Progress in Heterocyclic Chemistry

1st Edition, Volume 35 - November 16, 2023
Authors: Gordon Gribble, R Alan Aitken
Language: English
Paperback ISBN:
9 7 8 - 0 - 4 4 3 - 2 1 9 3 6 - 8
eBook ISBN:
9 7 8 - 0 - 4 4 3 - 2 1 9 3 5 - 1

Progress in Heterocyclic Chemistry (PHC), Volume 35 is the latest in this annual review series that contains both highlights of the previous year’s literature on hetero… Read more

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Progress in Heterocyclic Chemistry (PHC), Volume 35 is the latest in this annual review series that contains both highlights of the previous year’s literature on heterocyclic chemistry and articles on new and developing topics of particular interest to heterocyclic chemists. Chapters in this new release are all written by leading researchers in their field, constituting a systematic survey of the important original material reported in the literature of heterocyclic chemistry in 2021. As with previous volumes in the series, this book will enable academic and industrial chemists, and advanced students, to keep abreast of developments in heterocyclic chemistry.

Cover image
Title page
Table of Contents
Copyright
1. Progress in the synthesis of 4,5,6,7-tetrahydroindoles
1.1. Introduction
1.2. Intramolecular reactions leading to tetrahydroindoles
1.3. Intermolecular reactions leading to tetrahydroindoles
1.4. Processes of indole reduction (hydrogenation) and perhydroindole oxidation in the synthesis of 4,5,6,7-tetrahydroindoles
1.5. Conclusion
2. Heterocycles in polymers
2.1. Introduction
2.2. Heterocycle on the backbone of the polymer
2.3. Heterocycle not on the polymer backbone
2.4. Conclusions
3. Three-membered ring systems
3.1. Introduction
3.2. Epoxides
3.3. Aziridines
3.4. 2H-azirines
4. Four-membered ring systems
4.1. Introduction
4.2. Azetidines, azetines, and related systems
4.3. Monocyclic 2-azetidinones (β-lactams)
4.4. Fused β-lactams and spirocyclic β-lactams
4.5. Oxetanes, dioxetanes, and 2-oxetanones (β-lactones)
4.6. Sulfur, silicon, phosphorus heterocycles, and related systems. Miscellaneous
5.1. Five-membered ring systems: thiophenes and selenium/tellurium analogs and benzo analogs
5.1.1. Introduction
5.1.2. Thienyl and benzo[b]thienyl groups as substituents
5.1.3. Thiophene ring properties
5.1.4. Thiophene ring substitution
5.1.5. Thiophene ring synthesis
5.1.6. Reactions at thiophene side-chains
5.1.7. Thiophene oligomers
5.1.8. Thiophene polymers
5.1.9. Benzo[b]thiophenes—reactions
5.1.10. Benzo[b]thiophenes—ring synthesis
5.1.11. Selenophenes and tellurophenes reactions
5.1.12. Selenophenes and tellurophenes Ring synthesis
5.2. Five-membered ring systems: pyrroles and benzo analogs
5.2.1. Introduction
5.2.2. Synthesis of pyrroles
5.2.3. Reactions of pyrroles
5.2.4. Synthesis of indoles
5.2.5. Reactions of indoles
5.3. Five-membered ring systems: furans and benzofurans
5.3.1. Introduction
5.3.2. Furans
5.3.3. Benzo[b]furans
5.3.4. Dibenzofurans and their heteroaromatic analogues
5.4. Five-membered ring systems: with more than one N atom
5.4.1. Introduction
5.4.2. Pyrazoles and ring-fused derivatives
5.4.3. Imidazoles and ring-fused derivatives
5.4.4. 1,2,3-Triazoles and ring-fused derivatives
5.4.5. 1,2,4-triazoles and ring-fused derivatives
5.4.6. Tetrazoles and ring-fused derivatives
5.5. Five-membered ring systems: with O and S (Se, Te) atoms
5.5.1. 1,3-Dioxoles and dioxolanes
5.5.2. 1,3-Dithioles and dithiolanes
5.5.3. 1,3-Oxathioles and oxathiolanes
5.5.4. 1,2-Dioxolanes
5.5.5. 1,2-Dithioles and dithiolanes
5.5.6. 1,2-Oxathioles and oxathiolanes
5.5.7. Three heteroatoms
5.6. Five-membered ring systems with O and N atoms
5.6.1. Isoxazoles
5.6.2. Isoxazolines
5.6.3. Isoxazolidines
5.6.4. Oxazoles
5.6.5. Oxazolines
5.6.6. Oxazolidines
5.6.7. Oxadiazoles
6.1. Six-membered ring systems: pyridines and benzo derivatives
6.1.1. Introduction
6.1.2. Pyridines
6.1.3. Quinolines
6.1.4. Isoquinolines
6.2. Six-membered ring systems: diazines and benzo derivatives
6.2.1. Introduction
6.2.2. Pyridazines and benzo derivatives
6.2.3. Pyrimidines and benzo derivatives
6.2.4. Pyrazines and benzo derivatives
6.3. Triazines, tetrazines and fused ring polyaza systems
6.3.1. Introduction
6.3.2. Triazines
6.3.3. Tetrazines
6.3.4. Heptazines
6.3.5. Polyaza systems
6.4. Six-membered ring systems: With O and/or S atoms
6.4.1. Introduction
6.4.2. Heterocycles containing one oxygen atom
6.4.3. Heterocycles containing one or two sulfur atoms
6.4.4. Heterocycles containing two or more oxygen atoms
6.4.5. Heterocycles containing two sulfur atoms
6.4.6. Heterocycles containing both oxygen and sulfur in the same ring
7. Seven-membered rings
7.1. Introduction
7.2. Seven-membered systems containing one heteroatom
7.3. Seven-membered systems containing two heteroatoms
7.4. Seven-membered systems containing three or more heteroatoms
8. Eight-membered and larger rings
8.1. Introduction
8.2. Carbon–oxygen rings
8.3. Carbon–sulfur rings
8.4. Carbon–nitrogen rings
8.5. Carbon–sulfur–oxygen rings
8.6. Carbon–nitrogen–selenium/tellurium rings
8.7. Carbon–sulfur–selenium rings
8.8. Carbon–nitrogen–oxygen rings
8.9. Carbon–nitrogen–boron rings
8.10. Carbon–nitrogen–sulfur rings
8.11. Carbon–nitrogen–sulfur–metal rings
8.12. Carbon–nitrogen–sulfur–oxygen rings
8.13. Carbon–phosphorus rings
8.14. Carbon–metal rings
8.15. Carbon–oxygen–metal rings
8.16. Carbon–nitrogen–metal rings
Index

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Gordon Gribble

R Alan Aitken