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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Request a sales quoteProgress 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.
- Presents articles on new and developing topics of interest to heterocyclic chemists
- Provides a systematic survey of the important 2022 heterocyclic chemistry literature
- Includes contributions from leading researchers in the field
- Recognized as the premiere annual review of heterocyclic chemistry
The primary audience for this series includes Heterocyclic, Medicinal and Natural Product Chemists working in academia, Government laboratories, and industry, Given the wide breadth of heterocyclic chemistry, there is a vast secondary audience of scientists from other disciplines, including Organic and Analytical Chemists, Biochemists, Synthetic Chemists, Pharmaceutical Scientists and Chemical Engineers
- 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
- No. of pages: 700
- Language: English
- Edition: 1
- Volume: 35
- Published: November 16, 2023
- Imprint: Elsevier
- Paperback ISBN: 9780443219368
- eBook ISBN: 9780443219351
GG
Gordon Gribble
Gordon Gribble is the Dartmouth Professor of Chemistry at Dartmouth College, Hanover, USA. His research program covers several areas of organic chemistry, most of which involve synthesis, including novel indole chemistry, triterpenoid synthesis, DNA intercalation, and new synthetic methodology. Prof. Gribble also has a deep interest in naturally occurring organohalogen compounds and in the chemistry of wine and wine making.
Affiliations and expertise
Professor, Chemistry, Dartmouth College, Hanover, USARA
R Alan Aitken
Alan Aitken is a Professor of Organic Chemistry at the University of St Andrews, UK. Much of his research activity has been in the area of heterocyclic chemistry and he has been active in the International Society of Heterocyclic Chemistry, attending all but two of their biennial congresses since 1985, contributing an annual review chapter to Progress in Heterocyclic Chemistry since 1990 and being an elected member of their International Advisory Committee 1997–99 and 2011–17. Since 2018, he has been a member of the Executive Committee and Publicity Chair for ISHC.
Affiliations and expertise
Professor of Organic Chemistry, School of Chemistry, University of St Andrews, UKRead Progress in Heterocyclic Chemistry on ScienceDirect