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Advances in Heterocyclic Chemistry, Volume 141, latest release in this definitive series, combines descriptive synthetic chemistry and mechanistic insight to yield an understanding of how chemistry drives the preparation and useful properties of heterocyclic compounds.
Intro -- Advances in Heterocyclic Chemistry -- Copyright -- Contents -- Contributors -- Preface -- Chapter One: Recent advances in the synthesis of five-membered heterocycles via multicomponent and domino reactions (from ... -- 1. Introduction -- 2. Synthesis of five-membered heterocycles with one heteroatom -- 2.1. Five-membered rings containing nitrogen -- 2.2. Five-membered rings containing oxygen -- 2.3. Five-membered rings containing sulfur -- 3. Five-membered rings with two heteroatoms -- 3.1. Five-membered rings containing two nitrogens -- 3.2. Five-membered rings containing nitrogen and sulfur -- 3.3. Five-membered rings containing nitrogen and oxygen -- 3.4. Five-membered rings containing oxygen and sulfur -- 4. Five-membered rings with three heteroatoms -- 5. Five-membered rings with four heteroatoms -- 6. Five-membered rings via domino reaction -- 7. Conclusion -- References -- Chapter Two: Recent advances in application of the Stetter reaction in heterocyclic chemistry -- 1. Introduction -- 2. Synthesis of five-membered heterocycles -- 3. Synthesis of six-membered heterocycles -- 4. Conclusion -- Acknowledgment -- References -- Chapter Three: Recent developments in the Hantzsch synthesis of dihydropyridines -- 1. Introduction -- 2. Diverse synthesis of 1,4-dihydropyridines -- 2.1. Ionic liquid-based catalysts -- 2.2. Deep eutectic solvent-based catalysts -- 2.3. Heterogeneous catalyst -- 2.4. Nanoparticles -- 2.5. Magnetic nanoparticles -- 3. Microwave-assisted synthesis (MWAS) -- 4. Ultrasound-assisted synthesis (USAS) -- 5. Miscellaneous -- 6. Conclusion -- References -- Chapter Four: Recent developments in the chemistry of 1H- and 4H-1,2,4-triazoles -- 1. Introduction -- 2. Synthetic routes to 1H- and 4H-1,2,4-triazoles -- 2.1. Synthesis of monosubstituted-1H-1,2,4-triazoles -- 3. Synthesis of disubstituted-1,2,4-triazoles.
3.1. Synthesis of 5-aryl-4H-1,2,4-triazole-3-thiols -- 3.2. Electrosynthesis of 1,5-disubstituted-1H-1,2,4-triazoles -- 3.3. Synthesis 1,3- and 1,5-disubstituted-1H-1,2,4-triazoles -- 3.4. Synthesis of 3,4-diaryl-4H-1,2,4-triazoles -- 3.5. Synthesis of 3,5-disubstituted-1H(4H)-1,2,4-triazoles -- 4. Synthesis of trisubstituted-1,2,4-triazoles -- 4.1. Synthesis of 3-amino-4,5-disubstituted-1,2,4-triazoles -- 4.2. Synthesis of 4-amino-5-substituted-4H-1,2,4-triazole-3-thiols -- 4.3. Synthesis of 4-amino-3,5-diaryl-1,2,4-triazoles -- 4.4. Synthesis of 5-amino-1,3-disubstituted-1,2,4-triazoles -- 4.5. Synthesis of 1,3-disubstituted-1,2,4-triazole-5-thiols -- 4.6. Synthesis of 1,5-substituted-1H-1,2,4-triazole-3-thiols -- 4.7. Synthesis of 1,5-substituted-1H-1,2,4-triazole-3-selones -- 4.8. Synthesis of 4,5-disubstituted-1,2,4-triazole-3-thiols -- 4.9. Synthesis of 1,5-disubstituted-1H-1,2,4-triazole-3-carboxylates -- 4.10. Synthesis of 1,3,5-triaryl-1,2,4-triazoles -- 4.11. Synthesis of 3,4,5-trisubstituted-1,2,4-triazoles -- 5. Synthesis of tetrasubstituted-1,2,4-triazoles -- 5.1. Synthesis of 1,2,3,5-trisubstituted-1,2,4-triazoles -- 5.2. Synthesis of 2,4,5-trisubstituted-1,2,4-triazole-3-thiones -- 5.3. Synthesis of 1,4-disubstituted-1,2,4-triazolidine-3,5-diones -- 5.4. Synthesis of 2,4,5-trisubstituted-1,2,4-triazole-3-ones -- 5.5. Synthesis of 1,3,4,5-tetrasubstituted-1,2,4-triazoles -- 6. Conclusions -- References -- Index.
editors, Eric F. V. Scriven and Christopher A. Ramsden.
Includes bibliographical references and index.