4.5 1,2-Dioxetane...........................................................................................................................45
4.6 1,2-Dithiete...............................................................................................................................48
4.7 1,2-Dihydro-1,2-diazete............................................................................................................48
4.8 1,2-Diazetidine.........................................................................................................................49
References................................................................................................................................51
XII
Contents
5 Five-Membered Heterocycles.......................................................................................
.....................52
5.1 Furan............................................................................................................
5.2 Benzo[6]furan...........................................................................................................................
5.3 Isobenzofuran...........................................................................................................................^
5.4 Dibenzofuran............................................................................................................................^
5.5 Tetrahydrofuran........................................................................................................................^
5.6 Thiophene.................................................................................................................................^
5.7 Benzo[6]thiophene...................................................................................................................80
5.8 Benzo[c]thiophene....................................................................................................................82
5.9 2,5-Dihydrothiophene...............................................................................................................83
5.10 Thiolane....................................................................................................................................84
5.11 Selenophene..............................................................................................................................85
5.12 Pyrrole......................................................................................................................................86
5.13 Indole........................................................................................................................................99
5.14 Isoindole.................................................................................................................................110
5.15 Carbazole................................................................................................................................Ill
5.16 Pyrrolidine..............................................................................................................................114
5.17 Phosphole...............................................................................................................................116
5.18 1,3-Dioxolane.........................................................................................................................118
5.19 1,2-Dithiole.............................................................................................................................119
5.20 1,2-DithioIane.........................................................................................................................120
5.21 1,3-Dithiole.............................................................................................................................121
5.22 1,3-Dithiolane.........................................................................................................................122
5.23 Oxazole...................................................................................................................................122
5.24 Bcnzoxazole...........................................................................................................................132
5.25 4,5-Dihydrooxazole.............................................................................................................
5.26 Isoxazole........................................................................................................................................................................................................138
5.27 4,5-Dihydroisoxazole....................................................................................................................................................144
5.28 2,3-Dihydroisoxazole........................................................................................................................................147
5.29 Thiazole...................................................................
5.30 Benzothiazole..........................................................................................................^5
5.31 Penam..........................................................
5.32 Isothiazole....................................................
5.33 Imidazole...............
.............................................................................................................
5.34 Benzimidazole....................................................................................^
5.35 Imidazolidine....................................................................................g
5.36 Pyrazole.......
J .......................................................................................................................179
5.37 Indazole.......
.......................................................................................................................185
Contents XIII
5.38 4,5-Dihydropyrazole...............................................................................................................186
5.39 Pyrrolidine............................................................................................................................189
5.40 1,2,3-Oxadiazole....................................................................................................................191
5.41 1,2,5-Oxadiazole....................................................................................................................193
5.42 1,2,3-Thiadiazole....................................................................................................................196
5.43 1,2,4-Thiadiazole....................................................................................................................198
5.44 1,2,3-Triazole.........................................................................................................................200
5.45 Benzotriazole..........................................................................................................................205
5.46 1,2,4-Triazole.........................................................................................................................208
5.47 Tetrazole.................................................................................................................................212
References..............................................................................................................................218
6 Six-Membered Heterocycles.......................................................................................222
6.1 Pyrylium ion...........................................................................................................................222
6.2 2//-Pyran.................................................................................................................................231
6.3 2/7-Pyran-2-one......................................................................................................................233
6.4 3,4-Dihydro-2//-pyran............................................................................................................239
6.5 Tetrahydropyran.....................................................................................................................243
6.6 2//-Chromene.........................................................................................................................245
6.7 2//-Chromen-2-one.................................................................................................................247
6.8 1-Benzopyrylium ion..............................................................................................................252
6.9 4H-Pyran.................................................................................................................................255
6.10 4//-Pyran-4-one......................................................................................................................257
6.11 4//-Chromene.........................................................................................................................260
6.12 4//-Chromen-4-one.................................................................................................................261
6.13 Chroman.................................................................................................................................266
6.14 Pyridine...................................................................................................................................269
6.15 Pyridone..................................................................................................................................310
6.16 Quinoline................................................................................................................................316
6.17 Isoquinoline............................................................................................................................336
6.18 Quinolizinium ion..........*.......................................................................................................349
6.19 Dibenzopyridines....................................................................................................................353
6.20 Piperidine................................................................................................................................360
6.21 Phosphabenzene.....................................................................................................................365
6.22 1,4-Dioxin, 1,4-Dithiin, 1,4-Oxathiin....................................................................................369
6.23 1,4-Dioxane............................................................................................................................371
6.24 Oxazine...................................................................................................................................373
6.25 Morpholine.............................................................................................................................381
6.26 1,3-Dioxane............................................................................................................................383
XIV Contents___
6.27 ........................................................................................................................................387
6.28 Cepham...................................................................................................................................389
6.29 Pyridazine...............................................................................................................................393
6.30 Pyrimidine..............................................................................................................................398
6.31 Purine......................................................................................................................................408
6.32 Pyrazine..................................................................................................................................4^
6.33 Piperazine...............................................................................................................................4^2
6.34 Pteridine..................................................................................................................................4^5
6.35 Benzodiazine..........................................................................................................................430
6.36 1,2,3-Triazine.........................................................................................................................437
6.37 1,2,4-Triazine.........................................................................................................................440
6.38 1,3,5-Triazine.........................................................................................................................446
6.39 1,2,4,5-Tetrazine.....................................................................................................................451
References..............................................................................................................................457
7 Seven-Membered Heterocycles..................................................................................461
7.1 Oxepine..................................................................................................................................461
7.2 Thiepine..................................................................................................................................465
7.3 Azepine...................................................................................................................................466
7.4 Diazepines..............................................................................................................................472
References................................................................................................................................................................................................................473
8 Larger Ring Heterocycles............................................................................................480
8.1 Azocine................................................................................................................................4g0
8.2 Heteronines and Larger Ring Heterocycles................................................................................................................482
8.3 Tetrapyrroles..................................................................................................................................^
References................................................................................................................................4^4
9 Problems and Their Solutions........................................................................................................496
10 Indices........
.................................................................................................................... 545
10.1 General Subject Index......
................................................................................................... 545
10.2 Index of Named Reactions.
............................................................................................... 554
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| spelling | Eicher, Theophil 1932-2016 Verfasser (DE-588)12479274X aut The chemistry of heterocycles structure, reactions, syntheses, and applications Theophil Eicher ; Siegfried Hauptmann 2., completely rev., and enl. ed. Weinheim Wiley-VCH 2003 XVI, 556 S. txt rdacontent n rdamedia nc rdacarrier Chimie des composés hétérocycliques Compostos heterocíclicos larpcal Química larpcal Heterocyclic chemistry Heterocyclische Verbindungen (DE-588)4159726-6 gnd rswk-swf 1\p (DE-588)4123623-3 Lehrbuch gnd-content Heterocyclische Verbindungen (DE-588)4159726-6 s DE-604 Hauptmann, Siegfried 1931-2011 Verfasser (DE-588)120336855 aut Paralle Sprachausgabe deutsch Eicher, Theophil Chemie der Heterocyclen HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010344137&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk |
| spellingShingle | Eicher, Theophil 1932-2016 Hauptmann, Siegfried 1931-2011 The chemistry of heterocycles structure, reactions, syntheses, and applications Chimie des composés hétérocycliques Compostos heterocíclicos larpcal Química larpcal Heterocyclic chemistry Heterocyclische Verbindungen (DE-588)4159726-6 gnd |
| subject_GND | (DE-588)4159726-6 (DE-588)4123623-3 |
| title | The chemistry of heterocycles structure, reactions, syntheses, and applications |
| title_auth | The chemistry of heterocycles structure, reactions, syntheses, and applications |
| title_exact_search | The chemistry of heterocycles structure, reactions, syntheses, and applications |
| title_full | The chemistry of heterocycles structure, reactions, syntheses, and applications Theophil Eicher ; Siegfried Hauptmann |
| title_fullStr | The chemistry of heterocycles structure, reactions, syntheses, and applications Theophil Eicher ; Siegfried Hauptmann |
| title_full_unstemmed | The chemistry of heterocycles structure, reactions, syntheses, and applications Theophil Eicher ; Siegfried Hauptmann |
| title_short | The chemistry of heterocycles |
| title_sort | the chemistry of heterocycles structure reactions syntheses and applications |
| title_sub | structure, reactions, syntheses, and applications |
| topic | Chimie des composés hétérocycliques Compostos heterocíclicos larpcal Química larpcal Heterocyclic chemistry Heterocyclische Verbindungen (DE-588)4159726-6 gnd |
| topic_facet | Chimie des composés hétérocycliques Compostos heterocíclicos Química Heterocyclic chemistry Heterocyclische Verbindungen Lehrbuch |
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