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| Reihe | Springer Theses | 
|---|---|
| ISBN | 9789811097348 | 
| Sprache | Englisch | 
| Erscheinungsdatum | 07.07.2018 | 
| Genre | Chemie/Organische Chemie | 
| Verlag | Springer Singapore | 
| Lieferzeit | Lieferbar in 16 Werktagen | 
| Herstellerangaben | Anzeigen  Springer Nature Customer Service Center GmbH ProductSafety@springernature.com | 
This thesis focuses on NHC-catalyzed annulation of nitroalkenes, enals and α,β-unsaturated carboxylic acids. (1) NHCs were found to be efficient catalysts for the [4+2] annulation of β-substituted nitroalkenes. The scope of Rauhut–Currier reaction was successfully extended to the most challenging β-substituted alkenes by this method; (2) Enals were successfully used for [4+2] annulations with azodicarboxylates catalyzed by NHC via γ-addition. Highly enantiopure tetrahydropyridazinones and γ-amino acid derivatives could be easily prepared by subsequent transformations of the resulting dihydropyridazinones. (4) The readily available α,β-unsaturated carboxylic acids were first successfully employed to generate the α,β-unsaturated acyl azolium intermediates by using NHC for the enantioselective [3+2] and [3+3] annulations.
| Reihe | Springer Theses | 
|---|---|
| ISBN | 9789811097348 | 
| Sprache | Englisch | 
| Erscheinungsdatum | 07.07.2018 | 
| Genre | Chemie/Organische Chemie | 
| Verlag | Springer Singapore | 
| Lieferzeit | Lieferbar in 16 Werktagen | 
| Herstellerangaben | Anzeigen  Springer Nature Customer Service Center GmbH ProductSafety@springernature.com | 
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