Chemoselective Nucleophilic α-Amination of Amides / / by Miran Lemmerer

• Autore: Lemmerer Miran
• Pubblicazione: Wiesbaden : , : Springer Fachmedien Wiesbaden : , : Imprint : Springer Spektrum, , 2020
• Edizione: 1st ed. 2020.
• Descrizione fisica: 1 online resource (68 pages)
• Disciplina: 547.042
• Soggetto topico: Asymmetric synthesis; Chemical structure; Organic compounds - Synthesis; Chemistry; Asymmetric Synthesis; Structure And Bonding; Synthetic Chemistry Methodology; Reactive Precursor
• Nota di contenuto: Traditional Umpolung Reactions in Organic Chemistry -- Insight into Electrophilic Amide Activation -- Results and Discussion of a New α-Amination Method via Umpolung of Amides -- α-Arylation of Carbonlys via a Smiles Rearrangement.
• Sommario/riassunto: α-Amino carbonyl compounds are omnipresent in all living organisms, making their selective synthesis highly sought after. However, the synthesis of α-amino amides, a subclass of α-amino carbonyls, in the presence of other carbonyls is usually challenging, due to the required harsh conditions. Miran Lemmerer expands a novel chemoselective approach for the synthesis of these intriguing molecules together with Univ.-Prof. Dr. Nuno Maulide’s team. Contents Traditional Umpolung Reactions in Organic Chemistry Insight into Electrophilic Amide Activation Results and Discussion of a New α-Amination Method via Umpolung of Amides α-Arylation of Carbonlys via a Smiles Rearrangement Target Groups Scientists and students in the field of organic chemistry, especially in methodology development The Author Miran Lemmerer is currently pursuing his PhD studies under supervision of Prof. Dr. Nuno Maulide at the Department of Organic Chemistry, University of Vienna, Austria. .
• Titolo autorizzato: Chemoselective Nucleophilic α-Amination of Amides
• ISBN: 3-658-30020-5
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910410046703321
• Lo trovi qui: Univ. Federico II
• Serie: BestMasters, . 2625-3615