Brønsted acid catalyzed enantioselective addition of hydrazones to 3-indolylmethanols
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
In: 10.1039/D2QO00840H
- Ereignis
-
Veröffentlichung
- (wo)
-
Aachen
- (wer)
-
Universitätsbibliothek der RWTH Aachen
- (wann)
-
2022
- Urheber
- DOI
-
10.18154/RWTH-2022-07759
- URN
-
urn:nbn:de:101:1-2022082601261145482999
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:48 MEZ
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.
Beteiligte
- Mader, Steffen
- Maji, Modhu Sudan
- Atodiresei, Iuliana Luisa
- Rüping, Magnus
- Universitätsbibliothek der RWTH Aachen
Entstanden
- 2022
Ähnliche Objekte (12)
Brønsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement
Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones
Brønsted acid catalyzed asymmetric acetalizations
Desymmetrization of Oxabenzonorbornadienes through Brønsted Acid‐Catalyzed Enantioselective (3+2) Cycloaddition with Hydrazones
Iridium-Catalyzed Enantioselective 1,6-Addition
Enantioselective Reduction of Pyridines via Brønsted Acid Catalysis
The First Enantioselective Rhodium-Catalyzed 1,4-Addition
Brønsted Acid Catalyzed Asymmetric Silylation of Biaryl Diols
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Enol Catalysis – Enantioselective Transformations via Bifunctional Brønsted Acid Promoted Enolization
Brønsted Base‐Catalyzed Enantioselective α‐Functionalization of Carbonyl Compounds Involving π‐Extended Enolates
Brønsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement
Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones
Brønsted acid catalyzed asymmetric acetalizations
Desymmetrization of Oxabenzonorbornadienes through Brønsted Acid‐Catalyzed Enantioselective (3+2) Cycloaddition with Hydrazones
Iridium-Catalyzed Enantioselective 1,6-Addition
Enantioselective Reduction of Pyridines via Brønsted Acid Catalysis
The First Enantioselective Rhodium-Catalyzed 1,4-Addition
Brønsted Acid Catalyzed Asymmetric Silylation of Biaryl Diols
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Enol Catalysis – Enantioselective Transformations via Bifunctional Brønsted Acid Promoted Enolization
Brønsted Base‐Catalyzed Enantioselective α‐Functionalization of Carbonyl Compounds Involving π‐Extended Enolates
Brønsted Acid Catalyzed Enantioselective Indole Aza-Claisen Rearrangement
Asymmetric Brønsted Acid-catalyzed Intramolecular aza-Michael Reaction – Enantioselective Synthesis of Dihydroquinolinones
Brønsted acid catalyzed asymmetric acetalizations
Desymmetrization of Oxabenzonorbornadienes through Brønsted Acid‐Catalyzed Enantioselective (3+2) Cycloaddition with Hydrazones
Iridium-Catalyzed Enantioselective 1,6-Addition
Enantioselective Reduction of Pyridines via Brønsted Acid Catalysis
The First Enantioselective Rhodium-Catalyzed 1,4-Addition
Brønsted Acid Catalyzed Asymmetric Silylation of Biaryl Diols
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Brønsted Acid Catalyzed Asymmetric Synthesis of cis ‐Tetrahydrocannabinoids **
Enol Catalysis – Enantioselective Transformations via Bifunctional Brønsted Acid Promoted Enolization