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Progress in heterocyclic chemistry. Volume 30 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Gribble, Gordon W. (Editor ), Joule, J. A. (John Arthur) (Editor )
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Amsterdam, Netherlands : Elsevier, [2018]
Colección:Progress in Heterocyclic Chemistry ; Volume 30
Temas:
Acceso en línea:Texto completo
Texto completo
Tabla de Contenidos:
  • Front Cover
  • PROGRESS IN HETEROCYCLIC CHEMISTRY
  • PROGRESS IN HETEROCYCLIC CHEMISTRY
  • Copyright
  • CONTENTS
  • CONTRIBUTORS
  • FOREWORD
  • EDITORIAL ADVISORY BOARD MEMBERS PROGRESS IN HETEROCYCLIC CHEMISTRY
  • 1
  • Nitrogen-Philic Cyclization of Acyl Radicals Enables the Synthesis of Lactams
  • 1.1 INTRODUCTION
  • 1.1.1 Exo Cyclization of Acyl Radicals Onto Imine N-C Double Bond
  • 1.1.2 Endo Cyclization of Acyl Radicals Onto Imine CN Double Bond
  • 1.2 ACYL RADICAL CYCLIZATION ONTO AMINE NITROGEN
  • 1.3 ACYL RADICAL CYCLIZATION ONTO AZIDE NITROGEN
  • 1.4 SYNTHESIS OF LACTAMS VIA [2+2+1] CYCLOADDITION
  • 1.5 AMINOCARBONYLATION LEADING TO LACTAMS
  • 1.6 CONCLUSIONS
  • REFERENCES
  • 2
  • The Silyl-Prins Reaction as an Emerging Method for the Synthesis of Heterocycles
  • 2.1 INTRODUCTION
  • 2.2 SYNTHESIS OF OXACYCLES BY SILYL-PRINS CYCLIZATIONS WITH ALLYLSILANES
  • 2.2.1 Synthesis of Five-Membered Oxacycles
  • 2.2.2 Synthesis of Six-Membered Oxacycles
  • 2.2.2.1 Synthesis of Dihydropyrans and Tetrahydropyrans
  • 2.2.2.2 Synthesis of Methylenetetrahydropyrans
  • 2.3 SYNTHESIS OF SEVEN- TO TEN-MEMBERED OXACYCLES
  • 2.3.1 Oxepanes
  • 2.3.2 Oxocanes
  • 2.3.3 Macrocyclic Systems
  • 2.3.4 Synthesis of Bicycles
  • 2.4 SYNTHESIS OF OXACYCLES BY SILYL-PRINS CYCLIZATIONS WITH VINYLSILANES
  • 2.4.1 Synthesis of Five-Membered Oxacycles
  • 2.4.2 Synthesis of Six-Membered Oxacycles
  • 2.4.3 Synthesis of Seven-Membered Oxacycles
  • 2.4.4 Synthesis of Bicycles
  • 2.5 SYNTHESIS OF AZACYCLES BY SILYL-AZA-PRINS CYCLIZATIONS
  • 2.5.1 Allyl Silanes
  • 2.5.1.1 Five-Membered Azacycles
  • 2.5.1.2 Six-Membered Azacycles
  • 2.5.1.3 Seven-Membered Azacycles
  • 2.5.1.4 Bicyclic Systems
  • 2.5.2 Vinyl Silanes
  • 2.5.2.1 Six-Membered Azacycles
  • 2.5.2.2 Bicyclic Systems
  • 2.6 OTHER SILANES
  • 2.7 SUMMARY
  • REFERENCES
  • 3
  • Three-Membered Ring Systems
  • 3.1 INTRODUCTION.
  • 5.2.4.1.3 Intramolecular Type c
  • 5.2.4.1.4 Intramolecular Type e
  • 5.2.4.2 Intermolecular Approaches to Indoles
  • 5.2.4.2.1 Intermolecular Type ab
  • 5.2.4.2.2 Intermolecular Type ac
  • 5.2.4.2.3 Intermolecular Type bc
  • 5.2.4.2.4 Intermolecular Type ce
  • 5.2.4.2.5 Other Intermolecular Syntheses of Indole
  • 5.2.5 REACTIONS OF INDOLES
  • 5.2.5.1 Substitution at C2/C3
  • 5.2.5.1.1 C2 Substitution
  • 5.2.5.1.1.1 Directed C-H Functionalization
  • 5.2.5.1.1.2 Innate C-H Functionalization
  • 5.2.5.1.2 C2 Substitution, Ring-Forming
  • 5.2.5.1.3 C2-C3 Annulation/Functionalization
  • 5.2.5.1.4 C3 Substitution
  • 5.2.5.1.5 C3 Substitution, Ring-Forming
  • 5.2.5.2 Substitution at Nitrogen
  • 5.2.5.3 Functionalization of the Benzene Ring
  • 5.2.5.3.1 C-H Functionalization
  • 5.2.5.3.2 From Prefunctionalized Indoles (e.g., Halides, Triflates, etc.)
  • 5.2.6 ISATINS, OXINDOLES, INDOXYLS, AND SPIROOXINDOLES
  • 5.2.7 CARBAZOLES
  • 5.2.8 AZAINDOLES
  • 5.2.9 ISOINDOLES
  • REFERENCES
  • 5.3
  • Five-Membered Ring Systems: Furans and Benzofurans
  • 5.3.1 INTRODUCTION
  • 5.3.2 REACTIONS
  • 5.3.2.1 Furans
  • 5.3.3 SYNTHESIS
  • 5.3.3.1 Furans
  • 5.3.3.2 Benzo[b]furans and Related Compounds
  • ACKNOWLEDGMENTS
  • REFERENCES
  • 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
  • REFERENCES
  • 5.5
  • Five-Membered Ring Systems: With N and S Atoms
  • 5.5.1 INTRODUCTION
  • 5.5.2 THIAZOLES
  • 5.5.2.1 Synthesis of Thiazoles
  • 5.5.2.2 Synthesis of Thiazolines
  • 5.5.2.3 Synthesis of Benzothiazoles
  • 5.5.2.4 Reactions of Thiazoles and Fused Derivatives
  • 5.5.2.5 New Thiazole-Containing Natural Products.
  • 5.5.2.6 Biologically Active Thiazoles and Isothiazoles
  • 5.5.3 ISOTHIAZOLES
  • 5.5.4 THIADIAZOLES
  • REFERENCES
  • 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-DITHIOLES AND DITHIOLANES
  • 5.6.5 THREE HETEROATOMS
  • REFERENCES
  • 5.7
  • Five-Membered Ring Systems: With O and 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
  • REFERENCES
  • 6.1
  • Six-Membered Ring Systems: Pyridine and Benzo Derivatives
  • 6.1.1 INTRODUCTION
  • 6.1.2 PYRIDINES
  • 6.1.2.1 Preparation of Pyridines
  • 6.1.2.2 Reactions of Pyridines
  • 6.1.3 QUINOLINES
  • 6.1.3.1 Preparation of Quinolines
  • 6.1.3.2 Reactions of Quinolines
  • 6.1.4 ISOQUINOLINES
  • 6.1.4.1 Preparation of Isoquinolines
  • 6.1.4.2 Reactions of Isoquinolines
  • REFERENCES
  • 6.2
  • Six-Membered Ring Systems: Diazines and Benzo Derivatives
  • 6.2.1 Introduction
  • 6.2.2 Pyridazines and Benzo Derivatives
  • 6.2.2.1 Syntheses
  • 6.2.2.2 Reactions
  • 6.2.2.3 Applications
  • 6.2.3 Pyrimidines and Benzo Derivatives
  • 6.2.3.1 Syntheses
  • 6.2.3.2 Reactions
  • 6.2.3.3 Applications
  • 6.2.4 Pyrazines and Benzo Derivatives
  • 6.2.4.1 Syntheses
  • 6.2.4.2 Reactions
  • 6.2.4.3 Applications
  • References
  • 6.3
  • Triazines, Tetrazines, and Fused Ring Polyaza Systems
  • 6.3.1 INTRODUCTION
  • 6.3.2 TRIAZINES
  • 6.3.2.1 1,2,3-Triazines or v-Triazines and 1,2,4-Triazines or a-Triazines
  • 6.3.2.2 1,3,5-Triazines (s-Triazines)
  • 6.3.2.2.1 Chemistry
  • 6.3.2.2.2 Triazines for Material Chemistry
  • 6.3.2.2.3 Triazines for Biomedical and Related Applications
  • 6.3.2.2.4 Triazines for Fluorescence and Optics-Related Applications
  • 6.3.2.2.5 Miscellaneous
  • 6.3.3 TETRAZINES.
  • 6.3.3.1 Synthetic Chemistry
  • 6.3.3.2 Tetrazines for Click Chemistry and Related Applications
  • 6.3.3.3 Applications for Optics: New Dyes
  • 6.3.3.4 Miscellaneous
  • 6.3.4 FUSED HIGHER POLYAZAAROMATICS
  • 6.3.4.1 [6+5] Fused Systems: Purines and Related Heterocycles
  • 6.3.4.1.1 Purines and Related Heterocycles
  • 6.3.4.2 [6+6] Fused Systems: Pteridines and Related Heterocycles
  • 6.3.4.3 New Polyazafused Rings and Heptazines
  • REFERENCES
  • 6.4
  • Six-Membered Ring Systems: With O and/or S Atoms
  • 6.4.1 INTRODUCTION
  • 6.4.2 HETEROCYCLES CONTAINING ONE OXYGEN ATOM
  • 6.4.2.1 Pyrans
  • 6.4.2.2 [1]Benzopyrans and Dihydro[1]benzopyrans
  • 6.4.2.2.1 Chromenes and Chromans
  • 6.4.2.3 [2]Benzopyrans and Dihydro[2]benzopyrans
  • 6.4.2.3.1 Isochromenes and Isochromans
  • 6.4.2.4 Pyranones
  • 6.4.2.5 Coumarins
  • 6.4.2.6 Chromones and Chromanones
  • 6.4.2.7 Xanthenes and Xanthones
  • 6.4.3 HETEROCYCLES CONTAINING ONE OR TWO SULFUR ATOMS
  • 6.4.3.1 Thiopyrans and Analogs
  • 6.4.3.2 Dithiin Analogs
  • 6.4.4 HETEROCYCLES CONTAINING TWO OR MORE OXYGEN ATOMS
  • 6.4.4.1 Dioxanes
  • 6.4.5 HETEROCYCLES CONTAINING BOTH OXYGEN AND SULFUR IN THE SAME RING
  • 6.4.5.1 Oxathianes
  • REFERENCES
  • 7
  • Seven-Membered Rings
  • 7.1 INTRODUCTION
  • 7.2 SEVEN-MEMBERED SYSTEMS CONTAINING ONE HETEROATOM
  • 7.2.1 Azepanes and Derivatives
  • 7.2.2 Benzazepines and Derivatives
  • 7.2.3 Fused Azepanes and Derivatives
  • 7.2.4 Oxepanes and Fused Derivatives
  • 7.2.5 Thiepines and Fused Derivatives
  • 7.3 SEVEN-MEMBERED SYSTEMS CONTAINING TWO HETEROATOMS
  • 7.3.1 Diazepines and Fused Diazepines
  • 7.3.1.1 Benzodiazepines and Derivatives
  • 7.3.2 Oxazepanes and Fused Derivatives
  • 7.3.3 Thiazepines and Derivatives
  • 7.3.4 Dioxepines, Dithiepines, Oxathiepines, and Derivatives
  • 7.4 SEVEN-MEMBERED SYSTEMS CONTAINING THREE OR MORE HETEROATOMS.