Direct C(sp3)–H allylation of 2-alkylpyridines with Morita–Baylis–Hillman carbonates via a tandem nucleophilic substitution/aza-Cope rearrangement
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Direct C(sp3)–H allylation of 2-alkylpyridines with Morita–Baylis–Hillman carbonates via a tandem nucleophilic substitution/aza-Cope rearrangement ; volume:17 ; pages:2505-2510
Beilstein journal of organic chemistry ; 17, 2505-2510
- Klassifikation
-
Chemie
- DOI
-
10.3762/bjoc.17.167
- URN
-
urn:nbn:de:101:1-2021123009474896279663
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:32 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)
Palladium-Catalyzed Nucleophilic Allylation of Aldehydes or Aldimines
Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines
Bispalladacycle Catalyzed Nucleophilic Enantioselective Allylation of Aldehydes by Allylstannanes
Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Bromine-Radical-Mediated Site-Selective Allylation of C(sp3)–H Bonds
Regio- and Stereocontrolled Nucleophilic Trifluoromethylthiolation of Morita–Baylis–Hillman Carbonates
Bifunctional organocatalysis in the asymmetric Aza-Baylis-Hillman reaction
Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides
A redox-active diborane platform performs C(sp3)–H activation and nucleophilic substitution reactions
Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita–Baylis–Hillman alcohols
Palladium-Catalyzed Nucleophilic Allylation of Aldehydes or Aldimines
Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines
Bispalladacycle Catalyzed Nucleophilic Enantioselective Allylation of Aldehydes by Allylstannanes
Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Bromine-Radical-Mediated Site-Selective Allylation of C(sp3)–H Bonds
Regio- and Stereocontrolled Nucleophilic Trifluoromethylthiolation of Morita–Baylis–Hillman Carbonates
Bifunctional organocatalysis in the asymmetric Aza-Baylis-Hillman reaction
Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides
A redox-active diborane platform performs C(sp3)–H activation and nucleophilic substitution reactions
Et3B-mediated and palladium-catalyzed direct allylation of β-dicarbonyl compounds with Morita–Baylis–Hillman alcohols
Palladium-Catalyzed Nucleophilic Allylation of Aldehydes or Aldimines
Aza-Morita–Baylis–Hillman Synthesis of Benzoxazepines
Bispalladacycle Catalyzed Nucleophilic Enantioselective Allylation of Aldehydes by Allylstannanes
Palladium-Catalyzed Enantioselective Aza-Morita–Baylis–Hillman Reaction
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Gold (I)‐Catalyzed Nucleophilic Allylation of Azinium Ions with Allylboronates
Bromine-Radical-Mediated Site-Selective Allylation of C(sp3)–H Bonds
Regio- and Stereocontrolled Nucleophilic Trifluoromethylthiolation of Morita–Baylis–Hillman Carbonates
Bifunctional organocatalysis in the asymmetric Aza-Baylis-Hillman reaction
Synergistic catalysis for cascade allylation and 2-aza-cope rearrangement of azomethine ylides
A redox-active diborane platform performs C(sp3)–H activation and nucleophilic substitution reactions