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Progress in Heterocyclic Chemistry
1st Edition - October 27, 2014
Editors: Gordon Gribble, John A. Joule
Hardback ISBN:9780081000175
9 7 8 - 0 - 0 8 - 1 0 0 0 1 7 - 5
eBook ISBN:9780081000427
9 7 8 - 0 - 0 8 - 1 0 0 0 4 2 - 7
This is the 26th annual volume of Progress in Heterocyclic Chemistry and covers the literature published during 2013 on most of the important heterocyclic ring systems. This… Read more
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This is the 26th annual volume of Progress in Heterocyclic Chemistry and covers the literature published during 2013 on most of the important heterocyclic ring systems. This volume opens with two specialized reviews, not restricted to work published in 2013: ‘Recent Developments in the Synthesis of Cyclic Guanidine Alkaloids’ written by Matthew G. Donahue, and ‘Heterocyclic chemistry: a complete toolbox for nanostructured carbon materials’ written by Luisa Lascialfari, Stefano Fedeli, and Stefano Cicchi. The remaining chapters examine the 2013 literature on the common heterocycles in order of increasing ring size and the heteroatoms present.
Recognized as the premiere review of heterocyclic chemistry
Contributions from leading researchers in the field
Systematic survey of the important 2013 heterocyclic chemistry literature
Organic chemists, academic and industrial chemists, as well as advanced students
Foreword
Editorial Advisory Board Members Progress in Heterocyclic Chemistry
Chapter 1. Recent Developments in the Synthesis of Cyclic Guanidine Alkaloids
1.1. Introduction and Scope of the Review
1.2. Cyclic Guanidines in Organic Chemistry
1.3. Total Synthesis of Cyclic Guanidine Natural Products
1.4. Recently Isolated Natural Products and Medicinal Agents
Chapter 2. Heterocyclic Chemistry: A Complete Toolbox for Nanostructured Carbon Materials
2.1. Introduction
2.2. Three Membered Cycles
2.3. Five-Membered Heterocycles
2.4. Six-Membered Heterocycles
2.5. Seven-Membered Heterocycles
Chapter 3. Three-Membered Ring Systems
3.1. Introduction
3.2. Epoxides
3.3. Aziridines
Chapter 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 and Spirocyclic β-Lactams
4.5. Oxetanes, Dioxetanes, and 2-Oxetanones (β-Lactones)
4.6. Thietanes and Related Systems
4.7. Silicon and Phosphorus Heterocycles Miscellaneous
Chapter 5.1. Five-Membered Ring Systems: Thiophenes and Se/Te Derivatives
5.1.1. Introduction
5.1.2. Reviews and Books on Thiophene, Selenophene, and Tellurophene Chemistry
5.1.3. Synthesis of Thiophenes, Selenophenes, and Tellurophenes
5.1.4. Elaboration of Thiophenes and Benzothiophenes
5.1.5. Elaboration of Selenophenes and Benzoselenophenes
5.1.6. Synthesis of Thiophenes, Selenophenes, and Tellurophenes for Use in Material Science
5.1.7. Thiophenes, Selenophenes, and Tellurophenes in Medicinal and Environmental Chemistry
5.1.8. Selenophenes
Chapter 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
5.2.6. Isatins, Oxindoles, Indoxyls, and Spirooxindoles
5.2.7. Carbazoles
5.2.8. Azaindoles
5.2.9. Isoindoles
Chapter 5.3. Five-Membered Ring Systems: Furans and Benzofurans
5.3.1. Introduction
5.3.2. Reactions
5.3.3. Synthesis
Chapter 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
Chapter 5.5. Five-Membered Ring Systems
5.5.1. Introduction
5.5.2. Thiazoles
5.5.3. Isothiazoles
5.5.4. Thiadiazoles
5.5.5. Tellurazoles
Chapter 5.6. Five-Membered Ring Systems: With O and S (Se, Te) Atoms
5.6.1. 1,3-Dioxoles and Dioxolanes
5.6.2. 1,3-Dithioles and Dithiolanes
5.6.3. 1,3-Oxathioles and Oxathiolanes
5.6.4. 1,2-Dioxolanes
5.6.5. 1,2-Dithioles and Dithiolanes
5.6.6. Three Heteroatoms
Chapter 5.7. Five-Membered Ring Systems with O & N Atoms
5.7.1. Isoxazoles
5.7.2. Isoxazolines
5.7.3. Isoxazolidines
5.7.4. Oxazoles
5.7.5. Oxazolines
5.7.6. Oxazolidines
5.7.7. Oxadiazoles
Chapter 6.1. Six-Membered Ring Systems: Pyridine and Benzo Derivatives
6.1.1. Introduction
6.1.2. Overview of Pyridine and (Iso)Quinoline Uses
6.1.3. Synthesis of Pyridines
6.1.4. Reactions of Pyridines
6.1.5. Synthesis of (Iso)Quinolines
6.1.6. Reactions of (Iso)Quinolines
Chapter 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 Its Benzo Derivatives
Chapter 6.3. Triazines and Tetrazines
6.3.1. Triazines
6.3.2. Tetrazines
Chapter 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 Sulfur Atom
6.4.4. Heterocycles Containing Two or More Oxygen Atoms
6.4.5. Heterocycles Containing Both Oxygen and Sulfur in the Same Ring
Chapter 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
7.5. Future Directions
Chapter 8. Eight-Membered and Larger Rings
8.1. Introduction
8.2. Carbon–Oxygen Rings
8.3. Carbon–Nitrogen Rings
8.4. Carbon–Sulfur Rings
8.5. Carbon–Nitrogen–Selenium Rings
8.6. Carbon–Nitrogen–Oxygen Rings
8.7. Carbon–Nitrogen–Sulfur Rings
8.8. Carbon–Oxygen–Sulfur Rings
8.9. Carbon–Sulfur–Phosphorus Rings
8.10. Carbon–Boron–Sulfur–Oxygen Rings
8.11. Carbon–Nitrogen–Oxygen–Sulfur Rings
Index
No. of pages: 632
Language: English
Published: October 27, 2014
Imprint: Elsevier
Hardback ISBN: 9780081000175
eBook ISBN: 9780081000427
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, USA
JJ
John A. Joule
John Arthur Joule did his BSc, MSc, and PhD degrees at The University of Manchester, obtaining his PhD in 1961. He then undertook post-doctoral work at Princeton University and Stanford University, before joining the academic staff of the Chemistry Department at The University of Manchester in 1963, where he is currently a Professor. In 1996 he received an RSC Medal for Heterocyclic Chemistry.
Affiliations and expertise
Emeritus Professor, The University of Manchester, UK