Double Strain‐Release (3+3)‐Cycloaddition: Lewis Acid Catalyzed Reaction of Bicyclobutane Carboxylates and Aziridines
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Double Strain‐Release (3+3)‐Cycloaddition: Lewis Acid Catalyzed Reaction of Bicyclobutane Carboxylates and Aziridines ; day:11 ; month:12 ; year:2024 ; extent:7
Chemistry - a European journal ; (11.12.2024) (gesamt 7)
- Urheber
- DOI
-
10.1002/chem.202404099
- URN
-
urn:nbn:de:101:1-2412121318576.899047434939
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:28 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.
Beteiligte
- George, Malini
- Mindner, Jasper
- Wittmer, Silas
- Knyazev, Daniil A.
- Werz, Daniel B.
Ähnliche Objekte (12)
Double strain‐release (3+3)‐cycloaddition: Lewis acid catalyzed reaction of bicyclobutane carboxylates and aziridines
Novel gold-catalyzed rearrangement reactions and a platinum-catalyzed intermolecular (3+3) cycloaddition reaction
Enantioselective Intermolecular Ruthenium-Catalyzed Cycloaddition
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
Lewis base-catalyzed intermolecular triazene alkyne cycloaddition for late-stage functionalization and scaffold diversification
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Chiral Lewis Base Catalyzed Aldol Reaction of Unprotected Carboxylic Acids
Palladium-Catalyzed Vinyl-Substituted Trimethylenemethane Cycloaddition
Au-Catalyzed Diastereoselective [3+2] Cycloaddition
Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition
Gold(I)-catalyzed enantioselective cycloaddition reactions
Enantioselective Copper-Catalyzed Diels–Alder Cycloaddition
Double strain‐release (3+3)‐cycloaddition: Lewis acid catalyzed reaction of bicyclobutane carboxylates and aziridines
Novel gold-catalyzed rearrangement reactions and a platinum-catalyzed intermolecular (3+3) cycloaddition reaction
Enantioselective Intermolecular Ruthenium-Catalyzed Cycloaddition
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
Lewis base-catalyzed intermolecular triazene alkyne cycloaddition for late-stage functionalization and scaffold diversification
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Chiral Lewis Base Catalyzed Aldol Reaction of Unprotected Carboxylic Acids
Palladium-Catalyzed Vinyl-Substituted Trimethylenemethane Cycloaddition
Au-Catalyzed Diastereoselective [3+2] Cycloaddition
Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition
Gold(I)-catalyzed enantioselective cycloaddition reactions
Enantioselective Copper-Catalyzed Diels–Alder Cycloaddition
Double strain‐release (3+3)‐cycloaddition: Lewis acid catalyzed reaction of bicyclobutane carboxylates and aziridines
Novel gold-catalyzed rearrangement reactions and a platinum-catalyzed intermolecular (3+3) cycloaddition reaction
Enantioselective Intermolecular Ruthenium-Catalyzed Cycloaddition
Recent Developments in the Ruthenium‐Catalyzed Azide Alkyne Cycloaddition (RuAAC) Reaction
Lewis base-catalyzed intermolecular triazene alkyne cycloaddition for late-stage functionalization and scaffold diversification
Post‐Functionalization of Organoboranes by Cu‐Catalyzed Azide Alkyne (3+2)‐Cycloaddition Reaction
Chiral Lewis Base Catalyzed Aldol Reaction of Unprotected Carboxylic Acids
Palladium-Catalyzed Vinyl-Substituted Trimethylenemethane Cycloaddition
Au-Catalyzed Diastereoselective [3+2] Cycloaddition
Asymmetric Rhodium-Catalyzed [4+3] Cycloaddition
Gold(I)-catalyzed enantioselective cycloaddition reactions