Ishikawa | Superbases for Organic Synthesis | E-Book | sack.de
E-Book

E-Book, Englisch, 336 Seiten, E-Book

Ishikawa Superbases for Organic Synthesis

Guanidines, Amidines, Phosphazenes and Related Organocatalysts

E-Book, Englisch, 336 Seiten, E-Book

ISBN: 978-0-470-74086-6
Verlag: John Wiley & Sons
Format: PDF
Kopierschutz: Adobe DRM (»Systemvoraussetzungen)



Guanidines, amidines and phosphazenes have been attractingattention in organic synthesis due to their potential functionalityresulting from their extremely strong basicity. They are alsopromising catalysts because of their potential for easy molecularmodification, possible recyclability, and reduced or zero toxicity.Importantly, these molecules can be derived as natural products- valuable as scientists move towards "sustainablechemistry", where reagents and catalysts are derived frombiomaterial sources.
Superbases for Organic Synthesis is an essential guide tothese important molecules for preparative organic synthesis. Topicscovered include the following aspects:
* an introduction to organosuperbases
* physicochemical properties of organic superbases
* amidines and guanidines in organic synthesis
* phosphazene: preparation, reaction and catalytic role
* polymer-supported organosuperbases
* application of organosuperbases to total synthesis
* related organocatalysts: proton sponges and ureaderivatives
* amidines and guanidines in natural products and medicines
Superbases for Organic Synthesis is a comprehensive,authoritative and up-to-date guide to these important reagents fororganic chemists, drug discovery researchers and those interestedin the chemistry of natural products.
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Preface.
Acknowledgements.
List of Contributors.
1. General Aspects of Organosuperbases (TsutomuIshikawa).
2. Physicochemical Properties of Organic Superbases (DavorMargetic).
2.1 Introduction.
2.2 Proton sponges.
2.3 Amidines.
2.4 Guanidines.
2.5 Phosphazenes.
2.6 Guanidinophosphazenes.
2.7 Other Phosphorus Containing Superbases: Verkade'sProazaphosphatranes.
2.8 Theoretical Methods.
2.9 Concluding Remarks.
References.
3. Amidines in Organic Synthesis (Tsutomu Ishikawa and TakuyaKumamoto).
3.1 Introduction.
3.2 Preparation of Amidine.
3.3 Application of Amidines to Organic Synthesis.
3.4 Amidinium Salt: Design and Synthesis.
3.5 Concluding Remarks.
References.
4. Guanidines in Organic Synthesis (TsutomuIshikawa).
4.1. Introduction.
4.2. Preparation of Chiral Guanidines.
4.3 Guanidines as Synthetic Tools.
4.4 Guanidinium Salt.
4.5 Concluding Remarks.
References.
5. Phosphazene: Preparation, Reaction and Catalytic Role(Yoshinori Kondo).
5.1 Introduction.
5.2 Deprotonative Transformations Using StoichiometricPhosphazenes.
5.3 Transformation Using Phosphazene Catalyst.
5.4 Proazaphosphatrane Base (Verkade's Base).
5.5 Concluding Remarks.
References.
6. Polymer-supported Organosuperbases (HiyoshizoKotsuki).
6.1 Introduction.
6.2 Acylation reactions.
6.3 Alkylation Reactions.
6.4 Heterocyclization.
6.5 Miscellaneous.
6.6 Concluding Remarks.
References.
7. Application of Organosuperbases to Total Synthesis (KazuoNagasawa).
7.1 Introduction.
7.2 Carbon-carbon bond-forming reactions.
7.3 Deprotection.
7.4 Elimination.
7.5 Ether synthesis.
7.6 Heteroatom conjugate addition.
7.7 Isomerization.
7.8 Concluding Remarks.
References.
8. Related Organocatalysts (1): Proton Sponge (KazuoNagasawa).
8.1 Introduction.
8.2 Alkylation and Hetero Michael reaction.
8.3 Amide formation.
8.4 Carbon-carbon bond-forming reaction.
8.5 Palladium-catalyzed reaction.
8.6 Concluding Remarks.
References.
9. Related Organocatalysts (2): Urea Derivatives (WakaNakanishi).
9.1 Introduction.
9.2 Bisphenol as Organoacid Catalyst.
9.3 Urea and Thiourea as Achiral Catalysts.
9.4 Urea and Thiourea as Chiral Catalyst.
9.5 Concluding Remarks.
References.
10. Amidines and Guanidines in Natural Products and Medicines(Takuya Kumamoto).
10.1 Introduction.
10.2 Natural Amidine Derivatives.
10.3 Natural Guanidine Derivatives.
10.4 Medicinal Amidine and Guanidine Derivatives.
References.
11. Perspective (Tsutomu Ishikawa and DavorMargetic).


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