Annulation of 1H-pyrrole-2,3-diones by thioacetamide: an approach to 5-azaisatins
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Annulation of 1H-pyrrole-2,3-diones by thioacetamide: an approach to 5-azaisatins ; volume:15 ; pages:364-370
Beilstein journal of organic chemistry ; 15, 364-370
- Klassifikation
-
Chemie
- DOI
-
10.3762/bjoc.15.32
- URN
-
urn:nbn:de:101:1-2020010209552786554365
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
14.08.2025, 10:54 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)
![A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles](/assets/placeholder/searchResultMediaUnknown.png)
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
Synthesis of novel 1,5-diaryl-1H-pyrrole-2,3-diones
Synthesis of New 1-(4-Anilinophenyl)-1H-pyrrole-2,5-diones
Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of [e]-fused 1H-pyrrole-2,3-diones with thiourea
Organocatalytic asymmetric Henry reaction of 1H-pyrrole-2,3-diones with bifunctional amine-thiourea catalysts bearing multiple hydrogen-bond donors
Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives
Auto-Oxidation–Povarov Annulation Approach to Quinolines
Die Annulation
Die Annulation
[C]-anellierte 1H- [H-] und 2H-Pyrrole [H-Pyrrole]: 4,5-, 5,5-, 5,6- und 5,7-gliedrige [gliedrige] Hetarene
Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation
A Straightforward Synthesis of 2-(1-Vinyl-1H-pyrrol-2-yl)-1H-benzimidazoles from 1-Vinyl-1H-pyrrole-2-carbaldehydes and o-Phenylenediamine
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
Synthesis of novel 1,5-diaryl-1H-pyrrole-2,3-diones
Synthesis of New 1-(4-Anilinophenyl)-1H-pyrrole-2,5-diones
Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of [e]-fused 1H-pyrrole-2,3-diones with thiourea
Organocatalytic asymmetric Henry reaction of 1H-pyrrole-2,3-diones with bifunctional amine-thiourea catalysts bearing multiple hydrogen-bond donors
Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives
Auto-Oxidation–Povarov Annulation Approach to Quinolines
Die Annulation
Die Annulation
[C]-anellierte 1H- [H-] und 2H-Pyrrole [H-Pyrrole]: 4,5-, 5,5-, 5,6- und 5,7-gliedrige [gliedrige] Hetarene
Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation
A Straightforward Synthesis of 2-(1-Vinyl-1H-pyrrol-2-yl)-1H-benzimidazoles from 1-Vinyl-1H-pyrrole-2-carbaldehydes and o-Phenylenediamine
A facile approach to spiro[dihydrofuran-2,3'-oxindoles] via formal [4 + 1] annulation reaction of fused 1H-pyrrole-2,3-diones with diazooxindoles
Synthesis of novel 1,5-diaryl-1H-pyrrole-2,3-diones
Synthesis of New 1-(4-Anilinophenyl)-1H-pyrrole-2,5-diones
Facile regiodivergent synthesis of spiro pyrrole-substituted pseudothiohydantoins and thiohydantoins via reaction of [e]-fused 1H-pyrrole-2,3-diones with thiourea
Organocatalytic asymmetric Henry reaction of 1H-pyrrole-2,3-diones with bifunctional amine-thiourea catalysts bearing multiple hydrogen-bond donors
Recent advances in the tandem annulation of 1,3-enynes to functionalized pyridine and pyrrole derivatives
Auto-Oxidation–Povarov Annulation Approach to Quinolines
Die Annulation
Die Annulation
[C]-anellierte 1H- [H-] und 2H-Pyrrole [H-Pyrrole]: 4,5-, 5,5-, 5,6- und 5,7-gliedrige [gliedrige] Hetarene
Synthesis of cis-hydrindan-2,4-diones bearing an all-carbon quaternary center by a Danheiser annulation