Hochschulschrift
Development of new asymmetric organocatalytic domino reactions for the synthesis of (benzo-fused) five- and benzo-fused six-membered cyclic compounds
- Alternative title
-
Entwicklung neuer organokatalysierter Dominoreaktionen zur Synthese von benzopenta-, penta- und hexacyclischen Verbindungen
- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Notes
-
RWTH Aachen, Dissertation, 2015
- Classification
-
Chemie
- Event
-
Veröffentlichung
- (where)
-
Aachen
- (who)
-
Universitätsbibliothek der RWTH Aachen
- (when)
-
2016
- Creator
- Contributor
- URN
-
urn:nbn:de:hbz:82-rwth-2016-023506
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:44 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Object type
- Hochschulschrift
Associated
- Hristeva, Stanimira
- Enders, Dieter
- Albrecht, Markus
- Universitätsbibliothek der RWTH Aachen
Time of origin
- 2016
Other Objects (12)
Asymmetric synthesis with chemical and biological methods
Enantioselektive C-C-Verknüpfungen über metallierte chirale Hydrazone
Das Verhalten von Serumlipiden und Serumfettsäuren bei verschiedenen Graden der Koronarsklerose
Control of four stereocentres in a triple cascade organocatalytic reaction
Asymmetric synthesis in solution and under mechanochemical conditions
N-heterocyclic carbene - and copper-catalyzed asymmetric domino reactions
Development of novel asymmetric organocatalytic reactions based on ketimines and para-quinone
N-Heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions via homoenolates and azolium dienolates
N-heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions of enals and α-chloroaldehydes
Benzo-bi- und [Benzo-]tri-pyrone
Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives
Asymmetric Synthesis of Functionalized Dihydro- and Tetrahydropyrans via an Organocatalytic Domino Michael–Hemiacetalization Reaction
Asymmetric synthesis with chemical and biological methods
Enantioselektive C-C-Verknüpfungen über metallierte chirale Hydrazone
Das Verhalten von Serumlipiden und Serumfettsäuren bei verschiedenen Graden der Koronarsklerose
Control of four stereocentres in a triple cascade organocatalytic reaction
Asymmetric synthesis in solution and under mechanochemical conditions
N-heterocyclic carbene - and copper-catalyzed asymmetric domino reactions
Development of novel asymmetric organocatalytic reactions based on ketimines and para-quinone
N-Heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions via homoenolates and azolium dienolates
N-heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions of enals and α-chloroaldehydes
Benzo-bi- und [Benzo-]tri-pyrone
Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives
Asymmetric Synthesis of Functionalized Dihydro- and Tetrahydropyrans via an Organocatalytic Domino Michael–Hemiacetalization Reaction
Asymmetric synthesis with chemical and biological methods
Enantioselektive C-C-Verknüpfungen über metallierte chirale Hydrazone
Das Verhalten von Serumlipiden und Serumfettsäuren bei verschiedenen Graden der Koronarsklerose
Control of four stereocentres in a triple cascade organocatalytic reaction
Asymmetric synthesis in solution and under mechanochemical conditions
N-heterocyclic carbene - and copper-catalyzed asymmetric domino reactions
Development of novel asymmetric organocatalytic reactions based on ketimines and para-quinone
N-Heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions via homoenolates and azolium dienolates
N-heterocyclic carbene catalyzed asymmetric cycloaddition/annulation reactions of enals and α-chloroaldehydes
Benzo-bi- und [Benzo-]tri-pyrone
Asymmetric synthesis of pyrazoles and pyrazolones employing the reactivity of pyrazolin-5-one derivatives