- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- ISSN
-
2041-1723
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
online resource.
- Erschienen in
-
Cobalt-catalyzed branched selective hydroallylation of terminal alkynes ; volume:13 ; number:1 ; day:3 ; month:8 ; year:2022 ; pages:1-9 ; date:12.2022
Nature Communications ; 13, Heft 1 (3.8.2022), 1-9, 12.2022
- Urheber
-
Chen, Jieping
Ying, Jiale
Lu, Zhan
- Beteiligte Personen und Organisationen
-
SpringerLink (Online service)
- DOI
-
10.1038/s41467-022-32291-3
- URN
-
urn:nbn:de:101:1-2022101322565263998207
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:33 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
- Chen, Jieping
- Ying, Jiale
- Lu, Zhan
- SpringerLink (Online service)
Ähnliche Objekte (12)
Cobalt-Catalyzed Hydroboration of Alkynes
Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides
Cobalt catalyzed practical hydroboration of terminal alkynes with time-dependent stereoselectivity
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Cobalt-Catalyzed Reductive Coupling of Activated Alkenes with Alkynes
Cobalt-Catalyzed [3+2] Cycloaddition of Alkynes with Cyclic Enones
Rhodium‐Catalyzed Anti‐Markovnikov Transfer Hydroiodination of Terminal Alkynes **
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Efficient [(NHC)Au(NTf2)]-catalyzed hydrohydrazidation of terminal and internal alkynes
Reaction Pathways and Redox States in α‐Selective Cobalt‐Catalyzed Hydroborations of Alkynes
Cobalt-Catalyzed Hydroboration of Alkynes
Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides
Cobalt catalyzed practical hydroboration of terminal alkynes with time-dependent stereoselectivity
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Cobalt-Catalyzed Reductive Coupling of Activated Alkenes with Alkynes
Cobalt-Catalyzed [3+2] Cycloaddition of Alkynes with Cyclic Enones
Rhodium‐Catalyzed Anti‐Markovnikov Transfer Hydroiodination of Terminal Alkynes **
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Efficient [(NHC)Au(NTf2)]-catalyzed hydrohydrazidation of terminal and internal alkynes
Reaction Pathways and Redox States in α‐Selective Cobalt‐Catalyzed Hydroborations of Alkynes
Cobalt-Catalyzed Hydroboration of Alkynes
Cobalt-catalyzed hydrothiolation of alkynes for the diverse synthesis of branched alkenyl sulfides
Cobalt catalyzed practical hydroboration of terminal alkynes with time-dependent stereoselectivity
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Photoinduced Palladium‐Catalyzed Dicarbofunctionalization of Terminal Alkynes
Cobalt-Catalyzed Reductive Coupling of Activated Alkenes with Alkynes
Cobalt-Catalyzed [3+2] Cycloaddition of Alkynes with Cyclic Enones
Rhodium‐Catalyzed Anti‐Markovnikov Transfer Hydroiodination of Terminal Alkynes **
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Rhodium‐NHC‐Catalyzed gem ‐Specific O ‐Selective Hydropyridonation of Terminal Alkynes
Efficient [(NHC)Au(NTf2)]-catalyzed hydrohydrazidation of terminal and internal alkynes