Synthesis of Aziridines and Oxaziridines from Imines
- 1st Edition - January 13, 2024
- Author: Navjeet Kaur
- Language: English
- Paperback ISBN:9 7 8 - 0 - 4 4 3 - 2 2 0 5 9 - 3
- eBook ISBN:9 7 8 - 0 - 4 4 3 - 2 2 0 6 0 - 9
Synthesis of Aziridines and Oxaziridines from Imines describes both new and old methods for the synthesis of aziridines from imines and covers an important and rapidly growing b… Read more
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Request a sales quoteSynthesis of Aziridines and Oxaziridines from Imines describes both new and old methods for the synthesis of aziridines from imines and covers an important and rapidly growing branch of heterocyclic chemistry. Readers will have access to different methods and information allowing them to evaluate which method is most suitable for particular cases. Several important advances in this area have been witnessed in recent years and discovering efficient novel methods for the synthesis of aziridines has been very active field of research. Its powerful synthetic utility has been described by an overpowering amount of documentation on the approaches for the formation of aziridine.
The smallest possible saturated azaheterocycle, aziridine, is well-known to organic chemists for its tremendous potential in pharmaceutical chemistry and organic synthesis. The general biological importance of aziridines is proven by the fact that they found several uses as subunits in pharmacologically active compounds such as antitumor agents, enzyme inhibitors, and antibiotics. Although aziridines are highly reactive, this framework occurs in many synthetic compounds and the natural products of biological interest also contain aziridine skeleton in their structures.
- Focuses on the biological importance of different heterocycles
- Describes traditional and innovative methods for the synthesis of aziridines from imines
- Includes comparison amongst different methods, reagents, reaction conditions in tabulated forms, advantages, disadvantages, and critical analysis of different methodologies with respect to their comparison with green technique
- Cover image
- Title page
- Table of Contents
- Copyright
- About the author
- Preface
- Abbreviations
- 1. Aziridine synthesis from imines-I
- Abstract
- 1.1 Introduction
- 1.2 Synthesis of aziridines from imines
- 1.3 Synthesis of aziridines from two imines
- References
- 2. Aziridine synthesis from imines-II
- Abstract
- 2.1 Introduction
- 2.2 Synthesis of aziridines from imines and carbonyl compounds
- 2.3 Synthesis of aziridines from imines and halomethane compounds
- 2.4 Synthesis of aziridines from imines and sulfur-containing compounds
- References
- 3. Aziridine synthesis by condensation of phenylimines with ethyl diazoacetate
- Abstract
- 3.1 Introduction
- 3.2 Synthesis of aziridines from phenylimines and ethyl diazoacetate
- 3.3 Synthesis of aziridines from phenylimines and ethyl diazoacetate using boron trifluoride
- 3.4 Synthesis of aziridines from phenylimines and ethyl diazoacetate using imidazolium ionic liquids
- 3.5 Synthesis of aziridines from phenylimines and ethyl diazoacetate using pyridinium salts
- 3.6 Synthesis of aziridines from phenylimines and ethyl diazoacetate using VAPOL or VANOL
- References
- 4. Aziridine synthesis by metal-catalyzed condensation of phenylimines with ethyl diazoacetate
- Abstract
- 4.1 Introduction
- 4.2 Metal-catalyzed synthesis of aziridines from phenylimines and ethyl diazoacetate
- 4.3 Copper-catalyzed synthesis of aziridines from phenylimines and ethyl diazoacetate
- 4.4 Iron-catalyzed synthesis of aziridines from phenylimines and ethyl diazoacetate
- References
- 5. Aziridine synthesis by the addition of biphenyl imines to ethyl diazoacetate
- Abstract
- 5.1 Introduction
- 5.2 Synthesis of aziridines from biphenyl imines and ethyl diazoacetate
- 5.3 Synthesis of aziridines from biphenyl imines and ethyl diazoacetate using vaulted chiral ligands binaphthol (VANOL) and biphenanthrol (VAPOL)
- References
- 6. Aziridine synthesis by metal-catalyzed addition of biphenyl imines to ethyl diazoacetate
- Abstract
- 6.1 Introduction
- 6.2 Metal-catalyzed synthesis of aziridines from biphenyl imines and ethyl diazoacetate
- 6.3 Ruthenium-catalyzed synthesis of aziridines from biphenyl imines and ethyl diazoacetate
- References
- 7. Aziridine synthesis by condensation of imines with diazo compounds
- Abstract
- 7.1 Introduction
- 7.2 Synthesis of aziridines from diazoimines
- 7.3 Synthesis of aziridines from imines and diazo compounds
- 7.4 Synthesis of aziridines from imines and diazoacetamides
- 7.5 Synthesis of aziridines from imines and t-butyl diazoacetates
- References
- 8. Aziridine synthesis by condensation of imines with diazomethane
- Abstract
- 8.1 Introduction
- 8.2 Synthesis of aziridines from imines and diazomethane
- 8.3 Synthesis of aziridines from imines and trimethylsilyldiazomethane
- 8.4 Synthesis of aziridines from imines and phenyldiazomethane
- References
- 9. Aziridine synthesis by ring-closure of haloimines
- Abstract
- 9.1 Introduction
- 9.2 Synthesis of aziridines from haloimines
- References
- 10. Aziridine synthesis by ring-closure of imines and halo compounds
- Abstract
- 10.1 Introduction
- 10.2 Synthesis of aziridines from imines and halo compounds
- References
- 11. Aziridine synthesis by alkene-imine and alkyne-imine reactions
- Abstract
- 11.1 Introduction
- 11.2 Synthesis of aziridines from alkenes and imines
- 11.3 Synthesis of aziridines from alkynes and imines
- References
- 12. Oxaziridine synthesis from imines
- Abstract
- 12.1 Introduction
- 12.2 Synthesis of oxaziridines from imines
- 12.3 Synthesis of oxaziridines from imines using hydrogen peroxide
- 12.4 Synthesis of oxaziridines from imines using Oxone
- 12.5 Synthesis of oxaziridines from imines using peroxy acids
- References
- 13. Oxaziridine synthesis from imines using meta-chloroperoxybenzoic acid
- Abstract
- 13.1 Introduction
- 13.2 Synthesis of oxaziridines from imines using m-chloroperoxybenzoic acid
- References
- Index
- No. of pages: 352
- Language: English
- Edition: 1
- Published: January 13, 2024
- Imprint: Elsevier
- Paperback ISBN: 9780443220593
- eBook ISBN: 9780443220609
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