Tandem dinucleophilic cyclization of cyclohexane-1,3-diones with pyridinium salts
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Erschienen in
-
Tandem dinucleophilic cyclization of cyclohexane-1,3-diones with pyridinium salts ; volume:9 ; pages:1119-1126
Beilstein journal of organic chemistry ; 9, 1119-1126
- Klassifikation
-
Chemie
- DOI
-
10.3762/bjoc.9.124
- URN
-
urn:nbn:de:101:1-2013062612292
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:46 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Ähnliche Objekte (12)
Facile Synthesis of Spiro (cyclohexane-1,3’-indoline)-2,2’-diones
Cyclohexane-1,2-dione hydrolase : A new tool to degrade alicyclic compounds
Small gold nanoparticles for tandem cyclization/reduction and cyclization/hydroalkoxylation reactions
Tin powder-promoted allylation and cyclization of 2-(benzylideneamino) isoindoline-1,3-diones
Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides
Zur Pyrolyse oligomethylierter Cyclohexane
Dione
Dione
Synthesis of (±)-Chokol A by a Tandem Michael-Addition/Dieckmann Cyclization
Cyclohexane-1,2-Dione Hydrolase from Denitrifying Azoarcus sp. Strain 22Lin, a novel member of the Thiamine Diphosphate Enzyme family
Lecture 13. Conformations of Cyclohexane
Synthese und Eigenschaften makrozyklischer 4-Pyridinium-Redox-Systeme [Pyridinium-Redox-Systeme]
Facile Synthesis of Spiro (cyclohexane-1,3’-indoline)-2,2’-diones
Cyclohexane-1,2-dione hydrolase : A new tool to degrade alicyclic compounds
Small gold nanoparticles for tandem cyclization/reduction and cyclization/hydroalkoxylation reactions
Tin powder-promoted allylation and cyclization of 2-(benzylideneamino) isoindoline-1,3-diones
Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides
Zur Pyrolyse oligomethylierter Cyclohexane
Dione
Dione
Synthesis of (±)-Chokol A by a Tandem Michael-Addition/Dieckmann Cyclization
Cyclohexane-1,2-Dione Hydrolase from Denitrifying Azoarcus sp. Strain 22Lin, a novel member of the Thiamine Diphosphate Enzyme family
Lecture 13. Conformations of Cyclohexane
Synthese und Eigenschaften makrozyklischer 4-Pyridinium-Redox-Systeme [Pyridinium-Redox-Systeme]
Facile Synthesis of Spiro (cyclohexane-1,3’-indoline)-2,2’-diones
Cyclohexane-1,2-dione hydrolase : A new tool to degrade alicyclic compounds
Small gold nanoparticles for tandem cyclization/reduction and cyclization/hydroalkoxylation reactions
Tin powder-promoted allylation and cyclization of 2-(benzylideneamino) isoindoline-1,3-diones
Chemoenzymatic tandem cyclization for the facile synthesis of bicyclic peptides
Zur Pyrolyse oligomethylierter Cyclohexane
Dione
Dione
Synthesis of (±)-Chokol A by a Tandem Michael-Addition/Dieckmann Cyclization
Cyclohexane-1,2-Dione Hydrolase from Denitrifying Azoarcus sp. Strain 22Lin, a novel member of the Thiamine Diphosphate Enzyme family
Lecture 13. Conformations of Cyclohexane