| Description |
1 v. (various pagings) : illustrations ; 25 cm. |
| Note |
Includes index. |
| Contents |
1. Heterocyclic Chemistry -- 1.1. Introduction -- 2. Classification and Nomenclature -- 2.1. Classification -- 2.2. Nomenclature -- 2.2.1. Monocyclic Rings -- 2.2.2. Polycyclic Rings -- Problems -- 3. Three Membered Heterocyclic Compounds -- 3.1. Three membered Heterocylic compounds with one heteroatom -- 3.1.1. Oxiranes (Epoxides) -- 3.1.2. Aziridines -- 3.1.3. Thiiranes -- 3.1.4. Oxirenes -- 3.1.5. Azirines -- 3.1.6. Thiirenes -- 3.2. Three membered Heterocyclic compounds with two heteroatoms -- 3.2.1. Diaziridines -- 3.2.2. Diazirine -- 3.2.3. Oxaziridines -- 3.2.4. Dimethyldioxirane -- 3.2.5. Three membered Heterocycles fused to six membered ring -- 3.2.5.1. Benzooxiranes -- 3.2.5.2. Benzoaziridines -- 3.2.5.3. Benzothiiranes -- Problems -- 4. Four Membered Heterocyclic Compounds -- 4.1. Azetidines -- 4.2. Azetidinones ([beta]-Lactams) -- 4.3. Oxetanes -- 4.4. Oxetanones -- 4.5. Thietanes -- 4.6. Dioxetanes -- Problems -- 5. Five Membered Heterocyclic Compounds with One Heteroatom -- 5.1. Introduction -- 5.2. Furan -- 5.2.1. Dervatives of Furan -- 5.2.2. Benzofurans -- 5.2.2.1. Benzo [b] furans -- 5.2.2.2. Benzo [c] furans -- 5.2.2.3. Dibenzofurans -- 5.3. Pyrrole -- 5.3.1. Benzopyrroles -- 5.3.1.1. Benzo [b] pyrroles -- 5.3.1.2. Benzo [c] pyrroles -- 5.3.1.3. Indolizines -- 5.3.1.4. Dibenzopyrroles -- 5.4. Thiophenes -- 5.4.1. Benzothiophenes -- 5.4.1.1. Benzo [b] thiophene -- 5.4.1.2. Benzo [c] thiophene -- 5.4.1.3. Dibenzothiophene -- Problems -- 6. Five Membered Heterocyclic Compounds with Two Heteroatoms -- 6.1. Introduction -- 6.2. 1, 3-Azoles -- 6.2.1. Imidazoles -- 6.2.2. Oxazoles -- 6.2.2.1. Benzoxazoles -- 6.2.3. Thiazoles -- 6.2.3.1. Benzothiazoles -- 6.3. 1, 2-Azoles -- 6.3.1. Pyrazoles -- 6.3.2. Isoxazoles -- 6.3.3. Isothiazoles -- 6.3.3.1. Benzoisothiazole -- Problems -- 7. Five Membered Heterocycles with More than Two Heteroatom -- 7.1. Triazoles -- 7.1.1. 1,2,3-Triazoles -- 7.1.1.1. Benzotriazole -- 7.1.2. 1,2,4-Triazoles -- 7.2. Tetrazoles -- 7.2.1. 1,2,3,4-Tetrazoles -- 7.3. Oxadiazoles -- 7.3.1. 1,2,3-Oxadiazoles -- 7.3.2. 1,2,4-Oxadiazoles -- 7.3.3. 1,2,5-Oxadiazoles -- 7.3.4. 1,3,4-Oxadiazoles -- 7.4. Thiadiazoles -- 7.4.1. 1,2,3-Thiadiazoles -- 7.4.2. 1,2,4-Thiadiazoles -- 7.4.3. 1,2,5-Thiadiazoles -- 7.4.4. 1,3,4-Thiadiazoles -- 7.5. Tetrazole -- Problems -- 8. Six Membered Heterocyclic Compounds with One Heteroatom -- 8.1. Pyrans -- 8.1.1. Synthesis -- 8.1.1.1. Synthesis of 4H-pyrans ([gamma]-pyrans) -- 8.1.1.2. Synthesis of 2H-pyrones ([alpha]-pyrones) -- 8.1.2. Reactions -- 8.1.2.1. Reactions of 2-pyrones -- 8.1.2.2. Reactions of 4-pyrones -- 8.2. Benzopyrones -- 8.2.1. Benzo-[alpha]-pyrones -- 8.2.1.1. Coumarin -- Synthesis -- Reactions -- 8.2.1.2. 3-Hydroxycoumarins -- Synthesis -- Reactions -- 8.2.1.3. 4-Methylcoumarin -- Synthesis -- Reactions -- 8.2.1.4. 4-Phenylcoumarins -- Synthesis -- Reactions -- 8.2.1.5. 4-Hydroxycoumarin -- Synthesis -- Reactions -- 8.2.1.6. 3, 4-Dimethoxycoumarin -- 8.2.1.7. 4-Hydroxy-3-phenylcoumarins -- Synthesis -- Reactions -- 8.2.2. Benzo-[gamma]-pyrones -- 8.2.2.1. Chromones -- Synthesis -- 8.2.2.2. Flavones -- 8.2.2.3. Flavanones -- Synthesis -- 8.2.2.4. Isoflavones -- Synthesis -- 8.2.2.5. Anthocyanidins -- Synthesis -- 8.2.2.6. Xanthones -- Synthesis -- 8.3. Pyridine -- Nomenclature -- Synthesis -- Reactions -- 8.3.1. Pyridine N-Oxide -- 8.3.2. Comparison of the Basiely of Pyridine, Piperidine and Pyrrole -- 8.3.3. Condensed Six-membered Heterocycles -- 8.3.3.1. Quinoline -- Synthesis -- Reactions -- 8.3.3.2. Isoquinoline -- Synthesis -- Reactions -- 8.3.3.3. Acridine -- Synthesis -- Reactions -- 8.4. Spiroheterocycles -- 8.5. Bridged Heterocycles -- Problems -- 9. Six Membered Heterocyclic Compounds with More than One Heteroatom -- 9.1. Pyridazine -- Synthesis -- Reactions -- 9.2. Pyrimidines -- Synthesis -- Reactions -- 9.2.1. Pyrimidine Derivatives -- 9.2.1.1. Barbituric Acid -- 9.2.1.1.1. Derivatives of barbituric acid -- 9.2.2. Uracil -- 9.2.3. Thymine -- 9.2.4. Cytosine -- 9.2.5. Alloxan -- 9.2.6. Fused Pyrimidines (Purines) -- 9.2.6.1. Uric Acid -- 9.2.6.2. Purine -- Synthesis -- 9.2.6.3. Adenine -- 9.2.6.4. Hypoxanthine -- 9.2.6.5. Xanthine -- 9.2.6.5.1. Caffeine -- 9.2.6.5.2. Theobromine -- 9.2.6.5.3. Theophylline -- 9.3. Pyrazines -- Reactions -- 9.4. Benzodiazines -- 9.4.1. Cinnolines -- 9.4.2. Phthalazines -- 9.4.3. Quinazolines -- 9.4.4. Quinoxalines -- 9.4.5. Phenazines -- 9.5. Six-membered heterocyclic compounds containing one nitrogen and one oxygen or sulphur atom -- 9.5.1. Oxazines -- 9.5.2. Phenoxazines -- 9.5.3. Phenothiazines -- 9.6. Six membered heterocyclic compounds containing 3 or 4 Nitrogen -- 9.6.1. Triazines -- 9.6.2. Tetrazines -- 9.7. Pteridine -- Problems -- 10. Meso-ionic and Seven Membered Heterocycles -- [A]. Meso-ionic heterocycles -- 10.1. Introduction -- 10.2. Classification -- 10.3. Meso-ionic Heterocycles of Type I -- 10.3.1. 1, 3-Oxazolium-4-Olates -- Synthesis -- Reactions -- 10.3.2. 1, 3-Oxazolium-5-Olates -- Synthesis -- Reactions -- 10.3.3. 1, 3-Oxathiolium-4-Olates -- Synthesis -- Reactions -- 10.3.4. 1, 3-Oxathiolium-5-Olates -- Synthesis -- Reactions -- 10.3.5. 1, 3-Diazolium-4-Olates -- Synthesis -- Reactions -- 10.3.6. 1, 3-Diazolium-4-Aminides -- Synthesis -- Reactions -- 10.3.7. 1, 3-Dithio]ium-4-Olates -- Synthesis -- Reactions -- 10.3.8. 1, 2, 3-Oxadiazolium-5-Olates -- Reactions 10.13 -- 10.4. Meso-Ionic Heterocycles of type II -- 10.4.1. 1, 2-Diazolium-4-Aminides -- Synthesis -- Reactions -- 10.4.2. 1, 2-Dithioliura-4-Olates -- Synthesis -- Reactions -- 10.4.3. 1, 2, 3, 4-Tetrazolium-5-Thiolates -- Reactions -- [B]. Seven-Membered Heterocyclic compounds -- 10.5. Introduction -- 10.6. Azepines -- Synthesis of 1-Substituted Azepines -- Synthesis of 3H-Azepines -- Reactions -- 10.7. Oxepins -- Synthesis -- Reactions -- 10.8. Thiepins -- Synthesis -- Reactions -- 10.9. Diazepines -- Synthesis -- 10.10. Benzodiazepines -- Problems. |
| Subjects |
Heterocyclic chemistry.
|
| LC NO |
QD400 .A45 2013 |
| Dewey No |
547/.59 23 |
| OCLC # |
835914241 |
| ISBN |
1842657097 |
|
9781842657096 |
| Isn/Std # |
(OCoLC)835914241 |
|
