Zhang | The Chemistry of Zirconacycles and 2,6-Diazasemibullvalenes | E-Book | sack.de
E-Book

E-Book, Englisch, 173 Seiten, eBook

Reihe: Springer Theses

Zhang The Chemistry of Zirconacycles and 2,6-Diazasemibullvalenes

Synthesis, Structures, Reactions, and Applications in the Synthesis of Novel N-Heterocycles
2015
ISBN: 978-3-662-45021-5
Verlag: Springer
Format: PDF
Kopierschutz: 1 - PDF Watermark

Synthesis, Structures, Reactions, and Applications in the Synthesis of Novel N-Heterocycles

E-Book, Englisch, 173 Seiten, eBook

Reihe: Springer Theses

ISBN: 978-3-662-45021-5
Verlag: Springer
Format: PDF
Kopierschutz: 1 - PDF Watermark



In this thesis, the author introduces two strategies used to construct various types of N-heterocycles, based on the chemistry of zirconacycles and 2,6-diazasemibullvalenes. In the first part, the author presents the development of multi-component cyclization of a zirconacyclobutene-silacyclobutene fused compound, nitriles and unsaturated compounds. These reactions provide synthetically useful methodology for various N-heterocycles such as 3-acyl pyrrole, pyrrolo[3,2-d]pyridazine and dihydropyrroloazepine, which are all difficult to synthesize by other means. The isolation and characterization of the key three-fused-ring Zr/Si-containing intermediates are also described in detail. These results show that the zirconacyclobutene-silacyclobutene fused compound behaves as a “chemical transformer” upon treatment with various substrates via the “coordination-induced skeleton rearrangement” mechanism. In the second part, the author demonstrates the synthesis and isolation of a series of 2,6-diazasemibullvalenes (NSBVs) from the reaction of 1,4-dilithio-1,3-dienes and nitriles, highlighting the significant progress made for the first time in this work: (1) determination of X-ray crystal structure of a substituted 2,6-diazasemibullvalene; (2) measurement of the activation barrier of its rapid intramolecular aza-Cope rearrangement in solution; (3) exploration of several reaction types of NSBV with diverse ring-expansion products and “bowl-shape” or “cage-shape” N-containing polycyclic skeletons; (4) demonstration of the localized structure as the predominant form and the homoaromatic delocalized structure as a minor component in the equilibrium using theoretical analysis. Based on well-founded results, this work sheds new light on this controversial topic.
Zhang The Chemistry of Zirconacycles and 2,6-Diazasemibullvalenes jetzt bestellen!

Zielgruppe


Research


Autoren/Hrsg.


Weitere Infos & Material


Introduction to Zirconacycle Chemistry.- Zirconocene-Mediated Cyclization of Bis(alkynyl)silanes and Nitriles: Synthesis of N -Heterocycles and Isolation, Characterization and Synthetic Application of Zr/Si-containing Reactive Intermediates.- Bulky-Nitrile Coordination Induced Skeleton Rearrangement of Zr/Si-containing Metallacycles and Selective Synthesis of 5-Azaindoles.- Introduction to Semibullvalenes and Azasemibullvalenes.- 2,6-Diazasemibullvalenes: Synthesis, Structure, Theoretical Analysis and Computational Chemistry.- 2,6-Diazasemibullvalenes: Reaction Chemistry and Synthetic Application.



Ihre Fragen, Wünsche oder Anmerkungen
Vorname*
Nachname*
Ihre E-Mail-Adresse*
Kundennr.
Ihre Nachricht*
Lediglich mit * gekennzeichnete Felder sind Pflichtfelder.
Wenn Sie die im Kontaktformular eingegebenen Daten durch Klick auf den nachfolgenden Button übersenden, erklären Sie sich damit einverstanden, dass wir Ihr Angaben für die Beantwortung Ihrer Anfrage verwenden. Selbstverständlich werden Ihre Daten vertraulich behandelt und nicht an Dritte weitergegeben. Sie können der Verwendung Ihrer Daten jederzeit widersprechen. Das Datenhandling bei Sack Fachmedien erklären wir Ihnen in unserer Datenschutzerklärung.